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Tezės ŽMGK

  1. Ginevičienė, Valentina; Genetic biomarkers for musculoskeletal injuries in Lithuanian athletes. ISSN: 2570-5911 ; DOI: 10.29256/v.02.01.2018.escbm01. Biological markers in fundamental and clinical medicine. Brno : ESCBM. 2018, vol. 2, no 1, p. 6-7.
  2. Massidda, Myosotis; Mendez-Villanueva, Alberto; Ginevičienė, Valentina; Proia, Patrizia; Drozdovska, Svitlana; Dosenko, Victos; Piras, Francesco; Calo, Carla Maria; Stula, Alexander; Sawczuk, Marek; Cieszczyk, Pawel ; Scorcu, Marco; Association of MCT1 A1470T polymorphism (RS1049434) with forward football player status. ISSN: 1517-8692. Revista Brasileira de medicina do esporte. Sao Paulo, Sociedade Brasileira Medicina Esporte. 2018, vol. 24, no. 5, suppl., abstract no. 04, p. 4.
  3. Evelina Siavrienė (žodinis pranešimas), iRNR splaisingo variantų, susijusių su intelektine negalia ir įgimtomis anomalijomis, funkcinė analizė. Bioateitis: gamtos ir gyvybės mokslų perspektyvos : 11-oji jaunųjų mokslininkų konferencija, 2018 m. gruodžio 14 d.: pranešimų santraukos. Vilnius : Lietuvos mokslų akademijos leidykla. p. 6.
  4. Laura Pranckėnienė (žodinis pranešimas), A. Jakaitienė, V. Kučinskas, De novo mutacijų pasiskirstymas ir intensyvumas žmogaus genome (pacientų su intelektine negalia grupėje). Bioateitis: gamtos ir gyvybės mokslų perspektyvos : 11-oji jaunųjų mokslininkų konferencija, 2018 m. gruodžio 14 d.: pranešimų santraukos. Vilnius : Lietuvos mokslų akademijos leidykla. p. 8.
  5. Beata Aleksiūnienė (žodinis pranešimas), Laima Ambrozaitytė, Alma Molytė, Vaidutis Kučinskas, Algirdas Utkus, Retų kopijų skaičiaus pokyčių įvertinimas įgimtų širdies ydų grupėje. Bioateitis: gamtos ir gyvybės mokslų perspektyvos : 11-oji jaunųjų mokslininkų konferencija, 2018 m. gruodžio 14 d.: pranešimų santraukos. Vilnius : Lietuvos mokslų akademijos leidykla. p. 12.
  6. Baronas, Karolis; Rančelis, Tautvydas; Pranculis, Aidas; Domarkienė, Ingrida; Ambrozaitytė, Laima; Kučinskas, Vaidutis. Analysis of known genome variants related to alcohol use disorder in Lithuanian group and other European populations. ISSN: 1392-6470. Laboratorinė medicina. Vilnius : Lietuvos laboratorinės medicinos draugija. 2018, T. 20, Spec. suppl, p. s19.
  7. Rančelis, Tautvydas ; Ambrozaitytė, Laima ; Kavaliauskienė, Ingrida ; Domarkienė, Ingrida ; Kučinskas, Vaidutis.Whole exome sequencing methods aid in detecting more frequent pathogenic variants of rare diseases in small populations. ISSN: 1392-6470. Laboratorinė medicina. Vilnius : Lietuvos laboratorinės medicinos draugija. 2018, T. 20, Spec. suppl, p. s37.
  8. Ginevičienė, Valentina, Genetics of sports science and medicine. European journal of sports medicine. Athens : EFSMA. 2018, vol. 5, suppl. 2, p. 23, ISSN: 1792-4979.
  9. Ginevičienė, Valentina, Utkus, Algirdas, Jakaitienė, Audronė , Pushkarev, V, Dyatlov, D, Pushkarev, S, Lekontsev, E., Prevalence of risk alleles of COL1a1 and COL3a1 genetic variants in Lithuanian and Russian athletes. European journal of sports medicine. Athens : EFSMA. 2018, vol. 5, suppl. 2, p. 41-42. ISSN: 1792-4979.
  10. Žukauskaitė G, Ambrozaitytė L, Rančelis T, Kavaliauskienė I, Kučinskas V. Evaluation of Automated Next Generation Sequencing Data Analysis Pipeline. 14th Baltic congress of Laboratory medicine, May 10–12, 2018, Vilnius, Lietuva. Laboratorinė medicina 2018, Vol. 20, Special Supplement, p. 42, ISSN: 1392-6470.
  11. Jekaterina Byčkova, Gabrielė Černytė, Margarita Gromova, Silvija Kiverytė, Vaiva Mickevičienė, Violeta Mikštienė, Eugenijus Lesinskas. Aetiology of deafness and the effect on paediatric cochlear implantation outcomes. Acta medica Lituanica. Vilnius : Lietuvos mokslų akademijos leidykla. 2018, vol. 25, suppl. p. 50-51. ISSN: 1392-0138
  12. Violeta Mikštienė (žodinis pranešimas) “Genome editing in medicine: state of the art and perspectives”. Acta medica Lituanica. Vilnius : Lietuvos mokslų akademijos leidykla. 2018, vol. 25, suppl. 1. p. 36-37. ISSN: 1392-0138.
  13. Strupaitė, Rasa, Ambrozaitytė, Laima, Meškienė, Raimonda, Cimbalistienė, Loreta, Strupaitė-Šakalienė, Ieva, Utkus, Algirdas. Clinical heterogeneity of the Lithuanian retinitis pigmentosa group. Acta medica Lituanica. Vilnius : Lietuvos mokslų akademijos leidykla. 2018, vol. 25, suppl. 1. p. 41-42. ISSN: 1392-0138.
  14. B. Burnytė, L. Ambrozaitytė, K. Grigalionienė, A. Morkūnienė, K. Baronas, V. Kučinskas, A. Utkus. Peripheral neuropathies: Application of targeted next generation sequencing for Lithuanian patients cohort. American Society of Human Genetics 68th Annuall Meeting, San Diego, JAV, October 16-20, 2018, Poster Abstracts, 1132T, p.79.
  15. E. Siavrienė, G. Petraitytė, V. Mikštienė, T. Rančelis, Ž. Maldžienė, A. Morkūnienė , E. Preikšaitienė, V. Kučinskas. Novel c.5535-1G>A variant in a patient with a mild features of CHARGE syndrome. American Society of Human Genetics 68th Annuall Meeting, San Diego, JAV, October 16-20, 2018, Poster Abstracts, 1188W, p. 107
  16. Pranckėnienė, E. Preikšaitienė, V. Kučinskas, A. Reymond, L. Gueneau. De novo insertion in the CHD7 gene causing a CHARGE syndrome. American Society of Human Genetics 68th Annuall Meeting, San Diego, JAV, October 16-20, 2018, Poster Abstracts, 2098T, p. 1103.
  17. A. Urnikytė, M. Mondal, E. Bosch, A. Molytė, V. Kučinskas. Detecting signatures of adaptive positive selection from high–density genotyping data in the Lithuanian population. American Society of Human Genetics 68th Annuall Meeting, San Diego, JAV, October 16-20, 2018, Poster Abstracts, 2738F, p. 658.
  18. Burnytė B, Grigalionienė K, Cimbalistienė L, Vaitkevičius A, Petroška D, Kučinskas V, Utkus A, Phenotypic spectrum of patients harbouring the m.3243A>G mutation. Journal of Inherited Metabolic Disease (2018) 41 (suppl 1). Annual Symposium 4-7 September 2018, Athens, Greece. Abstracts, P 289, S159, https://doi.org/10.1007/s10545-018-0232-x.
  19. Birutė Burnytė, Kristina Grigalionienė, Arūnas Vaitkevičius, Donatas Petroška, Loreta Cimbalistienė, Vaidutis Kučinskas, Algirdas Utkus, Phenotypic heterogeneity in three patients with M.3243A>G mutation. Journal of Neuromuscular Diseases, vol.5, suppl. 1, S206. 15th International Congress on Neuromuscular Diseases, July 6-10, 2018 Vienna, Austria.
  20. Gasiūnienė, Monika, Petkus, Gintautas, Krasovskaja, Natalija, Utkus, Algirdas, Navakauskienė, Rūta, Investigation of TGF-β1 and Angiotensin II as potential cardiomyogenic differentiation inducers of human amniotic fluid mesenchymal stem cells. XVth International Conference of the Lithuanian Biochemical Society, Dubingiai, June 26-29, 2018 : the programme and abstract book. [Vilnius] : Lietuvos biochemikų draugija, 2018, 2018. p. 63-64. ISBN: 9786099603001.
  21. Gasiūnienė, Monika, Petkus, Gintautas, Krasovskaja, Natalija, Utkus, Algirdas, Navakauskienė, Rūta, Assessement of the efficacy of TGF-β1 and Angiotensin II to induce cardiomyogenic differentiation of human amniotic fluid-derived mesenchymal stem cells. FEBS Open Bio. Hoboken : Wiley. 2018, vol. 8, Suppl. S1, abstract no. ShT.37-2. p. 59-60. ISSN: 2211-5463 ; DOI: 10.1002/2211-5463.12449.
  22. Dlugauskas, Edgaras, Lengvenytė, Aistė, Strumila, Robertas, Utkus, Algirdas, Lithuanian CYP2D6 polymorphism analysis (pilot study). Psychiatry - shaping the future : 32nd Nordic congress of psychiatry, June 13-16, 2018, Reykjavik. Reykjavik : NCP, 2018. [p. 1].
  23. Braždžiūnaitė, B. Burnytė, U. Mickys, R. Meškienė, L. Ambrozaitytė, G. Pošiūnas, R. Čerkauskienė, L. Cimbalistienė, A. Utkus; A case of infantile systemic hyalinosis associated with a frameshift mutation in the ANTXR2 gene. European Human Genetics Conference, Milan, Italy, June 16-19, 2018. E-P04.05.
  24. E. M. Blažytė, V. G. Samsonė, A. Matulevičienė, B. Aleksiūnienė, B. Burnytė, E. Dagytė, B. Tumienė, A. Utkus; The spectrum of associated congenital malformations in Down syndrome: a retrospective Lithuanian cohort study. European Human Genetics Conference, Milan, Italy, June 16-19, 2018. E-P05.10.
  25. R. Marcinkutė, D. Braždžiūnaitė, N. Burokienė, V. Dirsė, E. Preikšaitienė, A. Utkus; A de novo 8q22.2q22.3 interstitial microdeletion in a girl with developmental delay and congenital defects. European Human Genetics Conference, Milan, Italy, June 16-19, 2018. E-P11.08.
  26. B. Aleksiūnienė, B. Tumienė, A. Utkus; AHDC1 gene truncating 1p36.11p35.3 microdeletion in a patient with developmental delay, dysmorphic features and congenital heart defects. European Human Genetics Conference, Milan, Italy, June 16-19, 2018. E-P11.09.
  27. V. Ginevičienė, A. Jakaitienė, I. Ašmenavičiūtė, A. Utkus, L. Tubelis; Investigation of MCT1 rs1049434, COL1A1 rs1800012 and COL3A1 rs1800255 variants related to susceptibility to injuries in professional football players. European Human Genetics Conference, Milan, Italy, June 16-19, 2018. E-P18.03.
  28. M. Petkevičienė, K. Šablauskas, R. Marcinkutė, M. Smirnova, J. Songailienė, A. Utkus; The Beginning of the Neonatal Screening for Congenital Adrenal Hyperplasia in Lithuania: Cut-off Limits Based on 27175 Infants. European Human Genetics Conference, Milan, Italy, June 16-19, 2018. P06.07C / C.
  29. E. Siavrienė, E. Preikšaitienė, Ž. Maldžienė, L. Ambrozaitytė, L. Gueneau, A. Reymond, V. Kučinskas. Microduplication of the 13q31.3 miR17~92 cluster results in a syndrome with features opposite to those associated with Feingold syndrome 2. European Human Genetics Conference, Milan, Italy, June 16-19, 2018. P08.02B/B.
  30. E. Dagytė, A. Matulevičienė, L. Ambrozaitytė, R. Laimutė, B. Aleksiūnienė, B. Burnytė, A. Utkus; 15q13.3 microdeletion and microduplication in patients with neurodevelopment disorders. European Human Genetics Conference, Milan, Italy, June 16-19, 2018. P08.03C / C.
  31. B. Burnytė, A. Morkunienė, L. Ambrozaitytė, V. Regelskytė, A. Vaitkevičius, V. Kučinskas, A. Utkus; A report of a family of intermediate Charcot-Marie-Tooth disease with concomitant mutations in the GNB4 and DNM2 genes. European Human Genetics Conference, Milan, Italy, June 16-19, 2018. P10.09A / A.
  32. A. Matulevičienė, K. Šiaurytė, L. Cimbalistienė, B. Burnytė, L. Ambrozaitytė, R. Meškienė, V. Kučinskas, A. Utkus; Three unrelated Lithuanian cases of oculodentodigital dysplasia: phenotypic analysis and comparison to the literature. European Human Genetics Conference, Milan, Italy, June 16-19, 2018. P11.067C / C.
  33. K. Šablauskas, B. Tumienė, A. Utkus; Machine learning approach for detecting epilepsy causing proteins using protein interaction data. European Human Genetics Conference, Milan, Italy, June 16-19, 2018. P16.25A / A.
  34. Siavrienė E, Preikšaitienė E, Kučinskas V. Functional genome analysis aiming to define the genetic cause of intellectual disability. Juvenes Pro Medicina, Lodz, Poland, May 25-26, 2018. ISBN 978-83-947627-1-1.
  35. Ginevičienė, Valentina; Jakaitienė, Audronė ; Ašmenavičiūtė, Ieva; Utkus, Algirdas. Prevalence of risk alleles in collagen-encoding genes variants in Lithuanian football players. Laboratorinė medicina. Vilnius: Lietuvos laboratorinės medicinos draugija. 2018, T. 20, Spec. suppl. p. s22. ISSN: 1392-6470.
  36. Siavrienė, Evelina, Preikšaitienė, Eglė, Kučinskas, Vaidutis. Functional Genome Analysis in Patients with Intellectual Disability. Laboratorinė medicina. Vilnius: Lietuvos laboratorinės medicinos draugija. 2018, T. 20, Spec. suppl. p. s2. ISSN: 1392-6470.
  37. Grigalionienė, Kristina; Burnytė, Birutė; Žukauskaitė, Gabrielė; Vansevičiūtė, Danutė; Utkus, Algirdas. Comprehensive analysis of mitochondrial DNA in patients with suspected mitochondrial disorder. Laboratorinė medicina. Vilnius: Lietuvos laboratorinės medicinos draugija. 2018, T. 20, Spec. suppl. p. s23. ISSN: 1392-6470.
  38. Burnytė, Birutė; Ambrozaitytė, Laima; Morkūnienė, Aušra; Baronas, Karolis; Kavaliauskienė, Ingrida; Kučinskas, Vaidutis; Utkus, Algirdas. Genetic diagnostic utility in a cohort of patients with hereditary neuropathy. Laboratorinė medicina. Vilnius: Lietuvos laboratorinės medicinos draugija. 2018, T. 20, Spec. suppl. p. s20. ISSN: 1392-6470.
  39. Ambrozaitytė, Laima; Grigalionienė, Kristina; Domarkienė, Ingrida; Gudlevičienė, Živilė; Utkus, Algirdas. Preimplantation genetic diagnostics - Lithuanian status. Laboratorinė medicina. Vilnius: Lietuvos laboratorinės medicinos draugija. 2018, T. 20, nr. 1(77). p. 113. ISSN: 1392-6470.
  40. Braždžiūnaitė, Deimantė; Cimbalistienė, Loreta; Ambrozaitytė, Laima; Utkus, Algirdas. Early puberty in Xp11.22p23 microduplication syndrome. Laboratorinė medicina. Vilnius: Lietuvos laboratorinės medicinos draugija. 2018, T. 20, nr. 1(77). p. 115. ISSN: 1392-6470.
  41. Burnytė, Birutė; Morkūnienė, Aušra; Ambrozaitytė, Laima; Baronas, Karolis; Kavaliauskienė, Ingrida; Sereikė, Ieva; Kučinskas, Vaidutis; Utkus, Algirdas. The MFN2 gene is rarely mutated in Lithuanian patients with Charcot–Marie–Tooth disease. Laboratorinė medicina. Vilnius: Lietuvos laboratorinės medicinos draugija. 2018, T. 20, Spec. supl. p. s21. ISSN: 1392-6470.
  42. Aleksiūnienė, Beata; Ambrozaitytė, Laima; Dagytė, Evelina; Laimutė, Rita; Molytė, Alma; Utkus, Algirdas. Identification of rare copy number variants in patients with congenital heart diseases. Laboratorinė medicina. Vilnius: Lietuvos laboratorinės medicinos draugija. 2018, T. 20, Spec. suppl. p. s18. ISSN: 1392-6470.
  43. Ambrozaitytė, Laima; Benušienė, Eglė; Krasovskaja, Natalija; Bakšienė, Marija; Butkevičienė, Eglė; Aleksiūnienė, Beata; Dagytė, Evelina; Grigalionienė, Kristina; Laimutė, Rita; Meškienė, Raimonda; Mikštienė, Violeta; Morkūnienė, Aušra ; Šliužas, Vytautas; Kučinskas, Vaidutis; Utkus, Algirdas. The complexity of genetic diagnostics of prenatal cases. Laboratorinė medicina. Vilnius: Lietuvos laboratorinės medicinos draugija. 2018, T. 20, Spec. suppl. p. s18. ISSN: 1392-6470.
  44. Mikštienė, Violeta; Jakaitienė, Audronė; Byčkova, Jekaterina; Preikšaitienė, Eglė; Burnytė, Birutė; Tumienė, Birutė; Matulevičienė, Aušra; Ambrozaitytė, Laima; Kavaliauskienė, Ingrida; Domarkienė, Ingrida; Rančelis, Tautvydas; Cimbalistienė, Loreta; Lesinskas, Eugenijus; Kučinskas, Vaidutis; Utkus, Algirdas. Genomics of congenital / hereditary hearing loss: Influence to pathogenesis and phenotypic manifestation in the Lithuanian population. Laboratorinė medicina. Vilnius: Lietuvos laboratorinės medicinos draugija. 2018, T. 20, Spec. suppl. p. s31. ISSN: 1392-6470.
  45. K. Baronas, E. Dagytė, E. Dlugauskas, L. Ambrozaitytė, A. Utkus, Clinical applications of pharmacogenetic testing. IX-oji tarptautinė mokslinė konferencija „Retų ligų gydymo inovacijos“, 2018 m. kovo 16 d., Vilnius. Laboratorinė medicina. 2018, t. 20, Nr. 1(77), p. 114.
