Albrecht Röpke

Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study

Anita Rauch, Dagmar Wieczorek, Elisabeth Graf et al. · The Lancet · 2012 · 1.1K citations · Full text

Genetic Mutations, Mendelian Disorder, Genetic Disorder +7

Derivation and Expansion Using Only Small Molecules of Human Neural Progenitors for Neurodegenerative Disease Modeling

Peter Reinhardt, Michael Glatza, Kathrin Hemmer et al. · PLoS ONE · 2013 · 464 citations · Full text

Phenotypic Screening, Neurodegenerative Disease Modeling, Molecular Biology +22

X-Linked <i>TEX11</i> Mutations, Meiotic Arrest, and Azoospermia in Infertile Men

Alexander N. Yatsenko, Andrew Georgiadis, Albrecht Röpke et al. · New England Journal of Medicine · 2015 · 333 citations · Full text

WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes

Axel Bohring, Thomas Stamm, Christiane Spaich et al. · The American Journal of Human Genetics · 2009 · 227 citations · Full text

Developmental Biology, Mendelian Disorder, Sex-biased Manifestation Pattern +11

Copy Number Variants in Patients with Severe Oligozoospermia and Sertoli-Cell-Only Syndrome

Frank Tüttelmann, Manuela Simoni, Sabine Kliesch et al. · PLoS ONE · 2011 · 149 citations · Full text