Seva Kashin

37.1k total citations · 1 hit paper
7 papers, 768 citations indexed

About

Seva Kashin is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Seva Kashin has authored 7 papers receiving a total of 768 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 2 papers in Genetics and 2 papers in Cancer Research. Recurrent topics in Seva Kashin's work include Genomics and Rare Diseases (2 papers), Pluripotent Stem Cells Research (2 papers) and CRISPR and Genetic Engineering (2 papers). Seva Kashin is often cited by papers focused on Genomics and Rare Diseases (2 papers), Pluripotent Stem Cells Research (2 papers) and CRISPR and Genetic Engineering (2 papers). Seva Kashin collaborates with scholars based in United States, United Kingdom and Australia. Seva Kashin's co-authors include Steven A. McCarroll, Robert E. Handsaker, Giulio Genovese, Vanessa Van Doren, Jennifer R. Berman, Nolan Kamitaki, Florian T. Merkle, Kevin Eggan, Sulagna Ghosh and Curtis J. Mello and has published in prestigious journals such as Nature, Cell and Nature Communications.

In The Last Decade

Seva Kashin

7 papers receiving 755 citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Long somatic DNA-repeat expansion drives neurodegeneration in Huntington’s disease

2025 45 citations Robert E. Handsaker, Seva Kashin et al. Cell profile →

Peers

Seva Kashin

MB

GENET

CR

PS

CMN

Joshua B. Black United States

Dekker C. Deacon United States

Gareth Palidwor Canada

Zi Yan United States

Avni Santani United States

Yelena Dayn United States

Filippo M. Cernilogar Germany

Ivana Barbaric United Kingdom

Shijie Li China

Joshua B. Black United States

Seva Kashin

887 ×1.7

MB

182 ×0.6

GENET

44 ×0.5

CR

57 ×0.8

PS

32 ×0.6

CMN

Citations per year, relative to Seva Kashin Seva Kashin (= 1×) peers Joshua B. Black

Countries citing papers authored by Seva Kashin

Since Specialization

Citations

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

Fields of papers citing papers by Seva Kashin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Seva Kashin

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

All Works

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7 of 7 papers shown

1.

Handsaker, Robert E., Seva Kashin, Nora Reed, et al.. (2025). Long somatic DNA-repeat expansion drives neurodegeneration in Huntington’s disease. Cell. 188(3). 623–639.e19. 45 indexed citations breakdown →

2.

Genovese, Giulio, Curtis J. Mello, Po‐Ru Loh, et al.. (2022). Chromosomal phase improves aneuploidy detection in non-invasive prenatal testing at low fetal DNA fractions. Scientific Reports. 12(1). 12025–12025. 1 indexed citations

3.

Merkle, Florian T., Sulagna Ghosh, Giulio Genovese, et al.. (2022). Whole-genome analysis of human embryonic stem cells enables rational line selection based on genetic variation. Cell stem cell. 29(3). 472–486.e7. 25 indexed citations

4.

Saunders, Arpiar, Kee Wui Huang, Adrienne C. Philson, et al.. (2022). Ascertaining cells’ synaptic connections and RNA expression simultaneously with barcoded rabies virus libraries. Nature Communications. 13(1). 6993–6993. 10 indexed citations

5.

Merkle, Florian T., Sulagna Ghosh, Nolan Kamitaki, et al.. (2017). Human pluripotent stem cells recurrently acquire and expand dominant negative P53 mutations. Nature. 545(7653). 229–233. 348 indexed citations

6.

Handsaker, Robert E., Tōnu Esko, Marcus A. Tuke, et al.. (2015). Structural forms of the human amylase locus and their relationships to SNPs, haplotypes and obesity. Nature Genetics. 47(8). 921–925. 98 indexed citations

7.

Handsaker, Robert E., Vanessa Van Doren, Jennifer R. Berman, et al.. (2015). Large multiallelic copy number variations in humans. Nature Genetics. 47(3). 296–303. 241 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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