Elena Repnikova

850 total citations
26 papers, 278 citations indexed

About

Elena Repnikova is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Elena Repnikova has authored 26 papers receiving a total of 278 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 9 papers in Molecular Biology and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Elena Repnikova's work include Genomic variations and chromosomal abnormalities (7 papers), Genomics and Rare Diseases (5 papers) and Prenatal Screening and Diagnostics (4 papers). Elena Repnikova is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Genomics and Rare Diseases (5 papers) and Prenatal Screening and Diagnostics (4 papers). Elena Repnikova collaborates with scholars based in United States, Russia and France. Elena Repnikova's co-authors include Vladislav M. Panin, Kate Koles, Mark J. Zoran, Michiko Nakamura, Haiwen Li, Galina Pavlova, Dmitry Lyalin, L. I. Korochkin, Shivarajan Amudhavalli and Lauren Grote and has published in prestigious journals such as Journal of Neuroscience, SHILAP Revista de lepidopterología and Blood.

In The Last Decade

Elena Repnikova

23 papers receiving 263 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Elena Repnikova United States 10 180 81 67 47 38 26 278
Sharmistha Mitra United States 9 128 0.7× 115 1.4× 43 0.6× 38 0.8× 13 0.3× 14 321
Gabriela Galiová Czechia 10 515 2.9× 69 0.9× 28 0.4× 29 0.6× 13 0.3× 12 591
Stine A. Mikkelsen Denmark 8 309 1.7× 25 0.3× 48 0.7× 78 1.7× 13 0.3× 9 409
Tae Ho Lee South Korea 8 87 0.5× 32 0.4× 66 1.0× 32 0.7× 25 0.7× 20 230
Anne‐Marie Birot France 10 406 2.3× 79 1.0× 18 0.3× 33 0.7× 9 0.2× 14 554
Andrea Harničarová Czechia 10 520 2.9× 65 0.8× 30 0.4× 21 0.4× 16 0.4× 11 601
Bin Xue China 10 228 1.3× 99 1.2× 38 0.6× 41 0.9× 15 0.4× 14 307
Sadie Miki Sakurada United States 7 160 0.9× 37 0.5× 26 0.4× 55 1.2× 15 0.4× 10 269
Mill W. Miller United States 13 457 2.5× 76 0.9× 88 1.3× 117 2.5× 9 0.2× 17 568
Rama Thimmapaya United States 9 344 1.9× 48 0.6× 26 0.4× 38 0.8× 64 1.7× 12 432

Countries citing papers authored by Elena Repnikova

Since Specialization
Citations

This map shows the geographic impact of Elena Repnikova'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 Elena Repnikova with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Elena Repnikova more than expected).

Fields of papers citing papers by Elena Repnikova

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Elena Repnikova. 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 Elena Repnikova. The network helps show where Elena Repnikova may publish in the future.