  46. D. Braždžiūnaitė, R. Laimutė, B. Aleksiūnienė, E. Dagytė, L. Ambrozaitytė, E. Benušienė, L. Cimbalistienė, A. Utkus, Molecular karyotyping: clinical utility and practice. IX-oji tarptautinė mokslinė konferencija „Retų ligų gydymo inovacijos“, 2018 m. kovo 16 d., Vilnius. Laboratorinė medicina. 2018, t. 20, Nr. 1(77), p. 115.
  47. R. Strupaitė, L. Ambrozaitytė, R. Meškienė, L. Cimbalistienė, I. Strupaitė-Šakalienė, A. Utkus, Overview of the Lithuanian retinitis pigmentosa group. IX-oji tarptautinė mokslinė konferencija „Retų ligų gydymo inovacijos“, 2018 m. kovo 16 d., Vilnius. Laboratorinė medicina. 2018, t. 20, Nr. 1(77), p. 117.
  48. K. Šiaurytė, A. Matulevičienė, A. Utkus, Dysmorphology today. IX-oji tarptautinė mokslinė konferencija „Retų ligų gydymo inovacijos“, 2018 m. kovo 16 d., Vilnius. Laboratorinė medicina. 2018, t. 20, Nr. 1(77), p. 118.
  49. R. Šalkevič, D. Jančauskaitė, V. Mikštienė, Ž. Katliorienė, V. Černiauskienė, J. Barysienė, Paveldimas CACNA1C geno pokyčių sukeltas QTc intervalo pailgėjimas aštuonerių metų berniukui. IX-oji tarptautinė mokslinė konferencija „Retų ligų gydymo inovacijos“, 2018 m. kovo 16 d., Vilnius. Laboratorinė medicina. 2018, t. 20, Nr. 1(77), p. 117.
  50. Ginevičienė, Valentina; Jakaitienė, Audronė; Milašius, Kazys; Tubelis, Linas; Lietuvos sportininkų PPAR genetinių variantų reikšmė raumenų darbingumui ir sveikatai. ISBN: 9789955155188. Fiziniai pratimai sveikatinimui ir reabilitacijai : III-oji mokslinė-praktinė konferencija : tezių knyga : 2017 m. gruodžio 8 d. Kaunas, Lietuva. Kaunas : Lietuvos sveikatos mokslų universitetas. Medicinos akademija. Sporto institutas, 2017. p. 12-14.
  51. Navikiene Jurate, Kalinauskiene Olga, Slepikiene Rita, Strupiene Laima, Liubsys Arunas, Burnyte Birute, Samaitiene Ruta, Two cases of age related epilepsy syndromes at the neonatal intensive care unit. 14th Conference of the Baltic Child Neurology Association, Program & abstracts, May 18-20, 2017, Riga, Latvia, p. 40.
  52. Utkus, Algirdas; Dlugauskas, Edgaras; Dagytė, Evelina. Pharmacogenomic testing for the Lithuanian depression patients. WPA inter zonal congress : oral session abstracts book, Vilnius, 3-6 May 2017. WPA, 2017. Abstract no PcA1-3. p. 3.
  53. Laura Pranckėnienė, A. Jakaitienė, L. Ambrozaitytė, V. Kučinskas. De novo mutacijų ir jų intensyvumo analizė lietuvių triadų grupėje. Jaunųjų mokslininkų konferencija Bioateitis: gamtos ir gyvybės mokslų perspektyvos, Pranešimų santraukos, p. 10-11, 2017.
  54. Birutė Tumienė, Aleš Maver, Borut Peterlin, Vaidutis Kučinskas, Algirdas Utkus, Genominių veiksnių įtaka epilepsijos genetinei etiologinei struktūrai ir diagnostikai. Jaunųjų mokslininkų konferencija Bioateitis: gamtos ir gyvybės mokslų perspektyvos, Pranešimų santraukos, p. 12-13, 2017.
  55. B. Burnytė, I. Kavaliauskienė, L. Ambrozaitytė, A. Morkūnienė, A. Matulevičienė, B. Tumienė, V. Kučinskas, A. Utkus. Phenotypical features and genetic findings in Lithuanian patients with CMTX1. American Society of Human Genetics 67th Annual Meeting; October 17–21, 2017, Orlando, Florida, abstract no. 1172T, p. 327.
  56. E. Preikšaitienė, N. Voisin, L. Gueneau, E. Benušienė, A. Reymond, V. Kučinskas. A novel missense variant in the POMK gene causes Walker-Warburg syndrome. American Society of Human Genetics 67th Annual Meeting; October 17–21, 2017, Orlando, Florida, abstract no. 1059F, p. 344.
  57. V. Kučinskas, L. Ambrozaitytė, L. Cimbalistienė, R. Strupaitė, R. Ašoklis, A. Utkus. Novel RS1 gene mutations of X-linked retinoschysis Lithuanian patients. American Society of Human Genetics 67th Annual Meeting; October 17–21, 2017, Orlando, Florida, abstract no. 1110F; p. 370.
  58. A. Urnikytė, A. Molytė, V. Kučinskas, Z. A. Kučinskienė. Recent changes in contemporary effective population size from identical by descent segments. American Society of Human Genetics 67th Annual Meeting; October 17–21, 2017, Orlando, Florida, abstract no. 2315T, p. 976.
  59. L. Pranckėnienė, A. Jakaitienė, L. Ambrozaitytė, I. Domarkienė, I. Kavaliauskienė, R. Meškienė, T. Rančelis, Z. A. Kučinskienė, V. Kučinskas. The composition and intensity of de novo mutations in the Lithuanian exome. American Society of Human Genetics 67th Annual Meeting; October 17–21, 2017, Orlando, Florida, abstract no. 2339T, p. 988.
  60. Lengvenytė, Aistė; Strumila, Robertas; Dlugauskas, Edgaras; Utkus, Algirdas; CYP450 enzymes genetic polymorphism influence on treatment of affective disorders. European psychiatry. Paris: Elsevier France, 2017, Vol. 41, suppl. p. s167-s168 [abstract no. ew0186]. ISSN: 0924-9338 ; DOI: 10.1016/j.eurpsy.2017.01.2055.
  61. Glemžaitė, Monika; Zubova, Anastasija; Krasovskaja, Natalija; Utkus, Algirdas; Navakauskienė, Rūta; DNMT and p53 inhibitors are potential cardiomyogenic differentiation inducers of human amniotic fluid derived mesenchymal stem cells. Journal of stem cell research & therapy. Hyderabad: OMICS International, 2017, Vol. 7, No. 8, suppl. p. 52. ISSN: 2157-7633.
  62. Glemžaitė, Monika, Baronaitė, Sandra, Zentelytė, Aistė, Savickienė, Jūratė, Krasovskaja, Natalija, Utkus, Algirdas, Navakauskienė, Rūta, Characteristics and differentiation potential of human amniotic fluid-derived mesenchymal stem cells. Hydra XIII: The European summer school on stem cells and regenerative medicine, 10-17 September, 2017, Greece: [abstracts]. Hydra, 2017. p. 28.
  63. Loreta Cimbalistienė, Birutė Burnytė, Vilija Černiauskienė, Aušra Morkūnienė, Laima Ambrozaitytė, Ramūnas Janavičius, Algirdas Utkus, Novel hemizygous mutation of TAZ gene in a boy with atypical Barth syndrome. Journal of Inborn Errors of Metabolism and Screening, 13th International Congress of Inborn Errors of Metabolism, Rio de Janeiro, Brasil, September 5-8, 2017, Special supplement with the abstracts, p. 242.
  64. Dlugauskas, Edgaras; Lengvenytė, Aistė; Strumila, Robertas; Utkus, Algirdas, Poor CYP2D6 and ultrarapid CYP2C19 metabolizer: Clinical challenge in psychiatric treatment. European psychiatry. Paris: Elsevier France, 2017, Vol. 41, suppl. p. s163. ISSN: 0924-9338; DOI: 10.1016/j.eurpsy.2017.01.2042.
  65. Burnytė Birutė, Grigalionienė Kristina, Burokienė Vilmanta, Besusparis Justinas, Ambrozaitytė Laima, Utkus Algirdas, Diagnostic management challenges in an infant with possible diagnosis of mitochondrial disease. 14th Conference of the Baltic Child Neurology Association, Program & abstracts, May 18-20, 2017, Riga, Latvia. p. 27.
  66. Stavusis Janis, Inashkina Inna, Pelnena Dita, Micule Ieva, Strautmanis Jurgis, Naudina Maruta, S., Krumina Astrida, Lace Baiba, Cimbalistienė Loreta, Kučinskas Vaidutis, Utkus Algirdas, Burnytė Birutė, Matulevičienė Aušra, Limb-Girdle muscular dystrophies - the current state in Latvia and Lithuania. 14th Conference of the Baltic Child Neurology Association, Program & abstracts, May 18-20, 2017, Riga, Latvia p. 49.
  67. Norvydas, Matas; Ginevičienė Valentina, Milašius, Kazys; Tubelis, Linas; Utkus, Algirdas; Relationship between CKM gene variant and physical performance phenotypes in Lithuanian elite athletes. Multiplicity of sport science in practice: 10th Baltic sport science conference: abstracts: April 26–28, 2017 Riga, Latvia. Riga: Latvian Academy of Sport Education, 2017. p. 53-54. ISBN: 9789934520334.
  68. Ginevičienė, Valentina; Drozdovska, S. B; Tubelis, Linas; Utkus, Algirdas; The association of MCT1 gene variant with football players status in Lithuanian and Ukrainian cohorts. Multiplicity of sport science in practice : 10th Baltic sport science conference : abstracts : April 26–28, 2017 Riga, Latvia. Riga : Latvian Academy of Sport Education, 2017. p. 115. ISBN: 9789934520334.
  69. Ginevičienė, Valentina, Jakaitienė, Audronė, Milašius, Kazys, Tubelis, Linas Utkus, Algirdas, Relationships between ACE, AGT, AGTR1, MB genotypes and physical performance phenotype in Lithuanian elite athletes. 8th international scientific conference on kinesiology: proceedings: Opatija, Croatia, 10-14 May, 2017 / editors-in-chief Dragan Milanović, Goran Sporiš, Sanja Šalaj and Dario Škegro. Zagreb: University of Zagreb, 2017. p. 85.
  70. Aistė Lengvenytė, Robertas Strumila, Edgaras Dlugauskas, Algirdas Utkus, Alvydas Navickas, The Beginning of Pharmacogenetic Research with Psychiatric Drugs in Lithuania. WPA INTER ZONAL CONGRESS, Vilnius, Lithuania, 3 – 6 May 2017, Poster abstracts book, p.18.
  71. Indrė Kotryna Pakutkaitė, Edgaras Dlugauskas, Viktorija Norkūnienė, Algirdas Utkus, Alvydas Navickas, Higher Rates of Depression among Huntington's Disease Gene Carriers. WPA INTER ZONAL CONGRESS, Vilnius, Lithuania, 3 – 6 May 2017, Poster abstracts book, p. 43.
  72. V. Šliužas, B. Aleksiūnienė, E. Dagytė, L. Ambrozaitytė, B. Tumienė, B. Burnytė, A. Utkus, 16p11.2 microdeletion and microduplication in two Lithuanian patients with speech delay. The European Human Genetics Conference 2017, May 27-30, 2017, Copenhagen, Denmark, E-P11.01.
  73. D. Braždžiūnaitė, B. Burnytė, B. Aleksiūnienė, K. Grigalionienė, L. Ambrozaitytė, V. Norkūnienė, A. Utkus, A case of syndromic split hand/foot malformation type 1 with de novo 7q21.3 deletion. The European Human Genetics Conference 2017, May 27-30, 2017, Copenhagen, Denmark, P11.109A.
  74. V. Mikštienė, J. Songailienė, J. Byčkova, G. Rutkauskienė, E. Jašinskienė, R. Verkauskienė, E. Lesinskas, A. Utkus, Effect of management of thiamine responsive megaloblastic anemia syndrome with sulbutiamine. The European Human Genetics Conference 2017, May 27-30, 2017, Copenhagen, Denmark, P06.52D.
  75. B. Aleksiūnienė, A. Matulevičienė, L. Ambrozaitytė, V. Jakutis, A. Utkus, Hypoplastic right ventricle, dysmorphic features and brain structural anomalies in a patient with a de novo 1p36.33p36.32 deletion. The European Human Genetics Conference 2017, May 27-30, 2017, Copenhagen, Denmark, E-P05.16.
  76. L. Cimbalistienė, A. Morkūnienė, A. Vaitkevičius, R. Praninskienė, L. Ambrozaitytė, A. Utkus, Phenotypic variability of myotonia congenita in Lithuanian three generation family with heterozygous mutation in CLCN1 gene. The European Human Genetics Conference 2017, May 27-30, 2017, Copenhagen, Denmark, P10.35C.
  77. Pranckėnienė, Laura; Jakaitienė, Audronė; Kučinskas, Vaidutis. An evaluation of de novo mutation content in the Lithuanian exome. The European Human Genetics Conference 2017, May 27-30, 2017, Copenhagen, Denmark. E-P18.26.
  78. Urnikytė, Alina; Molytė, Alma; Kučinskas; Vaidutis. Detecting the recent changes of effective population size in the Lithuanian population. The European Human Genetics Conference 2017, May 27-30, 2017, Copenhagen, Denmark, E-P18.14.
  79. Preikšaitienė, Eglė; Laimutė, Rita; Morkūnienė, Aušra; Utkus, Algirdas; Kučinskas Vaidutis. Developmental delay, congenital heart defect and cleft palate in a patient with 1q22q23.1 microdeletion. The European Human Genetics Conference 2017, May 27-30, 2017, Copenhagen, Denmark, E-P08.05.
  80. Gueneau L., Fish R., Shamseddin H., Voisin N., Tran Mau-Them F., Preiksaitiene E., Monroe G., Allias F., Ambosaidi Q., Ambrozaityte L., Cimbalistiene L., Delafontaine J., Guex N., Hashem M., Kurdi W., Pippucci T., Pradervand S., Roechert B., Van Hasselt P., Wiederkehr M., Wright C., DDD Study, Xenarios I., Van Haaften G., Shaw-Smith C., Schindewolf E., Neerman-Arbez M., Chelly J., Kucinskas V., Alkuraya F., Reymond A. KIAA1109 variants are associated with a severe disorder of brain development and arthrogryposis. The European Human Genetics Conference 2017, May 27-30, 2017, Copenhagen, Denmark, C20.4.
  81. Burnytė, Birutė; Kavaliauskienė, Ingrida; Molytė, Alma; Ambrozaitytė, Laima; Rančelis, Tautvydas; Morkūnienė, Aušra; Matulevičienė, Aušra; Tumienė, Birutė; Kučinskas, Vaidutis; Utkus, Algirdas. Novel mutations of the GJB1 gene associated with Charcot-Marie-Tooth type 1X in Lithuanian cohort. The European Human Genetics Conference 2017, May 27-30, 2017, Copenhagen, Denmark, P10.23C
  82. Matulevičienė, Aušra; Burnytė, Birutė; Kavaliauskienė, Ingrida; Meškienė, Raimonda; Matulevičiūtė, Rugilė; Aleksiūnienė, Beata; Ambrozaitytė, Laima; Utkus, Algirdas; Kučinskas, Vaidutis. Variable expressivity of the c.749C>G mutation in the FGFR3 gene in two unrelated families of Muenke syndrome. The European Human Genetics Conference 2017, May 27-30, 2017, Copenhagen, Denmark, E-P04.14
  83. Grigalionienė, Kristina; Burnytė, Birutė; Kučinskas, Vaidutis; Utkus, Algirdas. MtDNA sequence analysis in the group of Lithuanian patients with clinically suspected mitochondrial disease. The European Human Genetics Conference 2017, May 27-30, 2017, Copenhagen, Denmark, E-P06.32
  84. Juodišienė G., Jonaitė G., Doščūraitė J., Sakaitė I., Sudnickaitė U., Vaicenayičienė G., Kučinskas V., Karčiauskaitė D. Influence of psychosocial factors on blood biochemical markers in a healthy Lithuanian male population. 8th congress of European Atherosclerosis Society, 23 – 26 April, 2017, Prague, p. 156.
  85. Ginevičienė Valentina, Jakaitienė Audronė, Milašius Kazys, Tubelis, Linas, Utkus Algirdas, Genetic variants in myostatin gene and physical performance in Lithuanian athletes. British journal of sports medicine. 34th FIMS world sports medicine congress: 29 September - 2 October 2016, Ljubljana, Slovenia. London: BMJ publishing group Vol. 50, iss. 1 (Supplement) A41 (2016). p. [1]. ISSN: 0306-3674 ; DOI: 10.1136/bjsports-2016-097120.71.
  86. Birutė Burnytė, I. Uktverytė, L. Ambrozaitytė, V. Kučinskas, A. Utkus, Paveldimos neuropatijos: epidemiologinė ir mutacijų analizė GJB1 gene. LMA, Jaunųjų mokslininkų konferencijos Bioateitis: gamtos ir gyvybės mokslų perspektyvos pranešimų santraukos, 2016, p. 7-8.
  87. Edgaras Dlugauskas, Aistė Lengvenytė, Robertas Strumila, Algirdas Utkus, Farmakogenetika psichiatrijoje – kelias į individualizuotą gydymą. LMA, Jaunųjų mokslininkų konferencijos Bioateitis: gamtos ir gyvybės mokslų perspektyvos pranešimų santraukos, 2016, p. 8.
  88. Cimbalistienė, Loreta; Burnytė, Birutė; Songailienė, Jurgita; Urbonas, Vaidotas; Grabhorn, Enke; Hempel, Maja; Santer, Rene; Haack, Tobias; Prokisch, Holger. Mitochondrial infantile liver disease due to TRMU gene mutations: two cases with different outcome. Journal of inherited metabolic disease. Dordrecht : Springer. ISSN 0141-8955. 2016, 39, supplement 1, p. S157. DOI: 10.1007/s10545-016-9969-2.
  89. Mažeikienė, Asta; Karčiauskaitė, Dovilė; Burokienė, Neringa; Daunoravičius, Žydrūnas; Kučinskienė, Zita Aušrelė; Kučinskas, Vaidutis. Association of serum carotenoid concentration with single nucleotide polymorphisms in APOE, BCMO1, NPC1L1, CD36, GSTP1, ABCG5, FABP1, FABP2 and LIPC genes. Atherosclerosis. Shannon : Elsevier Ireland Ltd. ISSN 0021-9150. eISSN 1879-1484. 2016, Vol. 252, p. E79. DOI: 10.1016/j.atherosclerosis.2016.07.494.
  90. Germanas, Šarūnas. Two-stage variant calling method for next-generation sequencing experiments. Data analysis methods for software systems : 8th international workshop on data analysis methods for software systems, Druskininkai, December 1-3, 2016. Vilnius : Vilniaus universiteto leidykla, 2016. ISBN 9789986680611. p. 21.
  91. Sveikata, Tomas; Klimas, Dalius; Molytė, Alma; Kanopa, Paulius; Porvaneckas, Narūnas. What do surgeons know about evolution? Evoliucinė medicina: šiuolakinių sveikatos problemų evoliuciniai mechanizmai ir dėsningumai = Evolutionary medicine: pre-existing mechanisms and patterns of current health issues : trečioji tarptautinė konferencija, 2016 m. birželio mėn. 14-19 d. Vilnius : Vilniaus universitetas, 2016. ISBN 9786094597206. p. 75.
