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D Schellenberg

Showing results (441-450 of 467) with videos related to

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American Journal of Human Genetics|April 29, 2014
Convergence of genes and cellular pathways dysregulated in autism spectrum disordersDalila Pinto, Elsa Delaby, Daniele Merico, et al.
Nature Genetics|November 21, 2022
Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer's diseaseHenne Holstege, Marc Hulsman, Camille Charbonnier, et al.
Human Genetics|October 15, 2011
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorderJillian P Casey, Tiago Magalhaes, Judith M Conroy, et al.
Nature Genetics|February 16, 2010
Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusionsVivianna M Van Deerlin, Patrick M A Sleiman, Maria Martinez-Lage, et al.
Molecular Psychiatry|March 18, 2015
A novel Alzheimer disease locus located near the gene encoding tau proteinG Jun, C A Ibrahim-Verbaas, M Vronskaya, et al.
Nature Genetics|February 27, 2007
Mapping autism risk loci using genetic linkage and chromosomal rearrangements, Peter Szatmari, Andrew D Paterson, et al.
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.
Nature Genetics|March 13, 2026
A repeat expansion in GOLGA8A is a major risk factor for atypical frontotemporal lobar degeneration with ubiquitin-positive inclusionsWouter De Coster, Marleen Van den Broeck, Matt Baker, et al.
Molecular Psychiatry|December 5, 2024
X-chromosome-wide association study for Alzheimer's diseaseJulie Le Borgne, Lissette Gomez, Sami Heikkinen, et al.
Neurology|January 18, 2019
Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based settingGanesh Chauhan, Hieab H H Adams, Claudia L Satizabal, et al.
Pageof 47

Showing results (441-450 of 467) with videos related to

Sort By:
Pageof 47
American Journal of Human Genetics|April 29, 2014
Convergence of genes and cellular pathways dysregulated in autism spectrum disordersDalila Pinto, Elsa Delaby, Daniele Merico, et al.
Nature Genetics|November 21, 2022
Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer's diseaseHenne Holstege, Marc Hulsman, Camille Charbonnier, et al.
Human Genetics|October 15, 2011
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorderJillian P Casey, Tiago Magalhaes, Judith M Conroy, et al.
Nature Genetics|February 16, 2010
Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusionsVivianna M Van Deerlin, Patrick M A Sleiman, Maria Martinez-Lage, et al.
Molecular Psychiatry|March 18, 2015
A novel Alzheimer disease locus located near the gene encoding tau proteinG Jun, C A Ibrahim-Verbaas, M Vronskaya, et al.
Nature Genetics|February 27, 2007
Mapping autism risk loci using genetic linkage and chromosomal rearrangements, Peter Szatmari, Andrew D Paterson, et al.
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.
Nature Genetics|March 13, 2026
A repeat expansion in GOLGA8A is a major risk factor for atypical frontotemporal lobar degeneration with ubiquitin-positive inclusionsWouter De Coster, Marleen Van den Broeck, Matt Baker, et al.
Molecular Psychiatry|December 5, 2024
X-chromosome-wide association study for Alzheimer's diseaseJulie Le Borgne, Lissette Gomez, Sami Heikkinen, et al.
Neurology|January 18, 2019
Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based settingGanesh Chauhan, Hieab H H Adams, Claudia L Satizabal, et al.
Pageof 47