Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Shaun M Purcell

Showing results (81-90 of 101) with videos related to

Pageof 11
Sort By:
Genome Medicine|August 27, 2021
Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed programBrian E Cade, Jiwon Lee, Tamar Sofer, et al.
Science (New York, N.Y.)|May 9, 2015
Human genomics. Effect of predicted protein-truncating genetic variants on the human transcriptomeManuel A Rivas, Matti Pirinen, Donald F Conrad, et al.
Neuron|January 29, 2013
Rare complete knockouts in humans: population distribution and significant role in autism spectrum disordersElaine T Lim, Soumya Raychaudhuri, Stephan J Sanders, et al.
Human Molecular Genetics|November 8, 2018
Admixture mapping identifies novel loci for obstructive sleep apnea in Hispanic/Latino AmericansHeming Wang, Brian E Cade, Tamar Sofer, et al.
Nature Communications|August 15, 2019
Genome-wide association analysis of self-reported daytime sleepiness identifies 42 loci that suggest biological subtypesHeming Wang, Jacqueline M Lane, Samuel E Jones, et al.
Plos Genetics|April 17, 2019
Associations of variants In the hexokinase 1 and interleukin 18 receptor regions with oxyhemoglobin saturation during sleepBrian E Cade, Han Chen, Adrienne M Stilp, et al.
Biological Psychiatry|January 29, 2019
Contribution of Rare Copy Number Variants to Bipolar Disorder Risk Is Limited to Schizoaffective CasesAlexander W Charney, Eli A Stahl, Elaine K Green, et al.
Molecular Psychiatry|October 28, 2015
Genome-wide association study identifies SESTD1 as a novel risk gene for lithium-responsive bipolar disorderJ Song, S E Bergen, A Di Florio, et al.
Nature Neuroscience|March 15, 2016
Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disordersTarjinder Singh, Mitja I Kurki, David Curtis, et al.
Nature Neuroscience|September 27, 2016
Gene expression elucidates functional impact of polygenic risk for schizophreniaMenachem Fromer, Panos Roussos, Solveig K Sieberts, et al.
Pageof 11

Showing results (81-90 of 101) with videos related to

Sort By:
Pageof 11
Genome Medicine|August 27, 2021
Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed programBrian E Cade, Jiwon Lee, Tamar Sofer, et al.
Science (New York, N.Y.)|May 9, 2015
Human genomics. Effect of predicted protein-truncating genetic variants on the human transcriptomeManuel A Rivas, Matti Pirinen, Donald F Conrad, et al.
Neuron|January 29, 2013
Rare complete knockouts in humans: population distribution and significant role in autism spectrum disordersElaine T Lim, Soumya Raychaudhuri, Stephan J Sanders, et al.
Human Molecular Genetics|November 8, 2018
Admixture mapping identifies novel loci for obstructive sleep apnea in Hispanic/Latino AmericansHeming Wang, Brian E Cade, Tamar Sofer, et al.
Nature Communications|August 15, 2019
Genome-wide association analysis of self-reported daytime sleepiness identifies 42 loci that suggest biological subtypesHeming Wang, Jacqueline M Lane, Samuel E Jones, et al.
Plos Genetics|April 17, 2019
Associations of variants In the hexokinase 1 and interleukin 18 receptor regions with oxyhemoglobin saturation during sleepBrian E Cade, Han Chen, Adrienne M Stilp, et al.
Biological Psychiatry|January 29, 2019
Contribution of Rare Copy Number Variants to Bipolar Disorder Risk Is Limited to Schizoaffective CasesAlexander W Charney, Eli A Stahl, Elaine K Green, et al.
Molecular Psychiatry|October 28, 2015
Genome-wide association study identifies SESTD1 as a novel risk gene for lithium-responsive bipolar disorderJ Song, S E Bergen, A Di Florio, et al.
Nature Neuroscience|March 15, 2016
Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disordersTarjinder Singh, Mitja I Kurki, David Curtis, et al.
Nature Neuroscience|September 27, 2016
Gene expression elucidates functional impact of polygenic risk for schizophreniaMenachem Fromer, Panos Roussos, Solveig K Sieberts, et al.
Pageof 11