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Human Molecular Genetics
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February 17, 2018
Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma
Yukihiro Shiga, Masato Akiyama, Koji M Nishiguchi, et al.
Genetic Epidemiology
|
January 30, 2015
Meta-analysis of Genome-Wide Association Studies Identifies Novel Loci Associated With Optic Disc Morphology
Henriët Springelkamp, Aniket Mishra, Pirro G Hysi, et al.
Nature Communications
|
January 10, 2019
Author Correction: Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases
Adriana I Iglesias, Aniket Mishra, Veronique Vitart, et al.
Journal of Alzheimer'S Disease : JAD
|
September 18, 2010
The CALHM1 P86L polymorphism is a genetic modifier of age at onset in Alzheimer's disease: a meta-analysis study
Jean-Charles Lambert, Kristel Sleegers, Antonio González-Pérez, et al.
Brain : a Journal of Neurology
|
March 20, 2025
Novel modelling approaches to elucidate the genetic architecture of resilience to Alzheimer's disease
Jared M Phillips, Logan C Dumitrescu, Derek B Archer, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 14, 2010
Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration
Wei Chen, Dwight Stambolian, Albert O Edwards, et al.
Human Molecular Genetics
|
June 6, 2014
Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degeneration
Rinki Ratnapriya, Xiaowei Zhan, Robert N Fariss, et al.
Nature Communications
|
February 25, 2021
Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries
Puya Gharahkhani, Eric Jorgenson, Pirro Hysi, et al.
Nature Genetics
|
January 12, 2016
Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma
Jessica N Cooke Bailey, Stephanie J Loomis, Jae H Kang, et al.
Human Molecular Genetics
|
May 5, 2012
Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases
Giovanni Coppola, Subashchandrabose Chinnathambi, Jason JiYong Lee, et al.
Page
of 91
Search research articles
Search
Showing results (861-870 of 908) with videos related to
Sort By:
Page
of 91
Human Molecular Genetics
|
February 17, 2018
Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma
Yukihiro Shiga, Masato Akiyama, Koji M Nishiguchi, et al.
Genetic Epidemiology
|
January 30, 2015
Meta-analysis of Genome-Wide Association Studies Identifies Novel Loci Associated With Optic Disc Morphology
Henriët Springelkamp, Aniket Mishra, Pirro G Hysi, et al.
Nature Communications
|
January 10, 2019
Author Correction: Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases
Adriana I Iglesias, Aniket Mishra, Veronique Vitart, et al.
Journal of Alzheimer'S Disease : JAD
|
September 18, 2010
The CALHM1 P86L polymorphism is a genetic modifier of age at onset in Alzheimer's disease: a meta-analysis study
Jean-Charles Lambert, Kristel Sleegers, Antonio González-Pérez, et al.
Brain : a Journal of Neurology
|
March 20, 2025
Novel modelling approaches to elucidate the genetic architecture of resilience to Alzheimer's disease
Jared M Phillips, Logan C Dumitrescu, Derek B Archer, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 14, 2010
Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration
Wei Chen, Dwight Stambolian, Albert O Edwards, et al.
Human Molecular Genetics
|
June 6, 2014
Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degeneration
Rinki Ratnapriya, Xiaowei Zhan, Robert N Fariss, et al.
Nature Communications
|
February 25, 2021
Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries
Puya Gharahkhani, Eric Jorgenson, Pirro Hysi, et al.
Nature Genetics
|
January 12, 2016
Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma
Jessica N Cooke Bailey, Stephanie J Loomis, Jae H Kang, et al.
Human Molecular Genetics
|
May 5, 2012
Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases
Giovanni Coppola, Subashchandrabose Chinnathambi, Jason JiYong Lee, et al.
Page
of 91