The 2017 international classification of the Ehlers–Danlos syndromesFransiska Malfait, Brad T. Tinkle, Clair A. Francomano et al.|American Journal of Medical Genetics Part C Seminars in Medical Genetics|2017Cited by 1.9k
A nucleotide substitution in the promoter of human angiotensinogen is associated with essential hypertension and affects basal transcription in vitro.Ikuo Inoue, J.-M. Lalouel, Toshiaki Nakajima et al.|Journal of Clinical Investigation|1997Cited by 550
Dehydrated hereditary stomatocytosis linked to gain-of-function mutations in mechanically activated PIEZO1 ion channelsJuliette Albuisson, Ardem Patapoutian, Swetha E. Murthy et al.|Nature Communications|2013Cited by 383
Genetic Susceptibility for Human Familial Essential Hypertension in a Region of Homology with Blood Pressure Linkage on Rat Chromosome 10Cécile Julier, G. Mark Lathrop, Bernard Keavney et al.|Human Molecular Genetics|1997Cited by 178
Rare loss-of-function mutations of <i>PTGIR</i> are enriched in fibromuscular dysplasiaAdrien Georges, Nabila Bouatia‐Naji, Juliette Albuisson et al.|Cardiovascular Research|2020Cited by 32