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Nature Communications
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October 16, 2025
Genetic determinants and genomic consequences of non-leukemogenic somatic point mutations
Joshua S Weinstock, Sharjeel A Chaudhry, Maria Ioannou, 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 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 One
|
May 11, 2019
Mendelian randomization evaluation of causal effects of fibrinogen on incident coronary heart disease
Cavin K Ward-Caviness, Paul S de Vries, Kerri L Wiggins, et al.
Nature Communications
|
October 9, 2024
Rare variant contribution to the heritability of coronary artery disease
Ghislain Rocheleau, Shoa L Clarke, Gaëlle Auguste, et al.
Medrxiv : the Preprint Server for Health Sciences
|
August 30, 2023
Rare damaging <i>CCR2</i> variants are associated with lower lifetime cardiovascular risk
Marios K Georgakis, Rainer Malik, Omar El Bounkari, 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.
Journal of the American Heart Association
|
February 14, 2025
Unveiling the Genetic Landscape of Coronary Artery Disease Through Common and Rare Structural Variants
Kruthika R Iyer, Shoa L Clarke, Rodrigo Guarischi-Sousa, et al.
Circulation. Genomic and Precision Medicine
|
November 28, 2023
Type 2 Diabetes Modifies the Association of CAD Genomic Risk Variants With Subclinical Atherosclerosis
Natalie R Hasbani, Kenneth E Westerman, Soo Heon Kwak, et al.
Page
of 26
Search research articles
Search
Showing results (161-170 of 258) with videos related to
Sort By:
Page
of 26
Nature Communications
|
October 16, 2025
Genetic determinants and genomic consequences of non-leukemogenic somatic point mutations
Joshua S Weinstock, Sharjeel A Chaudhry, Maria Ioannou, 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 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 One
|
May 11, 2019
Mendelian randomization evaluation of causal effects of fibrinogen on incident coronary heart disease
Cavin K Ward-Caviness, Paul S de Vries, Kerri L Wiggins, et al.
Nature Communications
|
October 9, 2024
Rare variant contribution to the heritability of coronary artery disease
Ghislain Rocheleau, Shoa L Clarke, Gaëlle Auguste, et al.
Medrxiv : the Preprint Server for Health Sciences
|
August 30, 2023
Rare damaging <i>CCR2</i> variants are associated with lower lifetime cardiovascular risk
Marios K Georgakis, Rainer Malik, Omar El Bounkari, 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.
Journal of the American Heart Association
|
February 14, 2025
Unveiling the Genetic Landscape of Coronary Artery Disease Through Common and Rare Structural Variants
Kruthika R Iyer, Shoa L Clarke, Rodrigo Guarischi-Sousa, et al.
Circulation. Genomic and Precision Medicine
|
November 28, 2023
Type 2 Diabetes Modifies the Association of CAD Genomic Risk Variants With Subclinical Atherosclerosis
Natalie R Hasbani, Kenneth E Westerman, Soo Heon Kwak, et al.
Page
of 26