Kornelia Neveling

Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene

Alfons Meindl, Heide Hellebrand, Constanze Wiek et al. · Nature Genetics · 2010 · 727 citations

Breast Oncology, Somatic Variant, Cancer Pathology +9

Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer

Sarah Reid, Detlev Schindler, Helmut Hanenberg et al. · Nature Genetics · 2006 · 640 citations

Biallelic Mutations, Genetic Disorder, Genetics +6

Mutation of the RAD51C gene in a Fanconi anemia–like disorder

Fiona Vaz, Helmut Hanenberg, Beatrice Schuster et al. · Nature Genetics · 2010 · 402 citations

Genetic Disorder, Genetics, Molecular Biology +4

The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia

Orna Levran, Claire Attwooll, Rashida Henry et al. · Nature Genetics · 2005 · 365 citations

Genetics, Molecular Biology, Heme Signaling +3

A Post-Hoc Comparison of the Utility of Sanger Sequencing and Exome Sequencing for the Diagnosis of Heterogeneous Diseases

Kornelia Neveling, Ilse Feenstra, Christian Gilissen et al. · Human Mutation · 2013 · 336 citations · Full text

Exome Sequencing, Genetics, Genetic Epidemiology +23