Peter Huppke

Rett syndrome: Revised diagnostic criteria and nomenclature

Jeffrey L. Neul, Walter E. Kaufmann, Daniel G. Glaze et al. · Annals of Neurology · 2010 · 1.4K citations · Full text

Life Sciences, Genetics, Neurology +17

MECP2 Mutations in Sporadic Cases of Rett Syndrome Are Almost Exclusively of Paternal Origin

Ralf Ulrich Trappe, Franco Laccone, Joana Cobilanschi et al. · The American Journal of Human Genetics · 2001 · 283 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

Rett syndrome: analysis of MECP2 and clinical characterization of 31 patients

Peter Huppke · Human Molecular Genetics · 2000 · 246 citations

Life Sciences, Genetics, Molecular Genetics +17

Breathing dysfunctions associated with impaired control of postinspiratory activity in <i>Mecp2^−/y</i> knockout mice

Georg M. Stettner, Peter Huppke, Cornelia Brendel et al. · The Journal of Physiology · 2007 · 161 citations · Full text

Life Sciences, Neurobiology, Neuroscience +14

Mutations in SLC33A1 Cause a Lethal Autosomal-Recessive Disorder with Congenital Cataracts, Hearing Loss, and Low Serum Copper and Ceruloplasmin

Peter Huppke, Cornelia Brendel, Vera M. Kalscheuer et al. · The American Journal of Human Genetics · 2012 · 105 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14