VU Medicinos fakulteto autoriaus 'Beata Aleksiūnienė' publikacijų sąrašas

2022
1 Aleksiūnienė, Beata; Krasovskaja, Natalija; Benušienė, Eglė; Baronas, Karolis; Grigalionienė, Kristina; Meškienė, Raimonda; Utkus, Algirdas; Matulevičienė, Aušra. Familial cases with GPC3 mutations from Lithuanian cohort with overgrowth syndromes // EuroDysmorpho 2022: 32th European meeting on dysmorphology, September 14-17, 2022, Barcelona, Spain: abstract book : ERN-ITHACA. 2022, p. 34-35. Prieiga per internetą: <https://ern-ithaca.eu/wp-content/uploads/2022/09/ABSTRACT-BOOK-V4.pdf>.
2 Aleksiūnienė, Beata; Cimbalistienė, Loreta; Utkus, Algirdas. Novel SMARCA4 mutation identified in a patient with a mild phenotype of Coffin-Siris syndrome // European journal of human genetics: Abstracts from the 54th European Society of Human Genetics (ESHG) conference, August 28-31, 2021: e-Posters. London : Springer Nature. ISSN 1018-4813. eISSN 1476-5438. 2022, vol. 30, suppl. 1, art. no. P11.116.B, p. 364. DOI: 10.1038/s41431-021-01026-1. [DB: Science Citation Index Expanded (Web of Science)] [IF: 5.200; AIF: 5.050; Q1 (2022 InCities JCR SCIE)]

2021
1 Aleksiūnienė, Beata; Cimbalistienė, Loreta; Utkus, Algirdas. Novel SMARCA4 mutation identified in a patient with a mild phenotype of Coffin-Siris syndrome // ESHG 2021: virtual conference, August 28-31 : European Society of Human Genetics. 2021, p. [1]. Prieiga per internetą: <https://www.abstractsonline.com/pp8/#!/10372/presentation/1139>.
2 Šiaurytė, Kamilė; Aleksiūnienė, Beata; Matulevičienė, Aušra. Unknown case with complex heart, neurological and skeletal pathology // EuroDysmorpho 2021: 31th European meeting on dysmorphology, September 23-25, 2021, online: abstract book. 2021, p. 80.

2020
1 Aleksiūnienė, Beata; Tumienė, Birutė; Strupaitė-Šileikienė, Rasa; Utkus, Algirdas. Congenital bilateral iris coloboma in a patient with 16q23.1q23.2 deletion // European journal of human genetics: Abstracts from the 53rd European Society of Human Genetics (ESHG) Conference: e-Posters. London : Springer. ISSN 1018-4813. eISSN 1476-5438. 2020, vol. 28, suppl. 1, art. no. E-P02.04, p. 807. DOI: 10.1038/s41431-020-00741-5. [DB: Science Citation Index Expanded (Web of Science), Scopus] [IF: 4.246; AIF: 5.241; Q2 (2020 InCities JCR SCIE)]
2 Maldžienė, Živilė; Vaitėnienė, Evelina Marija; Aleksiūnienė, Beata; Utkus, Algirdas; Preikšaitienė, Eglė. A case report of familial 4q13.3 microdeletion in three individuals with syndromic intellectual disability // BMC medical genomics. London : BioMed Central Ltd. eISSN 1755-8794. 2020, vol. 13, iss. 1, art. no. 63, p. [1-6]. DOI: 10.1186/s12920-020-0711-4. [DB: Embase, Biological Abstracts, MEDLINE, Scopus, Science Citation Index Expanded (Web of Science)]
3 Aleksiūnienė, Beata; Tumienė, Birutė; Strupaitė-Šileikienė, Rasa; Utkus, Algirdas. Congenital bilateral iris coloboma in a patient with 16q23.1q23.2 deletion // ESHG 2020.2 - Live in Your Living Room : Virtual conference : June 6–9, 2020, Berlin, Germany / European Society for Human Genetics (ESHG). Berlin : European Society for Human Genetics (ESHG). 2020, abstract no. E-P02.04, p. 1. Prieiga per internetą: <https://www.abstractsonline.com/pp8/#!/9102/presentation/2355>.

