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Human Molecular Genetics|September 20, 2012
Inferring causality and functional significance of human coding DNA variantsShamil R SunyaevNature Structural & Molecular Biology|March 14, 2023
Revisiting mutagenesis at non-B DNA motifs in the human genomeR J McGinty, S R SunyaevFrontiers in Genetics|December 6, 2021
Maintenance of Complex Trait Variation: Classic Theory and Modern DataEvan M Koch, Shamil R SunyaevCurrent Protocols in Human Genetics|January 15, 2013
Predicting functional effect of human missense mutations using PolyPhen-2Ivan Adzhubei, Daniel M Jordan, Shamil R SunyaevAmerican Journal of Human Genetics|March 16, 2007
Most rare missense alleles are deleterious in humans: implications for complex disease and association studiesGregory V Kryukov, Len A Pennacchio, Shamil R SunyaevCurrent Opinion in Structural Biology|April 20, 2010
Human allelic variation: perspective from protein function, structure, and evolutionDaniel M Jordan, Vasily E Ramensky, Shamil R SunyaevPlos Genetics|February 7, 2009
Adaptive mutations in the JC virus protein capsid are associated with progressive multifocal leukoencephalopathy (PML)Shamil R Sunyaev, Alexey Lugovskoy, Kenneth Simon, et al.Communications Biology|March 5, 2021
Shared associations identify causal relationships between gene expression and immune cell phenotypesChristiane Gasperi, Sung Chun, Shamil R Sunyaev, et al.Proceedings of the National Academy of Sciences of the United States of America|January 7, 2012
The mystery of missing heritability: Genetic interactions create phantom heritabilityOr Zuk, Eliana Hechter, Shamil R Sunyaev, et al.American Journal of Human Genetics|January 15, 2022
StrVCTVRE: A supervised learning method to predict the pathogenicity of human genome structural variantsAndrew G Sharo, Zhiqiang Hu, Shamil R Sunyaev, et al.Pageof 11