B. Burnytė

发表

C. Fauth, H. Cavé, M. Tartaglia, 2020, European Journal of Human Genetics.

A. Ferlini, M. Neri, D. Vlodavets, 2020, Neurology Genetics.

A. Khrunin, S. Limborska, S. Pajusalu, 2022, Human mutation.

S. Waisbren, M. Hochuli, S. Wortmann, 2019, Orphanet Journal of Rare Diseases.

P. Lapunzina, E. Guillén-Navarro, A. Utkus, 2014, American journal of medical genetics. Part A.

V. Kučinskas, Evelina Dagytė, A. Utkus, 2015, Molecular Cytogenetics.

R. Ganetzky, H. Prokisch, E. Eklund, 2022, Genetics in medicine : official journal of the American College of Medical Genetics.

S. Scherer, A. Jordanova, J. Baets, 2022, Orphanet Journal of Rare Diseases.

A. Utkus, B. Burnytė, S. Rusonienė, 2016, Pediatric Rheumatology.

V. Kučinskas, A. Krūmiņa, A. Utkus, 2016, BMC Musculoskeletal Disorders.

S. Ehl, Miriam Heizmann, M. Nordenskjöld, 2018, The Journal of allergy and clinical immunology.

A. Utkus, B. Lāce, I. Inashkina, 2015, Acta neurologica Scandinavica.

G. Verkauskas, Vytis Kazlauskas, V. Bilius, 2022, Frontiers in Pediatrics.

Z. Krūmiņa, L. Pliss, Evelina Dagytė, 2018, Mitochondrial DNA. Part A, DNA mapping, sequencing, and analysis.

B. Burnytė, L. Ambrozaitytė, Rūta Praninskienė, 2017, Brain and Development.

Danutė Balkelienė, A. Utkus, B. Burnytė, 2022, Molecular genetics & genomic medicine.

A. Utkus, I. Adomaitienė, B. Burnytė, 2023, Neurology: Genetics.

A. Utkus, A. Morkūnienė, B. Burnytė, 2022, Brain and Development.

A. Utkus, B. Burnytė, L. Ambrozaitytė, 2023, Orphanet Journal of Rare Diseases.

B. Burnytė, Rūta Gegieckienė, Aurelija Kemezyte, 2023, BMC Pediatrics.

B. Burnytė, Vytautas Augustinavičius, Greta Asadauskaitė, 2023, Frontiers in neurology.

T. Meitinger, H. Prokisch, C. Sokollik, 2023, Hepatology.

B. Burnytė, Givi Lengvenis, Mantas Jokubaitis, 2024, Frontiers in neurology.