  92. Aušra Matulevičienė, Laima Ambrozaitytė, Aušra Morkūnienė, Hantingtono ligos patogenezės mechanizmai. Hantingtono ligos konferencija. Vilnius : Hantingtono ligos koordinacinis centras, 2016. p. 10-11.
  93. N. Voisin, H. Shamseddin, F.,Tran Mau Them, E. Preiksaitiene, R. Fish, L. Gueneau, L. Ambrozaityte, A. Morkuniene, N. Guex, B. Roechert, S. Pradervand, I. Xenarios, M., Neerman-Arbez, C. Shaw-Smith, V. Kucinskas, J. Chelly, F.S. Alkuraya, A.Reymond, KIAA1109 variants are associated with a severe syndromic brain development disorder with arthrogryposis. American Society of Human Genetics 66th Annual Meeting, October 18–22, 2016 VANCOUVER, CANADA PLATFORM ABSTRACTS, p. 80.
  94. B. Burnytė, L. Ambrozaitytė, V. Kučinskas, A. Utkus, Novel homozygous SPG11 mutation in the molecular diagnosis of hereditary spastic paraplegia. American Society of Human Genetics 66th Annual Meeting, October 18–22, 2016, Vancouver, Canada : poster abstracts. Vancouver : ASHG, 2016. p. 1356.
  95. L. Ambrozaitytė, B. Burnytė, L. Cimbalistienė, B. Tumienė, A. Utkus, I. Kavaliauskienė, T. Rančelis, V. Kučinskas, GNPTAB gene mutations in the Lithuanian mucolipidosis II and II/III patients. American Society of Human Genetics 66th Annual Meeting, October 18–22, 2016, Vancouver, Canada : poster abstracts. Vancouver : ASHG, 2016. p. 1449.
  96. A. Urnikytė, A. Molytė, E. Pranckevičienė, V. Kučinskas. Inference of evolutionary relationships among human populations based on the estimates of effective population size. American Society of Human Genetics 66th Annual Meeting, October 18–22, 2016, Vancouver, Canada : poster abstracts. Vancouver : ASHG, 2016. p. 491.
  97. Aušra Matulevičienė, Laima Ambrozaitytė, Rugilė Matulevičiūtė, Arūnas Liubšys, Algirdas Utkus, Vaidutis Kučinskas, A patent with Raine syndrome due to novel mutations in FAM20C gene. Twenty-seventh European meeting on dysmorphology, 7-9 September 2016, Le Bischenberg, France, p.4.
  98. Philippos Patsalis, George Koumbaris, Elena Kypri, Kyriakos Tsangaras, Achilleas Achilleos, Petros Mina, Maria Neofytou, Voula Velissariou, Georgia Christopoulou, Ioannis Kallikas, Alicia González-Liñán, Eglė Benušienė, ...... Elisavet Papageorgiou, Development of a novel targeted assay for non-invasive prenatal testing of fetal trisomies exhibits near-diagnostic accuracy. Prenatal Diagnosis 2016, 36(Suppl. 1), 23–84, P-147 p.67.
  99. V. Šliužas, Ž. Maldžienė, B. Burnytė, V. Kučinskas, A. Utkus, Patient With 22q11.2 Microdeletion and Atypical Clinical Features. The European Human Genetics Conference 2016, May 21-24, Barcelona, Spain. European journal of human genetics. London : Nature Publishing Group, 2016, Vol. 24, e-suppl. 1. p. 233. ISSN: 1018-4813.
  100. V. Mikštienė, I. Vebraitė, G. Alzbutas, T. Rančelis, A. Utkus, V. Popendikytė. Multiplex PCR and NGS in detection mutations of target genes associated with hearing loss. The European Human Genetics Conference 2016, May 21-24, Barcelona, Spain. European journal of human genetics. London : Nature Publishing Group, 2016, vol. 24, e-suppl. 1. p. 328-329. ISSN: 1018-4813.
  101. E. Benušienė, M. Rachlevičiūtė, A. Morkūnienė, L. Ambrozaitytė, A. Utkus, A novel TAZ gene mutation detected prenatally in a family with Barth syndrome. The European Human Genetics Conference 2016, May 21-24, Barcelona, Spain. European journal of human genetics. London : Nature Publishing Group, 2016, Vol. 24, e-suppl. 1. p. 408. ISSN: 1018-4813.
  102. D. Braždžiūnaitė, B. Burnytė, V. Šliužas, A. Utkus, Rare case of male infertility due to monosomy X and structural rearrangement of chromosome Y. The European Human Genetics Conference 2016, May 21-24, Barcelona, Spain. European journal of human genetics. London : Nature Publishing Group, 2016, Vol. 24, e-suppl. 1. p. 412. ISSN: 1018-4813.
  103. B. Burnytė, I. Inashkina, B. Lace, D. Pelnena, A. Molytė, K. Grigalionienė, V. Kučinskas, A. Utkus, Implementing the survey of disease natural history as a tool to collect complex information on mitochondrial patients in Lithuania and Latvia. The European Human Genetics Conference 2016, May 21-24, Barcelona, Spain. European journal of human genetics. London : Nature Publishing Group, 2016, vol. 24, e-Supplement 1. p. 431. ISSN: 1018-4813.
  104. B. Aleksiūnienė, L. Cimbalistienė, V. Dirsė, E. Gineikienė, R. Marcinkutė, A. Utkus, De novo 15q26.2q26.3 duplication and 15q26.3 deletion in a patient with an anomalous parietal sutures. The European Human Genetics Conference 2016, May 21-24, Barcelona, Spain. European journal of human genetics. London : Nature Publishing Group, 2016, Vol. 24, e-suppl. 1. p. 452-453. ISSN: 1018-4813.
  105. V. Ginevičienė, A. Jakaitienė, S. Drozdovska, L. Tubelis, V. Kučinskas, A. Utkus. Association analysis of five genes polymorphisms in two cohorts of European athletes. The European Human Genetics Conference 2016, May 21-24, Barcelona, Spain. European journal of human genetics. London : Nature Publishing Group, 2016, Vol. 24, e-Supplement 1. p. 482-483. ISSN: 1018-4813.
  106. Beata Aleksiūnienė, Laima Ambrozaitytė, Algirdas Utkus, Comparative whole genome hybridisation methods in molecular diagnostics. XIII Baltic Congress in Laboratory Medicine, Tartu, Estonia, May 12-14, 2016, Eesti Arst 2016; 95(suppl. 1), p.33, OP-16.
  107. V. Ginevičienė, E. Pranckevičienė, L. Tubelis, A. Utkus, V. Kučinskas, Association of gene variants with high-speed, strength and power sports in Lithuanians. The 9th Conference of the Baltic Sport Science Society, April 27–29, 2016, Kaunas, Lithuania. ABSTRACTS, p. 91.
  108. E. Preikšaitienė, Ž. Maldžienė, B. Aleksiūnienė, V. Kučinskas, Mild intellectual disability, congenital heart defect and skeletal abnormalities in three patients with 4q13.3 Microdeletion. The European Human Genetics Conference 2016, May 21-24, Barcelona, Spain. European journal of human genetics. London: Nature Publishing Group, 2016, 24, e-suppl.1. p. 224. ISSN: 1018-4813.
  109. A. Urnikytė, A. Molytė, E. Pranckevičienė, V. Kučinskas, Demographic inference of the Lithuanian population. The European Human Genetics Conference 2016, May 21-24, Barcelona, Spain. European journal of human genetics. London : Nature Publishing Group, 2016, Vol. 24, e-suppl. 1. p. 388. ISSN: 1018-4813.
  110. Laura Gudavičiūtė, Vaidutis Kučinskas, An evaluation of de novo mutation process intensity in the different regions of human genome. The 3rd International Conference Evolutionary Medicine: Pre-Existing Mechanisms and Patterns of Current Health Issues, 14th-19th of June, 2016, Vilnius University, Lithuania, p. 56, ISBN 978-609-459-720-6.
  111. Violeta Mikštienė, Audronė Jakaitienė, Jekaterina Byčkova, Eglė Gradauskienė, Eglė Preikšaitienė, Birutė Burnytė, Birutė Tumienė, Aušra Matulevičienė, Laima Ambrozaitytė, Ingrida Kavaliauskienė, Ingrida Domarkienė, Tautvydas Rančelis, Loreta Cimbalistienė, Eugenijus Lesinskas, Vaidutis Kučinskas, Algirdas Utkus, The High Frequency of GJB2 Gene Mutation C.313_326del14 Suggests Its Possible Origin in Ancestors of Lithuanian Population. The 3rd International Conference Evolutionary Medicine: Pre-Existing Mechanisms and Patterns of Current Health Issues, 14th-19th of June, 2016, Vilnius University, Lithuania, p. 65, ISBN 978-609-459-720-6.
  112. Rasa Strupaitė, Birutė Tumienė, Algirdas Utkus, Inherited Retinal Dystrophies – Case Series. The 3rd International Conference Evolutionary Medicine: Pre-Existing Mechanisms and Patterns of Current Health Issues, 14th-19th of June, 2016, Vilnius University, Lithuania, p. 74, ISBN 978-609-459-720-6.
  113. Edgaras Dlugauskas, Aistė Lengvenytė, Robertas Strumila, Algirdas Utkus, Influence of CYP450 Enzymes Genetic Polymorphism on Treatment of Depression and Bipolar disorder. The 3rd International Conference Evolutionary Medicine: Pre-Existing Mechanisms and Patterns of Current Health Issues, 14th-19th of June, 2016, Vilnius University, Vilnius, Lithuania, p. 89, ISBN 978-609-459-720-6.
  114. Lina Barauskienė, Ingrida Uktverytė, Raimonda Meškienė, Ingrida Domarkienė, Laima Ambrozaitytė, Justas Arasimavičius, Algimantas Irnius, Vaidutis Kučinskas, Association of Sweet Taste Perception in the General Population of Lithuanians. The 3rd International Conference Evolutionary Medicine: Pre-Existing Mechanisms and Patterns of Current Health Issues, 14th-19th of June, 2016, Vilnius University, Lithuania, p. 82, ISBN 978-609-459-720-6.
  115. Alina Urnikytė, Alma Molytė, Vaidutis Kučinskas, Recent Effective Population Size Estimated from Segments of Identity by Descent in the Lithuanian Population. The 3rd International Conference Evolutionary Medicine: Pre-Existing Mechanisms and Patterns of Current Health Issues, 14th-19th of June, 2016, Vilnius University, Lithuania, p. 77, ISBN 978-609-459-720-6.
  116. M. Aksenov, V. Ginevičienė, The myostatin gene K153R polymorphism in Russian and Lithuanian strength / power athletes. The 9th Conference of the Baltic Sport Science Society, April 27–29, 2016, Kaunas, Lithuania. ABSTRACTS, p. 92-93.
  117. Andrejus Coj, Zita Aušrelė Kučinskienė, Vaidutis Kučinskas, MMP-9 as a new marker to predict coronary heart disease in native Lithuanians. XIII Baltic Congress in Laboratory Medicine, Tartu, Estonia May 12-14, 2016, Eesti Arst 2016; 95(suppl. 1), p.47, PP-5.
  118. A. Urnikytė, I. Domarkienė, I. Uktverytė, L. Ambrozaitytė, R. Meškienė, V. Kučinskas, Genomic diversity and distribution of CNVs in Lithuanian population. European journal of human genetics. London : Nature Publishing Group, 2015, Vol. 23, Supplement 1. p. 332-333. ISSN: 1018-4813.
  119. Erinija Pranckevičienė, Laima Ambrozaitytė, Ingrida Uktverytė, Algirdas Utkus, Vaidutis Kučinskas. Galaxy in teaching computational methods of genome analysis for master degree students in Medical Genetics program at the Faculty of Medicine, Vilnius University. Galaxy Community Conference 2015, 6-8th July 2015, the Sainsbury Laboratory Norwich, UK.
  120. B. Tumienė, A. Maver, B. Peterlin, V. Kučinskas, A. Utkus, Molecular pathology of monogenic epilepsies. 7th Conference of Lithuanian Neuroscience Association, 27 November 2015, National Open Access Scholarly Communication and Information Center, Saulėtekio al. 5, Vilnius. Program and Abstracts, P 13., p.27, ISBN 978-609-459-605-6.
  121. Algirdas Utkus, Development, evolution and dysmorphology. The 8th Baltic Morphology Scientific Conference: Interdisciplinary Nature of Contemporary Morphology, the 12-14th of November, 2015, Vilnius, Lithuania, Abstracts, p. 35.
  122. Birutė Tumienė, Aleš Maver, Borut Peterlin, Vaidutis Kučinskas, Algirdas Utkus, Dissection of genetic architecture of epilepsies through exome sequencing studies. The 8th Baltic Morphology Scientific Conference: Interdisciplinary Nature of Contemporary Morphology, the 12-14th of November, 2015, Vilnius, Lithuania, Abstracts, p. 67.
  123. Pranckevičienė, E., Ginevičienė V., Milašius K., Utkus A., Decision tree learning rules to associate athletes phenotypes with genotypes in different sports. Sport science for sports practice and teacher's training, 8th conference of Baltic society of sport sciences, abstracts. April 22-24, 2015 Vilnius, Lithuania. Vilnius: Lietuvos edukologijos universiteto leidykla, 2015, p. 165-166, ISBN 9789955209881.
  124. Batkovskytė, D., Ginevičienė V., Utkus A., Tubelis L., Variation in the myostatin gene in Lithuanian elite athletes. Sport science for sports practice and teacher's training, 8th conference of Baltic society of sport sciences, abstracts. April 22-24, 2015 Vilnius, Lithuania. Vilnius, Lietuvos edukologijos universiteto leidykla, 2015, p. 24-25, ISBN 9789955209881.
  125. T. Rančelis, E. Pranckevičienė, A. Pranculis, V.Kučinskas, Comparison of SOLiD sequencing data analysis pipelines . European journal of human genetics. London, Nature Publishing Group. ISSN 1018-4813. Vol. 23, Supplement 1. 2015. p. 314-314.
  126. E. Benusiene, S. Tumene, A. Matuleviciene, R. Meskiene, V. Kučinskas. Prenatally suspected and after the birth confirmed Simpson-Golabi-Behmel syndrome: familial case / European journal of human genetics. London, Nature Publishing Group. ISSN 1018-4813. Vol. 23, Supplement 1. 2015. p. 70.
  127. V. Kučinskas, T. Rancelis, I. Domarkiene, E. Pranckeviciene, I. Uktveryte, L. Ambrozaityte. Profile of pathogenic alleles in healthy Lithuanian population / 65th Annual Meeting of The American Society of Human Genetics, October 6-10, 2015, Baltimore MD : poster abstracts. Baltimore, The American Society of Human Genetics. 2015. p. 483.
  128. Uktverytė, I. Domarkienė, L. Ambrozaitytė, R. Meškienė, V. Kasiulevičius, Z. A. Kučinskienė, V.Kučinskas. Large scale genotyping key to hidden genetic diversity of the population of Lithuania. European journal of human genetics. London, Nature Publishing Group. ISSN 1018-4813. Vol. 23, Supplement 1. 2015. p. 341.
  129. L. Ambrozaitytė, A. Morkūnienė, Ž. Čiuladaitė, E. Preikšaitienė, E. Pranckevičienė, T. Rančelis, L. Cimbalistienė, L. Gueneau, K. Männik, N. Voisin, A. Reymond, V.Kučinskas. UNIGENE: Familial intellectual disability in Lithuanian patients /European journal of human genetics. London, Nature Publishing Group. ISSN 1018-4813. Vol. 23, Supplement 1. 2015. p. 157.
  130. N. Voisin, L. Ambrozaityte, A. Morkuniene, L. Gueneau, K. Mannik, Z. Ciuladaite, E. Preiksaitiene, E. Pranckeviciene, T. Rancelis, L. Cimbalistiene, N. Guex, V.Kučinskas, A. Reymond. DCHS2, a novel autosomal recessive cause of Van Maldergem Syndrome /65th Annual Meeting of The American Society of Human Genetics, October 6-10, 2015, Baltimore MD : poster abstracts. Baltimore, The American Society of Human Genetics. 2015. p. 1080.
  131. Burnyte B., Peciuliene S., Gudaitiene R., Rusoniene S., Songailiene J., Liubsys A., Cimbalistiene L., Drazdiene N. Importance of early diagnosis and start of treatment in Mevalonate Kinase Deficiency (MKD) patients. Journal of inherited metabolic disease. Dordrecht, Springer. ISSN 0141-8955. Vol. 38, iss. 1, Supplement. 2015. P-706, p. 334.
  132. Ginevičienė V., Genetic Research in Sports Science: Actuality and Prospects. Sport science for sports practice and teacher's training : 8th conference of Baltic society of sport sciences: abstracts: April 22-24, 2015 Vilnius, Lithuania. Vilnius: Lietuvos edukologijos universiteto leidykla, 2015. p. 105-106.
  133. Tomas Sveikata, Narunas Porvaneckas, Alma Molytė, Algirdas Venalis.Total knee arthroplasty in the elderly. The 8th Baltic Morphology Scientific Conference: Interdisciplinary Nature of Contemporary Morphology, the 12-14th of November, 2015, Vilnius, Lithuania, Abstracts, p. 66.
  134. V.Ginevičienė V., Pranckevičienė E., Tubelis, L., Utkus A., Gene variants related to the sprint/power performance of the Lithuanian elite athletes. 9th European Congress on Sports Medicine, Antwerp, Belgium, 10 – 12 September, 2015. European journal of sports medicine Vol. 3 (suppl.1), 85-86 p.
  135. Tumienė B, Songailienė J, Preikšaitienė E, Čiuladaitė Z, Bandanskytė A, KučinskasV, Utkus A, Chromosomal aberrations mimicking mitochondrial disorders. SSIEM 2015: Annual Symposium of the Society for the Study of Inborn Errors of Metabolism, Lyon, France,1-4 September 2015. Journal of inherited metabolic disease. Dordrecht, Springer. ISSN 0141-8955. Vol. 38, iss. 1, suppl. 2015, P-395, p. S214.
  136. Mayr J A ., Burnyte B., Snariene R., Feichtinger R G., Zimmermann F A ., Lunzer V., Wortmann S. B., Baskirova I., Drazdiene N. , Algirdas Utkus, Sperl W., Lactic acidosis and neonatal death in patient with deficiency of the E2 subunit of the pyruvate dehydrogenase complex. SSIEM 2015: Annual Symposium of the Society for the Study of Inborn Errors of Metabolism, Lyon, France,1-4 September 2015. Journal of inherited metabolic disease. Dordrecht, Springer. ISSN 0141-8955. Vol. 38, iss. 1, suppl. 2015, P-362, p. S201.
