Author

Andrey K. Shevchenko

St Petersburg 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

Click to filter author papers

Genetic & Genomic Medicine· 1 Genomics· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 2 Approach:statistical model· 2 Assay:whole-genome sequencing· 2 Research Focus:GWAS / association mapping· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Collet DandaraiD· 2 shared Delesa Damena Mulisa· 2 shared Emile Rugamika ChimusaiD· 2 shared Max EssexiD· 2 shared Melvin M. LeteaneiD· 2 shared Prisca K. ThamiiD· 2 shared Simani GaseitsiweiD· 2 shared Stephen J. O’BrieniD· 2 shared

Activity by Year

2020-2020 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersGenetic & Genomic Medicine

Collet DandaraORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Whole Genome Rare-Variant Association Study of HIV-1 Progression in a Southern African Population

Prisca K. Thami, Wonderful Tatenda Choga, Delesa Damena Mulisa, Collet Dandara, Andrey K. Shevchenko, Melvin M. Leteane, Vlad Novitsky, Stephen J. O’Brien, Max Essex, Simani Gaseitsiwe, Emile Rugamika Chimusa

This study identifies rare genetic variants associated with HIV-1 progression in a Botswana population using whole genome sequencing and statistical analysis.

medRxiv · Dec 16, 2020 · PreprintGenetic & Genomic Medicine

Whole Genome Sequencing-based Characterization of Human Genome Variation and Mutation Burden in Botswana

The paper characterizes human genomic variations and mutation burden in Botswana using whole genome sequencing, identifying damaging variants and admixture patterns.

bioRxiv · Dec 15, 2020 · PreprintGenomics