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Showing results (871-880 of 908) with videos related to

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Human Molecular Genetics|January 12, 2017
New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristicsHenriët Springelkamp, Adriana I Iglesias, Aniket Mishra, et al.
JAMA Neurology|October 19, 2020
Novel Alzheimer Disease Risk Loci and Pathways in African American Individuals Using the African Genome Resources Panel: A Meta-analysisBrian W Kunkle, Michael Schmidt, Hans-Ulrich Klein, et al.
Nature Communications|September 23, 2014
Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous processHenriët Springelkamp, René Höhn, Aniket Mishra, et al.
Nature Genetics|January 8, 2013
Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconusYi Lu, Veronique Vitart, Kathryn P Burdon, et al.
Molecular Psychiatry|October 23, 2019
Correction: Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulationJoshua C Bis, Xueqiu Jian, Brian W Kunkle, et al.
Molecular Psychiatry|August 16, 2018
Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulationJoshua C Bis, Xueqiu Jian, Brian W Kunkle, et al.
Nature Genetics|September 1, 2014
Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucomaPirro G Hysi, Ching-Yu Cheng, Henriët Springelkamp, et al.
JAMA|February 23, 2021
Association of Rare CYP39A1 Variants With Exfoliation Syndrome Involving the Anterior Chamber of the Eye, Zheng Li, Zhenxun Wang, et al.
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.
Pageof 91

Showing results (871-880 of 908) with videos related to

Sort By:
Pageof 91
Human Molecular Genetics|January 12, 2017
New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristicsHenriët Springelkamp, Adriana I Iglesias, Aniket Mishra, et al.
JAMA Neurology|October 19, 2020
Novel Alzheimer Disease Risk Loci and Pathways in African American Individuals Using the African Genome Resources Panel: A Meta-analysisBrian W Kunkle, Michael Schmidt, Hans-Ulrich Klein, et al.
Nature Communications|September 23, 2014
Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous processHenriët Springelkamp, René Höhn, Aniket Mishra, et al.
Nature Genetics|January 8, 2013
Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconusYi Lu, Veronique Vitart, Kathryn P Burdon, et al.
Molecular Psychiatry|October 23, 2019
Correction: Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulationJoshua C Bis, Xueqiu Jian, Brian W Kunkle, et al.
Molecular Psychiatry|August 16, 2018
Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulationJoshua C Bis, Xueqiu Jian, Brian W Kunkle, et al.
Nature Genetics|September 1, 2014
Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucomaPirro G Hysi, Ching-Yu Cheng, Henriët Springelkamp, et al.
JAMA|February 23, 2021
Association of Rare CYP39A1 Variants With Exfoliation Syndrome Involving the Anterior Chamber of the Eye, Zheng Li, Zhenxun Wang, et al.
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.
Pageof 91