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Evaluation and comparison of short chain fatty acids composition in gut diseases

World journal of gastroenterology : WJG, 2019-09, Vol.25 (36), p.5543-5558

2019

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Detection rate of serrated polyps and serrated polyposis syndrome in colorectal cancer screening cohorts: a European overview

Gut, 2017-07, Vol.66 (7), p.1225

2017

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Familial risk-colorectal cancer: ESMO Clinical Practice Guidelines

Annals of oncology, 2013-10, Vol.24 Suppl 6, p.vi73-vi80

2013

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Declining detection rates for APC and biallelic MUTYH variants in polyposis patients, implications for DNA testing policy

European journal of human genetics : EJHG, 2020-02, Vol.28 (2), p.222-230

2020

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Features of Patients With Hereditary Mixed Polyposis Syndrome Caused by Duplication of GREM1 and Implications for Screening and Surveillance

Gastroenterology (New York, N.Y. 1943), 2017-06, Vol.152 (8), p.1876-1880.e1

2017

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Approach to screening for Familial Adenomatous Polyposis (FAP) in a cohort of 226 patients with Desmoid-type Fibromatosis (DF): experience of a specialist center in the UK

Familial cancer, 2022, Vol.21 (1), p.69-74

2022

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Cancer Risk in Patients With and Relatives of Serrated Polyposis Syndrome and Sporadic Sessile Serrated Lesions

The American journal of gastroenterology, 2022-02, Vol.117 (2), p.336-342

2022

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A novel AXIN2 germline variant associated with attenuated FAP without signs of oligondontia or ectodermal dysplasia

European journal of human genetics : EJHG, 2014-03, Vol.22 (3), p.423-426

2014

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High interobserver variability and frequent overdiagnosis of dysplasia in fundic gland polyps can be improved by detecting atypia on the surface epithelium and an abrupt transition to non‐neoplastic cells

Histopathology, 2022-01, Vol.80 (2), p.314-321

2022

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NTHL1 biallelic mutations seldom cause colorectal cancer, serrated polyposis or a multi-tumor phenotype, in absence of colorectal adenomas

Scientific reports, 2019-06, Vol.9 (1), p.9020-5, Article 9020

2019

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Novel APC gene mutations associated with protein alteration in diffuse type gastric cancer

BMC medical genetics, 2017-06, Vol.18 (1), p.61-61, Article 61

2017

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Desmoid tumor patients carry an elevated risk of familial adenomatous polyposis

Journal of surgical oncology, 2016-02, Vol.113 (2), p.209-212

2016

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Germline mutations in APC and MUTYH are responsible for the majority of families with attenuated familial adenomatous polyposis

Clinical genetics, 2007-05, Vol.71 (5), p.427-433

2007

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Genetic testing and phenotype in a large kindred with attenuated familial adenomatous polyposis

Gastroenterology (New York, N.Y. 1943), 2004-08, Vol.127 (2), p.444-451

2004

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Plasma Glycoprotein Profiling for Colorectal Cancer Biomarker Identification by Lectin Glycoarray and Lectin Blot

Journal of proteome research, 2008-04, Vol.7 (4), p.1693-1703

2008

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Multi-gene panel testing confirms phenotypic variability in MUTYH-Associated Polyposis

Familial cancer, 2019-04, Vol.18 (2), p.203-209

2019

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NTHL1-associate polyposis: first Australian case report

Familial cancer, 2019-04, Vol.18 (2), p.179-182

2019

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The Diagnostic Yield of Genetic Testing in Patients With Multiple Colorectal Adenomas: A Specialist Center Cohort Study

Clinical and translational gastroenterology, 2024-01, Vol.15 (1), p.e00645-e00645

2024

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The impact of screening and genetic registration on mortality and colorectal cancer incidence in familial adenomatous polyposis

Gut, 2010-10, Vol.59 (10), p.1378-1382

2010

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Germline mutation p.N363K in POLE is associated with an increased risk of colorectal cancer and giant cell glioblastoma

Familial cancer, 2019-04, Vol.18 (2), p.173-178

2019

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Unexplained polyposis: a challenge for geneticists, pathologists and gastroenterologists

Clinical genetics, 2012-01, Vol.81 (1), p.38-46

2012

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Intestinal and extraintestinal neoplasms in patients with NTHL1 tumor syndrome: a systematic review

Familial cancer, 2022-10, Vol.21 (4), p.453-462

2022

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Evaluation and comparison of short chain fatty acids composition in gut diseases

Detection rate of serrated polyps and serrated polyposis syndrome in colorectal cancer screening cohorts: a European overview

Familial risk-colorectal cancer: ESMO Clinical Practice Guidelines

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

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

Declining detection rates for APC and biallelic MUTYH variants in polyposis patients, implications for DNA testing policy

Features of Patients With Hereditary Mixed Polyposis Syndrome Caused by Duplication of GREM1 and Implications for Screening and Surveillance

Approach to screening for Familial Adenomatous Polyposis (FAP) in a cohort of 226 patients with Desmoid-type Fibromatosis (DF): experience of a specialist center in the UK

Cancer Risk in Patients With and Relatives of Serrated Polyposis Syndrome and Sporadic Sessile Serrated Lesions

A novel AXIN2 germline variant associated with attenuated FAP without signs of oligondontia or ectodermal dysplasia

High interobserver variability and frequent overdiagnosis of dysplasia in fundic gland polyps can be improved by detecting atypia on the surface epithelium and an abrupt transition to non‐neoplastic cells

NTHL1 biallelic mutations seldom cause colorectal cancer, serrated polyposis or a multi-tumor phenotype, in absence of colorectal adenomas

Novel APC gene mutations associated with protein alteration in diffuse type gastric cancer

Desmoid tumor patients carry an elevated risk of familial adenomatous polyposis

Germline mutations in APC and MUTYH are responsible for the majority of families with attenuated familial adenomatous polyposis

Genetic testing and phenotype in a large kindred with attenuated familial adenomatous polyposis

Plasma Glycoprotein Profiling for Colorectal Cancer Biomarker Identification by Lectin Glycoarray and Lectin Blot

Multi-gene panel testing confirms phenotypic variability in MUTYH-Associated Polyposis

Prevalence and Characteristics of MUTYH-Associated Polyposis in Patients with Multiple Adenomatous and Serrated Polyps

NTHL1-associate polyposis: first Australian case report

The Diagnostic Yield of Genetic Testing in Patients With Multiple Colorectal Adenomas: A Specialist Center Cohort Study

The impact of screening and genetic registration on mortality and colorectal cancer incidence in familial adenomatous polyposis

Germline mutation p.N363K in POLE is associated with an increased risk of colorectal cancer and giant cell glioblastoma

Unexplained polyposis: a challenge for geneticists, pathologists and gastroenterologists

Intestinal and extraintestinal neoplasms in patients with NTHL1 tumor syndrome: a systematic review

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