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F Sullivan

Showing results (1041-1050 of 1,111) with videos related to

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Molecular Psychiatry|November 12, 2024
Genome-wide copy number variation association study in anorexia nervosaAlicia Walker, Robert Karlsson, Jin P Szatkiewicz, et al.
Molecular Psychiatry|November 3, 2010
Genome-wide association study of major depressive disorder: new results, meta-analysis, and lessons learnedN R Wray, M L Pergadia, D H R Blackwood, et al.
Plos Genetics|February 14, 2015
A multi-megabase copy number gain causes maternal transmission ratio distortion on mouse chromosome 2John P Didion, Andrew P Morgan, Amelia M-F Clayshulte, et al.
Nature Genetics|April 15, 2014
Heritability and genomics of gene expression in peripheral bloodFred A Wright, Patrick F Sullivan, Andrew I Brooks, et al.
Science (New York, N.Y.)|April 27, 2023
Leveraging base-pair mammalian constraint to understand genetic variation and human diseasePatrick F Sullivan, Jennifer R S Meadows, Steven Gazal, et al.
Biorxiv : the Preprint Server for Biology|March 22, 2023
Leveraging Base Pair Mammalian Constraint to Understand Genetic Variation and Human DiseasePatrick F Sullivan, Jennifer R S Meadows, Steven Gazal, et al.
American Journal of Human Genetics|June 5, 2018
Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic SpectrumAndrea Ganna, F Kyle Satterstrom, Seyedeh M Zekavat, et al.
Nature Genetics|March 3, 2015
Analyses of allele-specific gene expression in highly divergent mouse crosses identifies pervasive allelic imbalanceJames J Crowley, Vasyl Zhabotynsky, Wei Sun, et al.
JAMA Psychiatry|January 18, 2013
Implication of a rare deletion at distal 16p11.2 in schizophreniaSaurav Guha, Elliott Rees, Ariel Darvasi, et al.
The Lancet. Psychiatry|June 29, 2025
The Psychiatric Genomics Consortium: discoveries and directionsArpana Agrawal, Cynthia M Bulik, Dawit Shawel Abebe, et al.
Pageof 112

Showing results (1041-1050 of 1,111) with videos related to

Sort By:
Pageof 112
Molecular Psychiatry|November 12, 2024
Genome-wide copy number variation association study in anorexia nervosaAlicia Walker, Robert Karlsson, Jin P Szatkiewicz, et al.
Molecular Psychiatry|November 3, 2010
Genome-wide association study of major depressive disorder: new results, meta-analysis, and lessons learnedN R Wray, M L Pergadia, D H R Blackwood, et al.
Plos Genetics|February 14, 2015
A multi-megabase copy number gain causes maternal transmission ratio distortion on mouse chromosome 2John P Didion, Andrew P Morgan, Amelia M-F Clayshulte, et al.
Nature Genetics|April 15, 2014
Heritability and genomics of gene expression in peripheral bloodFred A Wright, Patrick F Sullivan, Andrew I Brooks, et al.
Science (New York, N.Y.)|April 27, 2023
Leveraging base-pair mammalian constraint to understand genetic variation and human diseasePatrick F Sullivan, Jennifer R S Meadows, Steven Gazal, et al.
Biorxiv : the Preprint Server for Biology|March 22, 2023
Leveraging Base Pair Mammalian Constraint to Understand Genetic Variation and Human DiseasePatrick F Sullivan, Jennifer R S Meadows, Steven Gazal, et al.
American Journal of Human Genetics|June 5, 2018
Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic SpectrumAndrea Ganna, F Kyle Satterstrom, Seyedeh M Zekavat, et al.
Nature Genetics|March 3, 2015
Analyses of allele-specific gene expression in highly divergent mouse crosses identifies pervasive allelic imbalanceJames J Crowley, Vasyl Zhabotynsky, Wei Sun, et al.
JAMA Psychiatry|January 18, 2013
Implication of a rare deletion at distal 16p11.2 in schizophreniaSaurav Guha, Elliott Rees, Ariel Darvasi, et al.
The Lancet. Psychiatry|June 29, 2025
The Psychiatric Genomics Consortium: discoveries and directionsArpana Agrawal, Cynthia M Bulik, Dawit Shawel Abebe, et al.
Pageof 112