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Shamil R Sunyaev

Showing results (61-70 of 105) with videos related to

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Nature Communications|February 18, 2021
Population-specific causal disease effect sizes in functionally important regions impacted by selectionHuwenbo Shi, Steven Gazal, Masahiro Kanai, et al.
Nature|February 22, 2008
Proportionally more deleterious genetic variation in European than in African populationsKirk E Lohmueller, Amit R Indap, Steffen Schmidt, et al.
Elife|March 22, 2019
Polygenic adaptation on height is overestimated due to uncorrected stratification in genome-wide association studiesMashaal Sohail, Robert M Maier, Andrea Ganna, et al.
Central Asian Journal of Global Health|May 29, 2018
Individuality and temporal stability of the human gut microbiomeShinichi Sunagawa, Siegfried Schloissnig, Manimozhiyan Arumugam, et al.
Molecular Genetics & Genomic Medicine|October 6, 2015
Inherited CHST11/MIR3922 deletion is associated with a novel recessive syndrome presenting with skeletal malformation and malignant lymphoproliferative diseaseSameer S Chopra, Ignaty Leshchiner, Hatice Duzkale, et al.
Science (New York, N.Y.)|May 6, 2017
Negative selection in humans and fruit flies involves synergistic epistasisMashaal Sohail, Olga A Vakhrusheva, Jae Hoon Sul, et al.
Nature Communications|September 7, 2017
Identifying DNase I hypersensitive sites as driver distal regulatory elements in breast cancerMatteo D Antonio, Donate Weghorn, Agnieszka D Antonio-Chronowska, et al.
Nucleic Acids Research|December 3, 2025
FAVOR 2.0: A reengineered functional annotation of variants online resource for interpreting genomic variationHufeng Zhou, Vineet Verma, Xihao Li, et al.
Plos Genetics|March 8, 2013
Deleterious alleles in the human genome are on average younger than neutral alleles of the same frequencyAdam Kiezun, Sara L Pulit, Laurent C Francioli, et al.
Cell Genomics|June 22, 2026
NERINE reveals rare variant associations in gene networks across phenotypes and implicates an SNCA-PRL-LRRK2 subnetwork in Parkinson's diseaseSumaiya Nazeen, Xinyuan Wang, Autumn R Morrow, et al.
Pageof 11

Showing results (61-70 of 105) with videos related to

Sort By:
Pageof 11
Nature Communications|February 18, 2021
Population-specific causal disease effect sizes in functionally important regions impacted by selectionHuwenbo Shi, Steven Gazal, Masahiro Kanai, et al.
Nature|February 22, 2008
Proportionally more deleterious genetic variation in European than in African populationsKirk E Lohmueller, Amit R Indap, Steffen Schmidt, et al.
Elife|March 22, 2019
Polygenic adaptation on height is overestimated due to uncorrected stratification in genome-wide association studiesMashaal Sohail, Robert M Maier, Andrea Ganna, et al.
Central Asian Journal of Global Health|May 29, 2018
Individuality and temporal stability of the human gut microbiomeShinichi Sunagawa, Siegfried Schloissnig, Manimozhiyan Arumugam, et al.
Molecular Genetics & Genomic Medicine|October 6, 2015
Inherited CHST11/MIR3922 deletion is associated with a novel recessive syndrome presenting with skeletal malformation and malignant lymphoproliferative diseaseSameer S Chopra, Ignaty Leshchiner, Hatice Duzkale, et al.
Science (New York, N.Y.)|May 6, 2017
Negative selection in humans and fruit flies involves synergistic epistasisMashaal Sohail, Olga A Vakhrusheva, Jae Hoon Sul, et al.
Nature Communications|September 7, 2017
Identifying DNase I hypersensitive sites as driver distal regulatory elements in breast cancerMatteo D Antonio, Donate Weghorn, Agnieszka D Antonio-Chronowska, et al.
Nucleic Acids Research|December 3, 2025
FAVOR 2.0: A reengineered functional annotation of variants online resource for interpreting genomic variationHufeng Zhou, Vineet Verma, Xihao Li, et al.
Plos Genetics|March 8, 2013
Deleterious alleles in the human genome are on average younger than neutral alleles of the same frequencyAdam Kiezun, Sara L Pulit, Laurent C Francioli, et al.
Cell Genomics|June 22, 2026
NERINE reveals rare variant associations in gene networks across phenotypes and implicates an SNCA-PRL-LRRK2 subnetwork in Parkinson's diseaseSumaiya Nazeen, Xinyuan Wang, Autumn R Morrow, et al.
Pageof 11