Andreas Winterpacht

Mutations in LMX1B cause abnormal skeletal patterning and renal dysplasia in nail patella syndrome

Sandra D. Dreyer, Guang Zhou, Antonio Baldini et al. · Nature Genetics · 1998 · 526 citations

Renal Dysplasia, Mendelian Disorder, Genetic Disorder +6

Nuclear localization of the protein encoded by the Wilms’ tumor gene <i>WT1</i> in embryonic and adult tissues

Stefan Mundlos, Jerry Pelletier, André Darveau et al. · Development · 1993 · 315 citations

Genetics, Renal Pathology, Molecular Genetics +19

Deficiency of UBR1, a ubiquitin ligase of the N-end rule pathway, causes pancreatic dysfunction, malformations and mental retardation (Johanson-Blizzard syndrome)

Martin Zenker, Julia Mayerle, Markus M. Lerch et al. · Nature Genetics · 2005 · 270 citations

Protein Quality Control, Autoimmune Disease, Genetics +7

Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene

Bärbel Dittrich, Karin Buiting, Bernd Korn et al. · Nature Genetics · 1996 · 257 citations

Chromatin, Transcriptional Regulation, Developmental Biology +9

<i>PAX8</i>, a human paired box gene: isolation and expression in developing thyroid, kidney and Wilms’ tumors

Andrej Poleev, Helmut Fickenscher, Stefan Mundlos et al. · Development · 1992 · 227 citations