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Neil Risch

Showing results (131-140 of 146) with videos related to

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American Journal of Human Genetics|September 8, 2018
The Clinical Sequencing Evidence-Generating Research Consortium: Integrating Genomic Sequencing in Diverse and Medically Underserved PopulationsLaura M Amendola, Jonathan S Berg, Carol R Horowitz, et al.
Genomics|May 14, 2011
Next generation genome-wide association tool: design and coverage of a high-throughput European-optimized SNP arrayThomas J Hoffmann, Mark N Kvale, Stephanie E Hesselson, et al.
Nature Genetics|May 5, 2009
Narcolepsy is strongly associated with the T-cell receptor alpha locusJoachim Hallmayer, Juliette Faraco, Ling Lin, et al.
Pediatrics|January 19, 2017
Newborn Sequencing in Genomic Medicine and Public HealthJonathan S Berg, Pankaj B Agrawal, Donald B Bailey, et al.
Nature Genetics|April 12, 2022
Exome sequencing in bipolar disorder identifies AKAP11 as a risk gene shared with schizophreniaDuncan S Palmer, Daniel P Howrigan, Sinéad B Chapman, et al.
Clinical Trials (London, England)|July 3, 2013
The epilepsy phenome/genome project, Bassel Abou-Khalil, Brian Alldredge, et al.
Nature Genetics|December 21, 2010
Common variants in P2RY11 are associated with narcolepsyBirgitte R Kornum, Minae Kawashima, Juliette Faraco, 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.
Plos Genetics|May 12, 2018
Correction: Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populationsJingjing Liang, Thu H Le, Digna R Velez Edwards, et al.
Pageof 15

Showing results (131-140 of 146) with videos related to

Sort By:
Pageof 15
American Journal of Human Genetics|September 8, 2018
The Clinical Sequencing Evidence-Generating Research Consortium: Integrating Genomic Sequencing in Diverse and Medically Underserved PopulationsLaura M Amendola, Jonathan S Berg, Carol R Horowitz, et al.
Genomics|May 14, 2011
Next generation genome-wide association tool: design and coverage of a high-throughput European-optimized SNP arrayThomas J Hoffmann, Mark N Kvale, Stephanie E Hesselson, et al.
Nature Genetics|May 5, 2009
Narcolepsy is strongly associated with the T-cell receptor alpha locusJoachim Hallmayer, Juliette Faraco, Ling Lin, et al.
Pediatrics|January 19, 2017
Newborn Sequencing in Genomic Medicine and Public HealthJonathan S Berg, Pankaj B Agrawal, Donald B Bailey, et al.
Nature Genetics|April 12, 2022
Exome sequencing in bipolar disorder identifies AKAP11 as a risk gene shared with schizophreniaDuncan S Palmer, Daniel P Howrigan, Sinéad B Chapman, et al.
Clinical Trials (London, England)|July 3, 2013
The epilepsy phenome/genome project, Bassel Abou-Khalil, Brian Alldredge, et al.
Nature Genetics|December 21, 2010
Common variants in P2RY11 are associated with narcolepsyBirgitte R Kornum, Minae Kawashima, Juliette Faraco, 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.
Plos Genetics|May 12, 2018
Correction: Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populationsJingjing Liang, Thu H Le, Digna R Velez Edwards, et al.
Pageof 15