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Human Genetics
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January 24, 2019
Leveraging linkage evidence to identify low-frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing data
Karen Y He, Xiaoyin Li, Tanika N Kelly, et al.
Atherosclerosis
|
February 25, 2012
Genetic determinants of the ankle-brachial index: a meta-analysis of a cardiovascular candidate gene 50K SNP panel in the candidate gene association resource (CARe) consortium
Christina L Wassel, Claudia Lamina, Vijay Nambi, et al.
American Journal of Respiratory Cell and Molecular Biology
|
October 28, 2017
Multiethnic Meta-Analysis Identifies RAI1 as a Possible Obstructive Sleep Apnea-related Quantitative Trait Locus in Men
Han Chen, Brian E Cade, Kevin J Gleason, et al.
Nature Communications
|
October 3, 2024
Whole-genome sequencing in 333,100 individuals reveals rare non-coding single variant and aggregate associations with height
Gareth Hawkes, Robin N Beaumont, Zilin Li, et al.
Human Molecular Genetics
|
September 1, 2016
Fine-mapping, novel loci identification, and SNP association transferability in a genome-wide association study of QRS duration in African Americans
Daniel S Evans, Christy L Avery, Mike A Nalls, et al.
Nature Methods
|
December 31, 2025
cellSTAAR: incorporating single-cell-sequencing-based functional data to boost power in rare variant association testing of noncoding regions
Eric Van Buren, Yi Zhang, Xihao Li, et al.
HGG Advances
|
December 26, 2022
Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants
Kristin L Young, Virginia Fisher, Xuan Deng, et al.
Plos Genetics
|
February 25, 2011
Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project
Guillaume Lettre, Cameron D Palmer, Taylor Young, et al.
Nature Genetics
|
December 23, 2022
Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies
Xihao Li, Corbin Quick, Hufeng Zhou, et al.
Nature Genetics
|
August 26, 2020
Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale
Xihao Li, Zilin Li, Hufeng Zhou, et al.
Page
of 96
Search research articles
Search
Showing results (871-880 of 959) with videos related to
Sort By:
Page
of 96
Human Genetics
|
January 24, 2019
Leveraging linkage evidence to identify low-frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing data
Karen Y He, Xiaoyin Li, Tanika N Kelly, et al.
Atherosclerosis
|
February 25, 2012
Genetic determinants of the ankle-brachial index: a meta-analysis of a cardiovascular candidate gene 50K SNP panel in the candidate gene association resource (CARe) consortium
Christina L Wassel, Claudia Lamina, Vijay Nambi, et al.
American Journal of Respiratory Cell and Molecular Biology
|
October 28, 2017
Multiethnic Meta-Analysis Identifies RAI1 as a Possible Obstructive Sleep Apnea-related Quantitative Trait Locus in Men
Han Chen, Brian E Cade, Kevin J Gleason, et al.
Nature Communications
|
October 3, 2024
Whole-genome sequencing in 333,100 individuals reveals rare non-coding single variant and aggregate associations with height
Gareth Hawkes, Robin N Beaumont, Zilin Li, et al.
Human Molecular Genetics
|
September 1, 2016
Fine-mapping, novel loci identification, and SNP association transferability in a genome-wide association study of QRS duration in African Americans
Daniel S Evans, Christy L Avery, Mike A Nalls, et al.
Nature Methods
|
December 31, 2025
cellSTAAR: incorporating single-cell-sequencing-based functional data to boost power in rare variant association testing of noncoding regions
Eric Van Buren, Yi Zhang, Xihao Li, et al.
HGG Advances
|
December 26, 2022
Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants
Kristin L Young, Virginia Fisher, Xuan Deng, et al.
Plos Genetics
|
February 25, 2011
Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project
Guillaume Lettre, Cameron D Palmer, Taylor Young, et al.
Nature Genetics
|
December 23, 2022
Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies
Xihao Li, Corbin Quick, Hufeng Zhou, et al.
Nature Genetics
|
August 26, 2020
Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale
Xihao Li, Zilin Li, Hufeng Zhou, et al.
Page
of 96