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Patrick F Sullivan

Showing results (431-440 of 468) with videos related to

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Biological Psychiatry|October 2, 2019
Classical Human Leukocyte Antigen Alleles and C4 Haplotypes Are Not Significantly Associated With DepressionKylie P Glanville, Jonathan R I Coleman, Ken B Hanscombe, et al.
Molecular Psychiatry|October 9, 2019
Contributions of common genetic variants to risk of schizophrenia among individuals of African and Latino ancestryTim B Bigdeli, Giulio Genovese, Penelope Georgakopoulos, et al.
Science Translational Medicine|January 22, 2016
Quantifying prion disease penetrance using large population control cohortsEric Vallabh Minikel, Sonia M Vallabh, Monkol Lek, et al.
American Journal of Human Genetics|May 17, 2022
Genome-wide association meta-analysis identifies 48 risk variants and highlights the role of the stria vascularis in hearing lossNatalia Trpchevska, Maxim B Freidin, Linda Broer, et al.
Nature Genetics|October 27, 2009
Microduplications of 16p11.2 are associated with schizophreniaShane E McCarthy, Vladimir Makarov, George Kirov, et al.
Molecular Psychiatry|November 13, 2019
Genome-wide association study of panic disorder reveals genetic overlap with neuroticism and depressionAndreas J Forstner, Swapnil Awasthi, Christiane Wolf, et al.
Molecular Psychiatry|January 23, 2021
Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorderXiaoming Jia, Fernando S Goes, Adam E Locke, et al.
Molecular Psychiatry|March 6, 2021
Correction: Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorderXiaoming Jia, Fernando S Goes, Adam E Locke, et al.
JAMA Psychiatry|January 12, 2022
Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in SchizophreniaAntonio F Pardiñas, Sophie E Smart, Isabella R Willcocks, et al.
Nature Genetics|February 27, 2019
Identification of common genetic risk variants for autism spectrum disorderJakob Grove, Stephan Ripke, Thomas D Als, et al.
Pageof 47

Showing results (431-440 of 468) with videos related to

Sort By:
Pageof 47
Biological Psychiatry|October 2, 2019
Classical Human Leukocyte Antigen Alleles and C4 Haplotypes Are Not Significantly Associated With DepressionKylie P Glanville, Jonathan R I Coleman, Ken B Hanscombe, et al.
Molecular Psychiatry|October 9, 2019
Contributions of common genetic variants to risk of schizophrenia among individuals of African and Latino ancestryTim B Bigdeli, Giulio Genovese, Penelope Georgakopoulos, et al.
Science Translational Medicine|January 22, 2016
Quantifying prion disease penetrance using large population control cohortsEric Vallabh Minikel, Sonia M Vallabh, Monkol Lek, et al.
American Journal of Human Genetics|May 17, 2022
Genome-wide association meta-analysis identifies 48 risk variants and highlights the role of the stria vascularis in hearing lossNatalia Trpchevska, Maxim B Freidin, Linda Broer, et al.
Nature Genetics|October 27, 2009
Microduplications of 16p11.2 are associated with schizophreniaShane E McCarthy, Vladimir Makarov, George Kirov, et al.
Molecular Psychiatry|November 13, 2019
Genome-wide association study of panic disorder reveals genetic overlap with neuroticism and depressionAndreas J Forstner, Swapnil Awasthi, Christiane Wolf, et al.
Molecular Psychiatry|January 23, 2021
Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorderXiaoming Jia, Fernando S Goes, Adam E Locke, et al.
Molecular Psychiatry|March 6, 2021
Correction: Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorderXiaoming Jia, Fernando S Goes, Adam E Locke, et al.
JAMA Psychiatry|January 12, 2022
Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in SchizophreniaAntonio F Pardiñas, Sophie E Smart, Isabella R Willcocks, et al.
Nature Genetics|February 27, 2019
Identification of common genetic risk variants for autism spectrum disorderJakob Grove, Stephan Ripke, Thomas D Als, et al.
Pageof 47