Rabi Tawil

Mutations in Kir2.1 Cause the Developmental and Episodic Electrical Phenotypes of Andersen's Syndrome

Nikki Plaster, Rabi Tawil, Martin Tristani‐Firouzi et al. · Cell · 2001 · 998 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

A Unifying Genetic Model for Facioscapulohumeral Muscular Dystrophy

Richard J.L.F. Lemmers, Patrick J. van der Vliet, Rinse Klooster et al. · Science · 2010 · 783 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2

Richard J.L.F. Lemmers, Rabi Tawil, Lisa M. Petek et al. · Nature Genetics · 2012 · 664 citations

Life Sciences, Genetics, Molecular Genetics +12

Interferon‐α/β–mediated innate immune mechanisms in dermatomyositis

Steven A. Greenberg, Jack L. Pinkus, Geraldine S. Pinkus et al. · Annals of Neurology · 2005 · 612 citations

Medicine, Immunology, Pathology +17

Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome)

Martin Tristani‐Firouzi, Judy L. Jensen, Matthew R. Donaldson et al. · Journal of Clinical Investigation · 2002 · 539 citations · Full text

Medicine, Cardiology, Genetics +17