2019
1 Maldžienė, Živilė; Bulanovaitė, Elena; Aleksiūnienė, Beata; Utkus, Algirdas; Preikšaitienė, Eglė. 16p13.11-p12.3 microdeletion identified in a patient with sagittal craniosynostosis and developmental delay // Clinical dysmorphology. Philadelphia : Wolters Kluwer Health, Inc. ISSN 0962-8827. eISSN 1473-5717. 2019, vol. 28, no. 4, p. 195-197. DOI: 10.1097/MCD.0000000000000285. [DB: MEDLINE, Scopus, Science Citation Index Expanded (Web of Science)] [IF: 0.521; AIF: 4.091; Q4 (2019 InCities JCR SCIE)]
2 Braždžiūnaitė, Deimantė; Burnytė, Birutė; Cimbalistienė, Loreta; Tumienė, Birutė; Preikšaitienė, Eglė; Bikauskaitė-Valčiukė, Liucija; Maldžienė, Živilė; Dagytė, Evelina; Aleksiūnienė, Beata; Matulevičienė, Aušra; Utkus, Algirdas. Wolf-Hirschhorn syndrome: clinical and genetic data analysis of Lithuanian patients // European journal of human genetics: vol. 27, suppl. 2: Abstracts from the 52nd European Society of Human Genetics (ESHG) Conference: Posters. London : Nature Publishing Group. ISSN 1018-4813. eISSN 1476-5438. 2019, vol. 27, suppl. 2, p. 1896. DOI: 10.1038/s41431-019-0493-3. [DB: Scopus, Science Citation Index Expanded (Web of Science)] [IF: 3.657; AIF: 4.393; Q2 (2019 InCities JCR SCIE)]
3 Matulevičienė, Aušra; Burnytė, Birutė; Kavaliauskienė, Ingrida; Meškienė, Raimonda; Matulevičiūtė, R.; Aleksiūnienė, Beata; Ambrozaitytė, Laima; Utkus, Algirdas; Kučinskas, Vaidutis. Variable expressivity of the c.749 C > G mutation in the FGFR3 gene in two unrelated families of Muenke syndrome // European journal of human genetics: Abstracts from the 50th European Society of Human genetics conference: electronic posters. London : Springer. ISSN 1018-4813. eISSN 1476-5438. 2019, vol. 26, suppl., art. no. E-P04.14, p. 871-872. DOI: 10.1038/s41431-018-0248-6. [DB: Science Citation Index Expanded (Web of Science)] [IF: 3.657; AIF: 4.393; Q2 (2019 InCities JCR SCIE)]
4 Aleksiūnienė, Beata; Matulevičienė, Aušra; Ambrozaitytė, Laima; Jakutis, Virginijus; Utkus, Algirdas. Hypoplastic right ventricle, dysmorphic features and brain structural anomalies in a patient with a de novo 1p36.33p36.32 deletion // European journal of human genetics: Abstracts from the 50th European Society of Human genetics conference: electronic posters. London : Springer. ISSN 1018-4813. eISSN 1476-5438. 2019, vol. 26, suppl., art. no. E-P05.16, p. 879-880. DOI: 10.1038/s41431-018-0248-6. [DB: Science Citation Index Expanded (Web of Science)] [IF: 3.657; AIF: 4.393; Q2 (2019 InCities JCR SCIE)]
5 Blažytė, Evelina Marija; Šiaurytė, Kamilė; Matulevičienė, Aušra; Ambrozaitytė, Laima; Aleksiūnienė, B.; Burnytė, Birutė; Preikšaitienė, Eglė; Dagytė, Evelina; Tumienė, Birutė; Mikštienė, Violeta; Benušienė, Eglė; Krasovskaja, Natalija; Cimbalistienė, Loreta; Utkus, Algirdas. Genotype-phenotype analysis in 22q11.2 deletion/duplication groups // European journal of human genetics: vol. 27, suppl. 2: abstracts from the 52nd European Society of Human Genetics (ESHG) Conference. London : Springer. ISSN 1018-4813. eISSN 1476-5438. 2019, vol. 27, suppl. 2, p. 1869-1870. DOI: 10.1038/s41431-019-0493-3. [DB: Scopus, Science Citation Index Expanded (Web of Science)] [IF: 3.657; AIF: 4.393; Q2 (2019 InCities JCR SCIE)]
6 Dagytė, Evelina; Matulevičienė, Aušra; Ambrozaitytė, Laima; Laimutė, Rita; Aleksiūnienė, Beata; Burnytė, Birutė; Utkus, Algirdas. 15q13.3 microdeletion and microduplication in patients with neurodevelopment disorders // European journal of human genetics: Conference: 51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG), Milan, Italy, June 16-19, 2018. London : Nature Publishing Group. ISSN 1018-4813. eISSN 1476-5438. 2019, vol. 27, suppl. 1, art. no. P08.03C, p. 210-211. Prieiga per internetą: <https://www.nature.com/articles/s41431-019-0404-7> [žiūrėta 2021-03-09]. [DB: Science Citation Index Expanded (Web of Science)] [IF: 3.657; AIF: 4.393; Q2 (2019 InCities JCR SCIE)]
7 Blažytė, Evelina Marija; Samsonė, Viltė Gabrielė; Matulevičienė, Aušra; Aleksiūnienė, Beata; Burnytė, Birutė; Dagytė, Evelina; Tumienė, Birutė; Utkus, Algirdas. The spectrum of associated congenital malformations in Down syndrome: a retrospective Lithuanian cohort study // European journal of human genetics: Conference: 51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG), Milan, Italy, June 16-19, 2018. London : Nature Publishing Group. ISSN 1018-4813. eISSN 1476-5438. 2019, vol. 27, suppl. 1, art. no. E-P05.10, p. 920. Prieiga per internetą: <https://www.nature.com/articles/s41431-019-0408-3.pdf> [žiūrėta 2021-04-22]. [DB: Science Citation Index Expanded (Web of Science)] [IF: 3.657; AIF: 4.393; Q2 (2019 InCities JCR SCIE)]
8 Aleksiūnienė, Beata; Tumienė, Birutė; Utkus, Algirdas. AHDC1 gene truncating 1p36.11p35.3 microdeletion in a patient with developmental delay, dysmorphic features and congenital heart defects // European journal of human genetics: Conference: 51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG), Milan, Italy, June 16-19, 2018. London : Nature Publishing Group. ISSN 1018-4813. eISSN 1476-5438. 2019, vol. 27, suppl. 1, art. no. E-P11.09, p. 978. Prieiga per internetą: <https://www.nature.com/articles/s41431-019-0408-3.pdf> [žiūrėta 2021-04-22]. [DB: Science Citation Index Expanded (Web of Science)] [IF: 3.657; AIF: 4.393; Q2 (2019 InCities JCR SCIE)]

