Andrei Barysenka

2.5k total citations
14 papers, 238 citations indexed

About

Andrei Barysenka is a scholar working on Molecular Biology, Genetics and Hematology. According to data from OpenAlex, Andrei Barysenka has authored 14 papers receiving a total of 238 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 5 papers in Genetics and 4 papers in Hematology. Recurrent topics in Andrei Barysenka's work include Genetic Associations and Epidemiology (5 papers), Bioinformatics and Genomic Networks (4 papers) and Advanced Proteomics Techniques and Applications (2 papers). Andrei Barysenka is often cited by papers focused on Genetic Associations and Epidemiology (5 papers), Bioinformatics and Genomic Networks (4 papers) and Advanced Proteomics Techniques and Applications (2 papers). Andrei Barysenka collaborates with scholars based in Germany, Netherlands and United Kingdom. Andrei Barysenka's co-authors include Monika Stoll, Anika Witten, Arthur Gilly, Frank Rühle, Emmanouil Tsafantakis, Maria Karaleftheri, Eleftheria Zeggini, George Dedoussis, Nigel W. Rayner and Ulrike Nowak‐Göttl and has published in prestigious journals such as Nature Communications, Blood and PLoS ONE.

In The Last Decade

Andrei Barysenka

13 papers receiving 238 citations

Peers

Andrei Barysenka
Kristin G. Ardlie United States
Lo Wong Hong Kong
Shunji Shiohira Japan
Constança Coelho Portugal
Pardeep Aggarwal United States
Jiamin Cao China
Sofia Bosdotter Enroth Sweden
Kimberley Veraar Netherlands
Shira Ginsberg Israel
Shinya Ogasawara Japan
Kristin G. Ardlie United States
Andrei Barysenka
Citations per year, relative to Andrei Barysenka Andrei Barysenka (= 1×) peers Kristin G. Ardlie

Countries citing papers authored by Andrei Barysenka

Since Specialization
Citations

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

Fields of papers citing papers by Andrei Barysenka

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andrei Barysenka

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

All Works

14 of 14 papers shown
1.
Bocher, Ozvan, Urmo Võsa, Ene Reimann, et al.. (2024). Disentangling the consequences of type 2 diabetes on targeted metabolite profiles using causal inference and interaction QTL analyses. PLoS Genetics. 20(12). e1011346–e1011346. 1 indexed citations
2.
Isaacs, Aaron, Andrei Barysenka, Rachel M.A. ter Bekke, et al.. (2023). Standing genetic variation affects phenotypic heterogeneity in an SCN5A-mutation founder population with excess sudden cardiac death. Heart Rhythm. 20(5). 720–727. 1 indexed citations
3.
Gilly, Arthur, Lucija Klarić, Andrei Barysenka, et al.. (2022). Gene-based whole genome sequencing meta-analysis of 250 circulating proteins in three isolated European populations. Molecular Metabolism. 61. 101509–101509. 4 indexed citations
4.
Gerlini, Raffaele, Konstantinos Hatzikotoulas, Andrei Barysenka, et al.. (2022). Identifying causal serum protein–cardiometabolic trait relationships using whole genome sequencing. Human Molecular Genetics. 32(8). 1266–1275. 8 indexed citations
5.
Barysenka, Andrei, Pau Navarro, Xia Shen, et al.. (2021). Mapping the serum proteome to neurological diseases using whole genome sequencing. Nature Communications. 12(1). 7042–7042. 34 indexed citations
6.
Gilly, Arthur, Andrei Barysenka, Iris Fischer, et al.. (2020). Whole-genome sequencing analysis of the cardiometabolic proteome. Nature Communications. 11(1). 6336–6336. 61 indexed citations
7.
Witten, Anika, Frank Rühle, Andrei Barysenka, et al.. (2020). ADAMTS12, a new candidate gene for pediatric stroke. PLoS ONE. 15(8). e0237928–e0237928. 6 indexed citations
8.
Hatzikotoulas, Konstantinos, Cindy G. Boer, Lorraine Southam, et al.. (2020). Large-scale genome-wide meta-analyses provide insights for the development of new disease modifying targets for osteoarthritis. Osteoarthritis and Cartilage. 28. S54–S54.
9.
Schulz, Angela, Andreas Eisenreich, Andrei Barysenka, et al.. (2019). Analysis of the genomic architecture of a complex trait locus in hypertensive rat models links Tmem63c to kidney damage. eLife. 8. 23 indexed citations
10.
Witten, Anika, Maren Kasper, Martin Busch, et al.. (2019). Transcriptomic and proteomic analysis of iris tissue and aqueous humor in juvenile idiopathic arthritis-associated uveitis. Journal of Autoimmunity. 100. 75–83. 40 indexed citations
11.
Witten, Anika, Juliane Bolbrinker, Andrei Barysenka, et al.. (2018). Targeted resequencing of a locus for heparin-induced thrombocytopenia on chromosome 5 identified in a genome-wide association study. Journal of Molecular Medicine. 96(8). 765–775. 12 indexed citations
12.
Bekke, Rachel M.A. ter, Aaron Isaacs, Andrei Barysenka, et al.. (2017). Heritability in a SCN5A -mutation founder population with increased female susceptibility to non-nocturnal ventricular tachyarrhythmia and sudden cardiac death. Heart Rhythm. 14(12). 1873–1881. 16 indexed citations
13.
Rühle, Frank, Anika Witten, Andrei Barysenka, et al.. (2016). Rare genetic variants in SMAP1, B3GAT2, and RIMS1 contribute to pediatric venous thromboembolism. Blood. 129(6). 783–790. 17 indexed citations
14.
Stoll, Monika, et al.. (2016). Rare Variants in the ADAMTS13 Von Willebrand Factor–Binding Domain Contribute to Pediatric Stroke. Circulation Cardiovascular Genetics. 9(4). 357–367. 15 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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