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Michael C Mahaney

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Journal of Lipid Research|June 23, 2019

Rare DEGS1 variant significantly alters de novo ceramide synthesis pathwayNicholas B Blackburn, Laura F Michael, Peter J Meikle, et al.

Medrxiv : the Preprint Server for Health Sciences|August 30, 2023

Rare damaging CCR2 variants are associated with lower lifetime cardiovascular riskMarios 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 scaleXihao Li, Zilin Li, Hufeng Zhou, et al.

Circulation. Genomic and Precision Medicine|November 28, 2023

Type 2 Diabetes Modifies the Association of CAD Genomic Risk Variants With Subclinical AtherosclerosisNatalie R Hasbani, Kenneth E Westerman, Soo Heon Kwak, et al.

Genome Medicine|March 22, 2025

Rare damaging CCR2 variants are associated with lower lifetime cardiovascular riskMarios K Georgakis, Rainer Malik, Omar El Bounkari, et al.

Biorxiv : the Preprint Server for Biology|November 14, 2023

A statistical framework for powerful multi-trait rare variant analysis in large-scale whole-genome sequencing studiesXihao Li, Han Chen, Margaret Sunitha Selvaraj, et al.

Medrxiv : the Preprint Server for Health Sciences|May 5, 2025

Genome-wide association study and multi-ancestry meta-analysis identify common variants associated with carotid artery intima-media thicknessDevendra Meena, Jian Huang, Marjan Zare, 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 studyYuxuan 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 StudyYuxuan 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 studiesXihao Li, Han Chen, Margaret Sunitha Selvaraj, et al.

Pageof 13

Search research articles

Showing results (111-120 of 121) with videos related to

Sort By:

Pageof 13

Journal of Lipid Research|June 23, 2019

Rare DEGS1 variant significantly alters de novo ceramide synthesis pathwayNicholas B Blackburn, Laura F Michael, Peter J Meikle, et al.

Medrxiv : the Preprint Server for Health Sciences|August 30, 2023

Rare damaging CCR2 variants are associated with lower lifetime cardiovascular riskMarios 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 scaleXihao Li, Zilin Li, Hufeng Zhou, et al.

Circulation. Genomic and Precision Medicine|November 28, 2023

Type 2 Diabetes Modifies the Association of CAD Genomic Risk Variants With Subclinical AtherosclerosisNatalie R Hasbani, Kenneth E Westerman, Soo Heon Kwak, et al.

Genome Medicine|March 22, 2025

Rare damaging CCR2 variants are associated with lower lifetime cardiovascular riskMarios K Georgakis, Rainer Malik, Omar El Bounkari, et al.

Biorxiv : the Preprint Server for Biology|November 14, 2023

A statistical framework for powerful multi-trait rare variant analysis in large-scale whole-genome sequencing studiesXihao Li, Han Chen, Margaret Sunitha Selvaraj, et al.

Medrxiv : the Preprint Server for Health Sciences|May 5, 2025

Genome-wide association study and multi-ancestry meta-analysis identify common variants associated with carotid artery intima-media thicknessDevendra Meena, Jian Huang, Marjan Zare, 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 studyYuxuan 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 StudyYuxuan 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 studiesXihao Li, Han Chen, Margaret Sunitha Selvaraj, et al.

Pageof 13