Birutė Burnytė

677 total citations
28 papers, 194 citations indexed

About

Birutė Burnytė is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, Birutė Burnytė has authored 28 papers receiving a total of 194 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 10 papers in Genetics and 6 papers in Neurology. Recurrent topics in Birutė Burnytė's work include Neurological diseases and metabolism (5 papers), Mitochondrial Function and Pathology (4 papers) and Metabolism and Genetic Disorders (3 papers). Birutė Burnytė is often cited by papers focused on Neurological diseases and metabolism (5 papers), Mitochondrial Function and Pathology (4 papers) and Metabolism and Genetic Disorders (3 papers). Birutė Burnytė collaborates with scholars based in Lithuania, Latvia and United States. Birutė Burnytė's co-authors include Algirdas Utkus, Dalius Jatužis, Laima Ambrozaitytė, Pablo Lapunzina, Víctor L. Ruiz‐Pérez, María Juliana Ballesta‐Martínez, Vanesa López‐González, Víctor Martínez‐Glez, Eulalia Valencia and Ana M. Bueno and has published in prestigious journals such as SHILAP Revista de lepidopterología, Medicine and Cells.

In The Last Decade

Birutė Burnytė

25 papers receiving 194 citations

Peers

Birutė Burnytė

GENET

RHEUM

NEURO

Amjad Khan Pakistan

Laila Mahmoud Qatar

Piotr Gasperowicz Poland

Dhanya Lakshmi Narayanan India

Zhengjun Jia China

Arthur Sorlin France

Minal Menezes Australia

Érika L. Freitas Brazil

Shenela Lakhani United States

Shinobu Fukumura Japan

Amjad Khan Pakistan

Birutė Burnytė

170 ×1.7

124 ×1.8

GENET

20 ×0.7

RHEUM

6 ×0.3

13 ×0.6

NEURO

Citations per year, relative to Birutė Burnytė Birutė Burnytė (= 1×) peers Amjad Khan

Countries citing papers authored by Birutė Burnytė

Since Specialization

Citations

This map shows the geographic impact of Birutė Burnytė's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Birutė Burnytė with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Birutė Burnytė more than expected).

Fields of papers citing papers by Birutė Burnytė

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Birutė Burnytė. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Birutė Burnytė. The network helps show where Birutė Burnytė may publish in the future.

Co-authorship network of co-authors of Birutė Burnytė

This figure shows the co-authorship network connecting the top 25 collaborators of Birutė Burnytė. A scholar is included among the top collaborators of Birutė Burnytė based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Birutė Burnytė. Birutė Burnytė is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Burnytė, Birutė, et al.. (2024). Rapidly Progressing and Early-Onset Forms of Amyotrophic Lateral Sclerosis Caused by a Novel SOD1 Variant in a Lithuanian Family. Neurology Genetics. 10(6). e200217–e200217.

Burnytė, Birutė, et al.. (2023). Genotype-phenotype spectrum and prognosis of early-onset Marfan syndrome. BMC Pediatrics. 23(1). 539–539. 3 indexed citations

Burnytė, Birutė, et al.. (2023). Cerebellar Ataxia and Peripheral Neuropathy in a Family With PNPLA8 -Associated Disease. Neurology Genetics. 9(3). e200068–e200068. 6 indexed citations

Burnytė, Birutė, et al.. (2023). Wide diagnostic and genotypic spectrum in patients with suspected mitochondrial disease. Orphanet Journal of Rare Diseases. 18(1). 307–307. 4 indexed citations

Dasevičius, Darius, et al.. (2022). Early Bilateral Gonadoblastoma in a Patient with Mixed Gonadal Dysgenesis (Karyotype 45,X/46,XY): Case Report and Review of Literature. SHILAP Revista de lepidopterología. 29(2). 318–324.

Burnytė, Birutė, Els De Vriendt, Jonathan Baets, et al.. (2022). HINT1 neuropathy in Lithuania: clinical, genetic, and functional profiling. Orphanet Journal of Rare Diseases. 17(1). 374–374. 1 indexed citations

Utkus, Algirdas, et al.. (2022). Identification of a novel BICRA variant leading to the newly described Coffin–Siris syndrome 12. Brain and Development. 45(3). 185–190. 1 indexed citations

Burnytė, Birutė, et al.. (2022). Urine Biomarkers Combined With Ultrasound for the Diagnosis of Obstruction in Pediatric Hydronephrosis. Frontiers in Pediatrics. 9. 762417–762417. 4 indexed citations

Savige, Judy, Marius Miglinas, Edita Kazėnaitė, et al.. (2022). Identification of 27 Novel Variants in Genes COL4A3, COL4A4, and COL4A5 in Lithuanian Families With Alport Syndrome. Frontiers in Medicine. 9. 859521–859521. 2 indexed citations

10.

Meyer, Robert, Matthias Begemann, Alma Kuechler, et al.. (2021). One test for all: whole exome sequencing significantly improves the diagnostic yield in growth retarded patients referred for molecular testing for Silver–Russell syndrome. Orphanet Journal of Rare Diseases. 16(1). 42–42. 17 indexed citations

11.

Burnytė, Birutė, et al.. (2021). Ischemic Stroke Genetics: What Is New and How to Apply It in Clinical Practice?. Genes. 13(1). 48–48. 40 indexed citations

12.

Preikšaitienė, Eglė, et al.. (2021). Novel In-Frame Deletion in HTRA1 Gene, Responsible for Stroke at a Young Age and Dementia—A Case Study. Genes. 12(12). 1955–1955. 5 indexed citations

13.

Burnytė, Birutė, et al.. (2021). Compound heterozygous c.598_612del and c.1746-20C > G CAPN3 genotype cause autosomal recessive limb-girdle muscular dystrophy-1: a case report. BMC Musculoskeletal Disorders. 22(1). 1020–1020. 3 indexed citations

14.

Matulevičienė, Aušra, et al.. (2017). Opposite chromosome constitutions due to a familial translocation t(1;21)(q43;q22) in 2 cousins with development delay and congenital anomalies. Medicine. 96(16). e6521–e6521. 5 indexed citations

15.

Jakaitienė, Audronė, Eglė Preikšaitienė, Birutė Burnytė, et al.. (2016). The high frequency of GJB2 gene mutation c.313_326del14 suggests its possible origin in ancestors of Lithuanian population. BMC Genetics. 17(1). 45–45. 18 indexed citations

16.

Praninskienė, Rūta, et al.. (2016). Novel mutation in a patient with late onset GLUT1 deficiency syndrome. Brain and Development. 39(4). 352–355. 4 indexed citations

17.

Burnytė, Birutė, et al.. (2016). Perinatal manifestation of mevalonate kinase deficiency and efficacy of anakinra. Pediatric Rheumatology. 14(1). 19–19. 13 indexed citations

18.

Burnytė, Birutė, et al.. (2015). Clinical, cytogenetic and molecular study of a case of ring chromosome 10. Molecular Cytogenetics. 8(1). 29–29. 5 indexed citations

19.

Burnytė, Birutė, et al.. (2014). A novel de novo 2.5 Mb microdeletion of 7q22.1 harbours candidate gene for neurobehavioural disorders and mental retardation. Journal of Genetics. 93(2). 501–503. 2 indexed citations

20.

Guillén‐Navarro, Encarna, María Juliana Ballesta‐Martínez, Eulalia Valencia, et al.. (2014). Two mutations in IFITM5 causing distinct forms of osteogenesis imperfecta. American Journal of Medical Genetics Part A. 164(5). 1136–1142. 32 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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