Anthony Renwick
Ratings
0
Nobody has rated this yet. Be the first!
Works
12
Evaluation of Fanconi Anemia genes in familial breast cancer predisposition
The ICR639 CPG NGS validation series: A resource to assess analytical sensitivity of cancer predisposition gene testing
Corrigendum: Mutations in the PP2A regulatory subunit B family genes PPP2R5B, PPP2R5C and PPP2R5D cause human overgrowth
OpEx - a validated, automated pipeline optimised for clinical exome sequence analysis.
Germline RAD51C mutations confer susceptibility to ovarian cancer
A genome-wide association study identifies susceptibility loci for Wilms tumor
ICR142 Benchmarker: evaluating, optimising and benchmarking variant calling using the ICR142 NGS validation series
Predisposition gene identification in common cancers by exome sequencing: insights from familial breast cancer
PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene
Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles
