Author

Alex Fedotov

Columbia University

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Bioinformatics· 1 Genetic & Genomic Medicine· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Research Focus:database / resource· 2 Organism:human· 2 Approach:statistical model· 2 Assay:electronic health records· 1 Approach:experimental assay· 1 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1 Research Focus:software / tool· 1

Frequent Co-Authors

David R. CrossliniD· 3 shared Gail Pairitz JarvikiD· 3 shared Ali G. GharaviiD· 2 shared Chunhua WengiD· 2 shared David A. FaseliD· 2 shared Eric VenneriD· 2 shared Hakon H. HakonarsoniD· 2 shared Hana BangashiD· 2 shared

Activity by Year

2021-2022 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersGenetic & Genomic Medicine

David R. CrosslinORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Genome-wide polygenic score with APOL1 risk genotypes predicts chronic kidney disease across major continental ancestries

Atlas Khan, Michael C. Turchin, Amit Patki, Vinodh Srinivasasainagendra, Ning Shang, Rajiv Nadukuru, Alana C Jones, Edyta Małolepsza, Ozan Dikilitas, Iftikhar J. Kullo, Daniel J. Schaid, Elizabeth W. Karlson, Tian Ge, James B. Meigs, Jordan W. Smoller, , Krzysztof Kiryluk

This paper develops a genome-wide polygenic score for chronic kidney disease that incorporates APOL1 risk genotypes and shows consistent performance across four major continental ancestries.

Nature Medicine · Jun 16, 2022Peer-reviewedGenetic & Genomic Medicine

Neptune: An environment for the delivery of genomic medicine

Eric Venner, Victoria Yi, David R. Murdock, Sara E. Kalla, Tsung-Jung Wu, Aniko Sabo, Shoudong Li, Qingchang Meng, Tian Xia, Mullai Murugan, Michelle L. Cohen, Christie Kovar, Wei‐Qi Wei, Wendy K. Chung, Chunhua Weng, , Andrea L. Hartzler

Neptune delivers structured genomic data to EHR systems through customizable reports and variant reanalysis, supporting over 15,000 clinical reports.

Genetics in Medicine · Jul 13, 2021Peer-reviewedBioinformatics

Genomic Considerations for FHIR; eMERGE Implementation Lessons

Mullai Murugan, Lawrence J. Babb, Casey Overby Taylor, Luke V. Rasmussen, Robert R. Freimuth, Eric Venner, Fei Yan, Victoria Yi, Stephen J. Granite, Hana Zouk, Samuel Aronson, Kevin Power, Alex Fedotov, David R. Crosslin, David A. Fasel, , Richard A. Gibbs

This paper describes the implementation of HL7 FHIR standards for representing clinical genomics results in the eMERGE Networks, improving interoperability for genetic data management.

Journal of Biomedical Informatics · Apr 28, 2021Peer-reviewedGenomics