학술논문
Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases
Document Type
article
Author
Adrien Georges; Min-Lee Yang; Takiy-Eddine Berrandou; Mark K. Bakker; Ozan Dikilitas; Soto Romuald Kiando; Lijiang Ma; Benjamin A. Satterfield; Sebanti Sengupta; Mengyao Yu; Jean-François Deleuze; Delia Dupré; Kristina L. Hunker; Sergiy Kyryachenko; Lu Liu; Ines Sayoud-Sadeg; Laurence Amar; Chad M. Brummett; Dawn M. Coleman; Valentina d’Escamard; Peter de Leeuw; Natalia Fendrikova-Mahlay; Daniella Kadian-Dodov; Jun Z. Li; Aurélien Lorthioir; Marco Pappaccogli; Aleksander Prejbisz; Witold Smigielski; James C. Stanley; Matthew Zawistowski; Xiang Zhou; Sebastian Zöllner; FEIRI investigators; International Stroke Genetics Consortium (ISGC) Intracranial Aneurysm Working Group; MEGASTROKE; Philippe Amouyel; Marc L. De Buyzere; Stéphanie Debette; Piotr Dobrowolski; Wojciech Drygas; Heather L. Gornik; Jeffrey W. Olin; Jerzy Piwonski; Ernst R. Rietzschel; Ynte M. Ruigrok; Miikka Vikkula; Ewa Warchol Celinska; Andrzej Januszewicz; Iftikhar J. Kullo; Michel Azizi; Xavier Jeunemaitre; Alexandre Persu; Jason C. Kovacic; Santhi K. Ganesh; Nabila Bouatia-Naji
Source
Nature Communications, Vol 12, Iss 1, Pp 1-16 (2021)
Subject
Language
English
ISSN
2041-1723
Abstract
Fibromuscular dysplasia is a cardiovascular disease affecting mostly women with a mostly unknown genetic basis. Here the authors have performed a genome-wide association meta-analysis of Fibromuscular dysplasia to identify genetic loci, some of which are shared with common cardiovascular disease and traits.