2018
1 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. ISSN 1392-6470. 2018, T. 20, Spec. suppl. p. S18. Prieiga per internetą: <https://www.balm2018.lt/wp-content/uploads/2018/05/Lab_Med_2018_SPEC.pdf> [žiūrėta 2018-06-19]. [DB: Index Copernicus]
2 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. ISSN 1392-6470. 2018, T. 20, Spec. suppl. p. S18. Prieiga per internetą: <https://www.balm2018.lt/wp-content/uploads/2018/05/Lab_Med_2018_SPEC.pdf> [žiūrėta 2018-06-19]. [DB: Index Copernicus]
3 Braždžiūnaitė, Deimantė; Laimutė, Rita; Aleksiūnienė, Beata; Dagytė, Evelina; Ambrozaitytė, Laima; Benušienė, Eglė; Cimbalistienė, Loreta; Utkus, Algirdas. Molecular karyotyping: clinical utility and practice // Laboratorinė medicina. Vilnius : Lietuvos laboratorinės medicinos draugija. ISSN 1392-6470. 2018, T. 20, nr. 1, p. 115. [DB: Index Copernicus]
4 Aleksiūnienė, Beata; Preikšaitienė, Eglė; Morkūnienė, Aušra; Ambrozaitytė, Laima; Utkus, Algirdas. A de novo 1q22q23.1 interstitial microdeletion in a girl with intellectual disability and multiple congenital anomalies including congenital heart defect // Cytogenetic and genome research. Basel : Karger Publishers. ISSN 1424-8581. eISSN 1424-859X. 2018, vol. 154, no 1, p. 1-6. DOI: 10.1159/000486947. [IF: 1.423; AIF: 4.963; Q4 (2018 InCities JCR SCIE)]
5 Blažytė, Evelina Marija; Samsonė, Viltė Gabrielė; Matulevičienė, Aušra; Aleksiūnienė, Beata; Burnytė, Birutė; Dagytė, Evelina; Tumienė, Birutė; Utkus, Algirdas. The spectrum of associated congenital malformations in Down syndrome: a retrospective Lithuanian cohort study // European human genetics conference 2018 in conjunction with the European meeting on psychosocial aspects of genetics, Milan, Italy, June 16 - 19. Milan : ESHG. 2018, abstract no. E-P05.10, p. [1]. Prieiga per internetą: <http://www.abstractsonline.com/pp8/#!/4652/presentation/4399> [žiūrėta 2018-07-26].
6 Aleksiūnienė, Beata; Tumienė, Birutė; Utkus, Algirdas. AHDC1 gene truncating 1p36.11p35.3 microdeletion in a patient with developmental delay, dysmorphic features and congenital heart defects // European human genetics conference 2018 in conjunction with the European meeting on psychosocial aspects of genetics, Milan, Italy, June 16 - 19. Milan : ESHG. 2018, abstract no. E-P11.09, p. [1]. Prieiga per internetą: <http://www.abstractsonline.com/pp8/#!/4652/presentation/4798> [žiūrėta 2018-07-25].
7 Dagytė, Evelina; Matulevičienė, Aušra; Ambrozaitytė, Laima; Laimutė, Rita; Aleksiūnienė, Beata; Burnytė, Birutė; Utkus, Algirdas. 15q13.3 microdeletion and microduplication in patients with neurodevelopment disorders // European human genetics conference 2018 in conjunction with the European meeting on psychosocial aspects of genetics, Milan, Italy, June 16 - 19. Milan : ESHG. 2018, p. [1]. Prieiga per internetą: <http://www.abstractsonline.com/pp8/#!/4652/presentation/1772> [žiūrėta 2018-07-25].
8 Vaišvilas, Mantas; Dirsė, Vaidas; Aleksiūnienė, Beata; Tamulienė, Indrė; Cimbalistienė, Loreta; Utkus, Algirdas; Rascon, Jelena. Acute pre-B lymphoblastic leukemia and congenital anomalies in a child with a de novo 22q11.1q11.22 duplication // Balkan journal of medical genetics. Scopje : Macedonian Academy of Sciences and Arts. ISSN 1311-0160. 2018, vol. 21, iss. 1, p. 87-91. DOI: 10.2478/bjmg-2018-0002. [DB: MEDLINE, Scopus, Science Citation Index Expanded (Web of Science)] [IF: 0.769; AIF: 3.940; Q4 (2018 InCities JCR SCIE)]
9 Aleksiūnienė, Beata; Ambrozaitytė, Laima; Molytė, Alma; Kučinskas, Vaidutis; Utkus, Algirdas. 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. 2018, p. 12. Prieiga per internetą: <http://www.lma.lt/uploads/2017-12-07_BIOATEITIS_pranesimu_santraukos.pdf> [žiūrėta 2019-01-22].
10 Braždžiūnaitė, Deimantė; Burnytė, Birutė; Aleksiūnienė, Beata; Grigalionienė, Kristina; Ambrozaitytė, Laima; Norkūnienė, V.; Utkus, Algirdas. A case of syndromic split hand/foot malformation type 1 with de novo 7q21.3 deletion // European journal of human genetics: Abstracts from the 50th European Society of human genetics conference: posters, Copenhagen, Denmark, May 27–30, 2017. London : Springer. ISSN 1018-4813. eISSN 1476-5438. 2018, vol. 26, suppl., art. no. P11.109A, p. 502. DOI: 10.1038/s41431-018-0247-7. [DB: Science Citation Index Expanded (Web of Science)] [IF: 3.650; AIF: 4.178; Q2 (2018 InCities JCR SCIE)]