Co-authorship network of co-authors of Elena Repnikova

This figure shows the co-authorship network connecting the top 25 collaborators of Elena Repnikova. A scholar is included among the top collaborators of Elena Repnikova 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 Elena Repnikova. Elena Repnikova is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Repnikova, Elena, et al.. (2024). Pediatric spinal ependymoma with chromothripsis of chromosome 6: a case report and review of the literature . Journal of Medical Case Reports. 18(1). 95–95.
2.
Repnikova, Elena, et al.. (2024). P319: Expanding the phenotype of EIF3F-related neurodevelopmental disorder. SHILAP Revista de lepidopterología. 2. 101213–101213.
3.
Repnikova, Elena, Eric T. Rush, Jennifer M. Roberts, et al.. (2024). P398: A rare report of a child with mosaic trisomy 4. SHILAP Revista de lepidopterología. 2. 101292–101292.
4.
Cooley, Linda D., John Herriges, Lei Zhang, et al.. (2023). Integrated genetic profiling of archival pediatric high-grade glial tumors and reassessment with 2021 WHO classification of paediatric CNS tumours. Cancer Genetics. 274-275. 10–20. 2 indexed citations
5.
Cadieux‐Dion, Maxime, Emily Farrow, Isabelle Thiffault, et al.. (2022). Phenotypic expansion and variable expressivity in individuals with JARID2 ‐related intellectual disability: A case series. Clinical Genetics. 102(2). 136–141. 2 indexed citations
6.
Cadieux‐Dion, Maxime, John Herriges, Jeffrey Johnston, et al.. (2022). Clinical Validation of Genome Reference Consortium Human Build 38 in a Laboratory Utilizing Next-Generation Sequencing Technologies. Clinical Chemistry. 68(9). 1177–1183. 4 indexed citations
7.
Sharma, Sonal, et al.. (2021). Diagnostic yield of genetic testing in 324 infants with hypotonia. Clinical Genetics. 100(6). 752–757. 9 indexed citations
8.
Cadieux‐Dion, Maxime, Byunggil Yoo, Neil Miller, et al.. (2021). Factors Affecting Migration to GRCh38 in Laboratories Performing Clinical Next-Generation Sequencing. Journal of Molecular Diagnostics. 23(5). 651–657. 12 indexed citations
9.
Zhang, Lei, Linda D. Cooley, Elena Repnikova, et al.. (2020). Application of 2016 WHO classification in the diagnosis of paediatric high-grade MYC -negative mature B-cell lymphoma with Burkitt-like morphological features. Journal of Clinical Pathology. 73(9). 563–570. 4 indexed citations
10.
Repnikova, Elena, Jennifer Roberts, Midhat S. Farooqi, et al.. (2019). Clinical and molecular characterization of novel deletions causing epsilon gamma delta beta thalassemia: Report of two cases. Pathology - Research and Practice. 215(10). 152578–152578. 4 indexed citations
11.
Repnikova, Elena, Dmitry Lyalin, Kimberly S. McDonald, et al.. (2019). CNTN6 copy number variations: Uncertain clinical significance in individuals with neurodevelopmental disorders. European Journal of Medical Genetics. 63(1). 103636–103636. 5 indexed citations
12.
Cadieux‐Dion, Maxime, Nicole P. Safina, Kendra Engleman, et al.. (2018). Novel heterozygous pathogenic variants in CHUK in a patient with AEC-like phenotype, immune deficiencies and 1q21.1 microdeletion syndrome: a case report. BMC Medical Genetics. 19(1). 41–41. 6 indexed citations
13.
Roberts, Jennifer, et al.. (2018). Novel mosaic SRY gene deletions in three newborn males with variable genitourinary malformations. American Journal of Medical Genetics Part A. 176(9). 2017–2023. 1 indexed citations
14.
Repnikova, Elena, et al.. (2018). Biparental/androgenetic mosaicism in a male with features of overgrowth and placental mesenchymal dysplasia. Clinical Genetics. 94(6). 564–568. 11 indexed citations
15.
Grote, Lauren, Elena Repnikova, & Shivarajan Amudhavalli. (2015). Expanding the phenotype of feingold syndrome‐2. American Journal of Medical Genetics Part A. 167(12). 3219–3225. 13 indexed citations
16.
Repnikova, Elena, Jill A. Rosenfeld, Aimee McKinney, et al.. (2013). Characterization of copy number variation in genomic regions containing STR loci using array comparative genomic hybridization. Forensic Science International Genetics. 7(5). 475–481. 6 indexed citations
17.
Nakamura, Michiko, Elena Repnikova, Mandy Carnahan, et al.. (2013). The Role of Drosophila Cytidine Monophosphate-Sialic Acid Synthetase in the Nervous System. Journal of Neuroscience. 33(30). 12306–12315. 22 indexed citations
18.
Repnikova, Elena, Caroline Astbury, Shalini C. Reshmi, et al.. (2012). Microarray comparative genomic hybridization and cytogenetic characterization of tissue‐specific mosaicism in three patients. American Journal of Medical Genetics Part A. 158A(8). 1924–1933. 17 indexed citations
19.
Repnikova, Elena, Kate Koles, Michiko Nakamura, et al.. (2010). Sialyltransferase Regulates Nervous System Function in Drosophila. Journal of Neuroscience. 30(18). 6466–6476. 60 indexed citations
20.
Koles, Kate, Elena Repnikova, Galina Pavlova, L. I. Korochkin, & Vladislav M. Panin. (2008). Sialylation in protostomes: a perspective from Drosophila genetics and biochemistry. Glycoconjugate Journal. 26(3). 313–324. 37 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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