  137. Domarkienė, I. Uktverytė, L. Ambrozaitytė, R. Meškienė, N. Burokienė, V. Kasiulevičius, Z. A. Kučinskienė, V. Kučinskas. Evaluation of CVD genetic risk in the Lithuanian population / European journal of human genetics. London, Nature Publishing Group. ISSN 1018-4813. Vol. 23, Supplement 1. 2015. p. 330-331.
  138. B. Aleksiūnienė, R. Matulevičiūtė, Ž.Čiuladaitė, A. Matulevičienė, A. Utkus, V. Kučinskas, Coarctation of aorta with dysmorphic features in a patient with triplication of 15q26.1-q26.3: clinical and molecular analysis. 9-11 September, 2015; 26th European Meeting on Dysmorphology, Le Bischenberg, France, p.27.
  139. Matulevičienė, B. Aleksiūnienė, L. Tamulienė, A. Liubšys, Ž. Čiuladaitė, A. Utkus, V. Kučinskas. A novel de novo dup (4) (q28.2-qter) & del (8) (pter-p23.1) due to unbalanced translocation in a girl: clinical and molecular analysis. 9-11 September, 2015; 26th European Meeting on Dysmorphology, Le Bischenberg, France.
  140. V. Ginevičienė, A. Jakaitienė, L. Tubelis, A. Utkus, Do metabolic disease genes SNPs affect elite sports performance? European Journal of Human Genetics, vol . 23, suppl. 1, 2015, European Human Genetics Conference, June 6 - 9, 2015 Glasgow, Scotland, United Kingdom, Abstracts PS15.21, p. 303.
  141. V. Mikštienė, J. Byčkova, E. Gradauskienė, E. Lesinskas, A. Utkus, The contribution of GJB2 gene mutations to development of early onset hearing loss in affected group of patients in Lithuanian population. European Journal of Human Genetics, vol . 23, suppl. 1, 2015, European Human Genetics Conference, June 6 - 9, 2015 Glasgow, Scotland, United Kingdom, Abstracts PS02.29, p.78.
  142. E. Preikšaitienė, Ž. Čiuladaitė, B. Tumienė, A. Utkus, V. Kučinskas, Clinical and molecular delineation of the emerging 10q22.1q22.3 microdeletion syndrome. European Journal of Human Genetics, vol . 23, suppl. 1, 2015, European Human Genetics Conference, June 6 - 9, 2015 Glasgow, Scotland, United Kingdom, Abstracts J08.01, p.409.
  143. D. Vansevičiūtė, Ž. Čiuladaitė, B. Tumienė, A. Utkus, V. Kučinskas, De novo case of a mosaic ring supernumerary marker chromosome leading to trisomy of 8p11.22-q11.23 in a boy with development delay and corpus callosum hypoplasia. European Journal of Human Genetics, vol . 23, suppl. 1, 2015, European Human Genetics Conference, June 6 - 9, 2015 Glasgow, Scotland, United Kingdom, Abstracts J09.24, p. 417.
  144. B. Burnytė, I. Uktverytė, A. Vaitkevičius, L. Ambrozaitytė, V. Kučinskas, A. Utkus, GJB1 gene mutation c.34G>A in a Lithuanian family. European Journal of Human Genetics, vol . 23, suppl. 1, 2015, European Human Genetics Conference, June 6 - 9, 2015 Glasgow, Scotland, United Kingdom, Abstracts J10.08, p. 422.
  145. Ž. Čiuladaitė, E. Preikšaitienė, A. Utkus, V. Kučinskas, A deletion at 4p15.2 and disruption of PITX2 gene due to pericentric inversion in a patient with Axenfeld-Rieger syndrome and developmental delay. European Journal of Human Genetics, vol . 23, suppl. 1, 2015, European Human Genetics Conference, June 6 - 9, 2015 Glasgow, Scotland, United Kingdom, Abstracts PM13.22, p. 271.
  146. Lina Zabulienė, Airida Audronė Bagdžiūnienė, Birutė Burnytė, Ramūnas Janavičius, Jurgita Urbonienė, Algirdas Utkus, The Ehlers-Danlos syndrome and metastatic medullary thyroid carcinoma: a case report. Endocrine abstracts. Bristol, BioScientifica. ISSN 1470-3947. Vol. 37. 2015. Abstract no. EP1310.
  147. Birutė Tumienė, Algirdas Utkus, Algorithms for epilepsy genetic testing. Eesti Arst 2015; (Suppl.1): 1-88, 13th International Conference of Baltic Child Neurology Association, May 13-16, 2015, Tartu, p.53.
  148. Janis Stavusis, I. Inashkina, E. Jankevics, I. Radovica, I. Micule, J. Strautmanis, M. S. Naudina, A. Utkus, B. Burnytė, B. Lace, Variations in LGMD genes CAV3 and FKRP. Eesti Arst 2015; (Suppl.1): 1-88, 13th International Conference of Baltic Child Neurology Association, May 13-16, 2015, Tartu, p.21.
  149. B. Aleksiūnienė, A. Matulevičienė, E. Benušienė, Hypoplastic left heart syndrome in a case with partial 18p monosomy and partial 20q trisomy. European journal of human genetics. London, Nature Publishing Group. ISSN 1018-4813. 2014, Vol. 23, Supplement 1. 2015. p. 399-400.
  150. Matulevičienė, B. Aleksiūnienė, V. Mikštienė, N. Krasovskaja, L. Griškevičius, A. Utkus, V. Kučinskas. Dup (1) (q43–q44) & del (21) (q22.2–q22.3) characterized by facial dysmorphism, congenital heart defect and mental retardation. 10-12 September, 2014; 25th European meeting on dysmorphology, Le Bischenberg, France.
  151. Mažeikienė A., Jakaitienė A., Arasimavičius J., Domarkienė I., Uktverytė I., Ambrozaitytė L., Kučinskienė Z.A., Kučinskas V. Association of serum carotenoid concentrations with single nucleotide polymorphisms in APOE, BCMO1, HL and FABP genes. The 17th International Symposium on Carotenoids 2014, Utah, USA, June 29 – July 4.
  152. Mažeikienė A., Kučinskas V., Kučinskienė Z.A. Serum Carotenoid Concentrations in Ethnic Lithuanians. Tarptautinė konferencija „Evolutionary medicine: perspectives in understanding health and disease“, Vilnius, Lithuania, 2014 May 27-30.
  153. Valentina Ginevičienė, Audronė Jakaitienė, Algirdas Utkus, Vaidutis Kučinskas, Linas Tubelis, The effect of genetic variants on muscular performance and sprint/power phenotype. The 4th International Conference on Science and Applied Research, Post-Genome Methods of Analysis in Biology and Laboratory and Clinical Medicine, Kazan, Russia, October 29-November 1, 2014, Abstracts Book, p. 288-289.
  154. V. Šliužas, Ž. Čiuladaitė, E. Preikšaitienė, A. Utkus, Implication of cytogenetic methods in to clinical cytogenetic diagnostics: a case report. XII Baltic Congress in Laboratory Medicine, Riga, Latvia, September 18-20, 2014, Journal of International Education for Clinical Chemistry and laboratory Medicine (IECCLM) vol.1, no.1, Abstracts Book, p. 43, ISSN 2256-0092.
  155. E. Benušienė, E. Preikšaitienė, V. Šliužas, S. Tumėnė, Familial chromosomal translocation t(3;5)(q26.2;p14): clinical characterization of affected members with neural tube defect as a common clinical feature, European Human Genetics Conference 2014, May 31 - June 3, Milan, Italy, European Journal of Human genetics, vol. 22, suppl. 1, May 2014, P01.059-S, p. 61.
  156. E. Pranckevičienė, A. Pranculis, E. Preikšaitienė, V. Kučinskas, Computational pipeline to analyze genomic variants with respect to clinical phenotypes by mining literature. Study of genomic regions related to intellectual disability. European Human Genetics Conference 2014, May 31 - June 3, Milan, Italy, European Journal of Human genetics, vol. 22, suppl. 1, May 2014, P16.48-M, p. 314.
  157. V. Ginevičienė, G. Olšauskaitė, L. Tubelis, A. Utkus, The association of PPARD and PPARA gene variants with physical performance in Lithuanian elite athletes. European Human Genetics Conference 2014, May 31 - June 3, Milan, Italy, European Journal of Human genetics, vol. 22, suppl. 1, May 2014, J17.49, p. 506.
  158. N. Kapitanova, Ž. Čiuladaitė, B. Burnytė, A. Utkus, Clinical characterization of a patient with mosaic microdeletion 7q36.1-qter. European Human Genetics Conference 2014, May 31 - June 3, Milan, Italy, European Journal of Human genetics, vol. 22, suppl. 1, May 2014, J11.31, p. 450.
  159. Liaugaudienė, A. Utkus, Ž. Čiuladaitė, E. Preikšaitienė, A report of partial monosomy of distal 5p and partial trisomy of distal 19q in a family with Charcot-Marie-Tooth disease. European Human Genetics Conference 2014, May 31 - June 3, Milan, Italy, European Journal of Human genetics, vol. 22, suppl. 1, May 2014, J11.30, p. 449.
  160. Ž. Čiuladaitė, O. Liaugaudienė, A. Utkus, V. Kučinskas, An alternate unbalanced recombinants of chromosome 10 due to familial pericentric inversion. European Human Genetics Conference 2014, May 31 - June 3, Milan, Italy, European Journal of Human genetics, vol. 22, suppl. 1, May 2014, P11.124-M, p. 230.
  161. E. Preikšaitienė, A. Utkus, V. Kučinskas, Exon skipping mutation in collagen VI detected in a patient from Lithuania. European Human Genetics Conference 2014, May 31 - June 3, Milan, Italy, European Journal of Human genetics, vol. 22, suppl. 1, May 2014, P10.40-M, p. 204.
  162. V. Mikštienė, J. Songailienė, J. Byckova, G. Rutkauskienė, E. Jasinskienė, R. Verkauskienė, E. Lesinskas, A. Utkus, Rogers syndrome (thiamine responsive megaloblastic anemia syndrome): the success of multidisciplinary approach. European Human Genetics Conference 2014, May 31 - June 3, Milan, Italy, European Journal of Human genetics, vol. 22, suppl. 1, May 2014, P06.56-M, p. 138.
  163. V. Ginevičienė, S. B. Drozdovska, L. Tubelis, A. Utkus, The association of candidate gene polymorphisms with athlete status in the Lithuanian and Ukrainian cohorts. 7th Conference of Baltic Society of Sport Sciences (BSSS), Tartu, Estonia, May 7-9, 2014. Oral and poster presentations, Acta Kinesiologiae universitatis Tartuensis, vol.20, p. 89, University of Tartu Press, ISSN 1406-9822.
  164. V. Kučinskas, Ž. Čiuladaitė, A large-scale copy number variations in population of Lithuania. Human Genome Meeting 2014, 27-30 April 2014, CICG, Geneva, Switzerland, Final Programme and Abstract Book „Genome Variation and Human Health“, P226.
  165. Mažeikienė A., Jakaitienė A., Kučinskienė Z.A., Kučinskas V., Investigation of Lycopene Intake in the Different Lithuanian Ethnolinguistic Groups. Annals of Nutrition and Metabolism, vol.63, suppl.1, 2013, p.1225-1226, ISSN: 0250-6807.
  166. Čiuladaitė, Živilė, Kučinskas, Vaidutis, Nesubalansuotų struktūrinių chromosominių pokyčių paplitimas žmogaus genome. Bioateitis: gamtos ir gyvybės mokslų perspektyvos : 2013 m. jaunųjų mokslininkų konferencijos pranešimų santraukos. p. 13.
  167. Tumienė, Birutė, Preikšaitienė, Eglė, Utkus, Algirdas, Kasnauskienė, Jūratė, Čiuladaitė, Živilė, Šliužas, Vytautas, Lankutis, Kęstutis, Patsalis, Philippos C., Kučinskas, Vaidutis, Old and new cytogenetics in the evaluation of intellectual disabilities/developmental delays. Neurologijos seminarai. 2013, t. 17, priedas nr. 1 : 12th Conference of Baltic Child Neurology Association (BCNA), 30 May - 1 June, 2013, Kaunas, Lithuania. ISSN 1392-3064 p. S31.
  168. Pranculis, Aidas, Kučinskas, Vaidutis, Pharmacogenomic landscape of the Lithuanian population. Drug metabolism and drug interactions. 2013, vol. 28, no. 3 : Second ESPT Conference “Pharmacogenomics: From Cell to Clinic”, Lisbon, September 26–28, 2013 : congress abstracts.. ISSN 0792- p. A28.
  169. Mažeikienė, Asta, Kučinskienė, Zita Aušrelė, Kučinskas, Vaidutis, Association between serum lycopene concentration and cardiovascular morbidity. 6th Baltic Atherosclerosis Congress, October 11-12, 2013, Riga, Latvia : program and abstracts. p. 13.
  170. Domarkienė, Ingrida, Pranculis, Aidas, Germanas, Šarūnas, Jakaitienė, Audronė, Dženkevičiūtė, Vilma, Kučinskas, Vaidutis, Kučinskienė, Zita Aušrelė, Lithuanian way towards genomics of coronary heart disease. 6th Baltic Atherosclerosis Congress, October 11-12, 2013, Riga, Latvia : program and abstracts. p. 20.
  171. Cimbalistienė L., Ambrozaitytė L., Smirnova M., Utkus. Algorithm for identifying, diagnostic and management of hyperphenylalaninemia (HPA) in Lithuania. Nacionalinių veiklos, susijusios su retomis ligomis, planų ir strategijų įgyvendinimo aktualijos / The national activities related to rare diseases : programa ir tezės, 2013.11.14, Vilnius. p. 21.
  172. Anisko S., Utkus A., Miglinas M., Scientific Research on Rare Diseases. Nacionalinių veiklos, susijusios su retomis ligomis, planų ir strategijų įgyvendinimo aktualijos / The national activities related to rare diseases : programa ir tezės, 2013.11.14, Vilnius. p. 35.
  173. Cimbalistienė L., Ambrozaitytė L., Meškienė R., Smirnova M., Blau N., Utkus A., Tetrahydrobiopterin (BH4) deficiency in Lithuanian newborn screening. Journal of inherited metabolic disease. 2013, vol. 36, suppl. 2: 12th International Congress of Inborn Errors of Metabolism, 3-6 September 2013, Barcelona : abstracts book. ISSN 0141-8955 p. S116.
  174. V. Ginevičienė, Genetics in sport and relationships between genotypes – physical performance in Lithuanian elite athletes. VIII International Baltic Congress of Sport Medicine, 26-27 October 2013, Vilnius, Publication of Abstracts, edited by Dr. Žumbakytė-Šermuksnienė, p.23.
  175. V. Ginevičienė, A gene for sports: the effect of ten genetic variants on the physical performance of Lithuanian athletes. 6th Baltic Scientific Conference Sport Science for Sustainable Society, April 23-25, 2013, Riga, Latvia, Latvian Academy of Sport Education, Abstracts, p. 141, ISSN 1691-6220.
  176. Karandienė J., Cimbalistienė L., Endzinienė M., Nonketotic Hyperglycinemia: the first case in Lithuania. Nacionalinių veiklos, susijusios su retomis ligomis, planų ir strategijų įgyvendinimo aktualijos / The national activities related to rare diseases : programa ir tezės, 2013.11.14, Vilnius. p. 41.
  177. Ginevičienė V., Jakaitienė A., Milašius K., Tubelis L., Kučinskas V., Utkus A.,Variation of the HIF1A and MB Genes in Lithuanian Athletes. 18 th annual Congress of the European College of Sport Science, 26-29 June 2013, Barcelona, Spain, Book of Abstracts, Edited by Balague, N., Torrents, C., Vilanova, A., Cadefau, J., Tarrago, R., Tsolakidis, E., p. 132-133, ISBN 978-84-695-7786-8.
  178. Liaugaudienė, L. Cimbalistienė, Ž. Čiuladaitė, J. Kasnauskienė, E. Preikšaitienė, V. Kučinskas, New critical region for recently defined 4q21 microdeletion syndrome. European Journal of Human Genetics, vol.21, suppl. 2, June 2013, European Human Genetics Conference 2013, June 8 - 11, 2013, Palais des Congrès, Paris, France, Abstracts, P02.015, p.89.
  179. E. Preikšaitienė, A. Molytė, Ž. Čiuladaitė, J. Kasnauskienė, A. Utkus, V. Kučinskas, Phenomic clues to genomic variation in patients with developmental delay or intellectual disability. European Journal of Human Genetics, vol.21, suppl. 2, June 2013, European Human Genetics Conference 2013, June 8 - 11, 2013, Palais des Congrès, Paris, France, Abstracts, P05.088, p.176.
  180. V. Ginevičienė, A. Jakaitienė, K. Milašius, L. Tubelis, V. Kučinskas, A. Utkus, Association of hypoxia inducible factor-1 alpha gene polymorphism with physical performance in Lithuanian athletes. European Journal of Human Genetics, vol.21, suppl. 2, June 2013, European Human Genetics Conference 2013, June 8 - 11, 2013, Palais des Congrès, Paris, France, Abstracts, P16.061, p. 392.
  181. Uktverytė, R. Meškienė, L. Ambrozaitytė, I. Domarkienė, A. Pranculis, N.Burokienė, A. Coj, A. Mažeikienė, V. Kasiulevičius, Z. A. Kučinskienė, V. Kučinskas, LITGEN - revealing genetic structure of the population of Lithuania. European Journal of Human Genetics, vol.21, suppl. 2, June 2013, European Human Genetics Conference 2013, June 8 - 11, 2013, Palais des Congrès, Paris, France, Abstracts, P16.067, p. 394.
  182. Ž. Čiuladaitė, J. Kasnauskienė, Š. Germanas, A. Jakaitienė, V. Kučinskas, A genome -wide survey of copy number variations in population of Lithuania. European Journal of Human Genetics, vol.21, suppl. 2, June 2013, European Human Genetics Conference 2013, June 8 - 11, 2013, Palais des Congrès, Paris, France, Abstracts, J16.93, p. 573.
  183. V. Ginevičienė, A. Jakaitienė, A. Pranculis, K. Milašius, L.Tubelis, V. Kučinskas, A. Utkus, The myoglobin gene A79G polymorphism in Lithuanian athletes. 6th Baltic Scientific Conference Sport Science for Sustainable Society, April 23-25, 2013, Riga, Latvia, Latvian Academy of Sport Education, Abstracts, p. 161-162, ISSN 1691-6220.
  184. Ž. Čiuladaitė, V. Kučinskas, Analysis of rare copy number variants in healthy individuals and individuals with id. Joint Conference of HGM 2013 and 21st International Congress of Genetics GENETICS&GENOMICS of Global Health and Sustainability, 13-18 April 2013, The Sands Expo and Convention Center, Marina Bay Sands, Singapore, Abstract Book, p. 295-296.
  185. L. Cimbalistienė, O. Liaugaudienė, A. Utkus, Familial case of c.413T>C PHEX gene mutation leading to X-linked hypophosphatemic rickets. European Journal of Human Genetics, vol.21, suppl. 2, June 2013, European Human Genetics Conference 2013, June 8 - 11, 2013, Palais des Congrès, Paris, France, Abstracts, J09.27, p.520.
