Hereditary gastrointestinal cancers: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up†

Colorectal Cancer in Individuals With Familial Adenomatous Polyposis, Based on Analysis of the Danish Polyposis Registry

(2019) John Gásdal Karstensen et al.   Clinical Gastroenterology and Hepatology

Hereditary gastric cancer: what’s new? Update 2013–2018

(2019) Rachel S. van der Post et al.   Familial Cancer

Personalised surveillance for serrated polyposis syndrome: results from a prospective 5-year international cohort study

(2019) Arne GC Bleijenberg et al.   GUT

Opportunistic testing of BRCA1 , BRCA2 and mismatch repair genes improves the yield of phenotype driven hereditary cancer gene panels

(2019) Lídia Feliubadaló et al.   INTERNATIONAL JOURNAL OF CANCER

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

(2018) Amy Taylor et al.   JOURNAL OF MEDICAL GENETICS

Assessment of Tumor Sequencing as a Replacement for Lynch Syndrome Screening and Current Molecular Tests for Patients With Colorectal Cancer

(2018) Heather Hampel et al.   JAMA Oncology

High incidence of advanced colorectal neoplasia during endoscopic surveillance in serrated polyposis syndrome

(2018) Daniel Rodríguez-Alcalde et al.   ENDOSCOPY

Cancer Risks for PMS2-Associated Lynch Syndrome

(2018) Sanne W. ten Broeke et al.   JOURNAL OF CLINICAL ONCOLOGY

A Decision Analysis for Rectal-Sparing Familial Adenomatous Polyposis

(2018) Nelya Melnitchouk et al.   DISEASES OF THE COLON & RECTUM

Cancer risk and survival inpath_MMRcarriers by gene and gender up to 75 years of age: a report from the Prospective Lynch Syndrome Database

(2017) Pål Møller et al.   GUT

British Society of Gastroenterology position statement on serrated polyps in the colon and rectum

(2017) James E East et al.   GUT

Development and Validation of the PREMM5 Model for Comprehensive Risk Assessment of Lynch Syndrome

(2017) Fay Kastrinos et al.   JOURNAL OF CLINICAL ONCOLOGY

Cancer Susceptibility Gene Mutations in Individuals With Colorectal Cancer

(2017) Matthew B. Yurgelun et al.   JOURNAL OF CLINICAL ONCOLOGY

Nivolumab in patients with metastatic DNA mismatch repair-deficient or microsatellite instability-high colorectal cancer (CheckMate 142): an open-label, multicentre, phase 2 study

(2017) Michael J Overman et al.   LANCET ONCOLOGY

POLE and POLD1 screening in 155 patients with multiple polyps and early-onset colorectal cancer

(2017) Clara Esteban-Jurado et al.   Oncotarget

Prevalence and Spectrum of Germline Cancer Susceptibility Gene Mutations Among Patients With Early-Onset Colorectal Cancer

(2017) Rachel Pearlman et al.   JAMA Oncology

Cancer Risk in Families Fulfilling the Amsterdam Criteria for Lynch Syndrome

(2017) N. Jewel Samadder et al.   JAMA Oncology

Association of DNA Mismatch Repair and Mutations in BRAF and KRAS With Survival After Recurrence in Stage III Colon Cancers

(2017) Frank A. Sinicrope et al.   JAMA Oncology

Point Mutations in Exon 1B of APC Reveal Gastric Adenocarcinoma and Proximal Polyposis of the Stomach as a Familial Adenomatous Polyposis Variant

(2016) Jun Li et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Incidence of and survival after subsequent cancers in carriers of pathogenic MMR variants with previous cancer: a report from the prospective Lynch syndrome database

(2016) Pål Møller et al.   GUT

Benefit of Surveillance for Pancreatic Cancer in High-Risk Individuals: Outcome of Long-Term Prospective Follow-Up Studies From Three European Expert Centers

(2016) Hans Vasen et al.   JOURNAL OF CLINICAL ONCOLOGY

β-Catenin activation in fundic gland polyps, gastric cancer and colonic polyps in families afflicted by ‘gastric adenocarcinoma and proximal polyposis of the stomach’ (GAPPS)

(2016) Lucas A McDuffie et al.   JOURNAL OF CLINICAL PATHOLOGY

Impact of Chromoscopy on Adenoma Detection in Patients With Lynch Syndrome: A Prospective, Multicenter, Blinded, Tandem Colonoscopy Study

(2015) Gabriel Rahmi et al.   AMERICAN JOURNAL OF GASTROENTEROLOGY

ACG Clinical Guideline: Genetic Testing and Management of Hereditary Gastrointestinal Cancer Syndromes

(2015) Sapna Syngal et al.   AMERICAN JOURNAL OF GASTROENTEROLOGY

Phenotypic and genotypic characterisation of biallelic mismatch repair deficiency (BMMR-D) syndrome

(2015) Carol A. Durno et al.   EUROPEAN JOURNAL OF CANCER

POLE and POLD1 mutations in 529 kindred with familial colorectal cancer and/or polyposis: review of reported cases and recommendations for genetic testing and surveillance

(2015) Fernando Bellido et al.   GENETICS IN MEDICINE

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

Colorectal cancer risk factors in patients with serrated polyposis syndrome: a large multicentre study

(2015) Sabela Carballal et al.   GUT

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

A germline homozygous mutation in the base-excision repair gene NTHL1 causes adenomatous polyposis and colorectal cancer

