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International Journal of Epidemiology
|
January 19, 2012
Complement factor H genetic variant and age-related macular degeneration: effect size, modifiers and relationship to disease subtype
Reecha Sofat, Juan P Casas, Andrew R Webster, et al.
Nature Genetics
|
September 8, 2021
A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer's disease
Douglas P Wightman, Iris E Jansen, Jeanne E Savage, et al.
Communications Biology
|
December 14, 2020
Common variants in SOX-2 and congenital cataract genes contribute to age-related nuclear cataract
Ekaterina Yonova-Doing, Wanting Zhao, Robert P Igo, et al.
Nature Genetics
|
October 31, 2017
Exome chip meta-analysis identifies novel loci and East Asian-specific coding variants that contribute to lipid levels and coronary artery disease
Xiangfeng Lu, Gina M Peloso, Dajiang J Liu, et al.
Nature Genetics
|
October 31, 2017
Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology
Manuel A Ferreira, Judith M Vonk, Hansjörg Baurecht, et al.
Gut
|
April 23, 2021
Genome-wide analysis of 944 133 individuals provides insights into the etiology of haemorrhoidal disease
Tenghao Zheng, David Ellinghaus, Simonas Juzenas, et al.
Nature Genetics
|
April 23, 2026
Genomic analyses implicate hormonal and metabolic dysregulation in polycystic ovary syndrome
Loes M E Moolhuijsen, Jia Zhu, Benjamin H Mullin, et al.
Nature Communications
|
December 19, 2020
Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease
Jonas B Nielsen, Oren Rom, Ida Surakka, et al.
Nature Genetics
|
January 16, 2019
Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use
Mengzhen Liu, Yu Jiang, Robbee Wedow, et al.
Nature Genetics
|
April 29, 2020
Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility
Maria Teresa Landi, D Timothy Bishop, Stuart MacGregor, et al.
Page
of 16
Search research articles
Search
Showing results (141-150 of 156) with videos related to
Sort By:
Page
of 16
International Journal of Epidemiology
|
January 19, 2012
Complement factor H genetic variant and age-related macular degeneration: effect size, modifiers and relationship to disease subtype
Reecha Sofat, Juan P Casas, Andrew R Webster, et al.
Nature Genetics
|
September 8, 2021
A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer's disease
Douglas P Wightman, Iris E Jansen, Jeanne E Savage, et al.
Communications Biology
|
December 14, 2020
Common variants in SOX-2 and congenital cataract genes contribute to age-related nuclear cataract
Ekaterina Yonova-Doing, Wanting Zhao, Robert P Igo, et al.
Nature Genetics
|
October 31, 2017
Exome chip meta-analysis identifies novel loci and East Asian-specific coding variants that contribute to lipid levels and coronary artery disease
Xiangfeng Lu, Gina M Peloso, Dajiang J Liu, et al.
Nature Genetics
|
October 31, 2017
Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology
Manuel A Ferreira, Judith M Vonk, Hansjörg Baurecht, et al.
Gut
|
April 23, 2021
Genome-wide analysis of 944 133 individuals provides insights into the etiology of haemorrhoidal disease
Tenghao Zheng, David Ellinghaus, Simonas Juzenas, et al.
Nature Genetics
|
April 23, 2026
Genomic analyses implicate hormonal and metabolic dysregulation in polycystic ovary syndrome
Loes M E Moolhuijsen, Jia Zhu, Benjamin H Mullin, et al.
Nature Communications
|
December 19, 2020
Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease
Jonas B Nielsen, Oren Rom, Ida Surakka, et al.
Nature Genetics
|
January 16, 2019
Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use
Mengzhen Liu, Yu Jiang, Robbee Wedow, et al.
Nature Genetics
|
April 29, 2020
Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility
Maria Teresa Landi, D Timothy Bishop, Stuart MacGregor, et al.
Page
of 16