Kornelia Neveling
Radboud University Nijmegen(NL)Radboud University Medical Center(NL)
Publications by Year
Research Areas
DNA Repair Mechanisms, Retinal Development and Disorders, Genomic variations and chromosomal abnormalities, Genomics and Rare Diseases, CRISPR and Genetic Engineering
Most-Cited Works
- → Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene(2010)731 cited
- → Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer(2006)641 cited
- → Mutation of the RAD51C gene in a Fanconi anemia–like disorder(2010)403 cited
- → The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia(2005)365 cited
- → A Post-Hoc Comparison of the Utility of Sanger Sequencing and Exome Sequencing for the Diagnosis of Heterogeneous Diseases(2013)338 cited
- → Next‐generation genetic testing for retinitis pigmentosa(2012)284 cited
- → FANCI is a second monoubiquitinated member of the Fanconi anemia pathway(2007)277 cited