Jacques Barhanin

KCNQ1 Gain-of-Function Mutation in Familial Atrial Fibrillation

Yi-Han Chen, Shi-Jie Xu, Saı̈d Bendahhou et al. · Science · 2003 · 990 citations

A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome

Nathalie Neyroud, Frédérique Tesson, Isabelle Denjoy et al. · Nature Genetics · 1997 · 881 citations

Novel Mutation, Channelopathies, Cardiomyopathy +10

TWIK-1, a ubiquitous human weakly inward rectifying K+ channel with a novel structure.

Florian Lesage, Eric Guillemare, Michel Fink et al. · The EMBO Journal · 1996 · 544 citations · Full text

Signal Transduction, Molecular Physiology, Hyperpolarization (Biology) +12

Inner Ear Defects Induced by Null Mutationof the isk Gene

Douglas E. Vetter, Jeffrey R. Mann, Philine Wangemann et al. · Neuron · 1996 · 395 citations · Full text

Developmental Anomaly, Developmental Biology, Genetic Disorder +7

A Kir2.1 gain-of-function mutation underlies familial atrial fibrillation

Min Xia, Qingfeng Jin, Yusong He et al. · Biochemical and Biophysical Research Communications · 2005 · 373 citations

Molecular Physiology, Genetic Disorder, Genetics +4