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M Neale

Showing results (391-400 of 551) with videos related to

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Neuron|May 5, 2017
De Novo Coding Variants Are Strongly Associated with Tourette DisorderA Jeremy Willsey, Thomas V Fernandez, Dongmei Yu, et al.
Nature Genetics|September 29, 2015
Partitioning heritability by functional annotation using genome-wide association summary statisticsHilary K Finucane, Brendan Bulik-Sullivan, Alexander Gusev, et al.
American Journal of Human Genetics|December 3, 2014
Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseasesAlexander Gusev, S Hong Lee, Gosia Trynka, et al.
Medrxiv : the Preprint Server for Health Sciences|January 30, 2023
Fine-mapping across diverse ancestries drives the discovery of putative causal variants underlying human complex traits and diseasesKai Yuan, Ryan J Longchamps, Antonio F Pardiñas, et al.
Nature Genetics|December 6, 2023
Inferring compound heterozygosity from large-scale exome sequencing dataMichael H Guo, Laurent C Francioli, Sarah L Stenton, et al.
Psychological Medicine|September 18, 2018
Genetic influences on eight psychiatric disorders based on family data of 4 408 646 full and half-siblings, and genetic data of 333 748 cases and controlsE Pettersson, P Lichtenstein, H Larsson, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|July 19, 2017
Mutation intolerant genes and targets of FMRP are enriched for nonsynonymous alleles in schizophreniaGanna Leonenko, Alexander L Richards, James T Walters, et al.
Plos Genetics|January 27, 2015
No evidence for association of autism with rare heterozygous point mutations in Contactin-Associated Protein-Like 2 (CNTNAP2), or in Other Contactin-Associated Proteins or ContactinsJohn D Murdoch, Abha R Gupta, Stephan J Sanders, et al.
Science (New York, N.Y.)|April 14, 2022
Getting genetic ancestry right for science and societyAnna C F Lewis, Santiago J Molina, Paul S Appelbaum, et al.
Cell Genomics|August 21, 2023
Multi-ancestry meta-analysis identifies 5 novel loci for ischemic stroke and reveals heterogeneity of effects between sexes and ancestriesIda Surakka, Kuan-Han Wu, Whitney Hornsby, et al.
Pageof 56

Showing results (391-400 of 551) with videos related to

Sort By:
Pageof 56
Neuron|May 5, 2017
De Novo Coding Variants Are Strongly Associated with Tourette DisorderA Jeremy Willsey, Thomas V Fernandez, Dongmei Yu, et al.
Nature Genetics|September 29, 2015
Partitioning heritability by functional annotation using genome-wide association summary statisticsHilary K Finucane, Brendan Bulik-Sullivan, Alexander Gusev, et al.
American Journal of Human Genetics|December 3, 2014
Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseasesAlexander Gusev, S Hong Lee, Gosia Trynka, et al.
Medrxiv : the Preprint Server for Health Sciences|January 30, 2023
Fine-mapping across diverse ancestries drives the discovery of putative causal variants underlying human complex traits and diseasesKai Yuan, Ryan J Longchamps, Antonio F Pardiñas, et al.
Nature Genetics|December 6, 2023
Inferring compound heterozygosity from large-scale exome sequencing dataMichael H Guo, Laurent C Francioli, Sarah L Stenton, et al.
Psychological Medicine|September 18, 2018
Genetic influences on eight psychiatric disorders based on family data of 4 408 646 full and half-siblings, and genetic data of 333 748 cases and controlsE Pettersson, P Lichtenstein, H Larsson, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|July 19, 2017
Mutation intolerant genes and targets of FMRP are enriched for nonsynonymous alleles in schizophreniaGanna Leonenko, Alexander L Richards, James T Walters, et al.
Plos Genetics|January 27, 2015
No evidence for association of autism with rare heterozygous point mutations in Contactin-Associated Protein-Like 2 (CNTNAP2), or in Other Contactin-Associated Proteins or ContactinsJohn D Murdoch, Abha R Gupta, Stephan J Sanders, et al.
Science (New York, N.Y.)|April 14, 2022
Getting genetic ancestry right for science and societyAnna C F Lewis, Santiago J Molina, Paul S Appelbaum, et al.
Cell Genomics|August 21, 2023
Multi-ancestry meta-analysis identifies 5 novel loci for ischemic stroke and reveals heterogeneity of effects between sexes and ancestriesIda Surakka, Kuan-Han Wu, Whitney Hornsby, et al.
Pageof 56