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Showing results (911-920 of 1,171) with videos related to
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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.
European Journal of Preventive Cardiology
|
December 13, 2016
Genetic invalidation of Lp-PLA<sub>2</sub> as a therapeutic target: Large-scale study of five functional Lp-PLA<sub>2</sub>-lowering alleles
John M Gregson, Daniel F Freitag, Praveen Surendran, et al.
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.
Plos One
|
October 31, 2015
Drug-Gene Interactions of Antihypertensive Medications and Risk of Incident Cardiovascular Disease: A Pharmacogenomics Study from the CHARGE Consortium
Joshua C Bis, Colleen Sitlani, Ryan Irvin, et al.
Blood
|
July 26, 2018
DNA methylation age is associated with an altered hemostatic profile in a multiethnic meta-analysis
Cavin K Ward-Caviness, Jennifer E Huffman, Karl Everett, et al.
American Journal of Human Genetics
|
August 4, 2016
Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis
Linda M Polfus, Rajiv K Khajuria, Ursula M Schick, et al.
Nature Communications
|
March 27, 2026
An integrated germline and somatic genomic model for coronary artery disease
Xiong Yang, Min Seo Kim, Xinyu Zhu, et al.
The Journal of Clinical Endocrinology and Metabolism
|
January 12, 2018
Transethnic Evaluation Identifies Low-Frequency Loci Associated With 25-Hydroxyvitamin D Concentrations
Jaeyoung Hong, Kathryn E Hatchell, Jonathan P Bradfield, 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.
Plos One
|
June 19, 2013
Genetic loci for retinal arteriolar microcirculation
Xueling Sim, Richard A Jensen, M Kamran Ikram, et al.
Page
of 118
Search research articles
Search
Showing results (911-920 of 1,171) with videos related to
Sort By:
Page
of 118
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.
European Journal of Preventive Cardiology
|
December 13, 2016
Genetic invalidation of Lp-PLA<sub>2</sub> as a therapeutic target: Large-scale study of five functional Lp-PLA<sub>2</sub>-lowering alleles
John M Gregson, Daniel F Freitag, Praveen Surendran, et al.
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.
Plos One
|
October 31, 2015
Drug-Gene Interactions of Antihypertensive Medications and Risk of Incident Cardiovascular Disease: A Pharmacogenomics Study from the CHARGE Consortium
Joshua C Bis, Colleen Sitlani, Ryan Irvin, et al.
Blood
|
July 26, 2018
DNA methylation age is associated with an altered hemostatic profile in a multiethnic meta-analysis
Cavin K Ward-Caviness, Jennifer E Huffman, Karl Everett, et al.
American Journal of Human Genetics
|
August 4, 2016
Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis
Linda M Polfus, Rajiv K Khajuria, Ursula M Schick, et al.
Nature Communications
|
March 27, 2026
An integrated germline and somatic genomic model for coronary artery disease
Xiong Yang, Min Seo Kim, Xinyu Zhu, et al.
The Journal of Clinical Endocrinology and Metabolism
|
January 12, 2018
Transethnic Evaluation Identifies Low-Frequency Loci Associated With 25-Hydroxyvitamin D Concentrations
Jaeyoung Hong, Kathryn E Hatchell, Jonathan P Bradfield, 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.
Plos One
|
June 19, 2013
Genetic loci for retinal arteriolar microcirculation
Xueling Sim, Richard A Jensen, M Kamran Ikram, et al.
Page
of 118