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Steven Gazal

Showing results (31-40 of 98) with videos related to

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Medrxiv : the Preprint Server for Health Sciences|June 30, 2025
Pleiotropic heritability quantifies the shared genetic variance of common diseasesYujie Zhao, Benjamin Strober, Kangcheng Hou, et al.
Nature Genetics|June 9, 2026
Pleiotropic shared heritability quantifies the shared genetic variance of common diseasesYujie Zhao, Benjamin Strober, Kangcheng Hou, et al.
American Journal of Human Genetics|January 1, 2019
Leveraging Polygenic Functional Enrichment to Improve GWAS PowerGleb Kichaev, Gaurav Bhatia, Po-Ru Loh, et al.
Science (New York, N.Y.)|April 27, 2023
Mammalian evolution of human cis-regulatory elements and transcription factor binding sitesGregory Andrews, Kaili Fan, Henry E Pratt, et al.
RMD Open|October 27, 2017
Variants of genes implicated in type 1 interferon pathway and B-cell activation modulate the EULAR response to rituximab at 24 weeks in rheumatoid arthritisPierre-Antoine Juge, Steven Gazal, Arnaud Constantin, et al.
Nature Genetics|July 21, 2025
Improved multiancestry fine-mapping identifies cis-regulatory variants underlying molecular traits and disease riskZeyun Lu, Xinran Wang, Matthew Carr, et al.
Elife|March 20, 2023
The lingering effects of Neanderthal introgression on human complex traitsXinzhu Wei, Christopher R Robles, Ali Pazokitoroudi, et al.
Medrxiv : the Preprint Server for Health Sciences|May 3, 2024
Improved multi-ancestry fine-mapping identifies <i>cis</i>-regulatory variants underlying molecular traits and disease riskZeyun Lu, Xinran Wang, Matthew Carr, et al.
Nature Genetics|September 29, 2022
Identifying disease-critical cell types and cellular processes by integrating single-cell RNA-sequencing and human geneticsKarthik A Jagadeesh, Kushal K Dey, Daniel T Montoro, et al.
Biorxiv : the Preprint Server for Biology|November 30, 2021
Identifying disease-critical cell types and cellular processes across the human body by integration of single-cell profiles and human geneticsKarthik A Jagadeesh, Kushal K Dey, Daniel T Montoro, et al.
Pageof 10

Showing results (31-40 of 98) with videos related to

Sort By:
Pageof 10
Medrxiv : the Preprint Server for Health Sciences|June 30, 2025
Pleiotropic heritability quantifies the shared genetic variance of common diseasesYujie Zhao, Benjamin Strober, Kangcheng Hou, et al.
Nature Genetics|June 9, 2026
Pleiotropic shared heritability quantifies the shared genetic variance of common diseasesYujie Zhao, Benjamin Strober, Kangcheng Hou, et al.
American Journal of Human Genetics|January 1, 2019
Leveraging Polygenic Functional Enrichment to Improve GWAS PowerGleb Kichaev, Gaurav Bhatia, Po-Ru Loh, et al.
Science (New York, N.Y.)|April 27, 2023
Mammalian evolution of human cis-regulatory elements and transcription factor binding sitesGregory Andrews, Kaili Fan, Henry E Pratt, et al.
RMD Open|October 27, 2017
Variants of genes implicated in type 1 interferon pathway and B-cell activation modulate the EULAR response to rituximab at 24 weeks in rheumatoid arthritisPierre-Antoine Juge, Steven Gazal, Arnaud Constantin, et al.
Nature Genetics|July 21, 2025
Improved multiancestry fine-mapping identifies cis-regulatory variants underlying molecular traits and disease riskZeyun Lu, Xinran Wang, Matthew Carr, et al.
Elife|March 20, 2023
The lingering effects of Neanderthal introgression on human complex traitsXinzhu Wei, Christopher R Robles, Ali Pazokitoroudi, et al.
Medrxiv : the Preprint Server for Health Sciences|May 3, 2024
Improved multi-ancestry fine-mapping identifies <i>cis</i>-regulatory variants underlying molecular traits and disease riskZeyun Lu, Xinran Wang, Matthew Carr, et al.
Nature Genetics|September 29, 2022
Identifying disease-critical cell types and cellular processes by integrating single-cell RNA-sequencing and human geneticsKarthik A Jagadeesh, Kushal K Dey, Daniel T Montoro, et al.
Biorxiv : the Preprint Server for Biology|November 30, 2021
Identifying disease-critical cell types and cellular processes across the human body by integration of single-cell profiles and human geneticsKarthik A Jagadeesh, Kushal K Dey, Daniel T Montoro, et al.
Pageof 10