  186. B. Burnytė, G. Brusokienė, Ž. Čiuladaitė, N. Drazdienė, A. Utkus, Ring chromosome 6 in an infant with multiple congenital anomalies. European Journal of Human Genetics, vol.21, suppl. 2, June 2013, European Human Genetics Conference 2013, June 8 - 11, 2013, Palais des Congrès, Paris, France, Abstracts, J02.54, p.485.
  187. Morkūnienė, A. Matulevičienė, L. Ambrozaitytė, R. Meškienė, R. Meškauskas, A. Utkus, Frame shift mutation of the ZMPSTE24 gene in two siblings affected with restrictive dermopathy. European Journal of Human Genetics, vol.21, suppl. 2, June 2013, European Human Genetics Conference 2013, June 8 - 11, 2013, Palais des Congrès, Paris, France, Abstracts, P01.126, p.82.
  188. Birutė Burnytė, Laima Ambrozaitytė, Algirdas Utkus, Juvenile Huntington disease: case report. 12th Conference of Baltic Child Neurology Association (BCNA) 30 May-1 June, 2013, Kaunas. Neurologijos seminarai, T.17, Priedas Nr. 1, Vilnius „Rotas“, 2013, p. S43, ISSN 1392-3064.
  189. Jurecka, Agnieszka, Cimbalistienė Loreta, Gusina, Nina; et al., A Homozygous R152W Mutation is Associated with a Relatively Attenuated Phenotype of Mucopolysaccharidosis Type VI. Conference: 8th Annual World Symposium of the Lysosomal Disease, San Diego, FEB 07-10, 2012 , MOLECULAR GENETICS AND METABOLISM Volume: 105 Issue: 2 Pages: S38-S38 DOI: 10.1016/j.ymgme.2011.11.086 Published: FEB 2012.
  190. Cimbalistienė L., Burnytė B., Songailienė J., Liaugaudienė O., Kučinskas V., Inborn errors of metabolism (IEM) in Lithuania according to the data of center for Medical genetics. Annual Symposium of the Society for the Study of Inborn Errors of Metabolism, Birmingham, UK, 4-7 September 2012, Abstracts, Journal of Inherited Metabolic Disease, vol.35, suppl. 1, September 2012, Springer, p. 167, ISSN 0141-8955.
  191. Cimbalistienė L., Rimkus V., Songailienė J., Kučinskas V., Two-generational alkaptonuria in a non-consanguineous family from Lithuania. Annual Symposium of the Society for the Study of Inborn Errors of Metabolism, Birmingham, UK, 4-7 September 2012, Journal of Inherited Metabolic Disease, Abstracts, vol.35, suppl. 1, September 2012, Springer, p. 32, ISSN 0141-8955.
  192. Jurecka A., Zakharova E., Cimbalistienė L., Gusina N., Kulpanovich A., Golda A., Opoka-Winiarska V., Piotrowska E., Voskoboeva E., Tylki-Szymanska A., Attenuated phenotype in MPS VI (Maroteaux-Lamy) patients carrying the P.R152W mutation. Annual Symposium of the Society for the Study of Inborn Errors of Metabolism, Birmingham, UK, 4-7 September 2012, Abstracts, Journal of Inherited Metabolic Disease, vol.35, suppl. 1, September 2012, Springer, p. 90, ISSN 0141-8955.
  193. Jurecka A., Cimbalistienė L., Gusina N., Malinova V., Roždžynska-Swiątkowska A., Golda A., Kulpanovich A., Kaldenovna Abdilova G., Opoka-Winiarska V., Ounap K., Tylki-Szymanska A. Natural history, incidence and prevalence rates of mucopolysaccharidosis type VI in central and eastern Europe. Annual Symposium of the Society for the Study of Inborn Errors of Metabolism, Birmingham, UK, 4-7 September 2012, Abstracts, Journal of Inherited Metabolic Disease, vol.35, suppl. 1, September 2012, Springer, p. 90, ISSN 0141-8955.
  194. V. Kučinskas, I. Pepalytė, A. Pranculis, L. Bagdonaitė, V. Dženkevičiūtė, Z. A. Kučinskienė. Coronary artery disease genomics: CNV findings in the group of patients from Lithuania. The American Society of Human Genetics 62 nd Annual Meeting, San Francisco, November 6-10, 2012, ashg.org/2012meeting, 920T, p.147.
  195. Pranculis, I. Pepalytė, J. Arasimavičius, Z. A. Kučinskienė, V. Kučinskas. Pharmacogenomics of cardiovascular disease treatment in subjects from the Lithuanian population. The American Society of Human Genetics 62 nd Annual Meeting, San Francisco, November 6-10, 2012, ashg.org/2012meeting, 653T, p.136.
  196. Čiuladaitė, Živilė, Kučinskas, Vaidutis, DNR kopijų skaičiaus pokyčių tyrimas - naujas instrumentas genų kartografavime. Bioateitis: gamtos ir gyvybės mokslų perspektyvos : 2012 m. jaunųjų mokslininkų konferencijos pranešimų santraukos. p. 14.
  197. Molytė, Alma, Uktverytė, Ingrida, Kučinskas, Vaidutis, Kritinė genetinių ir geografinių atstumų analizė pagal Y chromosomos trumpus tandeminius pasikartojimus žmonių populiacijose. Bioateitis: gamtos ir gyvybės mokslų perspektyvos : 2012 m. jaunųjų mokslininkų konferencijos pranešimų santraukos. p. 15.
  198. V. Ginevičienė, A.Jakaitienė, K. Milašius, E. Petkus, L. Tubelis, V. Kučinskas, The impact of gene polymorphisms on Lithuanian elite athlete status and related phenotypes. III International Scientific-Practical Conference "Current scientific, practical and biomedical provision issues of qualified athletes' preparation" within the limits of the Congress „Sports Medicine. Sochi 2012”, Sochi, Russia, 20-23 June, 2012. Book of abstracts, p. 203-207.
  199. V. Ginevičienė, A.Jakaitienė, K. Milašius, E. Petkus, L. Tubelis, V. Kučinskas, Association of genes polymorphisms with physical performance of Lithuanian athletes. International Scientifically-Practical Conference "Regenerative medicine: topikalissues", Kyiv, Ukraine, 4-5 October 2012. Book of abstracts, vol. 18, p. 171-172.
  200. B. Burnytė, A. Utkus, H. Gabriel, V. Kučinskas, KID syndrome: multiple joint contractures in Lithuanian patient with GJB2 gene mutation. European Journal of Human Genetics: European Human Genetics Conference 2012, Niurnberg, Germany, June 23-26, abstracts : vol.20, suppl.1, p. 366.
  201. Alexandrou, J. Hettinger, C. Sismani, M. Badura-Stronka, J. Kasnauskienė, V.Kučinskas, C. Graziano, G. Romeo, A. Kurg, T. Sarkisian, Z. Sedlacek, L. Livshits, P. C. Patsalis, Screening of a European cohort of 150 male XLID patients using a custom-designed chromosome X exon-specific microarray. European Journal of Human Genetics: European Human Genetics Conference 2012, Niurnberg, Germany, June 23-26, abstracts : vol.20, suppl.1, p. 288-289.
  202. Graziano, E. Bonora, J. A. Hettinger, K. Männik, P. Magini, M. Badura-Stronka, E. Õiglane-Slik, J. Kasnauskienė, I. Lebedev, M. Havlovicova, D. Babikyan, L. A. Livshits, T. Sarkisian, A. Latos-Bieleńska, V. Kučinskas, Z. Sedlacek, P. C. Patsalis, A. Kurg, G.Romeo, CHERISH - Improving Diagnoses of Mental Retardation in Children in Eastern Europe and Central Asia through Genetic Characterisation and Bioinformatics/Statistics - a GENOMIC PROJECT. European Journal of Human Genetics: European Human Genetics Conference 2012, Niurnberg, Germany, June 23-26, abstracts : vol.20, suppl.1, p. 272-273.
  203. Uktverytė, M. Li, M. Stoneking, V. Kučinskas, mtDNA haplogroups in the population of Lithuania. European Journal of Human Genetics: European Human Genetics Conference 2012, Niurnberg, Germany, June 23-26, abstracts : vol.20, suppl.1, p. 257.
  204. V. Ginevičienė, A. Jakaitienė, L. Tubelis, V. Kučinskas, Association of ACE, PPARGC1A and PPARA Genotypes with Footballers Performance. European Journal of Human Genetics: European Human Genetics Conference 2012, Niurnberg, Germany, June 23-26, abstracts : vol.20, suppl.1, p. 212.
  205. Kashevarova, E. Tolmacheva, O. Salyukova, P. Magini, C. Graziano, G. Romeo, J.Kasnauskiene, V. Kučinskas, I. Lebedev, Mental retardation, speech delay, attention-deficiency/hyperactivity disorder, and delicate microangiopathy in a boy with 11p13 deletion, European Journal of Human Genetics: European Human Genetics Conference 2012, Niurnberg, Germany, June 23-26, abstracts : vol.20, suppl.1, p.121.
  206. Ž. Čiuladaitė, A. Utkus, J. Kasnauskienė, E. Preikšaitienė, A. Pečiulytė, V.Kučinskas, A de novo interstitial deletion at 1p36.11 in a patient presenting with severe psychomotor delay, sensoneural hearing loss, congenital heart defect and dysmorphic features. European Journal of Human Genetics: European Human Genetics Conference 2012, Niurnberg, Germany, June 23-26, abstracts : vol.20, suppl.1, p.112-113.
  207. Liaugaudienė, L. Cimbalistienė, Ž. Čiuladaitė, J. Kasnauskienė, E.Preikšaitienė, V. Kučinskas, De novo duplication 15q22.21-24 in patient with mental retardation, congenital heart defect and dysmorphic features. European Journal of Human Genetics: European Human Genetics Conference 2012, Niurnberg, Germany, June 23-26, abstracts : vol.20, suppl.1, p.67.
  208. E. Preikšaitienė, J. Kasnauskienė, Ž. Čiuladaitė, B. Tumienė, P. Patsalis, V. Kučinskas, A second case of 7p22.1 microduplication: clinical and molecular characterization. European Journal of Human Genetics: European Human Genetics Conference 2012, Niurnberg, Germany, June 23-26, abstracts : vol.20, suppl.1, p.53.
  209. Uktverytė, O. Balanovsky, S. Frolova, M. Kuznetsova, E. Balanovska, V. Kučinskas, Application of evolving Y chromosome genetic markers for analysis of Lithuanian population. Tarptautinė konferencija „Evoliucinė medicina: nauji senųjų problemų sprendimai”, 2012 m. birželio mėn. 12-15 d., Vilniaus universitetas, Lietuva, p. 46.
  210. Pranculis, I. Pepalytė, J. Arasimavičius, Z.A. Kučinskienė, V. Kučinskas, The evolution of pharmacogenes and their variants in the Lithuanian population. Tarptautinė konferencija „Evoliucinė medicina: nauji senųjų problemų sprendimai”, 2012 m. birželio mėn. 12-15 d., Vilniaus universitetas, Lietuva, p. 42.
  211. Pepalytė, I. Uktverytė, V. Dirsė, V. Kučinskas, Characteristics of the genomic structural variation in the Lithuanian population. Tarptautinė konferencija „Evoliucinė medicina: nauji senųjų problemų sprendimai”, 2012 m. birželio mėn. 12-15 d., Vilniaus universitetas, Lietuva, p. 65.
  212. Ž. Čiuladaitė, V. Kučinskas, Copy number variation: new insights in human genome diversity and intelectual disability. Tarptautinė konferencija „Evoliucinė medicina: nauji senųjų problemų sprendimai”, 2012 m. birželio mėn. 12-15 d., Vilniaus universitetas, Lietuva, p. 28.
  213. Loreta Cimbalistienė, Vytautas Rimkus, Jurgita Songailienė, Vaidutis Kučinskas, Two-generational alkaptonuria in a non-consanguineous family from Lithuania, 11th Baltic Congress of Laboratory Medicine, Vilnius, Radisson Blu Hotel Lietuva, 10-12 May 2012, Laboratorinė medicina, vol. 14, Special Supplement, p. 27, ISSN 1392-6470.
  214. Živilė Čiuladaitė, Jūratė Kasnauskienė, Vaidutis Kučinskas, Array-CGH for the detection of chromosomal imbalances associated with intelectual disability and multiple congenital anomalies, 11th Baltic Congress of Laboratory Medicine, Vilnius, Radisson Blu Hotel Lietuva, 10-12 May 2012, Laboratorinė medicina, vol. 14, Special Supplement, p. 27, ISSN 1392-6470.
  215. Valentina Ginevičienė, Audronė Jakaitienė, Kazys Milašius, Linas Tubelis, Vaidutis Kučinskas, Association of genes polymorphisms with aerobic and anaerobic performance of athletes, 11th Baltic Congress of Laboratory Medicine, Vilnius, Radisson Blu Hotel Lietuva, 10-12 May 2012, Laboratorinė medicina, vol. 14, Special Supplement, p. 31, ISSN 1392-6470.
  216. Raimonda Meškienė, Ingrida Uktverytė, Justas Arasimavičius, Laima Ambrozaitytė, Lina Viniarskaitė, Algimantas Irnius, Vaidutis Kučinskas, Research of the nutritional genomics markers specific in the population of Lithuania, 11th Baltic Congress of Laboratory Medicine, Vilnius, Radisson Blu Hotel Lietuva, 10-12 May 2012, Laboratorinė medicina, vol. 14, Special Supplement, p. 42, ISSN 1392-6470.
  217. Aidas Pranculis, Ingrida Pepalytė, Vilma Dženkevičiūtė, Loreta Bagdonaitė, Vaidutis Kučinskas, Zita Aušrelė Kučinskienė, A family based genomics and pharmacogenomics study of coronary artery disease in the patient group from the Lithuanian population, 11th Baltic Congress of Laboratory Medicine, Vilnius, Radisson Blu Hotel Lietuva, 10-12 May 2012, Laboratorinė medicina, vol. 14, Special Supplement, p. 45, ISSN 1392-6470.
  218. Eglė Preikšaitienė, Vaidutis Kučinskas, Genetic diagnostic workflow for patients with intellectual disability, 11th Baltic Congress of Laboratory Medicine, Vilnius, Radisson Blu Hotel Lietuva, 10-12 May 2012, Laboratorinė medicina, vol. 14, Special Supplement, p. 46, ISSN 1392-6470.
  219. Vytautas Šliužas, Živilė Čiuladaitė, Vaidutis Kučinskas, Frequency of chromosome involvement into major chromosome structure rearrangements, 11th Baltic Congress of Laboratory Medicine, Vilnius, Radisson Blu Hotel Lietuva, 10-12 May 2012, Laboratorinė medicina, vol. 14, Special Supplement, p. 51, ISSN 1392-6470.
  220. Uktverytė, O. Balanovsky, S. A. Frolova, M. A. Kuznetsova, E. V. Balanovska, V. Kučinskas, Analysis of the population of Lithuania using Y chromosome genetic markers, 11th Baltic Congress of Laboratory Medicine, Vilnius, Radisson Blu Hotel Lietuva, 10-12 May 2012, Laboratorinė medicina, vol. 14, Special Supplement, p. 54, ISSN 1392-6470.
  221. V. Kučinskas, J. Kasnauskienė, Ž. Čiuladaitė, E.Preikšaitienė, A. Alexandrou, G. Koumbaris, P. Patsalis, Pathogenic chromosomal aberrations in the families with Mental Retardation and developmental delay detected by array-CGH, (Abstract / Program Cytogenetics. Presented at the 12th International Congress of Human Genetics / 61st Annual Meeting of The American Society of Human Genetics, October 13, 2011, Montreal, Canada), p. 598.
  222. Eglė Preikšaitienė, Jūratė Kasnauskienė, Loreta Cimbalistienė, Živilė Čiuladaitė, Joe A.Hettinger, Carolina Sismani, Philippos C.Patsalis, Vaidutis Kučinskas. De novo 5Q35.3 duplikacija, lemianti Sotos sindromo klinikinį pasireiškimą, Jaunųjų mokslininkų konferencija „Bioateitis: gamtos ir gyvybės mokslų perspektyvos“, pranešimų santraukos, Vinius, 2011, p. 11.
  223. Cimbalistienė L., Songailienė J., Czartoryska B., Kučinskas V., Ruijter G. Excretion of chondroitin sulphate and heparin sulphate in patient with mucopolysacharidosis type VII (sly sindrome) case report, SSIEM Annual Symposium 2011, August 30- September 2, Geneva , Switzerland, Journal of Inherited Metabolic Disease, vol. 34, suppl.3, p. 215.
  224. Ginevičienė V., Jakaitienė A., Milašius K., Tūbelis L., Kučinskas V. Genetic diversity of Lithuanian Football players according to the position of play on the field, 16th Annual Congress of the European College of Sport Science, „New horizons from a world heritage city“, 6-9 July, 2011, Liverpool, United Kingdom, Book of Abstracts, p.571-572, ISBN 978-09568903-0-6.
  225. Ginevičienė V., Jakaitienė A., Milašius K., Tūbelis L., Kučinskas V. Association analysis of the ACE and ACTN3 polymorphisms with physical performance phenotypes in Lithuanian athletes. 4th Baltic conference in exercise and sport sciences, Tartu, Estonia, 7-9 April, 2011, Book of abstracts, vol.16 (suppl), p. 85.
  226. Ginevičienė V., Jakaitienė A., Milašius K., Tubelis L., Kučinskas V. Gene Variants Associated with Physical Performance in Lithuanian Athletes. V International Congress "People, Sport and Health" , Saint-Petersburg, Russia, 21-23 April, 2011, Proceedings of the Congress.
  227. Ginevičienė V., Tūbelis L., Kučinskas V. Genome characteristics of Lithuanian athletes. I International Congress „Medicine for sports“, 2011. Moscow, Russia, 19-20 September, 2011, Book of abstracts (Congress materials), p.130-134.
  228. Ginevičienė V., Pranculis A., Jakaitienė A., Kučinskas V. Genomic diversity and it’s impact on the physical capacity of Lithuanian athletes. II International Scientifically-Practical Conference "The High Technologies, Fundamental and Applied Researches in Physiology, Pharmacology and Medicine". St.- Petersburg, Russia, 26-28 October, 2011, Book of abstracts, p.190-191.
  229. Ž.Čiuladaitė, J.Kasnauskienė, A.Matulevičienė, E.Preikšaitienė, A.Alexandrou, P.C.Patsalis, V.Kučinskas, A microduplication of the critical Rubinstein – Taybi deletion region: a contiguous gene syndrome?, 8th European Cytogenetics Conference, 02-05 July 2011, Porto, Portugal, Chromosome Research, vol.19, suppl.1, p. S61, ISSN 0967-3849.
