С.А. Федорова

8.5k total citations
65 papers, 576 citations indexed

About

С.А. Федорова is a scholar working on Genetics, Molecular Biology and Sensory Systems. According to data from OpenAlex, С.А. Федорова has authored 65 papers receiving a total of 576 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Genetics, 18 papers in Molecular Biology and 14 papers in Sensory Systems. Recurrent topics in С.А. Федорова's work include Forensic and Genetic Research (22 papers), Hearing, Cochlea, Tinnitus, Genetics (14 papers) and Connexins and lens biology (12 papers). С.А. Федорова is often cited by papers focused on Forensic and Genetic Research (22 papers), Hearing, Cochlea, Tinnitus, Genetics (14 papers) and Connexins and lens biology (12 papers). С.А. Федорова collaborates with scholars based in Russia, France and United Kingdom. С.А. Федорова's co-authors include Э. К. Хуснутдинова, Richard Villems, Nikolay A. Barashkov, Marina Bermisheva, Olga L. Posukh, Lilya U. Dzhemileva, Р. И. Хусаинова, М. И. Воевода, L. P. Osipova and Siiri Rootsi and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and International Journal of Molecular Sciences.

In The Last Decade

С.А. Федорова

51 papers receiving 545 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
С.А. Федорова Russia 12 308 171 119 95 67 65 576
V. Ferák Slovakia 11 442 1.4× 305 1.8× 57 0.5× 100 1.1× 28 0.4× 21 937
Nikolay A. Barashkov Russia 10 59 0.2× 158 0.9× 156 1.3× 14 0.1× 81 1.2× 49 287
Denis Pierron France 15 160 0.5× 268 1.6× 26 0.2× 27 0.3× 11 0.2× 28 533
Mari Nelis Estonia 13 306 1.0× 183 1.1× 8 0.1× 22 0.2× 3 0.0× 35 567
Nance We United States 12 185 0.6× 205 1.2× 41 0.3× 5 0.1× 17 0.3× 38 498
Kate van Duijn Netherlands 7 338 1.1× 236 1.4× 5 0.0× 24 0.3× 3 0.0× 7 644
Dean Phelan Australia 11 180 0.6× 188 1.1× 51 0.4× 5 0.1× 23 0.3× 15 398
Missy Dixon United States 6 430 1.4× 361 2.1× 5 0.0× 66 0.7× 6 0.1× 8 839
Jeffery R. Gulcher Iceland 6 136 0.4× 45 0.3× 3 0.0× 28 0.3× 3 0.0× 7 361
Inger Larsson Sweden 11 36 0.1× 72 0.4× 11 0.1× 6 0.1× 6 0.1× 28 464

Countries citing papers authored by С.А. Федорова

Since Specialization
Citations

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

Fields of papers citing papers by С.А. Федорова

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by С.А. Федорова. 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 С.А. Федорова. The network helps show where С.А. Федорова may publish in the future.

Co-authorship network of co-authors of С.А. Федорова

This figure shows the co-authorship network connecting the top 25 collaborators of С.А. Федорова. A scholar is included among the top collaborators of С.А. Федорова 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 С.А. Федорова. С.А. Федорова 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.
Федорова, С.А., et al.. (2024). Search for factors increasing the risk of developing anxiety and depressive disorders in the Yakut population. Yakut Medical Journal. 88(4). 16–20.
2.
Федорова, С.А., et al.. (2024). Y-chromosomal STRs Mutation Rates in the Yakut Population. Russian Journal of Genetics. 60(4). 533–542.
3.
Федорова, С.А., et al.. (2023). The Y-Chromosome Lineage Variation in Ancient and Modern Populations of the Sakha (Yakuts). Russian Journal of Genetics. 59(6). 544–550.
4.
Alekseev, Anatoly N., et al.. (2023). The Genetic History of the Russian Old Settlers of the Arctic Coast of Yakutia from the Village Russkoye Ust’ye. Генетика. 59(9). 1070–1077.
5.
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Kushniarevich, Alena, Gabriel Minárik, Ľudevít Kádaši, et al.. (2021). A common founder effect of the splice site variant c.-23 + 1G > A in GJB2 gene causing autosomal recessive deafness 1A (DFNB1A) in Eurasia. Human Genetics. 141(3-4). 697–707. 3 indexed citations
7.
Barashkov, Nikolay A., et al.. (2021). The Russian Old-Settlers in the Arctic Coast of Eastern Siberia: Family Name Diversity in the Context of Their Origin. Sustainability. 13(19). 10895–10895. 3 indexed citations
8.
Barashkov, Nikolay A., Fedor A. Konovalov, Igor V. Morozov, et al.. (2021). Autosomal recessive cataract (CTRCT18) in the Yakut population isolate of Eastern Siberia: a novel founder variant in the FYCO1 gene. European Journal of Human Genetics. 29(6). 965–976. 11 indexed citations
9.
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Duchesne, Sylvie, Patrice Gérard, Jean‐Luc Fausser, et al.. (2020). The genetic legacy of legendary and historical Siberian chieftains. Communications Biology. 3(1). 581–581. 9 indexed citations
11.
Sabbagh, Audrey, Jean‐Luc Fausser, Friso Palstra, et al.. (2020). The limitations of kinship determinations using STR data in ill-defined populations. International Journal of Legal Medicine. 134(6). 1981–1990. 12 indexed citations
12.
Yakovleva, Anna, et al.. (2019). Indicators of lipid peroxidation in the organism of relocated residents of Yakutia. Yakut Medical Journal. 60–63. 1 indexed citations
13.
Crubézy, Éric, et al.. (2019). Persistence and Disappearance of Traditional Patrilocality. Sibirica. 18(1). 53–70. 3 indexed citations
14.
Barashkov, Nikolay A., et al.. (2019). Selective Heterozygous Advantage of Carriers of с.-23+1G>A Mutation in GJB2 Gene Causing Autosomal Recessive Deafness 1A. Bulletin of Experimental Biology and Medicine. 167(3). 380–383. 3 indexed citations
15.
Barashkov, Nikolay A., Igor V. Morozov, Alexander A. Bondar, et al.. (2017). A novel pathogenic variant c.975G>A (p.Trp325*) in the POU3F4 gene in Yakut family (Eastern Siberia, Russia) with the X-linked deafness-2 (DFNX2). International Journal of Pediatric Otorhinolaryngology. 104. 94–97. 7 indexed citations
16.
Magnaval, Jean‐François, Isabelle Leparc-Goffart, Richard Fabre, et al.. (2016). A Serological Survey About Zoonoses in the Verkhoyansk Area, Northeastern Siberia (Sakha Republic, Russian Federation). Vector-Borne and Zoonotic Diseases. 16(2). 103–109. 9 indexed citations
17.
18.
Dzhemileva, Lilya U., Nikolay A. Barashkov, Olga L. Posukh, et al.. (2010). Carrier frequency of GJB2 gene mutations c.35delG, c.235delC and c.167delT among the populations of Eurasia. Journal of Human Genetics. 55(11). 749–754. 28 indexed citations
19.
Zhivotovsky, Lev A., et al.. (2008). An STR database on the Volga-Ural population. Forensic Science International Genetics. 3(4). e133–e136. 6 indexed citations
20.
Rootsi, Siiri, Lev A. Zhivotovsky, Marián Baldovič, et al.. (2006). A counter-clockwise northern route of the Y-chromosome haplogroup N from Southeast Asia towards Europe. European Journal of Human Genetics. 15(2). 204–211. 120 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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