2017
1 Aleksiūnienė, Beata; Matulevičiūtė, Rugilė; Matulevičienė, Aušra; Burnytė, Birutė; Krasovskaja, Natalija; Ambrozaitytė, Laima; Mikštienė, Violeta; Dirsė, Vaidas; Utkus, Algirdas; Kučinskas, Vaidutis. Opposite chromosome constitutions due to a familial translocation t(1;21)(q43;q22) in 2 cousins with development delay and congenital anomalies: a case report // Medicine (Baltimore). Philadelphia : Lippincott Williams & Wilkins. ISSN 0025-7974. eISSN 1536-5964. 2017, Vol. 96, no 16, Art. no e6521 [p. 1-6]. DOI: 10.1097/MD.0000000000006521. [DB: Science Citation Index Expanded (Web of Science), Scopus, CAB Abstracts, Embase, MEDLINE] [IF: 2.028; AIF: 4.640; Q2 (2017 InCities JCR SCIE)]
2 Šliužas, Vytautas; Aleksiūnienė, Beata; Dagytė, Evelina; Ambrozaitytė, Laima; Tumienė, Birutė; Burnytė, Birutė; Utkus, Algirdas. 16p11.2 microdeletion and microduplication in two Lithuanian patients with speech delay // European human genetics conference 2017, Copenhagen, Denmark, May 27-30. Copenhagen : ESHG. 2017, abstract no. E-P11.01. Prieiga per internetą: <http://www.abstractsonline.com/Plan/ViewAbstract.aspx?sKey=b92ea822-f3b4-480e-9df7-6a4f558bd64c&cKey=b6069b02-982c-46c4-8f03-f0b2b77c5ebd&mKey={15A3630E-7769-4D64-A80A-47F190AC2F4F}> [žiūrėta 2017-09-27].
3 Braždžiūnaitė, Deimantė; Burnytė, Birutė; Aleksiūnienė, Beata; Grigalionienė, Kristina; Ambrozaitytė, Laima; Norkūnienė, Valerija; Utkus, Algirdas. A case of syndromic split hand/foot malformation type 1 with de novo 7q21.3 deletion // European human genetics conference 2017, Copenhagen, Denmark, May 27-30. Copenhagen : ESHG. 2017, abstract no. P11.109A, [1 p.]. Prieiga per internetą: <http://www.abstractsonline.com/Plan/ViewAbstract.aspx?sKey=5ceff91c-a4bf-4aba-bcc0-877da2315b85&cKey=6f21b67d-3233-4580-98e3-13d0ad6261f3&mKey={15A3630E-7769-4D64-A80A-47F190AC2F4F}> [žiūrėta 2017-09-28].
4 Aleksiūnienė, Beata; Matulevičienė, Aušra; Ambrozaitytė, Laima; Jakutis, Virginijus; Utkus, Algirdas. Hypoplastic right ventricle, dysmorphic features and brain structural anomalies in a patient with a de novo 1p36.33p36.32 deletion // European human genetics conference 2017, Copenhagen, Denmark, May 27-30. Copenhagen : ESHG. 2017, abstract no. E-P05.16. Prieiga per internetą: <http://www.abstractsonline.com/Plan/ViewAbstract.aspx?sKey=93d402d3-cf3b-4df4-9e30-3de4ac5a135f&cKey=8b454268-9c3d-4e31-902e-06f2510a147b&mKey=15a3630e-7769-4d64-a80a-47f190ac2f4f> [žiūrėta 2017-10-02].
5 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 // European human genetics conference 2017, Copenhagen, Denmark, May 27-30. Copenhagen : ESHG. 2017, abstract no. E-P04.14. Prieiga per internetą: <http://www.abstractsonline.com/Plan/ViewAbstract.aspx?sKey=bba53598-181c-4525-a44f-643ebb9088e3&cKey=1d10f7e1-d9cf-4da2-910b-aad3dc1b6308&mKey=15a3630e-7769-4d64-a80a-47f190ac2f4f> [žiūrėta 2017-10-03].

