
Shamil Sunyaev
Harvard University · Biomedical Informatics
Active 1997–2025
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About
Shamil Sunyaev, PhD, is a Professor of Biomedical Informatics at Harvard Medical School and a Professor of Medicine at Brigham and Women’s Hospital. He is a computational genomicist and geneticist whose research encompasses many aspects of population genetic variation, including the origin of mutations, the effect of allelic variants on molecular function, population and evolutionary genetics, and the genetics of human complex and Mendelian traits. He has developed several computational and statistical methods that are widely adopted by the community. Dr. Sunyaev obtained his PhD in molecular biophysics from the Moscow Institute of Physics and Technology and completed his postdoctoral training in bioinformatics at the European Molecular Biology Laboratory (EMBL). He is an Institute Member at the Broad Institute of MIT and Harvard and co-organizes the Boston Evolutionary Genomics Supergroup.
Research topics
- Biology
- Genetics
- Internal medicine
- Medicine
- Cell biology
- Bioinformatics
- Computational biology
- Demography
- Biochemistry
- Evolutionary biology
Selected publications
A cross-disorder dosage sensitivity map of the human genome
Cell · 2022 · 356 citations
Identification of cancer driver genes based on nucleotide context
Nature Genetics · 2020-02-01 · 273 citations
articleOpen accessSenior authorThe landscape of tolerated genetic variation in humans and primates
Science · 2023-06-01 · 173 citations
articleOpen accessPersonalized genome sequencing has revealed millions of genetic differences between individuals, but our understanding of their clinical relevance remains largely incomplete. To systematically decipher the effects of human genetic variants, we obtained whole-genome sequencing data for 809 individuals from 233 primate species and identified 4.3 million common protein-altering variants with orthologs in humans. We show that these variants can be inferred to have nondeleterious effects in humans ba…
Cell · 2022 · 162 citations
Proceedings of the National Academy of Sciences · 2020 · 110 citations
), which suggest that variation in DNM rate is significantly shaped by nonadditive genetic effects and the environment.
Recent grants
The origin, the function and the phenotypic impact of human alleles
NIH · $7.2M · 2018–2028
NIH · $1.9M · 2018
Functional and population genetic architectures of complex disease
NIH · $8.7M · 2013–2027
Frequent coauthors
- 174 shared
Susan Redline
Massachusetts General Hospital
- 142 shared
Brian E. Cade
Brigham and Women's Hospital
- 108 shared
Tamar Sofer
Hadassah Medical Center
- 106 shared
Sung Chun
Brigham and Women's Hospital
- 106 shared
Jerome I. Rotter
UCLA Medical Center
- 104 shared
Richa Saxena
Harvard University
- 100 shared
Daniel J. Balick
Brigham and Women's Hospital
- 95 shared
Heming Wang
Brigham and Women's Hospital
Labs
Sunyaev LabPI
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