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 · 261 citations · Full text

Developmental Biology, Mendelian Disorder, Genetic Disorder +8

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 · 239 citations · Full text

Allelic Variant, Developmental Biology, Genetics +7

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

Genome Instability, Somatic Variant, Genetic Disorder +10

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

Loss of DNA Mismatch Repair Proteins in Skin Tumors From Patients With Muir–Torre Syndrome and MSH2 or MLH1 Germline Mutations

Micaela Mathiak, Arno Rütten, Elisabeth Mangold et al. · The American Journal of Surgical Pathology · 2002 · 175 citations

Genome Instability, Somatic Variant, Genetic Disorder +13