Andrey Khrunin

17.9k total citations
39 papers, 536 citations indexed

About

Andrey Khrunin is a scholar working on Genetics, Molecular Biology and Cancer Research. According to data from OpenAlex, Andrey Khrunin has authored 39 papers receiving a total of 536 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Genetics, 20 papers in Molecular Biology and 5 papers in Cancer Research. Recurrent topics in Andrey Khrunin's work include Genetic Associations and Epidemiology (11 papers), Forensic and Genetic Research (11 papers) and Glutathione Transferases and Polymorphisms (9 papers). Andrey Khrunin is often cited by papers focused on Genetic Associations and Epidemiology (11 papers), Forensic and Genetic Research (11 papers) and Glutathione Transferases and Polymorphisms (9 papers). Andrey Khrunin collaborates with scholars based in Russia, United Kingdom and United States. Andrey Khrunin's co-authors include Limborskaia Sa, Vera Gorbunova, Alexey Moisseev, D. V. Khokhrin, Dmitry A. Verbenko, Andres Metspalu, P. A. Slominsky, Evelin Mihailov, James A. Knowles and Anton Valouev and has published in prestigious journals such as Nucleic Acids Research, PLoS ONE and International Journal of Molecular Sciences.

In The Last Decade

Andrey Khrunin

37 papers receiving 519 citations

Peers

Andrey Khrunin
Jeannette F. Korczak United States
Sabine Preisler-Adams Germany
Josephine Addai United States
T Noguchi France
James T. Lu United States
Tuomo Mantere Finland
Toshiro Mizuno Japan
Virginia Speare United States
Heather Pierce United States
Shane M. Colley Australia
Jeannette F. Korczak United States
Andrey Khrunin
Citations per year, relative to Andrey Khrunin Andrey Khrunin (= 1×) peers Jeannette F. Korczak

Countries citing papers authored by Andrey Khrunin

Since Specialization
Citations

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

Fields of papers citing papers by Andrey Khrunin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andrey Khrunin

This figure shows the co-authorship network connecting the top 25 collaborators of Andrey Khrunin. A scholar is included among the top collaborators of Andrey Khrunin 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 Andrey Khrunin. Andrey Khrunin 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.
Khrunin, Andrey, et al.. (2025). Determinant-based grouping of SNPs and its application for detecting disease-associated genomic loci. NAR Genomics and Bioinformatics. 7(1). lqaf024–lqaf024.
2.
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Khrunin, Andrey, et al.. (2023). The Study of the Association of Polymorphisms in LSP1, GPNMB, PDPN, TAGLN, TSPO, and TUBB6 Genes with the Risk and Outcome of Ischemic Stroke in the Russian Population. International Journal of Molecular Sciences. 24(7). 6831–6831. 5 indexed citations
4.
Filippenkov, Ivan B., et al.. (2023). Are Ischemic Stroke and Alzheimer’s Disease Genetically Consecutive Pathologies?. Biomedicines. 11(10). 2727–2727. 3 indexed citations
5.
Sa, Limborskaia, et al.. (2023). Evaluation of Density-Based Spatial Clustering for Identifying Genomic Loci Associated with Ischemic Stroke in Genome-Wide Data. International Journal of Molecular Sciences. 24(20). 15355–15355. 4 indexed citations
6.
Fedorova, Larisa, et al.. (2022). Analysis of Common SNPs across Continents Reveals Major Genomic Differences between Human Populations. Genes. 13(8). 1472–1472. 9 indexed citations
7.
Khrunin, Andrey, et al.. (2020). imputeqc: an R package for assessing imputation quality of genotypes and optimizing imputation parameters. BMC Bioinformatics. 21(S12). 304–304. 8 indexed citations
8.
Khrunin, Andrey, et al.. (2020). Genomic landscape of the signals of positive natural selection in populations of Northern Eurasia: A view from Northern Russia. PLoS ONE. 15(2). e0228778–e0228778. 5 indexed citations
9.
Krūmiņa, Astrīda, Liāna Pliss, Gunita Zariņa, et al.. (2018). Population Genetics of Latvians in the Context of Admixture between North-Eastern European Ethnic Groups. Proceedings of the Latvian Academy of Sciences Section B Natural Exact and Applied Sciences. 72(3). 131–151. 3 indexed citations
10.
Khrunin, Andrey, Dmitry Pushkarev, D. V. Khokhrin, et al.. (2016). Reconstructing genetic history of Siberian and Northeastern European populations. Genome Research. 27(1). 1–14. 49 indexed citations
11.
Khokhrin, D. V., et al.. (2013). Pharmacogenomics of cisplatin-based chemotherapy in ovarian-cancer patients from Yakutia. Molecular Genetics Microbiology and Virology. 28(4). 137–140. 6 indexed citations
12.
Khrunin, Andrey, D. V. Khokhrin, Tōnu Esko, et al.. (2013). A Genome-Wide Analysis of Populations from European Russia Reveals a New Pole of Genetic Diversity in Northern Europe. PLoS ONE. 8(3). e58552–e58552. 41 indexed citations
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Khokhrin, D. V., et al.. (2012). Association of polymorphisms in glutathione-S-Transferase and DNA repair genes with ovarian cancer risk in the Russian population. Russian Journal of Genetics. 48(7). 764–766. 12 indexed citations
15.
Sa, Limborskaia, et al.. (2011). Specificity of genetic diversity in D1S80 revealed by SNP–VNTR haplotyping. Annals of Human Biology. 38(5). 564–569. 5 indexed citations
16.
Khrunin, Andrey, Alexey Moisseev, Vera Gorbunova, & Limborskaia Sa. (2009). Genetic polymorphisms and the efficacy and toxicity of cisplatin-based chemotherapy in ovarian cancer patients. The Pharmacogenomics Journal. 10(1). 54–61. 155 indexed citations
17.
Flegontova, Olga, et al.. (2009). Haplotype frequencies at the DRD2 locus in populations of the East European Plain. BMC Genetics. 10(1). 62–62. 7 indexed citations
18.
Krjutškov, Kaarel, Reidar Andreson, Reedik Mägi, et al.. (2008). Development of a single tube 640-plex genotyping method for detection of nucleic acid variations on microarrays. Nucleic Acids Research. 36(12). e75–e75. 30 indexed citations
19.
Khrunin, Andrey, et al.. (2007). Regional differences in the genetic variability of Finno‐Ugric speaking Komi populations. American Journal of Human Biology. 19(6). 741–750. 8 indexed citations
20.
Khrunin, Andrey, et al.. (2005). p53 polymorphisms in Russia and Belarus: correlation of the 2-1-1 haplotype frequency with longitude. Molecular Genetics and Genomics. 272(6). 666–672. 18 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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