2016
1 Aleksiūnienė, Beata; Ambrozaitytė, Laima; Utkus, Algirdas. Comparative whole genome hybridisation methods in molecular diagnostics // Eesti arst. Tartu : Eesti Arstide Liit. ISSN 0235-8026. 2016, Vol. 95, Suppl. 1, p. 33. [DB: Embase, INIS Collection Search]
2 Preikšaitienė, Eglė; Maldžienė, Živilė; Aleksiūnienė, Beata; Kučinskas, Vaidutis. Mild intellectual disability, congenital heart defect and skeletal abnormalities in three patients with 4q13.3 microdeletion // European journal of human genetics: The European Human Genetics Conference, 2016, May 21-24, Barcelona, Spain : abstracts book. London : Nature Publishing Group. ISSN 1018-4813. eISSN 1476-5438. 2016, vol. 24, e-suppl.1, p. 224. Prieiga per internetą: <https://www.eshg.org/fileadmin/www.eshg.org/conferences/2016/downloads/ESHG2016_Abstracts_final.pdf> [žiūrėta 2016-08-31]. [DB: MEDLINE, Science Citation Index Expanded (Web of Science)] [IF: 4.287; AIF: 4.136; Q1 (2016 InCities JCR SCIE)]
3 Aleksiūnienė, Beata; Cimbalistienė, Loreta; Dirsė, Vaidas; Gineikienė, Eglė; Marcinkutė, Rūta; Utkus, Algirdas. De novo 15q26.2q26.3 duplication and 15q26.3 deletion in a patient with an anomalous parietal sutures // European journal of human genetics: The European Human Genetics Conference, 2016, May 21-24, Barcelona, Spain : abstracts book. London : Nature Publishing Group. ISSN 1018-4813. eISSN 1476-5438. 2016, vol. 24, e-suppl. 1, p. 452-453. Prieiga per internetą: <https://www.eshg.org/fileadmin/www.eshg.org/conferences/2016/downloads/ESHG2016_Abstracts_final.pdf>. [DB: MEDLINE, Science Citation Index Expanded (Web of Science)] [IF: 4.287; AIF: 4.136; Q1 (2016 InCities JCR SCIE)]

