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H Geschwind

Showing results (791-800 of 809) with videos related to

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Human Molecular Genetics|July 31, 2012
Individual common variants exert weak effects on the risk for autism spectrum disordersRichard Anney, Lambertus Klei, Dalila Pinto, et al.
Medrxiv : the Preprint Server for Health Sciences|July 9, 2024
Deciphering Distinct Genetic Risk Factors for FTLD-TDP Pathological Subtypes via Whole-Genome SequencingCyril Pottier, Fahri Küçükali, Matt Baker, et al.
Plos Genetics|November 3, 2022
Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics InitiativeGuillaume Butler-Laporte, Gundula Povysil, Jack A Kosmicki, et al.
Cell Genomics|February 13, 2023
Global Biobank Meta-analysis Initiative: Powering genetic discovery across human diseaseWei Zhou, Masahiro Kanai, Kuan-Han H Wu, et al.
Human Molecular Genetics|July 29, 2010
A genome-wide scan for common alleles affecting risk for autismRichard Anney, Lambertus Klei, Dalila Pinto, et al.
Nature|June 10, 2010
Functional impact of global rare copy number variation in autism spectrum disordersDalila Pinto, Alistair T Pagnamenta, Lambertus Klei, et al.
Nature Genetics|April 5, 2011
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's diseaseAdam C Naj, Gyungah Jun, Gary W Beecham, et al.
JAMA Neurology|September 10, 2014
Effects of multiple genetic loci on age at onset in late-onset Alzheimer disease: a genome-wide association studyAdam C Naj, Gyungah Jun, Christiane Reitz, et al.
Neurology|June 23, 2012
Novel late-onset Alzheimer disease loci variants associate with brain gene expressionMariet Allen, Fanggeng Zou, High Seng Chai, et al.
JAMA Neurology|December 23, 2014
Rarity of the Alzheimer disease-protective APP A673T variant in the United StatesLi-San Wang, Adam C Naj, Robert R Graham, et al.
Pageof 81

Showing results (791-800 of 809) with videos related to

Sort By:
Pageof 81
Human Molecular Genetics|July 31, 2012
Individual common variants exert weak effects on the risk for autism spectrum disordersRichard Anney, Lambertus Klei, Dalila Pinto, et al.
Medrxiv : the Preprint Server for Health Sciences|July 9, 2024
Deciphering Distinct Genetic Risk Factors for FTLD-TDP Pathological Subtypes via Whole-Genome SequencingCyril Pottier, Fahri Küçükali, Matt Baker, et al.
Plos Genetics|November 3, 2022
Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics InitiativeGuillaume Butler-Laporte, Gundula Povysil, Jack A Kosmicki, et al.
Cell Genomics|February 13, 2023
Global Biobank Meta-analysis Initiative: Powering genetic discovery across human diseaseWei Zhou, Masahiro Kanai, Kuan-Han H Wu, et al.
Human Molecular Genetics|July 29, 2010
A genome-wide scan for common alleles affecting risk for autismRichard Anney, Lambertus Klei, Dalila Pinto, et al.
Nature|June 10, 2010
Functional impact of global rare copy number variation in autism spectrum disordersDalila Pinto, Alistair T Pagnamenta, Lambertus Klei, et al.
Nature Genetics|April 5, 2011
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's diseaseAdam C Naj, Gyungah Jun, Gary W Beecham, et al.
JAMA Neurology|September 10, 2014
Effects of multiple genetic loci on age at onset in late-onset Alzheimer disease: a genome-wide association studyAdam C Naj, Gyungah Jun, Christiane Reitz, et al.
Neurology|June 23, 2012
Novel late-onset Alzheimer disease loci variants associate with brain gene expressionMariet Allen, Fanggeng Zou, High Seng Chai, et al.
JAMA Neurology|December 23, 2014
Rarity of the Alzheimer disease-protective APP A673T variant in the United StatesLi-San Wang, Adam C Naj, Robert R Graham, et al.
Pageof 81