Michel van Geel

Comprehensive analysis of the gene encoding filaggrin uncovers prevalent and rare mutations in ichthyosis vulgaris and atopic eczema

Aileen Sandilands, Ana Terron-Kwiatkowski, Peter Hull et al. · Nature Genetics · 2007 · 660 citations

Allergy, Atopic Dermatitis, Genetic Disorder +11

Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis

Yaran Wen, Yang Liu, Yiming Xu et al. · Nature Genetics · 2009 · 208 citations

Inhibitory Upstream Orf, Genetic Disorder, Natural Sciences +8

A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome

Maurice A. M. Van Steensel, Michel van Geel, Peter M. Steijlen et al. · Journal of Investigative Dermatology · 2002 · 166 citations · Full text

Pathology, Novel Connexin 26, Dermatology +4

Evidence of digenic inheritance in Alport syndrome

Maria Antonietta Mencarelli, Laurence Heidet, Helen Storey et al. · Journal of Medical Genetics · 2015 · 159 citations · Full text

A Modular, Positive Selection Bacterial Artificial Chromosome Vector with Multiple Cloning Sites

Eirik Frengen, Dieter Weichenhan, Baohui Zhao et al. · Genomics · 1999 · 148 citations

Biology, Engineering, Multiple Cloning Sites +9