Hadas Lahat

A Missense Mutation in a Highly Conserved Region of CASQ2 Is Associated with Autosomal Recessive Catecholamine-Induced Polymorphic Ventricular Tachycardia in Bedouin Families from Israel

Hadas Lahat, Elon Pras, Tsviya Olender et al. · The American Journal of Human Genetics · 2001 · 649 citations · Full text

Medicine, Cardiology, Genetics +13

Autosomal Recessive Catecholamine- or Exercise-Induced Polymorphic Ventricular Tachycardia

Hadas Lahat, Michael Eldar, Etgar Levy‐Nissenbaum et al. · Circulation · 2001 · 269 citations · Full text

Medicine, Cardiology, Genetics +15

Point Mutation in the HCN4 Cardiac Ion Channel Pore Affecting Synthesis, Trafficking, and Functional Expression Is Associated With Familial Asymptomatic Sinus Bradycardia

Eyal Nof, David Luria, Dovrat Brass et al. · Circulation · 2007 · 178 citations

Natural Sciences, Cardiology, Genetics +17

Hypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosin

Etgar Levy‐Nissenbaum, Regina C. Betz, Moshe Frydman et al. · Nature Genetics · 2003 · 176 citations

Medicine, Dermatology, Genetics +8

Megalencephalic leukoencephalopathy with subcortical cysts; a founder effect in Israeli patients and a higher than expected carrier rate among Libyan Jews

Bruria Ben‐Zeev, Etgar Levy‐Nissenbaum, Hadas Lahat et al. · Human Genetics · 2002 · 43 citations

Medicine, Neurology, Neuroscience +10