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Showing results (441-450 of 552) with videos related to

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Nature Neuroscience|November 8, 2016
Ultra-rare disruptive and damaging mutations influence educational attainment in the general populationAndrea Ganna, Giulio Genovese, Daniel P Howrigan, et al.
Nature Genetics|December 25, 2012
Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretionJeroen R Huyghe, Anne U Jackson, Marie P Fogarty, et al.
Cell Reports|September 27, 2018
De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in PathogenesisSheng Wang, Jeffrey D Mandell, Yogesh Kumar, et al.
Ebiomedicine|April 16, 2025
Genome-wide association meta-analyses of drug-resistant epilepsyCostin Leu, Andreja Avbersek, Remi Stevelink, et al.
Nature Genetics|September 26, 2022
Identification of shared and differentiating genetic architecture for autism spectrum disorder, attention-deficit hyperactivity disorder and case subgroupsManuel Mattheisen, Jakob Grove, Thomas D Als, et al.
Nature|November 12, 2025
Rare genetic variants confer a high risk of ADHD and implicate neuronal biologyDitte Demontis, Jinjie Duan, Yu-Han H Hsu, et al.
Nature Communications|September 5, 2014
Clozapine-induced agranulocytosis is associated with rare HLA-DQB1 and HLA-B allelesJacqueline I Goldstein, L Fredrik Jarskog, Chris Hilliard, et al.
Biorxiv : the Preprint Server for Biology|April 22, 2024
The landscape of regional missense mutational intolerance quantified from 125,748 exomesKatherine R Chao, Lily Wang, Ruchit Panchal, et al.
Cell Reports|December 20, 2018
De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in PathogenesisSheng Wang, Jeffrey D Mandell, Yogesh Kumar, et al.
Biological Psychiatry|April 29, 2008
Linkage to chromosome 1p36 for attention-deficit/hyperactivity disorder traits in school and home settingsKaixin Zhou, Philip Asherson, Pak Sham, et al.
Pageof 56

Showing results (441-450 of 552) with videos related to

Sort By:
Pageof 56
Nature Neuroscience|November 8, 2016
Ultra-rare disruptive and damaging mutations influence educational attainment in the general populationAndrea Ganna, Giulio Genovese, Daniel P Howrigan, et al.
Nature Genetics|December 25, 2012
Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretionJeroen R Huyghe, Anne U Jackson, Marie P Fogarty, et al.
Cell Reports|September 27, 2018
De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in PathogenesisSheng Wang, Jeffrey D Mandell, Yogesh Kumar, et al.
Ebiomedicine|April 16, 2025
Genome-wide association meta-analyses of drug-resistant epilepsyCostin Leu, Andreja Avbersek, Remi Stevelink, et al.
Nature Genetics|September 26, 2022
Identification of shared and differentiating genetic architecture for autism spectrum disorder, attention-deficit hyperactivity disorder and case subgroupsManuel Mattheisen, Jakob Grove, Thomas D Als, et al.
Nature|November 12, 2025
Rare genetic variants confer a high risk of ADHD and implicate neuronal biologyDitte Demontis, Jinjie Duan, Yu-Han H Hsu, et al.
Nature Communications|September 5, 2014
Clozapine-induced agranulocytosis is associated with rare HLA-DQB1 and HLA-B allelesJacqueline I Goldstein, L Fredrik Jarskog, Chris Hilliard, et al.
Biorxiv : the Preprint Server for Biology|April 22, 2024
The landscape of regional missense mutational intolerance quantified from 125,748 exomesKatherine R Chao, Lily Wang, Ruchit Panchal, et al.
Cell Reports|December 20, 2018
De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in PathogenesisSheng Wang, Jeffrey D Mandell, Yogesh Kumar, et al.
Biological Psychiatry|April 29, 2008
Linkage to chromosome 1p36 for attention-deficit/hyperactivity disorder traits in school and home settingsKaixin Zhou, Philip Asherson, Pak Sham, et al.
Pageof 56