  230. Matulevičienė, V.Dirsė, V.Kučinskas, Duplication of chromosome 15q22 in patient with severe dysmorphic features. European Journal of Human Genetics: European Human Genetisc Conference 2011, Amsterdam, The Netherlands, May 28-31, abstracts : vol.19, suppl.2, p.83-84.
  231. L.Cimbalistienė, V.Dirsė, V.Kučinskas, Report of a Jacobsen syndrome with a mild facial dysmorphism, severe hearing impairment and thrombocytopenia. European Journal of Human Genetics: European Human Genetisc Conference 2011, Amsterdam, The Netherlands, May 28-31, abstracts : vol.19, suppl.2, p.97-98.
  232. E.Preikšaitienė, J.Kasnauskienė, Ž.Čiuladaitė,V.Dirsė, L.Cimbalistienė, A.Utkus, A.Matulevičienė, B.Tumienė, P.Magini, J.Baptista, P.Patsalis, A.Kurg, V.Kučinskas, Clinical features associated with submicroscopic chromosomal aberrations in patients with mental retardation/developmental delay. European Journal of Human Genetics: European Human Genetisc Conference 2011, Amsterdam, The Netherlands, May 28-31, abstracts : vol.19, suppl.2, p.107.
  233. V.Dirsė, J.Kasnauskienė, A.Utkus, E.Preikšaitienė, Ž.Čiuladaitė, K.Männik, A.Kurg, V.Kučinskas, A de novo 1.8 Mb 17q21.33 microdeletion detected by SNP-CGH in patient with mental retardation and dysmorphic features. European Journal of Human Genetics: European Human Genetisc Conference 2011, Amsterdam, The Netherlands, May 28-31, abstracts : vol.19, suppl.2, p.132-133.
  234. J.Kasnauskienė, Ž. Čiuladaitė, E.Preikšaitienė, J.Hettinger, P.C.Patsalis, V.Kučinskas, De novo deletion 10p14 in patient with mental retardation, speech impairment and hypothyroidism. European Journal of Human Genetics: European Human Genetisc Conference 2011, Amsterdam, The Netherlands, May 28-31, abstracts : vol.19, suppl.2, p.133.
  235. B.Burnytė, A.Matulevičienė, V.Dirsė, V.Kučinskas, Inherited complex mosaicism associated with fragile site at 16q22. European Journal of Human Genetics: European Human Genetisc Conference 2011, Amsterdam, The Netherlands, May 28-31, abstracts : vol.19, suppl.2, p.142.
  236. V.Šliužas, V.Dirsė, Ž.Čiuladaitė, B.Aleksiūnienė, V.Kučinskas, Subtelomeric fluorescence in situ hybridization in clinical cytogenetics: results of analysis of Lithuanian patients, European Journal of Human Genetics: European Human Genetisc Conference 2011, Amsterdam, The Netherlands, May 28-31, abstracts : vol.19, suppl.2, p. 148.
  237. Ž.Čiuladaitė, A.Matulevičienė, J.Kasnauskienė, B.Aleksiūnienė, V.Kučinskas, Small supernumerary marker chromosome derived from chromosome 3 in patient with severe psychomotor developmental delay and dysmorphism. European Journal of Human Genetics: European Human Genetisc Conference 2011, Amsterdam, The Netherlands, May 28-31, abstracts : vol.19, suppl.2, p.150.
  238. V.Ginevičienė, A.Jakaitienė, L.Tubelis, V.Kučinskas, Impact of polygenic profile to the performance of endurance and strength/power athletes. European Journal of Human Genetics: European Human Genetisc Conference 2011, Amsterdam, The Netherlands, May 28-31, abstracts : vol.19, suppl.2, p. 259.
  239. Pranculis, V.Ginevičienė, V.Kučinskas, AGTR1 c. *86A>C and AGT c.620C> T polymorphism genotypes and the aerobic capacity of elite Lithuanian atletes. European Journal of Human Genetics: European Human Genetisc Conference 2011, Amsterdam, The Netherlands, May 28-31, abstracts : vol.19, suppl.2, p. 265.
  240. T.Nikopensius, L.Ambrozaitytė, T.Jagomägi, M.Saag, A.Matulevičienė, V.Kučinskas, A.Metspalu, FN1 and TIMP2 polymorphisms are associated with nonsyndromic cleft lip with or without cleft palate. European Journal of Human Genetics: European Human Genetisc Conference 2011, Amsterdam, The Netherlands, May 28-31, abstracts : vol.19, suppl.2, p. 281.
  241. Pepalytė, K.Grigalionienė, Ž.Petrulionienė, L.Bagdonaitė, Z.A.Kučinskienė, V.Kučinskas, Common genetic variants in ITGA2, IL1B, ALOX5AP, OR13G1, MMP9 genes that participate in oxidative stress and influence atherosclerosis phenotype formation. European Journal of Human Genetics: European Human Genetisc Conference 2011, Amsterdam, The Netherlands, May 28-31, abstracts : vol.19, suppl.2, p. 272.
  242. Uktverytė, O.Balanovsky, S.Frolova, M.Kuznetsova, E.Balanovska, V.Kučinskas, The place of the population of Lithuania between Northern and Eastern Europe: Y chromosome analysis. European Journal of Human Genetics: European Human Genetisc Conference 2011, Amsterdam, The Netherlands, May 28-31, abstracts : vol.19, suppl.2, p. 345.
  243. Živilė Čiuladaitė, Jūratė Kasnauskienė, Agnė Pečiulytė, Philippos Patsalis, Vaidutis Kučinskas. Patogeninių kartotinių sekų reikšmė protinės raidos atsilikimo etiopatogenezėje. IV nacionalinė doktorantų mokslinė konferencija „Mokslas – sveikatai“, 2011, balandžio 7 d., Konferencijų tezių rinkinys, 90-91 p., Kaunas ISBN-9955-15-196-8.
  244. L.Cimbalistienė, B.Tumienė, A.Utkus, V.Kučinskas, H.Brackman, R.Santer. Fanconi- Bickel syndrome: three unrelated cases from Northern and Eastern Europe with the same novel mutation of the SLC2A2 gene. Journal of Inherited Metabolic Disease, 2010, vol.33, suppl. 1, p.70, ISSN:0141-8955.
  245. L.Ambrozaitytė, I.Uktverytė, A.Timinskas, A.Utkus, A.Matulevičienė, V.Kučinskas. Analysis of the variety of sequence variants of SOS1 gene in cleft lip and/or palate patients of Lithuania. The American Society of Human Genetics 60th Annual Meeting, November 2-6, 2010, Washington, poster abstracts: p.295.
  246. J.Kasnauskienė, Ž.Čiuladaitė, A.Alexandrou, G.Koumbaris, P.C.Patsalis, V.Kučinskas. Chromosomal aberrations delineated by aCGH and RT-PCR in the families with Mental Retardation. The American Society of Human Genetics 60th Annual Meeting, November 2-6, 2010, Washington, poster abstracts: p. 381.
  247. V.Kučinskas, V.Dirsė, A.Utkus, E.Preikšaitienė, J.Kasnauskienė, K.Männik, A.Kurg. Genome-wide detection of CNVs in Lithuanian patients with mental retardation. The American Society of Human Genetics 60th Annual Meeting, November 2-6, 2010, Washington, poster abstracts: p. 538.
  248. T.Esko, R.Mägi,, M.Nelis, P.Palta, F.Zimprich, D.Toncheva, M.Macek, l.Peltonen, M.Lathrop, M.Krawczak, T.Meitinger, B.Melegh, D.Toniolo, P.Gasparini, J.Klovins, V. Kučinskas, J.Lubinski, S.Limborska, S.Antonarakis, A.Franke, M.Remm, A.Metspalu. Runs Of Homozygozity in European Outbred Populations and Applications For Genome-Wide Association Analyzes. The American Society of Human Genetics 60th Annual Meeting, November 2-6, 2010, Washington, poster abstracts: p. 808.
  249. V.Kučinskas, Understanding a genome seqence: The genomes of the Lithuanians. International Student’s Conference of Natural Sciences The COINS 2010, Faculty of Natural Sciences Vilnius University, Vilnius, 2010, September 21-25, Lithuania (žodinis pranešimas).
  250. Ambrozaitytė, Laima, Uktverytė, Ingrida, Kasnauskienė, Jūratė, Matulevičienė, Aušra, Kučinskas, Vaidutis, Lūpos ir (arba) gomurio nesuaugimų genominiai tyrimai Lietuvos pacientų grupėje. Mokslas - žmonių sveikatai : 3-oji nacionalinė mokslinė konferencija, 2010 m. balandžio 7 d.: pranešimų tezės. ISBN 9789955151784 p. 68.
  251. L.Cimbalistienė, V.Šliužas, V.Kučinskas, Report of a patient with a 46, XY, 9p- constitution due to a paternal t(5;9) translocation. European Journal of Human Genetics: European Human Genetisc Conference 2010, Gothenburg, Sweden, 2010, June 12-15, abstracts : vol.18, suppl.1, p. 113.
  252. T.Esko, G.Escramis, R.Rabionet, P.Palta, F.Zimprich, D.Toncheva, M.Macek, L.Peltonen, B.Melegh, D.Toniolo, P.Gasparini, J.Klovins, V.Kučinskas, J.Lubinski, S.Limborska, S.E.Antonarakis, C.M. van Duijn, M.Remm, X.Estivill, A.Metspalu, Copy number variable regions in 13 European populations. European Journal of Human Genetics: European Human Genetisc Conference 2010, Gothenburg, Sweden, 2010, June 12-15, abstracts : vol.18, suppl.1, p. 32 (žodinis pranešimas).
  253. Ginevičienė, Valentina, Milašius, Kazys, Kučinskas, Vaidutis, Sportininkų individualaus genomo įvertinimas svarbus sporto teorijai, praktikai ir medicinai. Mokslas - žmonių sveikatai : 3-oji nacionalinė mokslinė konferencija, 2010 m. balandžio 7 d.: pranešimų tezės. ISBN 9789955151784 p. 15.
  254. V.Ginevičienė, L.Tubelis, V.Kučinskas, The effect of peroxisome proliferator– activated receptors polymorphisms on the physical performance of Lithuanian athletes. European Journal of Human Genetics: European Human Genetisc Conference 2010, Gothenburg, Sweden, 2010, June 12-15, abstracts : vol.18, suppl.1, p. 210.
  255. C.Graziano, E.Bonora, P.Magini, J.Baptista, G.Tortora, S.Miccoli, P.C.Patsalis, J.A.Hettinger, V.Anastasiadou, L.Kousoulidou, A.Kurg, K.Mnnik, S.Parkel, O.Zilina, m.Noukas, E.Oiglane-Slik, V.Kučinskas, J.Kasnauskienė, I.Labedev, A.Latos-Bielenska, M.Badura-Stronka, B.Budny, Z.Sedlacek, M.Havlovicova, M.Vlckova, M.Hancarova, T.Sarkisian, D.Babikyan, S.Midyan, L.A.Livshits, A.Cuppoletti, G.Romeo, CHERISH-Improving Diagnoses of Mental Retardation in Children in Eastern Europe and Central Asia through Genetic Characterisation and Bioinformatics/Statistics. European Journal of Human Genetics: European Human Genetisc Conference 2010, Gothenburg, Sweden, 2010, June 12-15, abstracts : vol.18, suppl.1, p. 86.
  256. Kasnauskienė, Jūratė, Grigalionienė, Kristina, Ambrozaitytė, Laima, Kučinskienė, Z.A., Kučinskas, Vaidutis, Mutations and SNPs spectrum for monogenic and common disorders in Lithuania: creation strategy for diagnostic and prognostic testing. Human Variome Project Implementation  Integration Meeting, 10 th – 14 th May 2010 UNESCO Paris France.
  257. Matulevičienė, B.Aleksiūnienė, V.Dirsė, V.Kučinskas, A de novo partial trisomy of distal 6p in patient with severe dysmorphic features. European Journal of Human Genetics: European Human Genetisc Conference 2010, Gothenburg, Sweden, 2010, June 12-15, abstracts : vol.18, suppl.1, p. 73.
  258. E.Preikšaitienė, L.Cimbalistienė, P.Magini, V.Kučinskas, Mental retardation in a patient with 14q32.33 and 19p13.3 microdeletions characterized using array-based CGH. European Journal of Human Genetics: European Human Genetisc Conference 2010, Gothenburg, Sweden, 2010, June 12-15, abstracts : vol.18, suppl.1, p. 119.
  259. Pranculis, V.Ginevičienė, V.Kučinskas, Association of ACTN3 genetic variants with physical performance of Lithuanian athletes. European Journal of Human Genetics: European Human Genetisc Conference 2010, Gothenburg, Sweden, 2010, June 12-15, abstracts : vol.18, suppl.1, p. 201.
  260. V.Šliužas, Ž.Čiuladaitė, V.Kučinskas, Chromosomes involment in to chromosomal structure rearrangemens frequency in Lithuania. European Journal of Human Genetics: European Human Genetisc Conference 2010, Gothenburg, Sweden, 2010, June 12-15, abstracts : vol.18, suppl.1, p. 110.
  261. V.Dirsė, Ž.Čiuladaitė, A.Utkus, K.Männik, A.Kurg, V.Kučinskas, Structural rearrangements of chromosome 8p23.1-p23.3 related to mental retardation. European Journal of Human Genetics: European Human Genetisc Conference 2010, Gothenburg, Sweden, 2010, June 12-15, abstracts : vol.18, suppl.1, p. 119.
  262. Cimbalistienė L., Kasnauskienė J., Blau N., Kučinskas V. The first case of DHPR deficiency in Lithuania. MOLECULAR GENETICS AND METABOLISM. 2009, vol 98, iss. 1-2, p. 21-21, ISSN: 1096-7192.
  263. Cimbalistienė L., Smirnova M., Zamkauskienė D., Kasnauskienė J., Kučinskas V. Results of Mass neonatal Screening in Lithuania. JOURNAL OF INHERITED METABOLIC DISEASE. 2005, vol. 28, suppl. 1, p. 5-5, ISSN: 0141-8955. (Įtraukta į ISI 2009 m).
  264. Metspalu A., Nelis M., Magi R., Palta P., Zimprich F., Toncheva D., Peltonen L., Lathrop M., Meitinger T., Melegh B., Toniolo D., Gasparini P., Klovins J., Kučinskas V., Lubinsky J., Limborska S., Estivill X., Antonarakis S., van Duijn C., Macek M., Krawczak M., Remm M., Esko T. Genetic Variation Based on SNPs, CNVs and RoHs in European Populations. The American Society of Human Genetics Conference , 59th Annual Meeting, 2009,Honolulu, Havaii, October 20-24.
  265. Kučinskas V., Grigalionienė K., Laucevičius A., Kučinskienė Z.A. Association studies of candidate genes involved in oxidative stress regulation pathways in Lithuanian population. The American Society of Human Genetics Conference , 59th Annual Meeting, 2009, Honolulu, Havaii, October 20-24.
  266. Tumienė B., Drazdienė N., Kučinskas V., Dallapiccola B. Congenital craniolacunia without any associated developmental defect. European Human Genetics Conference 2009, Vienna, Austria, May 23-26, European Journal of Human Genetics: vol.17, suppl. 2, p. 60.
  267. Matulevičienė A., Ambrozaitytė L., Preikšaitienė E., Utkus A., Linkevičienė L., Aleksiūnienė B., Dagytė E., Čiuladaitė Ž., Šliužas V., Kučinskas V. Spectrum of oral clefts in the light of contemporary research study. European Human Genetics Conference 2009, Vienna, Austria, May 23-26, European Journal of Human Genetics: vol.17, suppl. 2, p.74.
  268. Aleksiūnienė B., Utkus A., Kučinskas V. A de novo double translocations 3;14 and 6;20 in a patient with mental retardation and microcephaly. European Human Genetics Conference 2009, Vienna, Austria, May 23-26, European Journal of Human Genetics: vol.17, suppl. 2, p.128.
  269. Kasnauskienė J., Krasovskaja N., Kučinskas V. Rapid prenatal of chromosome aneuploidy by QT-PCR. European Human Genetics Conference 2009, Vienna, Austria, May 23-26, European Journal of Human Genetics: vol.17, suppl. 2, p. 164.
  270. Ambrozaitytė L., Matulevičienė A., Kučinskas V. Investigation of three candidate genes in the cleft lip and/or palate patients group of Lithuania. European Human Genetics Conference 2009, Vienna, Austria, May 23-26, European Journal of Human Genetics: vol.17, suppl. 2, p.237.
  271. Ginevičienė V., Kasnauskienė J., Kučinskas V. The PPARGC1A G1444A polymorphism in Lithuanian professional athletes and the general population. European Human Genetics Conference 2009, Vienna, Austria, May 23-26, European Journal of Human Genetics: vol.17, suppl. 2, p23.
  272. Cimbalistienė, Loreta, Songailienė, Jurgita, Czartoryska, Barbara, Kučinskas, Vaidutis. Phenotype variability in six cases with MPS VI in Lithuania. Journal of inherited metabolic disease. 2008, vol. 31, suppl. 1 p. 123.
  273. Kučinskas, Vaidutis, Ambrozaitytė, Laima, Matulevičienė, Aušra, Preikšaitienė, Eglė. Scan of 640 SNPs of 43 candidate cleft lip or palate genes in the nonsyndromic cleft lip or palate patients of Lithuania. ASHG 58th annual meeting, Philadelphia, November 11-15, 2008 : abstracts. Philadelphia, 2008 p. 391.
  274. Cimbalistienė, Loreta, Lehnert, Willy, Huoponen, Kirsi, Kučinskas, Vaidutis. A case of lysinuric protein intolerance presenting with hepatosplenomegaly. Journal of inherited metabolic disease. 2008, vol. 31, suppl. 1 p. 107.
  275. Kučinskas, Vaidutis, Grigalionienė, Kristina, Timinskas, Albertas, Laucevičius, Aleksandras, Kučinskienė, Zita Aušrelė. Association study of susceptibility to atherosclerosis and myocardial infarction using 150 genetics markers. Genetics - understanding living systems : XX international congress of genetics, Berlin, July 12-17, 2008 : abstract book. Berlin, 2008 p. 107.
  276. Aleksiūnienė, Beata, Krasovskaja, Natalija, Kučinskas, Vaidutis. Prenatal findings: a foetus with trisomy of 22 chromosome. European journal of human genetics : European human genetics conference 2008, Barcelona, Spain, 2008, May 31 - June 3 : abstracts. 2008, vol. 16, suppl. 2 p. 167.
  277. Ambrozaitytė, Laima, Matulevičienė, Aušra, Kučinskas, Vaidutis. Association study of microsattelite markers of five candidate loci in the cleft lip and palate patients of Lithuania. European journal of human genetics : European human genetics conference 2008, Barcelona, Spain, 2008, May 31 - June 3 : abstracts. 2008, vol. 16, suppl. 2 p. 300.
