Hildegunn Høberg‐Vetti

Mutational Signature Analysis Reveals NTHL1 Deficiency to Cause a Multi-tumor Phenotype

Judith E. Grolleman, Richarda M. de Voer, Fadwa A. Elsayed et al. · Cancer Cell · 2019 · 175 citations · Full text

Medicine, Molecular Biology, Molecular Genetics +12

Melanoma prone families with <i>CDK4</i> germline mutation: phenotypic profile and associations with <i>MC1R</i> variants

Hanne Puntervoll, Xiaohong R. Yang, Hildegunn Høberg‐Vetti et al. · Journal of Medical Genetics · 2013 · 136 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Ask Rosa – The making of a digital genetic conversation tool, a chatbot, about hereditary breast and ovarian cancer

Elen Siglen, Hildegunn Høberg‐Vetti, Aslaug Beathe Forberg Lunde et al. · Patient Education and Counseling · 2021 · 92 citations · Full text

Computing, Biomedical Informatics, Computer Science +17

BRCA1/2 testing in newly diagnosed breast and ovarian cancer patients without prior genetic counselling: the DNA-BONus study

Hildegunn Høberg‐Vetti, Cathrine Bjorvatn, Bent Fiane et al. · European Journal of Human Genetics · 2015 · 76 citations · Full text

Life Sciences, Genetics, Oncology +15

BRCA Testing by Single-Molecule Molecular Inversion Probes

Kornelia Neveling, Arjen R. Mensenkamp, Ronny Derks et al. · Clinical Chemistry · 2016 · 66 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17