2015
1 Aleksiūnienė, Beata; Matulevičiūtė, Rugilė; Čiuladaitė, Živilė; Matulevičienė, Aušra; Utkus, Algirdas; Kučinskas, Vaidutis. Coarctation of aorta with dysmorphic features in a patient with triplication of 15q26.1-q26.3: clinical and molecular analysis // Twenty-sixth European meeting on dysmorphology, 9-11 September 2015, Strasbourg, France. Strassbourg : EuroDysmorpho. 2015, p. 27.
2 Matulevičienė, Aušra; Aleksiūnienė, Beata; Tamulienė, Laima; Liubšys, Arūnas; Čiuladaitė, Živilė; Utkus, Algirdas; Kučinskas, Vaidutis. 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 // Twenty-sixth European meeting on dysmorphology, 9-11 September 2015, Le Bischenberg. Le Bischenberg. 2015, p. 28.
3 Aleksiūnienė, Beata; Matulevičienė, Aušra; Benušienė, Eglė. Hypoplastic left heart syndrome in a case with partial 18p monosomy and partial 20q trisomy // European journal of human genetics: European Human Genetics conference 2015, June 6-9, Glasgow, United Kingdom : abstracts. London : Nature Publishing Group. ISSN 1018-4813. 2015, Vol. 23, Supplement 1, p. 399-400. [DB: Science Citation Index Expanded (Web of Science), MEDLINE] [IF: 4.580; AIF: 4.099; Q1 (2015 InCities JCR SCIE)]

2014
1 Matulevičienė, Aušra; Aleksiūnienė, Beata; Mikštienė, Violeta; Krasovskaja, Natalija; Griškevičius, Laimonas; Utkus, Algirdas; Kučinskas, Vaidutis. Dup (1) (q43–q44) & del (21) (q22.2–q22.3) characterized by facial dysmorphism, congenital heart defect and mental retardation // Twenty-fifth European Meeting on Dysmorphology, 10-12 September 2014, Strasbourg, France. Strassbourg : EuroDysmorpho. 2014, p. 45.
2 Aleksiūnienė, Beata; Utkus, Algirdas; Tarutis, Virgilijus. Įgimtos širdies ydos: genetinė etiologija ir diagnostika // Sveikatos mokslai / Sveikatos apsaugos ministerija. Vilnius : Sveikata. ISSN 1392-6373. 2014, vol. 24, nr. 2, p. 105-112. DOI: 10.5200/sm-hs.2014.033. [DB: Index Copernicus]

2012
1 Čiuladaitė, Živilė; Preikšaitienė, Eglė; Kasnauskienė, Jūratė; Utkus, Algirdas; Cimbalistienė, Loreta; Matulevičienė, Aušra; Pečiulytė, Agnė; Ambrozaitytė, Laima; Aleksiūnienė, Beata; Dirsė, Vaidas; Kučinskas, Vaidutis. Molekulinis kariotipavimas ir intelektinės negalios genetinės priežastys: klinikiniai atvejai = Molecular karyotyping and genetic etiology of intellectual disability: case reports // Sveikatos mokslai / Sveikatos apsaugos ministerija. Vilnius : Sveikata. ISSN 1392-6373. 2012, vol. 22, nr. 1, p. 67-72. Prieiga per internetą: <http://sm-hs.eu/index.php/smhs/article/view/251/pdf_1> [žiūrėta 2012-02-02]. [DB: Index Copernicus]

2011
1 Šliužas, Vytautas; Dirsė, Vaidas; Čiuladaitė, Živilė; Aleksiūnienė, Beata; Kučinskas, Vaidutis. Subtelomeric fluorescence in situ hybridization in clinical cytogenetics: results of analysis of Lithuanian patients // European journal of human genetics. London : Nature Publishing Group. ISSN 1018-4813. 2011, vol. 19, suppl. 2, p. 148. [DB: Science Citation Index Expanded (Web of Science), MEDLINE] [IF: 4.400; AIF: 4.314; Q1 (2011 InCities JCR SCIE)]
2 Čiuladaitė, Živilė; Matulevičienė, Aušra; Kasnauskienė, Jūratė; Aleksiūnienė, Beata; Kučinskas, Vaidutis. Small supernumerary marker chromosome derived from chromosome 3 in patient with severe psychomotor developmental delay and dysmorphism // European journal of human genetics : European human genetics conference 2011, Amsterdam, The Netherlands, 2011, May 28-31 : abstracts. London : Nature Publishing Group. ISSN 1018-4813. 2011, vol. 19, suppl. 2, p. 150. [DB: Science Citation Index Expanded (Web of Science), MEDLINE] [IF: 4.400; AIF: 4.314; Q1 (2011 InCities JCR SCIE)]
3 Dirsė, Vaidas; Šliužas, Vytautas; Čiuladaitė, Živilė; Aleksiūnienė, Beata; Kučinskas, Vaidutis. Subtelomeric fluorescence in situ hybridization in clinical cytogenetics: results of analysis of Lithuanian patients = Subtelomerų fluorescencinės in situ hibridizacijos metodas klinikinėje citogenetikoje: Lietuvos pacientų tyrimų rezultatai // Biologija. Vilnius : Lietuvos mokslų akademijos leidykla. ISSN 1392-0146. 2011, vol. 57, nr. 1, p. 8-14. Prieiga per internetą: <http://www.lmaleidykla.lt/ojs/index.php/biologija/article/view/871/324> [žiūrėta 2012-09-17]. [DB: CAB Abstracts, VINITI, TOC Premier, Current Abstracts (EBSCO), Zoological Record]
4 Dzingelevičius, Nerijus; Maruška, Audrius; Ragažinskienė, Ona; Obelevičius, Kęstutis. Optimization of hop essential oil extraction by means of supercritical CO2 = Apynių eterinių aliejų ekstrakcijos superkritiniu CO2 optimizavimas // Biologija. Vilnius : Lietuvos mokslų akademijos leidykla. ISSN 1392-0146. 2011, vol. 57, nr. 2, p. 63-69. Prieiga per internetą: <http://www.lmaleidykla.lt/ojs/index.php/biologija/article/view/1830/740> [žiūrėta 2017-10-24]. [DB: Academic Search Complete, CAB Abstracts, VINITI, TOC Premier, Current Abstracts (EBSCO), Zoological Record]