  278. Ambrozaitytė, Laima, Kasnauskienė, Jūratė, Uktverytė, Ingrida, Šliužas, Vytautas, Matulevičienė, Aušra, Preikšaitienė, Eglė, Utkus, Algirdas, Kučinskas, Vaidutis. Genomic investigation of Lithuanian patients with cleft lip and/or palate. Stomatologija. 2008, t. 10, suppl. 5 : 3-oji Baltijos šalių odontologijos mokslinė konferencija, 2008 m. lapkričio 6-8 d., Vilnius p. 14-15.
  279. Cimbalistienė, Loreta, Černiauskienė, Vilija, Kučinskas, Vaidutis. The first case of Berardinelli-Seip congenital lypodystrophy reported in Lithuania. European journal of human genetics : European human genetics conference 2008, Barcelona, Spain, 2008, May 31 - June 3 : abstracts. 2008, vol. 16, suppl. 2 p. 94.
  280. Dagytė, Evelina, Cimbalistienė, Loreta, Kučinskas, Vaidutis. A girl with ring chromosome 5. European journal of human genetics : European human genetics conference 2008, Barcelona, Spain, 2008, May 31 - June 3 : abstracts. 2008, vol. 16, suppl. 2 p. 163.
  281. Gabriel, H., Kukučkova, M., Utkus, Algirdas, Kučinskas, Vaidutis, Lott, A., Gencik, M. Multi-copy amplification of the exon 2 of the dystrophin gene in a Duchenne muscular dystrophy patient: a new approach by Oligo-Array-CGH. European journal of human genetics : European human genetics conference 2008, Barcelona, Spain, 2008, May 31 - June 3 : abstracts. 2008, vol. 16, suppl. 2 p. 400-401.
  282. Ginevičienė, Valentina, Kasnauskienė, Jūratė, Kučinskas, Vaidutis. The ACE I/D polymorphism in Lithuanian professional athletes. European journal of human genetics: European human genetics conference 2008, Barcelona, Spain, 2008, May 31 – June 3: abstracts. 2008, vol. 16, suppl. 2 p. 363.
  283. Janavičius, Ramūnas, Kasnauskienė, Jūratė, Kučinskas, Vaidutis. Novel and common BRCA1 mutations in familial breast/ovarian cancer patients from Lithuania. European journal of human genetics : European human genetics conference 2008, Barcelona, Spain, 2008, May 31 - June 3 : abstracts. 2008, vol. 16, suppl. 2 p. 199.
  284. Kučinskas, Vaidutis, Grigalionienė, Kristina, Timinskas, Albertas, Laucevičius, Aleksandras, Kučinskienė, Zita Aušrelė. Association study of susceptibility to atherosclerosis and myocardial infarction using 150 genetics markers. Genetics - understanding living systems : XX international congress of genetics, Berlin, July 12-17, 2008 : abstract book. Berlin, 2008 p. 107.
  285. Preikšaitienė, Eglė, Matulevičienė, Aušra, Utkus, Algirdas, Kučinskas, Vaidutis. Clinical heterogeneity in cases of oral clefts with multiple congenital anomalies. European journal of human genetics : European human genetics conference 2008, Barcelona, Spain, 2008, May 31 - June 3 : abstracts. 2008, vol. 16, suppl. 2 p. 112-113.
  286. Matulevičienė, Aušra, Aleksiūnienė, Beata, Krasovskaja, Natalija, Preikšaitienė, Eglė, Kučinskas, Vaidutis. Rare unbalenced aberration of chromosome 18 in patient with severe dysmorphic features and poor prognosis. European journal of human genetics : European human genetics conference 2008, Barcelona, Spain, 2008, May 31 - June 3 : abstracts. 2008, vol. 16, suppl. 2 p. 152.
  287. Kučinskas, Vaidutis, Grigalionienė, Kristina, Kasnauskienė, Jūratė, Laucevičius, Aleksandras, Kučinskienė, Zita Aušrelė. Association studies of atherogenesis candidate gene involved in oxidative stress regulation and oxidative homeostasis pathways. 5th international symposium on genetics, health and disease, February 17-19, 2008, Amritsar (India) : abstracts. Amritsar, 2008 p. 21.
  288. Tumienė, Birutė, Cimbalistienė, Loreta, Jakutovič, Marija, Černiauskienė, Vilija, Songailienė, Jurgita, Czartoryska B., Malecka J., Beck M., Kučinskas, Vaidutis. Six cases of mucolipidoses II and III: Range of clinical severity and previously not described symptoms. Journal of inherited metabolic disease. 2007, vol. 30, suppl. 1. ISSN 0141-8955 p. 100-101.
  289. Matulevičienė, Aušra, Aleksiūnienė, Beata, Krasovskaja, Natalija, Kučinskas, Vaidutis. Down syndrome as a result of a 3:1 segregation of t(5,21) in the mother. Conference Information: 6th European Cytogenetics Conference, JUL 07-10, 2007 Istanbul, TURKEY. Chromosome research. 2007, vol. 15, suppl. 1. ISSN 0967-3849 p. 45-46.
  290. Matulevičienė, Aušra, Songailienė, Jurgita, Bierau, J., Kučinskas, Vaidutis, Spaapen, L. Severe neurological symptoms conceal inheritable disorder caused by partial deficiency of hypoxanthine-guanine phosphoribosyltransferase as Lesch Nyhan syndrome variant - The first case detected in Lithuania. Journal of inherited metabolic disease. 2007, vol. 30, suppl. 1. ISSN 0141-8955 p. 135.
  291. Cimbalistienė, Loreta, Jakutovič, Marija, Tumienė, Birutė, Songailienė, Jurgita, Kučinskas, Vaidutis. alpha-Mannosidosis presenting with two different clinical phenotypes. Journal of inherited metabolic disease. 2007, vol. 30, suppl. 1. ISSN 0141-8955 p. 112.
  292. Aleksiūnienė, Beata, Cimbalistienė, Loreta, Zarakauskaitė, Eglė, Kučinskas, Vaidutis. Down-Turner syndrome: a case report. Conference Information: 6th European Cytogenetics Conference, JUL 07-10, 2007 Istanbul, TURKEY. Chromosome research. 2007, vol. 15, suppl. 1. ISSN 0967-3849 p. 47.
  293. Šliužas V., Cimbalistenė L., Kučinskas V. Terminal deletion of chromosome 18q in a patient with multiple congenital malformations including mental retardation. Conference Information: 6th European Cytogenetics Conference, JUL 07-10, 2007 Istanbul, TURKEY, CHROMOSOME RESEARCH, 2007, vol 15 p. 54-55 : Suppl. 1 ISSN 0967-3849.
  294. Aleksiūnienė, Beata, Janavičius, Ramūnas, Cimbalistienė, Loreta, Kučinskas, Vaidutis. Phenotypic characteristics of 9p deletion syndrom: a case report. European journal of human genetics: European human genetics conference 2007, Nice, France, 2007, June 16-19. 2007, vol. 15, suppl. 1. ISSN 1018-4813 p. 106.
  295. Kirchengast S., Kučinskas, Vaidutis. Importance of old and new genetic/genomic markers in understanding of population structure and main microevolutionary forces in its formation. Antropologija ir medicinos praktika: tarptautinė mokslinė konferencija, Vilnius, 2007 rugsėjo 20-26 d. = Antropology and medical practice.
  296. Končiūtė, Kristina, Kučinskas, Vaidutis, Janavičius, Ramūnas, Kučinskienė, Zita Aušrelė, Timinskas, Albertas, Allele frequencies for 150 genetic markers of oxidative stress and myocardial infarction in Lithuania. European journal of human genetics: European human genetics conference 2007, Nice, France, 2007, June 16-19. 2007, vol. 15, suppl. 1. ISSN 1018-4813 p. 300.
  297. Krasovskaja, Natalija, Benušienė, Eglė, Butkevičienė, Eglė, Kučinskas, Vaidutis. Prenatal diagnosis of chromosomal abnormalities in Lithuania. European journal of human genetics: European human genetics conference 2007, Nice, France, 2007, June 16-19. 2007, vol. 15, suppl. 1. ISSN 1018-4813 p. 132.
  298. Kučinskas, Vaidutis, Končiūtė, Kristina, Utkus, Algirdas. Cystic fibrosis studies: an individual spectrum of CFTR gene mutations in Lithuania. European journal of human genetics: European human genetics conference 2007, Nice, France, 2007, June 16-19. 2007, vol. 15, suppl. 1. ISSN 1018-4813 p. 188.
  299. Matulevičienė, Aušra, Aleksiūnienė, Beata, Zarakauskaitė, Eglė, Kučinskas, Vaidutis. The patient with severe dysmorphic features and chromosomes abnormality with unidentified marker. European journal of human genetics: European human genetics conference 2007, Nice, France, 2007, June 16-19. 2007, vol. 15, suppl. 1. ISSN 1018-4813 p. 56.
  300. Morkūnienė, Aušra, Ambrozaitytė, Laima, Utkus, Algirdas, Kučinskas, Vaidutis. IRF6 gene’s nucleotide sequence changies in patients with nonsyndromic orofacial clefting from Lithuania. European journal of human genetics: European human genetics conference 2007, Nice, France, 2007, June 16-19. 2007, vol. 15, suppl. 1. ISSN 1018-4813 p. 206.
  301. Songailienė, Jurgita, Matulevičienė, Aušra, Bierau J., Kučinskas, Vaidutis, Spaapen L. Partial hypoxanthine-guanine phosphoribosyltransferase deficiency as Lesch-Nyhan syndrome variant - the first case detected in Lithuania. European journal of human genetics: European human genetics conference 2007, Nice, France, 2007, June 16-19. 2007, vol. 15, suppl. 1. ISSN 1018-4813 p. 203.
  302. Zarakauskaitė, Eglė, Matulevičienė, Aušra, Utkus, Algirdas, Linkevičienė, Laura, Kučinskas, Vaidutis. Orofacial clefts with associated anomalies in Lithuania. European journal of human genetics: European human genetics conference 2007, Nice, France, 2007, June 16-19. 2007, vol. 15, suppl. 1. ISSN 1018-4813 p. 81.
  303. Tumienė, Birutė, Utkus, Algirdas, Čerkauskienė, Rimantė, Becker R., Reardon W., Janavičius, Ramūnas, Songailienė, Jurgita, Spaapen L.J.M., Kučinskas, Vaidutis. Dental symptoms - clue to the diagnosis of hypophosphatasia of childhood type. European journal of human genetics: European human genetics conference 2007, Nice, France, 2007, June 16-19. 2007, vol. 15, suppl. 1. ISSN 1018-4813 p. 67.
  304. Kučinskas, Vaidutis, Končiūtė, Kristina, Utkus, Algirdas. Cystic fibrosis studies: an individual spectrum of CFTR gene mutations in Lithuania. European journal of human genetics: European human genetics conference 2007, Nice, France, 2007, June 16-19. 2007, vol. 15, suppl. 1. ISSN 1018-4813 p. 188.
  305. Kasnauskienė, Jūratė, Kučinskas, Vaidutis, Steponavičiūtė, Danguolė. Training non-MD medical geneticists: suggestions from Lithuania. European journal of human genetics: European human genetics conference 2007, Nice, France, 2007, June 16-19. 2007, vol. 15, suppl. 1. ISSN 1018-4813 p. 328.
  306. Janavičius, Ramūnas, Kasnauskienė, Jūratė, Ostapenko, Valerijus, Kučinskas, Vaidutis. Adaptation of hereditary breast/ovarian cancer genetic counselling and testing service in Lithuania. European journal of human genetics: European human genetics conference 2007, Nice, France, 2007, June 16-19. 2007, vol. 15, suppl. 1. ISSN 1018-4813 p. 158.
  307. Cimbalistienė, Loreta, Lehnert, Willy, Huoponen, K., Kučinskas, Vaidutis. A case of lysinuric protein intolerance presenting with hepatosplenomegaly. Laboratorinė medicina. 2006, nr. 1 : 8th Baltic Congress of laboratory medicine, Vilnius 2006. ISSN 1392-6470 p. 19.
  308. Utkus A., Končiūtė K., Tulevičienė B. J., Kučinskas V. Two cases with progressive movement disorder: form undiagnosed condition to confirming juvenile form of Huntington‘s disease. European Human Genetics Conference 2006, European meeting on Psychosocial Aspects of Genetics. RAI Congress Center Amsterdam, The Netherlands, Saturday May 6 – Tuesday May 9, 2006. European Journal of Human Genetics, 2006 vol 14 Suppl 1 ISSN 1018-4813 p. 130-131.
  309. Kučinskas V., Steponavičiūtė D., Morkūnienė A., Chung M., Šliužas V., Chen Y. J., Linkevičienė L., Utkus A. Investigation of the genetics basis of oral-facial clefting in humans. European Human Genetics Conference 2006, European meeting on Psychosocial Aspects of Genetics. RAI Congress Center Amsterdam, The Netherlands, Saturday May 6 – Tuesday May 9, 2006. European journal of human genetics. 2006, vol. 14, suppl. 1. ISSN 1018-4813 p. 348.
  310. Butkevičienė E., Krasovskaja N., Kučinskas V. The meaning of informed consent for congenital anomalies after IVF. European Human Genetics Conference 2006, European meeting on Psychosocial Aspects of Genetics. RAI Congress Center Amsterdam, The Netherlands, Saturday May 6 – Tuesday May 9, 2006. European journal of human genetics. 2006, vol. 14, suppl. 1. ISSN 1018-4813 p. 113.
  311. Aleksiūnienė B., Matulevičienė A., Kučinskas V. The familial reciprocal translocation t (2;6) (q21; p25) associated with wide spectrum of phenotypic signs – from normal to severe malformations. European Human Genetics Conference 2006, European meeting on Psychosocial Aspects of Genetics. RAI Congress Center Amsterdam, The Netherlands, Saturday May 6 – Tuesday May 9, 2006. European journal of human genetics. 2006, vol. 14, suppl. 1. ISSN 1018-4813 p. 185.
  312. Matulevičienė A., Aleksiūnienė B., Zarakauskaitė E., Kučinskas V. The partial trisomy for the distal short arm of chromosome 6 (region pter→p21) in a girl with psychomotor development delay and dysmorphic features. European Human Genetics Conference 2006, European meeting on Psychosocial Aspects of Genetics. RAI Congress Center Amsterdam, The Netherlands, Saturday May 6 – Tuesday May 9, 2006. European journal of human genetics. 2006, vol. 14, suppl. 1. ISSN 1018-4813 p. 122.
  313. Cimbalistienė L., Šliužas V., Tumienė B., Kučinskas V. Two different chromosomal anomalies in siblings: Klinefelter sindrome and del (18) (q21). European human genetics Conference 2006, European meeting on Psychosocial Aspects of Genetics. RAI Congress Center Amsterdam, The Netherlands, Saturday May 6 – Tuesday May 9, 2006. European Journal of Human Genetics, vol. 14, suppl. 1. ISSN 1018-4813 p. 113.
  314. Kučinskas V., Steponavičiūtė D., Andrulionis G. The Value of Free and Informed Consent in Genomic research and Development of Personalized Medicine // International IIth Congress of Human Genetics, August 6-10, 2006 Brisbane Australia. p. 320.
  315. Kučinskas V., Steponavičiūtė D., Morkūnienė A., Chung M. Y., Šliužas V., Chen Y. J., Linkevičienė L., Utkus A. Locating Genes for Oral-Facial Clefting in humans // International symposium on Human Genomics and Public health and XXXI Annual Conference of Indian sodiety of Human Genetics. NATIONAL Centre of Applied Genetics School of Life Sciences, Jawaharlal Nehru university, New Delhi, February 27 – March 1, 2006. Program and abstracts volume, 1(29), p. 7-8.
  316. Aleksiūnienė B., Matulevičienė A., Kučinskas V. Three Different Balanced translocations Present the Same Phenotypic Signs of Down Sindrome // Laboratorinė medicina. 2006, nr. 1 : 8th Baltic Congress of laboratory medicine, Vilnius 2006. ISSN 1392-6470 p. 16.
  317. Dagytė E., Aleksiūnienė B., Krasovskaja N., Kučinskas V. Rezults of Cytogenetic Prenatal Diagnosis in Lithuania from 2002-2005 // Laboratorinė medicina. 2006, nr. 1 : 8th Baltic Congress of laboratory medicine, Vilnius 2006. ISSN 1392-6470 p. 19.
  318. Dagytė E., Utkus A., Kučinskas V. A Girl with Familial Unbalanced Translocation der (14)t(10;14)(q26.1;q13) mat // Laboratorinė medicina. 2006, nr. 1 : 8th Baltic Congress of laboratory medicine, Vilnius 2006. ISSN 1392-6470 p. 19.
  319. Končiūtė K., Morkūnienė A., Kasnauskienė J., Kučinskas V. Identification of BCR-ABL Translocation using RT-PCR Technique for Diagnosis of CML and All // Laboratorinė medicina. 2006, nr. 1 : 8th Baltic Congress of laboratory medicine, Vilnius 2006. ISSN 1392-6470 p. 31.
  320. Matulevičienė A., Aleksiūnienė B., Kučinskas V. The Familial Reciprocal translocation i(8;10) (q24.1;q21.3) Associated with Spectrum of Phenotypic Signs of Trichorhinophalangeal sindrome, Type I // Laboratorinė medicina. 2006, nr. 1 : 8th Baltic Congress of laboratory medicine, Vilnius 2006. ISSN 1392-6470 p. 35.
  321. Morkūnienė A., Končiūtė K., Kasnauskienė J., Kučinskas V. QF-PCR in Prenatal diagnosis of Fetal 13, 18, 21 Chromosomal Aneuploidies // Laboratorinė medicina. 2006, nr. 1 : 8th Baltic Congress of laboratory medicine, Vilnius 2006. ISSN 1392-6470 p. 35.
  322. Smirnova M., Kasnauskienė J., Songailienė J., Kučinskas V. Results of Mass neonatal Screening in Lithuania // Laboratorinė medicina. 2006, nr. 1 : 8th Baltic Congress of laboratory medicine, Vilnius 2006. ISSN 1392-6470 p. 46.
  323. Steponavičiūtė D., Kučinskas V. Problems in Genetic Testing in Lithuania // Laboratorinė medicina. 2006, nr. 1 : 8th Baltic Congress of laboratory medicine, Vilnius 2006. ISSN 1392-6470 p. 47.
  324. Šliužas V., Kučinskas V. Application of Comparative Genomic hybridization (CGH) in Patiems with Syndromic Malformations // Laboratorinė medicina. 2006, nr. 1 : 8th Baltic Congress of laboratory medicine, Vilnius 2006. ISSN 1392-6470 p. 47.
  325. Kučinskas V., Šliužas V., Utkus A., Cimbalistienė L. Mosaic chromosome 21 abnormality in the patient with syndromic cleft lip and cleft palate. CHROMOSOME RESEARCH, 2005 vol: 13 p: 41-41 Suppl. 1.
  326. Končiūtė K., Utkus A., Kučinskas V. 90% CFTR gene mutations identified in cystic fibrosis patients from Lithuania: two novel frameshift mutations // 8th International Symposium for Cystic fibrosis, Prague, Czech Republic, 4-5 February, 2005. Program and Abstracts, Abstract 15.
