Samuel M Lockhart
9PUBLICATIONS
64CO-AUTHORS
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Publications (9)
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|Jan 05, 2026
Human genetics suggests differing causal pathways from HMGCR inhibition to coronary artery disease and type 2 diabetes.Seongwon Hwang, Ville Karhunen, Ashish Patel
|Nov 05, 2025
Rare Variants in HTRA1, SGTB, and RBM12 Confer Risk of Atherosclerotic Cardiovascular Disease Independent of Traditional Cardiovascular Risk Factors.Sam M Lockhart, Anuradhika Puri, Yajie Zhao
|Oct 10, 2025
Population-scale gene-based analysis of whole-genome sequencing provides insights into metabolic health.Yajie Zhao, Sam Lockhart, Jimmy Liu
|Mar 04, 2025
Effects of Rare Coding Variants in Severe Early-Onset Obesity Genes in the Population-Based UK Biobank Study.Raina Y Jia, Sam Lockhart, Brian Y H Lam
|Sep 25, 2024
Damaging mutations in liver X receptor-α are hepatotoxic and implicate cholesterol sensing in liver health.Sam M Lockhart, Milan Muso, Ilona Zvetkova
|Dec 13, 2023
GDF15 linked to maternal risk of nausea and vomiting during pregnancy.M Fejzo, N Rocha, I Cimino
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Frequent Collaborators
6 joint publications
Stephen O'Rahilly
4 joint publications
Yajie Zhao
4 joint publications
John R B Perry
3 joint publications
Felix R Day
3 joint publications
Katherine Kentistou
3 joint publications
Ken K Ong
2 joint publications
Brian Y H Lam
2 joint publications
Eugene J Gardner
2 joint publications
Vladimir Saudek
1 joint publications
Stephen Burgess
