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Nature Communications
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December 19, 2020
Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease
Jonas B Nielsen, Oren Rom, Ida Surakka, et al.
Human Molecular Genetics
|
April 12, 2015
A common variant near TGFBR3 is associated with primary open angle glaucoma
Zheng Li, R Rand Allingham, Masakazu Nakano, et al.
Medrxiv : the Preprint Server for Health Sciences
|
September 4, 2023
WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELE
Xinruo Zhang, Jennifer A Brody, Mariaelisa Graff, et al.
Nature Communications
|
April 11, 2025
Whole genome sequencing analysis of body mass index identifies novel African ancestry-specific risk allele
Xinruo Zhang, Jennifer A Brody, Mariaelisa Graff, et al.
Nature Genetics
|
February 24, 2015
A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome
Tin Aung, Mineo Ozaki, Takanori Mizoguchi, et al.
Cell Genomics
|
May 9, 2022
Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed
Margaret A Taub, Matthew P Conomos, Rebecca Keener, et al.
Biological Psychiatry
|
December 6, 2021
Enhancing Discovery of Genetic Variants for Posttraumatic Stress Disorder Through Integration of Quantitative Phenotypes and Trauma Exposure Information
Adam X Maihofer, Karmel W Choi, Jonathan R I Coleman, et al.
Nature Communications
|
October 10, 2019
International meta-analysis of PTSD genome-wide association studies identifies sex- and ancestry-specific genetic risk loci
Caroline M Nievergelt, Adam X Maihofer, Torsten Klengel, et al.
Nature
|
February 11, 2021
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program
Daniel Taliun, Daniel N Harris, Michael D Kessler, et al.
Nature
|
December 8, 2022
Genetic diversity fuels gene discovery for tobacco and alcohol use
Gretchen R B Saunders, Xingyan Wang, Fang Chen, et al.
Page
of 46
Search research articles
Search
Showing results (441-450 of 454) with videos related to
Sort By:
Page
of 46
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.
Human Molecular Genetics
|
April 12, 2015
A common variant near TGFBR3 is associated with primary open angle glaucoma
Zheng Li, R Rand Allingham, Masakazu Nakano, et al.
Medrxiv : the Preprint Server for Health Sciences
|
September 4, 2023
WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELE
Xinruo Zhang, Jennifer A Brody, Mariaelisa Graff, et al.
Nature Communications
|
April 11, 2025
Whole genome sequencing analysis of body mass index identifies novel African ancestry-specific risk allele
Xinruo Zhang, Jennifer A Brody, Mariaelisa Graff, et al.
Nature Genetics
|
February 24, 2015
A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome
Tin Aung, Mineo Ozaki, Takanori Mizoguchi, et al.
Cell Genomics
|
May 9, 2022
Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed
Margaret A Taub, Matthew P Conomos, Rebecca Keener, et al.
Biological Psychiatry
|
December 6, 2021
Enhancing Discovery of Genetic Variants for Posttraumatic Stress Disorder Through Integration of Quantitative Phenotypes and Trauma Exposure Information
Adam X Maihofer, Karmel W Choi, Jonathan R I Coleman, et al.
Nature Communications
|
October 10, 2019
International meta-analysis of PTSD genome-wide association studies identifies sex- and ancestry-specific genetic risk loci
Caroline M Nievergelt, Adam X Maihofer, Torsten Klengel, et al.
Nature
|
February 11, 2021
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program
Daniel Taliun, Daniel N Harris, Michael D Kessler, et al.
Nature
|
December 8, 2022
Genetic diversity fuels gene discovery for tobacco and alcohol use
Gretchen R B Saunders, Xingyan Wang, Fang Chen, et al.
Page
of 46