  327. Cimbalistienė L., Vasiliauskienė I., Tumienė B., Kučinskas V. A diagnosis of LCHAD deficiency made 8 years after a child’s death // European Human Genetics Conference 2005. Prague, Czech Republic, May 7-10, 2005. European Journal of Human Genetics, vol. 13, Suppl. 1, Abstract P0037, p. 88. ISSN 1018-4813.
  328. Posmyk R., Panasiuk B., Latos-Bielenska A., Wolnik-Brzozowska D., Piotrowicz M., Kučinskas V., Korniszewski L., Kozak-Klonowska B., Sorbaj-Sucharska G., Midro A.T. A quantitative definition of monosomy 5p syndrome // European Human Genetics Conference 2005. Prague, Czech Republic, May 7-10, 2005. European Journal of Human Genetics, vol. 13, Suppl. 1, Abstract P0176, p. 117. ISSN 1018-4813.
  329. Utkus A., Linkevičienė L., Kučinskas V. Oral clefts: associations with epidemiological and clinical characteristics among newborns in Lithuania, 1993-1997 // European Human Genetics Conference 2005. Prague, Czech Republic, May 7-10, 2005. European Journal of Human Genetics, vol. 13, Suppl. 1, Abstract P0194, p. 121. ISSN 1018-4813.
  330. Matulevičienė A., Kučinskas V. An eleven year old girl from Northern Lithuania with confirmed early-onset torsion dystonia // European Human Genetics Conference 2005. Prague, Czech Republic, May 7-10, 2005. European Journal of Human Genetics, vol. 13, Suppl. 1, Abstract P0254, p. 134. ISSN 1018-4813.
  331. Benušienė E., Kučinskas V. Prenatal diagnosis of Osteogenesis imperfecta in Lithuania // European Human Genetics Conference 2005. Prague, Czech Republic, May 7-10, 2005. European Journal of Human Genetics, vol. 13, Suppl. 1, Abstract P0435, p. 173. ISSN 1018-4813.
  332. Kasnauskienė J., Mikštienė V., Kučinskas V. Mutation screening in MSX1 gene in non-syndromic cleft lip and palate patients // European Human Genetics Conference 2005. Prague, Czech Republic, May 7-10, 2005. European Journal of Human Genetics, vol. 13, Suppl. 1, Abstract P0780, p. 248. ISSN 1018-4813.
  333. Končiūtė K., Utkus A., Kučinskas V. Two novel CFTR gene mutations identified in cystic fibrosis patients from Lithuania: can the 4171insCCTA mutation be associated with low sweat chloride level? // European Human Genetics Conference 2005. Prague, Czech Republic, May 7-10, 2005. European Journal of Human Genetics, vol. 13, Suppl. 1, Abstract P0827, p. 259. ISSN 1018-4813.
  334. Morkūnienė A., Utkus A., Kasperavičiūtė D., Linkevičienė L., Kučinskas V. Linking TGFA gene to Cleft Lip with or without Cleft Palate // European Human Genetics Conference 2005. Prague, Czech Republic, May 7-10, 2005. European Journal of Human Genetics, vol. 13, Suppl. 1, Abstract P1092, p. 318. ISSN 1018-4813.
  335. Kučinskas V., Andrulionis G., Steponavičiūtė D. The meaning of free and informed consent in biomedical research personalizing medicine // Personalized Medicine Europe: Health, Genes and Society. Tel Aviv, Israel, June 19-21, 2005. Personalized Medicine, vol. 2, No. 2, 2005. ISSN 1741-0541 p. 158.
  336. Barzda A., Kučinskas V., Bartkevičiūtė R., Abaravičius A., Krasauskienė A., Olechnovič M. Iodine dietary patterns in Lithuanian population. Annals of nutritions & metabolism: abstracts of 18th international congress of nutrition, September 19-23, 2005, South Africa. Basel : Karger, 2005, p. 155.
  337. Cimbalistienė L., Smirnova M., Zamkauskienė D., Kasnauskienė J., Kučinskas V. Results of mass neontal screening in Lithuania // Journal of inherited metabolic disease. ISSN 0141-8955. 2005, vol. 28, suppl. 1, p. 5. (2009 įtraukta į ISI).
  338. Kučinskas V., Morkūnienė A., Kasperavičiūtė D., Utkus A., Linkevičienė L. Linking candidate-genes to orofacial clefts in Lithuania population // The American society of human genetics 55th annual meeting: abstracts, October 25-29, 2005, USA, p. 300.
  339. Kučinskas V. Genomo įvairovė: lietuviai Europoje // Lietuvių genomo kilmė: [konferencijos pranešimų santraukos]. Vilnius : Lietuvos Mokslų akademijos leidykla, 2005, p. 3-4.
  340. Kučinskienė, Zita Aušrelė, Kučinskas, Vaidutis, Laucevičius, Aleksandras, Steponavičiūtė, Danguolė. Atherogen study in Lithuania: pathogenetic mechanisms of atherosclerosis determined by human genome diversity // Advances in cardiology research: molecular and genetic bases of cardiovascular diseases: program and abstracts. Bratislava, 2005, p. 27.
  341. Kasperavičiūtė D., Stoneking M., Kučinskas V. Genetic composition of the Lithuanians revealed by mitochondrial DNA and Y chromosome variation // Human Genome Meeting 2004. Berlin, Germany, April 4-7, 2004, Abstract 373, p. 141.
  342. Kasperavičiūtė D., Stoneking M., Kučinskas V. Genetic components of the Lithuanian population revealed by mitochondrial and Y chromosome variation // 200 Years of Lithuanian Anthropology: Modern Trends, History, Relation to Medical Practice and Humanities. Vilnius, Lithuania, October 27-29, 2004. p. 39.
  343. Benušienė E., Kučinskas V. Spectrum of mutations in COL1A1 gene and genotype-phenotype correlation in 79 patients with osteogenesis imperfecta // The 7th Baltic Congress in Laboratory Medicine. Pärnu, Estonia, September 9-11, 2004. p. 99.
  344. Juščienė D., Zamkauskienė D., Kučinskas V. Screening for congenital hypothyroidism used as an indicator for assessing the degree of iodine deficiency in Lithuania // The 7th Baltic Congress in Laboratory Medicine. Pärnu, Estonia, September 9-11, 2004. p. 110.
  345. Kasperavičiūtė D., Stoneking M., Kučinskas V. Genetic composition of the Lithuanians revealed by mitochondrial DNA and Y chromosome variation // Human Genome Meeting 2004. Berlin, Germany, April 4-7, 2004, Abstract 373, p. 141.
  346. Kučinskas, Vaidutis, Kasperavičiūtė, Dalia, Ambrasienė, Daiva, Stoneking, Mark. Y chromosome and mitochondrial DNA variation and the origin of Lithuanians / American journal of human genetics. 2003, vol. 73, no. 5, suppl.. ISSN 0002-9297 p. 379.
  347. Kučinskas V., Kasperavičiūtė D., Ambrasienė D., Stoneking M. Analysis of mitochondrial DNA and Y chromosome diversity in Lithuanian population // Eur J Hum Genet, 2003, vol. 11, suppl. 1, abstract P840, p. 244.
  348. Kučinskas V., Kasperavičiūtė D., Ambrasienė D., Stoneking M. Mitochondrial DNA and Y chromosome diversity and origins of Lithuanians // XIX International Congress of Genetics. Genomes-the Linkage to Life. Abstracts and Posters, 2003. Australia.
  349. Kasperavičiūtė D., Kučinskas V. Analysis of mitochondrial DNA and Y chromosome in Lithuanian population // Genetics of Complex Diseases and Isolated Populations. Book of Abstracts. Tortoli’, Sardinia, Italy, 23–30 May 2003, poster 53, p. 19.
  350. Kučinskas V., Benušienė E. Nine novel COLA1 gene mutations in Lithuanian patients with osteogenesis imperfecta // Human Genome Meeting 2003, Cancun, Mexico, April 27-30, 2003. Programme and Abstract book: Cancun, 2003, p. 59.
  351. Kasperavičiūtė D., Kučinskas V. Human mitochondrial DNA control region sequence variations in Lithuanian population, Conference Information: European-Society-of-Human-Genetics European Human Genetics Conference in Conjuction With European Meeting on Psychosocial Aspects of Genetics, MAY 25-28, 2002 STRASBOURG, FRANCE, EUROPEAN JOURNAL OF HUMAN GENETICS vol: 10 p: 175-175 suppl. 1, ISSN 1018-4813.
  352. Kasnauskienė, Jūratė, Cimbalistienė, Loreta, Kučinskas, Vaidutis. PAH gene mutations identified in Lithuania. European journal of human genetics. 2002, vol. 10: European Human Genetics Conference 2002 in conjunction with the European meeting on psychosocial aspects of genetics 2002, May 25-29, Strasbourg, p. 238.
  353. Benušienė, Eglė, Kučinskas, Vaidutis, Slibinskas, Rimantas, Kasperavičiūtė, Dalia. Clinical and molecular characterisation of osteogenesis imperfecta in patients from Lithuania. European journal of human genetics. 2002, vol. 10, suppl. 1. ISSN 1018-4813 p. 242.
  354. Kučinskas, Vaidutis, Steponavičiūtė, Danguolė, Giannattasio, Sergio, Lugovska, Rita, Zschocke, Johannes. Quality assurance in molecular genetic testing in a monogenic disease: lessons from testing in phenylketonuria / Laboratorinė medicina. 2002, spec. nr. ISSN 1392-6470 p.20.
  355. Ambrasienė D., Kučinskas V. Population data of Y-chromosomal STRs in the Lithuanian population // European Journal of Human Genetics, 2002, vol. 10, suppl. 1, p. 176.
  356. Jusienė R., Cimbalistienė L., Juščienė D., Kučinskas V. Psychological problems of children with inherited diseases // The 3d Genetical Congress of Baltic States, Vilnius, Lithuania, October 10-12, 2002. Program and abstracts; Vilnius, 2002, p. 48-49.
  357. Steponavičiūtė D., Kučinskas V. External quality assessment schemes in molecular genetic testing. EQA-PKU // The 3d Genetical Congress of Baltic States, Vilnius, Lithuania, October 10-12, 2002. Program and abstracts; Vilnius, 2002, p. 49.
  358. Kasnauskienė J., Cimbalistienė L., Kučinskas V. A molecular survey of phenylketonuria in Lithuania: identification of spectrum and frequency of PAH gene mutations // The 3d Genetical Congress of Baltic States, Vilnius, Lithuania, October 10-12, 2002. Program and abstracts; Vilnius, 2002, p.50.
  359. Benušienė E., Kučinskas V. Screening for mutations in collagen I coding genes // The 3d Genetical Congress of Baltic States, Vilnius, Lithuania, October 10-12, 2002. Program and abstracts; Vilnius, 2002, p.50.
  360. Ambrasienė D., Kučinskas V. Genetic diversity analysis of the Lithuanian human population using Y-chromosome molecular markers // The 3d Genetical Congress of Baltic States, Vilnius, Lithuania, October 10-12, 2002. Program and abstracts; Vilnius, 2002, p.51.
  361. Kučinskas V., Giannattasio S., Lugovska R., Steponavičiūtė D., Zschocke J. Quality assurance in molecular genetic testing in phenylketonuria // The 18th International Congress of Clinical Chemistry and Laboratory Medicine, Kyoto, Japan, October 20-25, 2002. Poster Abstracts; Kyoto, 2002, p. S144.
  362. Kučinskas V., Steponavičiūtė D. External quality assessment in molecular genetic testing // The 6th Baltic Congress for Laboratory Medicine, Riga, Latvia, May 30 – June 1, 2002. Abstracts Volume; Riga, 2002, p. 14.
  363. Kasnauskienė J., Cimbalistienė L., Kučinskas V. PAH gene mutations identified in Lithuanian PKU patients // The 6th Baltic Congress for Laboratory Medicine, Riga, Latvia, May 30 – June 1, 2002. Abstracts Volume; Riga, 2002, p. 35.
  364. Ambrasienė D., Kučinskas V. Genetic analysis of the Y-chromosomal STR loci in the Lithuanian population // The 6th Baltic Congress for Laboratory Medicine, Riga, Latvia, May 30 – June 1, 2002. Abstracts Volume; Riga, 2002, p. 39.
  365. Kasperavičiūtė, Dalia, Kučinskas, Vaidutis. Human mitochondrial DNA control region sequence variations in Lithuanian population / European journal of human genetics. 2002, vol. 10, suppl. 1. ISSN 1018-4813 p. 175.
  366. Kasperavičiūtė, Dalia, Kučinskas, Vaidutis, Features of the human mitochondrial DNA control region sequences in two Lithuanian etnolinguistic subgroups / Molecular ecology, evolution and systematics : conference abstractbook, Birštonas, Lithuania, April 20-23, 2002. p. 20-21.
  367. Ambrasienė, Daiva, Kučinskas, Vaidutis. The investigation of genetic variability of the Lithuanian human population by using Y chromosome molecular markers / Molecular ecology, evolution and systematics : conference abstractbook, Birštonas, Lithuania, April 20-23, 2002. p. 10-11.
  368. Kučinskas, Vaidutis, Benušienė, Eglė, Kasperavičiūtė, Dalia, Slibinskas, Rimantas. Identification of novel mutations in the COL1A1 gene / American journal of human genetics. 2001, vol. 69, no 4. ISSN 0002-9297 p. 593.
  369. Cimbalistienė L., Kučinskas V., Vasiliauskienė I., Lehnert W. The first four cases of ornithine transcarbamylase deficiency detected in Lithuania / 6th International Conference of Baltic Child Neurology Association, Kaunas, Lithuania, June 13-16, 2001 // 6th International Conference of Baltic Child Neurology Association. Program and Abstracts 2001, p. 94.
  370. Utkus A., Jurgelevičius V., Kučinskas V. Autosomal recessive syndrome of cerebellar ataxia and hypogonadotropic hypogonadism / 6th International Conference of Baltic Child Neurology Association, Kaunas, Lithuania, June 13-16, 2001 // 6th International Conference of Baltic Child Neurology Association. Program and Abstracts; Kaunas, 2001, p. 176.
  371. Jurgelevičius V., Kučinskas V., Cimbalistienė L. Pattern of deletions in the dystrophin gene Duchenne/Becker muscular dystrophy in patients from Lithuania / 6th International Conference of Baltic Child Neurology Association, Kaunas, Lithuania, June 13-16, 2001 // 6th International Conference of Baltic Child Neurology Association. Program and Abstracts 2001, p. 178.
  372. Jusiene R., Cimbalistiene L., Kučinskas V. Psychosocial problems of Lithuanian PKU children / 7th European Congress of Psychology, London, UK, July 1-6, 2001 // / 7th European Congress of Psychology. Book of Abstracts; London, 2001, p.149.
  373. Ambrasienė D., Kučinskas V. Analysis of the biallelic Y-chromosome polymorphisms in the Lithuanian population // EUROMEDLAB 2001, Prague, Chec Republic, May 26–31, 2001. Clin. Chem. Lab. Med., 2001, vol. 39, special supplement, p. S 304, abstract No. PO-Q003.
  374. Benušienė E., Utkus A., Butkevičienė E., Kučinskas V., Bartsch O. Familial report of unbalanced X;22 translocation // 12th Fetal Cell Workshop, Prague, Czech Republic, May 12–13, 2001 / Satellite Symposium of the 10th International Congress of Human Genetics 2001, Vienna, Austria, May 15–19, 2001. Abstract Book, p. 77.
  375. Ambrasienė D., Kučinskas V. Y chromosomal polymorphisms in two Lithuanian ethnolinguistic subgroups // 10th International Congress of Human Genetics 2001, Vienna, Austria, May 15–19. Eur. J. Hum. Genet., 2001, vol. 9, Supplement 1, p. 292, Abstract No. P0985.
  376. Kučinskas V., Jurgelevičius V., Steponavičiūtė D., Giannattasio S., Lattanzio P., Marra E., Lugovska R., Pronina N., Zschocke J. Molecular genetic testing in phenylketonuria: a model to assess the quality control system for monogenic disease // 10th International Congress of Human Genetics 2001, Vienna, Austria, May 15–19. Eur. J. Hum. Genet., 2001, vol. 9, Supplement 1, p. 299, Abstract No. P1020.
  377. Benušienė E., Kasperavičiūtė D., Kučinskas V. Mutation analysis in patients with osteogenesis imperfecta: identification of five novel mutatons // 10th International Congress of Human Genetics 2001, Vienna, Austria, May 15–19. Eur. J. Hum. Genet., 2001, vol. 9, Supplement 1, p. 300, Abstract No. P1024.
  378. Kasperavičiūte D., Ambrasienė D., Arčiulienė J.-V., Kučinskas V. A novel nonsense mutation in the RP1 gene causing autosomal dominant retinitis pigmentosa in a Lithuanian family // 10th International Congress of Human Genetics 2001, Vienna, Austria, May 15–19. Eur. J. Hum. Genet., 2001, vol. 9, Supplement 1, p. 392, Abstract No. P1482.
  379. Kasnauskienė J., Cimbalistienė L., Kučinskas V. Rare mutations in PKU patients from Lithuania // 10th International Congress of Human Genetics 2001, Vienna, Austria, May 15–19. Eur. J. Hum. Genet., 2001, vol. 9, Supplement 1, p. 406, Abstract No. P1556.
  380. Kasnauskienė J., Kučinskas V. Eight rare mutations in PKU patients from Lithuania. In: Programme and Abstract Book / HGM2001 Human Genome Meeting. Edinburgh, Scotland, April 19–22, 2001. Abstract No. 56, p. 16.
  381. Kučinskas, Vaidutis, Kaubrys, Gintaras Ferdinandas, Budrys, Valmantas, Jatužis, Dalius, Mameniškienė, Rūta, Songailienė, Jurgita, Kučinskienė, Zita Aušrelė, Alzeimer’s disease and vascular dementia: relationship to apolipoprotein E genotype and athereosclerosis /, Journal of the neurological sciences. 2001, vol. 187, suppl. 1: Abstracts of the XVII World Congress of Neurology, London, 17-22 June, 2001, [P0148]. ISSN 0022-510X.
  382. Budrys, Valmantas, Kaubrys, Gintaras Ferdinandas, Jatužis, Dalius, Mameniškienė, R., Songailienė, Jurgita, Kučinskienė, Zita Aušrelė, Kučinskas, Vaidutis. Vascular dementia and ishemic cerebrovascular disease: relationship to apolipoprotein E e2 allele and atherosclerosis severity /, Journal of the neurological sciences. 2001, vol. 187, suppl. 1: Abstracts of the XVII World Congress of Neurology, London, 17-22 June, 2001, [P0149]. ISSN 0022-510X.
  383. Ambrasienė, Daiva, Kučinskas, Vaidutis. Population data of Y- chromosomal STRs in the Lithuanian population, The second European-American intensive course in clinical and forensic genetics: final program and abstracts, September 3-14, 2001, Dubrovnik, Croatia.
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