Consensus for genes to be included on cancer panel tests offered by UK genetics services: guidelines of the UK Cancer Genetics Group

Validation of Recently Proposed Colorectal Cancer Susceptibility Gene Variants in an Analysis of Families and Patients—a Systematic Review

(2017) Peter Broderick et al.   GASTROENTEROLOGY

CDH1 germline mutations: different syndromes, same management?

(2017) Patrick R Benusiglio   GENETICS IN MEDICINE

Associations Between Cancer Predisposition Testing Panel Genes and Breast Cancer

(2017) Fergus J. Couch et al.   JAMA Oncology

Expanding the genotype–phenotype spectrum in hereditary colorectal cancer by gene panel testing

(2016) Anna Rohlin et al.   Familial Cancer

Incorporating truncating variants in PALB2, CHEK2 and ATM into the BOADICEA breast cancer risk model

(2016) Andrew J. Lee et al.   GENETICS IN MEDICINE

Rare non-epithelial ovarian neoplasms: Pathology, genetics and treatment

(2016) William D. Foulkes et al.   GYNECOLOGIC ONCOLOGY

No evidence that protein truncating variants inBRIP1are associated with breast cancer risk: implications for gene panel testing

(2016) Douglas F Easton et al.   JOURNAL OF MEDICAL GENETICS

Multigene testing of moderate-risk genes: be mindful of the missense

(2016) E L Young et al.   JOURNAL OF MEDICAL GENETICS

NCCN Guidelines Insights: Genetic/Familial High-Risk Assessment: Breast and Ovarian, Version 2.2017

(2016) Mary B. Daly et al.   Journal of the National Comprehensive Cancer Network

Counselling framework for moderate-penetrance cancer-susceptibility mutations

(2016) Nadine Tung et al.   Nature Reviews Clinical Oncology

Cancer incidence and survival in Lynch syndrome patients receiving colonoscopic and gynaecological surveillance: first report from the prospective Lynch syndrome database

(2015) Pål Møller et al.   GUT

Targeted massively parallel sequencing of a panel of putative breast cancer susceptibility genes in a large cohort of multiple-case breast and ovarian cancer families

(2015) Jun Li et al.   JOURNAL OF MEDICAL GENETICS

Hereditary diffuse gastric cancer: updated clinical guidelines with an emphasis on germlineCDH1mutation carriers

(2015) Rachel S van der Post et al.   JOURNAL OF MEDICAL GENETICS

Germline Mutations in the BRIP1, BARD1, PALB2, and NBN Genes in Women With Ovarian Cancer

(2015) Susan J. Ramus et al.   JNCI-Journal of the National Cancer Institute

Prediction of Breast Cancer Risk Based on Profiling With Common Genetic Variants

(2015) Nasim Mavaddat et al.   JNCI-Journal of the National Cancer Institute

Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer

(2015) Kyriaki Michailidou et al.   NATURE GENETICS

Gene-Panel Sequencing and the Prediction of Breast-Cancer Risk

(2015) Douglas F. Easton et al.   NEW ENGLAND JOURNAL OF MEDICINE

Germline Mutations in the BRIP1, BARD1, PALB2, and NBN Genes in Women With Ovarian Cancer

(2015) Susan J. Ramus et al.   JNCI-Journal of the National Cancer Institute

Prediction of Breast Cancer Risk Based on Profiling With Common Genetic Variants

(2015) Nasim Mavaddat et al.   JNCI-Journal of the National Cancer Institute

Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts

(2013) Hans F A Vasen et al.   GUT

EPCAM deletion carriers constitute a unique subgroup of Lynch syndrome patients

(2012) Marjolijn J. L. Ligtenberg et al.   Familial Cancer

Peutz-Jeghers syndrome: a systematic review and recommendations for management

(2010) A. D. Beggs et al.   GUT

Guidelines for colorectal cancer screening and surveillance in moderate and high risk groups (update from 2002)

(2010) S. R. Cairns et al.   GUT

TP53 germline mutation testing in 180 families suspected of Li-Fraumeni syndrome: mutation detection rate and relative frequency of cancers in different familial phenotypes

(2010) M. W. G. Ruijs et al.   JOURNAL OF MEDICAL GENETICS

Guidelines for the clinical management of familial adenomatous polyposis (FAP)

(2008) H. F. A. Vasen et al.   GUT