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Nature Genetics
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September 4, 2012
Common variants at 6p21.1 are associated with large artery atherosclerotic stroke
Elizabeth G Holliday, Jane M Maguire, Tiffany-Jane Evans, 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.
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.
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.
Plos Genetics
|
June 27, 2009
NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE Consortium
Nancy L Heard-Costa, M Carola Zillikens, Keri L Monda, 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 Communications
|
December 9, 2022
Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program
Marsha M Wheeler, Adrienne M Stilp, Shuquan Rao, et al.
Circulation Research
|
December 25, 2018
PATJ Low Frequency Variants Are Associated With Worse Ischemic Stroke Functional Outcome
Marina Mola-Caminal, Caty Carrera, Carolina Soriano-Tárraga, 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.
Nature Communications
|
October 9, 2024
Rare variant contribution to the heritability of coronary artery disease
Ghislain Rocheleau, Shoa L Clarke, Gaëlle Auguste, et al.
Page
of 46
Search research articles
Search
Showing results (351-360 of 457) with videos related to
Sort By:
Page
of 46
Nature Genetics
|
September 4, 2012
Common variants at 6p21.1 are associated with large artery atherosclerotic stroke
Elizabeth G Holliday, Jane M Maguire, Tiffany-Jane Evans, 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.
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.
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.
Plos Genetics
|
June 27, 2009
NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE Consortium
Nancy L Heard-Costa, M Carola Zillikens, Keri L Monda, 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 Communications
|
December 9, 2022
Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program
Marsha M Wheeler, Adrienne M Stilp, Shuquan Rao, et al.
Circulation Research
|
December 25, 2018
PATJ Low Frequency Variants Are Associated With Worse Ischemic Stroke Functional Outcome
Marina Mola-Caminal, Caty Carrera, Carolina Soriano-Tárraga, 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.
Nature Communications
|
October 9, 2024
Rare variant contribution to the heritability of coronary artery disease
Ghislain Rocheleau, Shoa L Clarke, Gaëlle Auguste, et al.
Page
of 46