Roland Kruse

Loss-of-Function Mutations in the Keratin 5 Gene Lead to Dowling-Degos Disease

Regina C. Betz, Laura Planko, Sibylle Eigelshoven et al. · The American Journal of Human Genetics · 2006 · 267 citations · Full text

Life Sciences, Genetics, Molecular Genetics +4

Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia

Axel M. Hillmer, S. Hanneken, Sibylle Ritzmann et al. · The American Journal of Human Genetics · 2005 · 245 citations · Full text

Medicine, Dermatology, Genetics +17

Muir-Torre Phenotype Has a Frequency of DNA Mismatch-Repair-Gene Mutations Similar to That in Hereditary Nonpolyposis Colorectal Cancer Families Defined by the Amsterdam Criteria

Roland Kruse, Arno Rütten, Christof Lamberti et al. · The American Journal of Human Genetics · 1998 · 234 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

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 · 212 citations

Life Sciences, Genetics, Molecular Genetics +9

Hypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosin

Etgar Levy‐Nissenbaum, Regina C. Betz, Moshe Frydman et al. · Nature Genetics · 2003 · 176 citations

Medicine, Dermatology, Genetics +8