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Bernie Devlin

Showing results (131-140 of 165) with videos related to

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Nature Genetics|May 16, 2019
Publisher Correction: Gene expression imputation across multiple brain regions provides insights into schizophrenia riskLaura M Huckins, Amanda Dobbyn, Douglas M Ruderfer, et al.
Alzheimer'S & Dementia (New York, N. Y.)|May 24, 2024
Genetic associations with psychosis and affective disturbance in Alzheimer's diseaseInga Margret Antonsdottir, Byron Creese, Lambertus Klei, et al.
Cell Reports|October 7, 2014
De novo insertions and deletions of predominantly paternal origin are associated with autism spectrum disorderShan Dong, Michael F Walker, Nicholas J Carriero, et al.
Cell Reports|April 9, 2020
Whole-Genome and RNA Sequencing Reveal Variation and Transcriptomic Coordination in the Developing Human Prefrontal CortexDonna M Werling, Sirisha Pochareddy, Jinmyung Choi, et al.
Cell|November 26, 2013
Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autismA Jeremy Willsey, Stephan J Sanders, Mingfeng Li, et al.
Plos Genetics|April 18, 2013
Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controlsLi Liu, Aniko Sabo, Benjamin M Neale, et al.
Nature|April 13, 2012
De novo mutations revealed by whole-exome sequencing are strongly associated with autismStephan J Sanders, Michael T Murtha, Abha R Gupta, et al.
Science (New York, N.Y.)|December 15, 2018
Genome-wide de novo risk score implicates promoter variation in autism spectrum disorderJoon-Yong An, Kevin Lin, Lingxue Zhu, et al.
Biological Psychiatry|April 25, 2006
Evaluation of a susceptibility gene for schizophrenia: genotype based meta-analysis of RGS4 polymorphisms from thirteen independent samplesMichael E Talkowski, Howard Seltman, Anne S Bassett, et al.
Gastroenterology|August 6, 2016
A Pleiotropic Missense Variant in SLC39A8 Is Associated With Crohn's Disease and Human Gut Microbiome CompositionDalin Li, Jean-Paul Achkar, Talin Haritunians, et al.
Pageof 17

Showing results (131-140 of 165) with videos related to

Sort By:
Pageof 17
Nature Genetics|May 16, 2019
Publisher Correction: Gene expression imputation across multiple brain regions provides insights into schizophrenia riskLaura M Huckins, Amanda Dobbyn, Douglas M Ruderfer, et al.
Alzheimer'S & Dementia (New York, N. Y.)|May 24, 2024
Genetic associations with psychosis and affective disturbance in Alzheimer's diseaseInga Margret Antonsdottir, Byron Creese, Lambertus Klei, et al.
Cell Reports|October 7, 2014
De novo insertions and deletions of predominantly paternal origin are associated with autism spectrum disorderShan Dong, Michael F Walker, Nicholas J Carriero, et al.
Cell Reports|April 9, 2020
Whole-Genome and RNA Sequencing Reveal Variation and Transcriptomic Coordination in the Developing Human Prefrontal CortexDonna M Werling, Sirisha Pochareddy, Jinmyung Choi, et al.
Cell|November 26, 2013
Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autismA Jeremy Willsey, Stephan J Sanders, Mingfeng Li, et al.
Plos Genetics|April 18, 2013
Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controlsLi Liu, Aniko Sabo, Benjamin M Neale, et al.
Nature|April 13, 2012
De novo mutations revealed by whole-exome sequencing are strongly associated with autismStephan J Sanders, Michael T Murtha, Abha R Gupta, et al.
Science (New York, N.Y.)|December 15, 2018
Genome-wide de novo risk score implicates promoter variation in autism spectrum disorderJoon-Yong An, Kevin Lin, Lingxue Zhu, et al.
Biological Psychiatry|April 25, 2006
Evaluation of a susceptibility gene for schizophrenia: genotype based meta-analysis of RGS4 polymorphisms from thirteen independent samplesMichael E Talkowski, Howard Seltman, Anne S Bassett, et al.
Gastroenterology|August 6, 2016
A Pleiotropic Missense Variant in SLC39A8 Is Associated With Crohn's Disease and Human Gut Microbiome CompositionDalin Li, Jean-Paul Achkar, Talin Haritunians, et al.
Pageof 17