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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.1225-1232

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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Attenuated adenomatous polyposis with MSH6 variation: Two case reports

Medicine (Baltimore), 2024-07, Vol.103 (27), p.e38791

2024

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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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The Effect of Metformin in Treatment of Adenomas in Patients with Familial Adenomatous Polyposis

Cancer prevention research (Philadelphia, Pa.), 2021-05, Vol.14 (5), p.563-572

2021

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

Clinical gastroenterology and hepatology, 2019-10, Vol.17 (11), p.2294-2300.e1

2019

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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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Desmoids and Genotype in Familial Adenomatous Polyposis

Diseases of the colon & rectum, 2015-04, Vol.58 (4), p.444-448

2015

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Feasibility of Cold Snare Polypectomy for Multiple Duodenal Adenomas in Patients with Familial Adenomatous Polyposis: A Pilot Study

Digestive diseases and sciences, 2016-09, Vol.61 (9), p.2755-2759

2016

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Colonic manifestations of PTEN hamartoma tumor syndrome: Case series and systematic review

World journal of gastroenterology : WJG, 2014-02, Vol.20 (7), p.1833-1838

2014

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Gene Expression Profiling of Desmoid Tumors by cDNA Microarrays and Correlation with Progression-Free Survival

Clinical cancer research, 2015-09, Vol.21 (18), p.4194-4200

2015

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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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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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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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Identification of a novel GREM1 duplication in a patient with multiple colon polyps

Familial cancer, 2019-01, Vol.18 (1), p.63-66

2019

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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

Attenuated adenomatous polyposis with MSH6 variation: Two case reports

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

The Effect of Metformin in Treatment of Adenomas in Patients with Familial Adenomatous Polyposis

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

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

Desmoids and Genotype in Familial Adenomatous Polyposis

Feasibility of Cold Snare Polypectomy for Multiple Duodenal Adenomas in Patients with Familial Adenomatous Polyposis: A Pilot Study

Colonic manifestations of PTEN hamartoma tumor syndrome: Case series and systematic review

Gene Expression Profiling of Desmoid Tumors by cDNA Microarrays and Correlation with Progression-Free Survival

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

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

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

Identification of a novel GREM1 duplication in a patient with multiple colon polyps

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