Genetic Susceptibility for Human Familial Essential Hypertension in a Region of Homology with Blood Pressure Linkage on Rat Chromosome 10
Cécile Julier(Centre for Human Genetics), G. Mark Lathrop(Centre for Human Genetics), Philippe Froguel(European Genomic Institute for Diabetes), Florent Soubrier(Inserm), Bernard Keavney(Manchester Academic Health Science Centre), Gilberto Velho(Inserm), Xavier Jeunemaı̂tre(Délégation Paris 5), Thuỳ Anh Bùi(Manchester Academic Health Science Centre), Peter J. Ratcliffe(University of Oxford), Joseph D. Terwilliger(Centre for Human Genetics), Daniel E. Weeks(University of Pittsburgh), Marc Délepine(Centre National de Recherche en Génomique Humaine), Pierre Corvol(Collège de France), Sean Davis(University Medical Center)
Cited by 178
Related Papers
Adiponectin stimulates glucose utilization and fatty-acid oxidation by activating AMP-activated protein kinase
|Nature Medicine|2002|4.2k
A mutation in the human leptin receptor gene causes obesity and pituitary dysfunction
|Nature|1998|2.4k
The 2017 international classification of the Ehlers–Danlos syndromes
|American Journal of Medical Genetics Part C Seminars in Medical Genetics|2017|1.9k
Global birth prevalence of congenital heart defects 1970–2017: updated systematic review and meta-analysis of 260 studies
|International Journal of Epidemiology|2019|1.4k