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Nature Genetics|November 24, 2020
Common variants in signaling transcription-factor-binding sites drive phenotypic variability in red blood cell traitsAvik Choudhuri, Eirini Trompouki, Brian J Abraham, et al.Plos Genetics|October 30, 2016
PHACTR1 Is a Genetic Susceptibility Locus for Fibromuscular Dysplasia Supporting Its Complex Genetic Pattern of InheritanceSoto Romuald Kiando, Nathan R Tucker, Luis-Jaime Castro-Vega, et al.Cardiovascular Research|June 13, 2020
Rare loss-of-function mutations of PTGIR are enriched in fibromuscular dysplasiaAdrien Georges, Juliette Albuisson, Takiy Berrandou, et al.Nature Communications|December 23, 2015
Exome-wide association analysis reveals novel coding sequence variants associated with lipid traits in ChineseClara S Tang, He Zhang, Chloe Y Y Cheung, et al.Nature Communications|October 16, 2021
Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseasesAdrien Georges, Min-Lee Yang, Takiy-Eddine Berrandou, et al.Nature Genetics|May 29, 2023
Genome-wide association meta-analysis of spontaneous coronary artery dissection identifies risk variants and genes related to artery integrity and tissue-mediated coagulationDavid Adlam, Takiy-Eddine Berrandou, Adrien Georges, et al.American Journal of Human Genetics|July 1, 2014
Effects of long-term averaging of quantitative blood pressure traits on the detection of genetic associationsSanthi K Ganesh, Daniel I Chasman, Martin G Larson, et al.American Journal of Human Genetics|December 27, 2016
Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in ErythropoiesisFrank J A van Rooij, Rehan Qayyum, Albert V Smith, et al.Pageof 14