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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.
Cell Genomics
|
January 8, 2024
Genome-wide study investigating effector genes and polygenic prediction for kidney function in persons with ancestry from Africa and the Americas
Odessica Hughes, Amy R Bentley, Charles E Breeze, et al.
American Journal of Human Genetics
|
October 6, 2023
Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study
Yuxuan Wang, Margaret Sunitha Selvaraj, Xihao Li, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 10, 2023
Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed Whole Genome Sequencing Study
Yuxuan Wang, Margaret Sunitha Selvaraj, Xihao Li, 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.
Biorxiv : the Preprint Server for Biology
|
April 17, 2026
The Common Fund Data Ecosystem (CFDE)
Julie A Jurgens, Andreas Bueckle, Jeet Vora, et al.
Diabetes
|
June 11, 2026
Colocalization of eQTLs With Type 2 Diabetes and Glycemic Traits Using Whole-Genome Sequences in Diverse Populations From the NHLBI Trans-Omics in Precision Medicine (TOPMed) Program
Ningyuan Wang, Daniel A DiCorpo, Yixin Zhang, et al.
Nature Human Behaviour
|
August 4, 2022
Rare genetic variants explain missing heritability in smoking
Seon-Kyeong Jang, Luke Evans, Allison Fialkowski, et al.
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of 54
Search research articles
Search
Showing results (521-530 of 534) with videos related to
Sort By:
Page
of 54
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.
Cell Genomics
|
January 8, 2024
Genome-wide study investigating effector genes and polygenic prediction for kidney function in persons with ancestry from Africa and the Americas
Odessica Hughes, Amy R Bentley, Charles E Breeze, et al.
American Journal of Human Genetics
|
October 6, 2023
Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study
Yuxuan Wang, Margaret Sunitha Selvaraj, Xihao Li, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 10, 2023
Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed Whole Genome Sequencing Study
Yuxuan Wang, Margaret Sunitha Selvaraj, Xihao Li, 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.
Biorxiv : the Preprint Server for Biology
|
April 17, 2026
The Common Fund Data Ecosystem (CFDE)
Julie A Jurgens, Andreas Bueckle, Jeet Vora, et al.
Diabetes
|
June 11, 2026
Colocalization of eQTLs With Type 2 Diabetes and Glycemic Traits Using Whole-Genome Sequences in Diverse Populations From the NHLBI Trans-Omics in Precision Medicine (TOPMed) Program
Ningyuan Wang, Daniel A DiCorpo, Yixin Zhang, et al.
Nature Human Behaviour
|
August 4, 2022
Rare genetic variants explain missing heritability in smoking
Seon-Kyeong Jang, Luke Evans, Allison Fialkowski, et al.
Page
of 54