Samuel M Lockhart

11PUBLICATIONS
85CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Cardiology (incl. cardiovascular diseases)Cancer geneticsPsychosocial aspects of childbirth and perinatal mental healthPredictive and prognostic markers
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Publications (11)

|Sep 25, 2026
Genome-wide mapping of common and rare variant effects on adiposity across childhood.

|Jul 30, 2026
Statin Use and Genetically Predicted HMG-CoA Reductase Inhibition in Relation to Clonal Hematopoiesis.

|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

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Frequent Collaborators

7 joint publications

Stephen O'Rahilly

5 joint publications

Yajie Zhao

5 joint publications

John R B Perry

4 joint publications

Felix R Day