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Benjamin M Neale

Showing results (111-120 of 293) with videos related to

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Molecular Psychiatry|February 25, 2021
Correction to: Attention-deficit/hyperactivity disorder and lifetime cannabis use: genetic overlap and causalityMaría Soler Artigas, Cristina Sánchez-Mora, Paula Rovira, et al.
Biorxiv : the Preprint Server for Biology|April 22, 2024
Blended Genome Exome (BGE) as a Cost Efficient Alternative to Deep Whole Genomes or ArraysMatthew DeFelice, Jonna L Grimsby, Daniel Howrigan, et al.
Journal of the American Academy of Child and Adolescent Psychiatry|August 25, 2010
Family-based genome-wide association scan of attention-deficit/hyperactivity disorderEric Mick, Alexandre Todorov, Susan Smalley, et al.
Nature Communications|December 14, 2025
Complex genetic effects linked to plasma protein abundance in the UK BiobankArnor I Sigurdsson, Justus F Gräf, Zhiyu Yang, et al.
Human Molecular Genetics|June 26, 2009
Common body mass index-associated variants confer risk of extreme obesityChris Cotsapas, Elizabeth K Speliotes, Ida J Hatoum, et al.
Bioinformatics (Oxford, England)|July 31, 2012
zCall: a rare variant caller for array-based genotyping: genetics and population analysisJacqueline I Goldstein, Andrew Crenshaw, Jason Carey, et al.
Nature Genetics|February 14, 2017
Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samplesJack A Kosmicki, Kaitlin E Samocha, Daniel P Howrigan, et al.
Nature Genetics|April 11, 2018
Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insightsAlexander Gusev, Nicholas Mancuso, Hyejung Won, et al.
Medrxiv : the Preprint Server for Health Sciences|May 1, 2026
Phenome-derived polygenic scores and social determinants jointly shape context-dependent disease riskYing Wang, Buu Truong, Wenhan Lu, et al.
American Journal of Human Genetics|May 2, 2026
Meta-analysis across six global biobanks identifies recessive coding associations with complex traits and diseasesFrederik H Lassen, Georgios Kalantzis, Andrea Eoli, et al.
Pageof 30

Showing results (111-120 of 293) with videos related to

Sort By:
Pageof 30
Molecular Psychiatry|February 25, 2021
Correction to: Attention-deficit/hyperactivity disorder and lifetime cannabis use: genetic overlap and causalityMaría Soler Artigas, Cristina Sánchez-Mora, Paula Rovira, et al.
Biorxiv : the Preprint Server for Biology|April 22, 2024
Blended Genome Exome (BGE) as a Cost Efficient Alternative to Deep Whole Genomes or ArraysMatthew DeFelice, Jonna L Grimsby, Daniel Howrigan, et al.
Journal of the American Academy of Child and Adolescent Psychiatry|August 25, 2010
Family-based genome-wide association scan of attention-deficit/hyperactivity disorderEric Mick, Alexandre Todorov, Susan Smalley, et al.
Nature Communications|December 14, 2025
Complex genetic effects linked to plasma protein abundance in the UK BiobankArnor I Sigurdsson, Justus F Gräf, Zhiyu Yang, et al.
Human Molecular Genetics|June 26, 2009
Common body mass index-associated variants confer risk of extreme obesityChris Cotsapas, Elizabeth K Speliotes, Ida J Hatoum, et al.
Bioinformatics (Oxford, England)|July 31, 2012
zCall: a rare variant caller for array-based genotyping: genetics and population analysisJacqueline I Goldstein, Andrew Crenshaw, Jason Carey, et al.
Nature Genetics|February 14, 2017
Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samplesJack A Kosmicki, Kaitlin E Samocha, Daniel P Howrigan, et al.
Nature Genetics|April 11, 2018
Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insightsAlexander Gusev, Nicholas Mancuso, Hyejung Won, et al.
Medrxiv : the Preprint Server for Health Sciences|May 1, 2026
Phenome-derived polygenic scores and social determinants jointly shape context-dependent disease riskYing Wang, Buu Truong, Wenhan Lu, et al.
American Journal of Human Genetics|May 2, 2026
Meta-analysis across six global biobanks identifies recessive coding associations with complex traits and diseasesFrederik H Lassen, Georgios Kalantzis, Andrea Eoli, et al.
Pageof 30