Lejin Wang

Calcium-sensitive potassium channelopathy in human epilepsy and paroxysmal movement disorder

Wei Du, Jocelyn F. Bautista, Huanghe Yang et al. · Nature Genetics · 2005 · 577 citations

Medicine, Neurology, Neuroscience +16

Mutation of MEF2A in an Inherited Disorder with Features of Coronary Artery Disease

Lejin Wang, Sarah E. Topol, Eric J. Topol et al. · Science · 2003 · 386 citations · Full text

Medicine, Cardiology, Genetics +17

Mutation in Nuclear Pore Component NUP155 Leads to Atrial Fibrillation and Early Sudden Cardiac Death

Xianqin Zhang, Shenghan Chen, Shin Yoo et al. · Cell · 2008 · 277 citations · Full text

Medicine, Cardiology, Genetics +14

Identification of a novel GPR143 mutation in a large Chinese family with congenital nystagmus as the most prominent and consistent manifestation

Jing Yu Liu, Xiang Ren, Xiufeng Yang et al. · Journal of Human Genetics · 2007 · 70 citations

Life Sciences, Genetics, Molecular Genetics +14

T14484C and T14502C in the mitochondrial ND6 gene are associated with Leber’s hereditary optic neuropathy in a Chinese family

Shirong Zhang, Lejin Wang, Yansheng Hao et al. · Mitochondrion · 2008 · 38 citations

Medicine, Genetics, Molecular Genetics +16