Heidemarie Kreimer-Erlacher

Mutation analyses in 17 patients with deficiency in acid β-galactosidase: three novel point mutations and high correlation of mutation W273L with Morquio disease type B

Eduard Paschke, Ivica Milos, Heidemarie Kreimer-Erlacher et al. · Human Genetics · 2001 · 59 citations

Genetic Disorder, Genetics, Pathogenesis +9

Ultraviolet Exposure as the Main Initiator of p53 Mutations in Basal Cell Carcinomas from Psoralen and Ultraviolet A-Treated Patients with Psoriasis

Hannes Seidl, Heidemarie Kreimer-Erlacher, Barbara Bäck et al. · Journal of Investigative Dermatology · 2001 · 50 citations · Full text

Basal Cell Carcinomas, P53 Mutations, Medicine +6

High Mutation Frequency at Ha-ras Exons 1-4 in Squamous Cell Carcinomas from PUVA-treated Psoriasis Patients¶

Heidemarie Kreimer-Erlacher, Hannes Seidl, Barbara Bäck et al. · Photochemistry and Photobiology · 2001 · 45 citations

High Frequency of Ultraviolet Mutations at the INK4a-ARF Locus in Squamous Cell Carcinomas from Psoralen-Plus-Ultraviolet-A-Treated Psoriasis Patients

Heidemarie Kreimer-Erlacher, Hannes Seidl, Barbara Bäck et al. · Journal of Investigative Dermatology · 2003 · 35 citations · Full text

Medicine, Pathology, Clinical Dermatology +8

The Ultraviolet Fingerprint Dominates the Mutational Spectrum of the p53 and Ha-ras Genes in Psoralen + Ultraviolet A Keratoses from Psoriasis Patients

Peter Wolf, Heidemarie Kreimer-Erlacher, Hannes Seidl et al. · Journal of Investigative Dermatology · 2004 · 21 citations · Full text

Psoriasis Patients, Skin Cancer, Genetics +10