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Nature|December 10, 2014
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarctionRon Do, Nathan O Stitziel, Hong-Hee Won, et al.
American Journal of Human Genetics|February 11, 2014
Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterolLeslie A Lange, Youna Hu, He Zhang, et al.
Nature Genetics|September 22, 2009
Identification of seven new prostate cancer susceptibility loci through a genome-wide association studyRosalind A Eeles, Zsofia Kote-Jarai, Ali Amin Al Olama, et al.
Medrxiv : the Preprint Server for Health Sciences|September 4, 2023
WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELEXinruo Zhang, Jennifer A Brody, Mariaelisa Graff, et al.
Nature Communications|April 11, 2025
Whole genome sequencing analysis of body mass index identifies novel African ancestry-specific risk alleleXinruo Zhang, Jennifer A Brody, Mariaelisa Graff, et al.
Brain : a Journal of Neurology|August 1, 2024
Relevance of genetic testing in the gene-targeted trial era: the Rostock Parkinson's disease studyAna Westenberger, Volha Skrahina, Tatiana Usnich, et al.
Nature Communications|January 30, 2015
Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibilityJennifer Wessel, Audrey Y Chu, Sara M Willems, et al.
Nature|February 2, 2017
Rare and low-frequency coding variants alter human adult heightEirini Marouli, Mariaelisa Graff, Carolina Medina-Gomez, et al.
Nature Genetics|June 5, 2019
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesityValérie Turcot, Yingchang Lu, Heather M Highland, et al.
Nature Genetics|December 24, 2017
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesityValérie Turcot, Yingchang Lu, Heather M Highland, et al.
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