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Medrxiv : the Preprint Server for Health Sciences
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May 3, 2024
Genomic and phenotypic correlates of mosaic loss of chromosome Y in blood
Yasminka A Jakubek, Xiaolong Ma, Adrienne M Stilp, et al.
Nature Communications
|
May 21, 2026
Co-occurring clonal hematopoiesis exhibits strong selection and high leukemia risk
Kara M Barnao, Aubrey K Hubbard, Irenaeus C C Chan, et al.
American Journal of Human Genetics
|
January 14, 2025
Genomic and phenotypic correlates of mosaic loss of chromosome Y in blood
Yasminka A Jakubek, Xiaolong Ma, Adrienne M Stilp, et al.
Nature Methods
|
October 27, 2022
A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies
Zilin Li, Xihao Li, Hufeng Zhou, et al.
BMC Genomics
|
February 20, 2022
Rare coding variants in RCN3 are associated with blood pressure
Karen Y He, Tanika N Kelly, Heming Wang, et al.
American Journal of Epidemiology
|
April 16, 2021
A System for Phenotype Harmonization in the National Heart, Lung, and Blood Institute Trans-Omics for Precision Medicine (TOPMed) Program
Adrienne M Stilp, Leslie S Emery, Jai G Broome, et al.
Plos Genetics
|
December 24, 2019
Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations
Madeline H Kowalski, Huijun Qian, Ziyi Hou, et al.
Biorxiv : the Preprint Server for Biology
|
February 7, 2023
Structural variation across 138,134 samples in the TOPMed consortium
Goo Jun, Adam C English, Ginger A Metcalf, et al.
Nature Computational Science
|
February 7, 2025
A statistical framework for multi-trait rare variant analysis in large-scale whole-genome sequencing studies
Xihao Li, Han Chen, Margaret Sunitha Selvaraj, et al.
Nature Communications
|
October 11, 2022
Whole genome sequence analysis of blood lipid levels in >66,000 individuals
Margaret Sunitha Selvaraj, Xihao Li, Zilin Li, et al.
Page
of 68
Search research articles
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Showing results (591-600 of 677) with videos related to
Sort By:
Page
of 68
Medrxiv : the Preprint Server for Health Sciences
|
May 3, 2024
Genomic and phenotypic correlates of mosaic loss of chromosome Y in blood
Yasminka A Jakubek, Xiaolong Ma, Adrienne M Stilp, et al.
Nature Communications
|
May 21, 2026
Co-occurring clonal hematopoiesis exhibits strong selection and high leukemia risk
Kara M Barnao, Aubrey K Hubbard, Irenaeus C C Chan, et al.
American Journal of Human Genetics
|
January 14, 2025
Genomic and phenotypic correlates of mosaic loss of chromosome Y in blood
Yasminka A Jakubek, Xiaolong Ma, Adrienne M Stilp, et al.
Nature Methods
|
October 27, 2022
A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies
Zilin Li, Xihao Li, Hufeng Zhou, et al.
BMC Genomics
|
February 20, 2022
Rare coding variants in RCN3 are associated with blood pressure
Karen Y He, Tanika N Kelly, Heming Wang, et al.
American Journal of Epidemiology
|
April 16, 2021
A System for Phenotype Harmonization in the National Heart, Lung, and Blood Institute Trans-Omics for Precision Medicine (TOPMed) Program
Adrienne M Stilp, Leslie S Emery, Jai G Broome, et al.
Plos Genetics
|
December 24, 2019
Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations
Madeline H Kowalski, Huijun Qian, Ziyi Hou, et al.
Biorxiv : the Preprint Server for Biology
|
February 7, 2023
Structural variation across 138,134 samples in the TOPMed consortium
Goo Jun, Adam C English, Ginger A Metcalf, et al.
Nature Computational Science
|
February 7, 2025
A statistical framework for multi-trait rare variant analysis in large-scale whole-genome sequencing studies
Xihao Li, Han Chen, Margaret Sunitha Selvaraj, et al.
Nature Communications
|
October 11, 2022
Whole genome sequence analysis of blood lipid levels in >66,000 individuals
Margaret Sunitha Selvaraj, Xihao Li, Zilin Li, et al.
Page
of 68