Search filters

List of works by Roland Kruse

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

scholarly article published in Nature Genetics

Follow-up study of the first genome-wide association scan in alopecia areata: IL13 and KIAA0350 as susceptibility loci supported with genome-wide significance

scientific article

Genetic variants in CTLA4 are strongly associated with alopecia areata

article

Genetic variation in the human androgen receptor gene is the major determinant of common early-onset androgenetic alopecia

scientific article

Genome-wide pooling approach identifies SPATA5 as a new susceptibility locus for alopecia areata

scientific article published on 26 October 2011

Genome-wide scan and fine-mapping linkage study of androgenetic alopecia reveals a locus on chromosome 3q26

scientific article

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

scientific article (publication date: June 2003)

Loss-of-Function Mutations in the Filaggrin Gene and Alopecia Areata: Strong Risk Factor for a Severe Course of Disease in Patients Comorbid for Atopic Disease

article

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

scientific article published on 4 January 2009

Marie Unna hereditary hypotrichosis: Identification of a U2HR mutation in the family from the original 1925 report

Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia

Reply

Susceptibility variants for male-pattern baldness on chromosome 20p11.

scientific article