Finn C. Nielsen
Copenhagen University Hospital(DK)Rigshospitalet(DK)
Publications by Year
Research Areas
BRCA gene mutations in cancer, CRISPR and Genetic Engineering, DNA Repair Mechanisms, Genetics, Bioinformatics, and Biomedical Research, Genetic Associations and Epidemiology
Most-Cited Works
- → Pathology of Breast and Ovarian Cancers among BRCA1 and BRCA2 Mutation Carriers: Results from the Consortium of Investigators of Modifiers of BRCA1 / 2 (CIMBA)(2012)655 cited
- → Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2(2011)118 cited
- → Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2mutation carriers(2012)96 cited
- → Functional characterization of BRCA1 gene variants by mini-gene splicing assay(2014)82 cited
- → Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers(2014)69 cited
- → BRCA1 and BRCA2 mutations in Danish families with hereditary breast and/or ovarian cancer(2008)53 cited
- → The silent mutation nucleotide 744 G → A, Lys172Lys, in exon 6 of BRCA2 results in exon skipping(2009)35 cited
- → An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers(2015)34 cited
- → Next-Generation Sequencing–Based Detection of Germline Copy Number Variations in BRCA1 / BRCA2(2017)29 cited
- → Splicing analysis of 14 BRCA1 missense variants classifies nine variants as pathogenic(2015)27 cited