2010
1 Matulevičienė, Aušra; Aleksiūnienė, Beata; Dirsė, Vaidas; Kučinskas, Vaidutis. A de novo partial trisomy of distal 6p in patient with severe dysmorphic features // European journal of human genetics. London : Nature Publishing Group. ISSN 1018-4813. 2010, vol. 18, suppl. 1, p. 73-74. Prieiga per internetą: <https://www.eshg.org/fileadmin/www.eshg.org/abstracts/ESHG2010Abstracts.pdf> [žiūrėta 2018-08-14]. [DB: Science Citation Index Expanded (Web of Science), MEDLINE] [IF: 4.380; AIF: 4.510; Q1 (2010 InCities JCR SCIE)]

2009
1 Skeivalas, Jonas; Utkus, Algirdas; Aleksiūnienė, Beata. Fotogrametrijos skaitiniai metodai atliekant chromosomų vaizdų analizę // Geodezija ir kartografija. Vilnius : Technika. ISSN 1392-1541. 2009, t. 35, nr. 4, p. 118-119. DOI: 10.3846/1392-1541.2009.35.118-125. [DB: Compendex, Scopus, GEOPHOKA, Current Abstracts]
2 Matulevičienė, Aušra; Ambrozaitytė, Laima; Preikšaitienė, Eglė; Utkus, Algirdas; Linkevičienė, Laura; Aleksiūnienė, Beata; Dagytė, Evelina; Čiuladaitė, Živilė; Šliužas, Vytautas; Kučinskas, Vaidutis. Spectrum of oral clefts in the light of contemporary research study // European journal of human genetics. London : Nature Publishing Group. ISSN 1018-4813. 2009, vol. 17, suppl. 2, p. 74. Prieiga per internetą: <https://www.eshg.org/fileadmin/www.eshg.org/abstracts/ESHG2009Abstracts.pdf> [žiūrėta 2018-11-21]. [DB: Science Citation Index Expanded (Web of Science), MEDLINE] [IF: 3.564; AIF: 4.368; Q2 (2009 InCities JCR SCIE)]
3 Aleksiūnienė, Beata; Utkus, Algirdas; Kučinskas, Vaidutis. A de novo double translocations 3;14 and 6;20 in a patient with mental retardation and microcephaly // European journal of human genetics. London : Nature Publishing Group. ISSN 1018-4813. 2009, vol. 17, suppl. 2, p. 128. Prieiga per internetą: <https://www.eshg.org/fileadmin/www.eshg.org/abstracts/ESHG2009Abstracts.pdf> [žiūrėta 2018-11-21]. [DB: Science Citation Index Expanded (Web of Science), MEDLINE] [IF: 3.564; AIF: 4.368; Q2 (2009 InCities JCR SCIE)]

