GENETIC ASSOCIATION STUDIES OF FIBROMUSCULAR DYSPLASIA IDENTIFY NEW RISK LOCI AND SHARED GENETIC BASIS WITH MORE COMMON VASCULAR DISEASES
Adrien Georges(Inserm), Nabila Bouatia‐Naji(Délégation Paris 5), Kristina L. Hunker(Michigan Medicine), Mark K. Bakker(Utrecht University), Ernst Rietzschel(Ghent University Hospital), Ewa Warchol Celinska(Inserm), Marco Pappaccogli(Cliniques Universitaires Saint-Luc), Alexandre Persu(Cliniques Universitaires Saint-Luc), Xavier Jeunemaı̂tre(Délégation Paris 5), Andrzej Januszewicz(Hypertension Institute), Ynte M. Ruigrok(University Medical Center Utrecht), Benjamin A. Satterfield(Mayo Clinic in Arizona), Min‐Lee Yang(University of Michigan), Jeffrey W. Olin(Icahn School of Medicine at Mount Sinai), Michel Azizi(Inserm), Santhi K. Ganesh(University of Michigan), Sebanti Sengupta(University of Michigan), Aleksander Prejbisz(Institute of Cardiology), Iftikhar J. Kullo(Medical College of Wisconsin), Lijiang Ma(Columbia University Irving Medical Center), Laurence Amar(Unit of Functional and Adaptive Biology), Ozan Dikilitas(Mayo Clinic), Takiy-Eddine Berrandou(Inserm), Heather L. Gornik(Asia Society), Jason C. Kovacic(Victor Chang Cardiac Research Institute), Aurélien Lorthioir(Assistance Publique – Hôpitaux de Paris)
Cited by 2
Related Papers
Recommendations for Cardiac Chamber Quantification by Echocardiography in Adults: An Update from the American Society of Echocardiography and the European Association of Cardiovascular Imaging
|Journal of the American Society of Echocardiography|2015|18k
Recommendations for Cardiac Chamber Quantification by Echocardiography in Adults: An Update from the American Society of Echocardiography and the European Association of Cardiovascular Imaging
|European Heart Journal - Cardiovascular Imaging|2015|8.3k
The 2017 international classification of the Ehlers–Danlos syndromes
|American Journal of Medical Genetics Part C Seminars in Medical Genetics|2017|1.9k
A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants
|Nature Genetics|2015|1.6k
Genome-wide association study of blood pressure and hypertension
|Nature Genetics|2009|1.4k