(2015) Robbert D A Weren et al.   NATURE GENETICS

PD-1 Blockade in Tumors with Mismatch-Repair Deficiency

(2015) Dung T. Le et al.   NEW ENGLAND JOURNAL OF MEDICINE

Hereditary Diffuse Gastric Cancer Syndrome

(2015) Samantha Hansford et al.   JAMA Oncology

Cáncer colorrectal familiar y hereditario

(2014) Francesc Balaguer   Gastroenterologia y Hepatologia

Colon and Endometrial Cancers With Mismatch Repair Deficiency Can Arise From Somatic, Rather Than Germline, Mutations

(2014) Sigurdis Haraldsdottir et al.   GASTROENTEROLOGY

BRCA1, BRCA2, PALB2 and CDKN2A mutations in familial pancreatic cancer: a PACGENE study

(2014) David B. Zhen et al.   GENETICS IN MEDICINE

Diagnostic criteria for constitutional mismatch repair deficiency syndrome: suggestions of the European consortium ‘Care for CMMRD’ (C4CMMRD)

(2014) Katharina Wimmer et al.   JOURNAL OF MEDICAL GENETICS

Guidelines for surveillance of individuals with constitutional mismatch repair-deficiency proposed by the European Consortium “Care for CMMR-D” (C4CMMR-D)

(2014) H F A Vasen et al.   JOURNAL OF MEDICAL GENETICS

Pancreatic cancer risk in hereditary pancreatitis

(2014) Frank U. Weiss   Frontiers in Physiology

Prevalence of Germline PTEN, BMPR1A, SMAD4, STK11, and ENG Mutations in Patients With Moderate-Load Colorectal Polyps

(2013) Joanne Ngeow et al.   GASTROENTEROLOGY

Germline Mutations in Oncogene-Induced Senescence Pathways Are Associated With Multiple Sessile Serrated Adenomas

(2013) Manish K. Gala et al.   GASTROENTEROLOGY

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

High prevalence of serrated polyposis syndrome in FIT-based colorectal cancer screening programmes: Table 1

(2012) Leticia Moreira et al.   GUT

International Cancer of the Pancreas Screening (CAPS) Consortium summit on the management of patients with increased risk for familial pancreatic cancer

(2012) Marcia Irene Canto et al.   GUT

Prevalence and Phenotypes of APC and MUTYH Mutations in Patients With Multiple Colorectal Adenomas

(2012) Shilpa Grover et al.   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

Identification of Lynch Syndrome Among Patients With Colorectal Cancer

(2012) Leticia Moreira et al.   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

Colorectal and Other Cancer Risks for Carriers and Noncarriers From Families With a DNA Mismatch Repair Gene Mutation: A Prospective Cohort Study

(2012) Aung Ko Win et al.   JOURNAL OF CLINICAL ONCOLOGY

Risks of Less Common Cancers in Proven Mutation Carriers With Lynch Syndrome

(2012) Christoph Engel et al.   JOURNAL OF CLINICAL ONCOLOGY

Pancreatic cancer risk in Peutz-Jeghers syndrome patients: a large cohort study and implications for surveillance

(2012) Susanne E Korsse et al.   JOURNAL OF MEDICAL GENETICS

History, Pathogenesis, and Management of Familial Gastric Cancer: Original Study of John XXIII's Family

(2012) Giovanni Corso et al.   Biomed Research International

Gastric adenocarcinoma and proximal polyposis of the stomach (GAPPS): a new autosomal dominant syndrome

(2011) D L Worthley et al.   GUT

Microsatellite Instability, Prognosis and Drug Sensitivity of Stage II and III Colorectal Cancer: More Complexity to the Puzzle

(2011) S. Tejpar et al.   JNCI-Journal of the National Cancer Institute

Long-term effect of aspirin on cancer risk in carriers of hereditary colorectal cancer: an analysis from the CAPP2 randomised controlled trial

(2011) John Burn et al.   LANCET

One to 2-Year Surveillance Intervals Reduce Risk of Colorectal Cancer in Families With Lynch Syndrome

(2010) Hans F.A. Vasen et al.   GASTROENTEROLOGY

Increased colorectal cancer risk during follow-up in patients with hyperplastic polyposis syndrome: a multicentre cohort study

(2009) K. S. Boparai et al.   GUT

Ten Years After Mutation Testing for Lynch Syndrome: Cancer Incidence and Outcome in Mutation-Positive and Mutation-Negative Family Members

(2009) Heikki J. Järvinen et al.   JOURNAL OF CLINICAL ONCOLOGY

Extra-Intestinal Manifestations of Familial Adenomatous Polyposis

(2008) Emma J. Groen et al.   ANNALS OF SURGICAL ONCOLOGY

Cardiovascular Risk of Celecoxib in 6 Randomized Placebo-Controlled Trials

(2008) Scott D. Solomon et al.   CIRCULATION

Screening for urinary tract cancer with urine cytology in Lynch syndrome and familial colorectal cancer

(2008) T. Myrhøj et al.   Familial Cancer

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

(2008) H. F. A. Vasen et al.   GUT

Feasibility of Screening for Lynch Syndrome Among Patients With Colorectal Cancer

(2008) Heather Hampel et al.   JOURNAL OF CLINICAL ONCOLOGY