2008
1 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: vol. 16, suppl. 2: European human genetics conference 2008, Barcelona, Spain, 2008, May 31 - June 3 : abstracts. London : Nature Publishing Group. ISSN 1018-4813. 2008, vol. 16, suppl. 2, p. 152. Prieiga per internetą: <https://www.eshg.org/fileadmin/www.eshg.org/abstracts/ESHG2008Abstracts.pdf> [žiūrėta 2019-09-11]. [DB: Science Citation Index Expanded (Web of Science), MEDLINE] [IF: 3.925; AIF: 4.298; Q2 (2008 InCities JCR SCIE)]
2 Aleksiūnienė, Beata; Krasovskaja, Natalija; Kučinskas, Vaidutis. Prenatal findings: a foetus with trisomy of 22 chromosome // European journal of human genetics: vol. 16, suppl. 2 : European human genetics conference 2008, Barcelona, Spain, 2008, May 31 - June 3 : abstracts. London : Nature Publishing Group. ISSN 1018-4813. 2008, vol. 16, suppl. 2, p. 167. Prieiga per internetą: <https://www.eshg.org/fileadmin/www.eshg.org/abstracts/ESHG2008Abstracts.pdf> [žiūrėta 2019-09-11]. [DB: Science Citation Index Expanded (Web of Science), MEDLINE] [IF: 3.925; AIF: 4.298; Q2 (2008 InCities JCR SCIE)]

2007
1 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. London : Nature Publishing Group. ISSN 1018-4813. 2007, vol. 15, suppl. 1, p. 106. [DB: Science Citation Index Expanded (Web of Science), MEDLINE] [IF: 4.003; AIF: 4.316; Q2 (2007 InCities JCR SCIE)]
2 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. London : Nature Publishing Group. ISSN 1018-4813. 2007, vol. 15, suppl. 1, p. 56. Prieiga per internetą: <https://www.eshg.org/fileadmin/www.eshg.org/abstracts/ESHG2007Abstracts.pdf>. [DB: Science Citation Index Expanded (Web of Science), MEDLINE] [IF: 4.003; AIF: 4.316; Q2 (2007 InCities JCR SCIE)]
3 Aleksiūnienė, Beata; Cimbalistienė, Loreta; Zarakauskaitė, Eglė; Kučinskas, Vaidutis. Down-Turner syndrome: a case report // Chromosome research. ISSN 0967-3849. 2007, vol. 15, suppl. 1, p. 47. [DB: SpringerLink, Science Citation Index Expanded (Web of Science)] [IF: 3.469; AIF: 4.316; Q2 (2007 InCities JCR SCIE)]
4 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 // Chromosome research. ISSN 0967-3849. 2007, vol. 15, suppl. 1, p. 45-46. [DB: SpringerLink, Science Citation Index Expanded (Web of Science)] [IF: 3.469; AIF: 4.316; Q2 (2007 InCities JCR SCIE)]

2006
1 Aleksiūnienė, Beata; Matulevičienė, Aušra; Kučinskas, Vaidutis. The familial reciprocal translocation t(2;6) (p21;p25) associated with wide spectrum of phenotypics signs - from normal to severe malformations // European journal of human genetics. London : Nature Publishing Group. ISSN 1018-4813. 2006, vol. 14, suppl. 1, p. 185. [IF: 3.697; AIF: 4.370; Q2 (2006 InCities JCR SCIE)]
2 Aleksiūnienė, Beata; Matulevičienė, Aušra; Kučinskas, Vaidutis. Three different balanced translocations present the same phenotypic signs of Down syndrome // Laboratorinė medicina: Nr. 1 : 8th Baltic Congress of laboratory medicine, Vilnius 2006. Vilnius : Lietuvos laboratorinės medicinos draugija : Lietuvos žmogaus genetikos draugija : Nacionalinė laboratorijų tiekėjų asociacija (NLTA). ISSN 1392-6470. 2006, Nr. 1, p. 16. [DB: Index Copernicus]
3 Dagytė, Evelina; Aleksiūnienė, Beata; Krasovskaja, Natalija; Kučinskas, Vaidutis. Results of cytogenetic prenatal diagnosis in Lithuania from 2002-2005 // Laboratorinė medicina: Nr. 1 : 8th Baltic Congress of laboratory medicine, Vilnius 2006. Vilnius : Lietuvos laboratorinės medicinos draugija : Lietuvos žmogaus genetikos draugija : Nacionalinė laboratorijų tiekėjų asociacija (NLTA). ISSN 1392-6470. 2006, Nr. 1, p. 19. [DB: Index Copernicus]
4 Matulevičienė, Aušra; Aleksiūnienė, Beata; Kučinskas, Vaidutis. The familial reciprocal translocation t(8;10)(q24.1;q21.3) associated with spectrum of phenotypic signs of trichorhinophalangeal syndrome, type I // Laboratorinė medicina: Nr. 1 : 8th Baltic Congress of laboratory medicine, Vilnius 2006. Vilnius : Lietuvos laboratorinės medicinos draugija : Lietuvos žmogaus genetikos draugija : Nacionalinė laboratorijų tiekėjų asociacija (NLTA). ISSN 1392-6470. 2006, Nr. 1, p. 35. [DB: Index Copernicus]