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Shamil R Sunyaev

Showing results (41-50 of 105) with videos related to

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Nature Genetics|February 21, 2017
Limited statistical evidence for shared genetic effects of eQTLs and autoimmune-disease-associated loci in three major immune-cell typesSung Chun, Alexandra Casparino, Nikolaos A Patsopoulos, et al.
Human Mutation|January 22, 2016
Pathogenicity Interpretation in the Age of Precision Medicine: The 2015 Annual Scientific Meeting of the Human Genome Variation SocietyWilliam S Oetting, Steven E Brenner, Anthony J Brookes, et al.
Nature|February 20, 2015
Cell-of-origin chromatin organization shapes the mutational landscape of cancerPaz Polak, Rosa Karlić, Amnon Koren, et al.
Bioinformatics Advances|October 10, 2024
FAVOR-GPT: a generative natural language interface to whole genome variant functional annotationsThomas Cheng Li, Hufeng Zhou, Vineet Verma, et al.
Nature Genetics|January 26, 2016
Genes with monoallelic expression contribute disproportionately to genetic diversity in humansVirginia Savova, Sung Chun, Mashaal Sohail, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 21, 2014
Searching for missing heritability: designing rare variant association studiesOr Zuk, Stephen F Schaffner, Kaitlin Samocha, et al.
Medrxiv : the Preprint Server for Health Sciences|December 25, 2025
Learning Patient Similarity from Genomics for Precision OncologyMaha Shady, Brendan Reardon, Sharon Jiang, et al.
Science (New York, N.Y.)|April 7, 2022
Genome-wide analysis of somatic noncoding mutation patterns in cancerFelix Dietlein, Alex B Wang, Christian Fagre, et al.
Nature Biotechnology|December 17, 2013
Reduced local mutation density in regulatory DNA of cancer genomes is linked to DNA repairPaz Polak, Michael S Lawrence, Eric Haugen, et al.
Biorxiv : the Preprint Server for Biology|June 22, 2026
Inference of elevated mutation rates and variant effects using 700k exomesPrathitha Kar, Mikhail A Moldovan, Jeremy Guez, et al.
Pageof 11

Showing results (41-50 of 105) with videos related to

Sort By:
Pageof 11
Nature Genetics|February 21, 2017
Limited statistical evidence for shared genetic effects of eQTLs and autoimmune-disease-associated loci in three major immune-cell typesSung Chun, Alexandra Casparino, Nikolaos A Patsopoulos, et al.
Human Mutation|January 22, 2016
Pathogenicity Interpretation in the Age of Precision Medicine: The 2015 Annual Scientific Meeting of the Human Genome Variation SocietyWilliam S Oetting, Steven E Brenner, Anthony J Brookes, et al.
Nature|February 20, 2015
Cell-of-origin chromatin organization shapes the mutational landscape of cancerPaz Polak, Rosa Karlić, Amnon Koren, et al.
Bioinformatics Advances|October 10, 2024
FAVOR-GPT: a generative natural language interface to whole genome variant functional annotationsThomas Cheng Li, Hufeng Zhou, Vineet Verma, et al.
Nature Genetics|January 26, 2016
Genes with monoallelic expression contribute disproportionately to genetic diversity in humansVirginia Savova, Sung Chun, Mashaal Sohail, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 21, 2014
Searching for missing heritability: designing rare variant association studiesOr Zuk, Stephen F Schaffner, Kaitlin Samocha, et al.
Medrxiv : the Preprint Server for Health Sciences|December 25, 2025
Learning Patient Similarity from Genomics for Precision OncologyMaha Shady, Brendan Reardon, Sharon Jiang, et al.
Science (New York, N.Y.)|April 7, 2022
Genome-wide analysis of somatic noncoding mutation patterns in cancerFelix Dietlein, Alex B Wang, Christian Fagre, et al.
Nature Biotechnology|December 17, 2013
Reduced local mutation density in regulatory DNA of cancer genomes is linked to DNA repairPaz Polak, Michael S Lawrence, Eric Haugen, et al.
Biorxiv : the Preprint Server for Biology|June 22, 2026
Inference of elevated mutation rates and variant effects using 700k exomesPrathitha Kar, Mikhail A Moldovan, Jeremy Guez, et al.
Pageof 11