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WWP1 Gain-of-Function Inactivation of PTEN in Cancer Predisposition

The New England journal of medicine, 2020-05, Vol.382 (22), p.2103-2116

2020

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Natural history of colonic polyposis in young patients with familial adenomatous polyposis

Gastrointestinal endoscopy, 2018-10, Vol.88 (4), p.726-733

2018

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The Second Allele: A Key to Understanding the Timing of Sporadic and Hereditary Colorectal Tumorigenesis

Genes, 2021-09, Vol.12 (10), p.1515

2021

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Web-Based Model for Predicting Time to Surgery in Young Patients with Familial Adenomatous Polyposis: An Internally Validated Study

The American journal of gastroenterology, 2018-12, Vol.113 (12), p.1881-1890

2018

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S620 Clinically Actionable Findings on Surveillance EGD in Asymptomatic Patients With Lynch Syndrome

The American journal of gastroenterology, 2021-10, Vol.116 (1), p.S281-S282

2021

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Compound heterozygous MSH3 germline variants and associated tumor somatic DNA mismatch repair dysfunction

NPJ precision oncology, 2024-01, Vol.8 (1), p.12-5, Article 12

2024

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Proximal colon cancers and the serrated pathway: a systematic analysis of precursor histology and BRAF mutation status

Modern pathology, 2012-10, Vol.25 (10), p.1423-1431

2012

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Hereditary colorectal cancer syndromes and genetic testing

Journal of surgical oncology, 2015-01, Vol.111 (1), p.103-111

2015

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Lynch syndrome screening in newly diagnosed colorectal cancer in general pathology practice: From the revised Bethesda guidelines to a universal approach

Scandinavian journal of gastroenterology, 2011-11, Vol.46 (11), p.1340-1348

2011

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Malignancy risk in individuals with familial adenomatous polyposis receiving biologics and immunomodulators

Familial cancer, 2022-04, Vol.21 (2), p.189-195

2022

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A Multi-Institutional Cohort of Therapy-Associated Polyposis in Childhood and Young Adulthood Cancer Survivors

Cancer prevention research (Philadelphia, Pa.), 2020-03, Vol.13 (3), p.291-298

2020

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Primer on Hereditary Cancer Predisposition Genes Included Within Somatic Next-Generation Sequencing Panels

JCO precision oncology, 2019-12 (3), p.1-11

2019

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SMAD4 mutation and the combined syndrome of juvenile polyposis syndrome and hereditary haemorrhagic telangiectasia

Thorax, 2010-08, Vol.65 (8), p.745-746

2010

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Diagnosis of “Tumor Lynch” syndrome: implications for clinical management

Journal of the American College of Surgeons, 2014-10, Vol.219 (4), p.e79-e79

2014

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The impact of clinical decision making in a molecular tumor board at a tertiary care center

Journal of clinical oncology, 2021-05, Vol.39 (15_suppl), p.3128-3128

2021

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2894 The Gastrointestinal Phenotype of Cowden’s Syndrome and Effects of Surveillance

The American journal of gastroenterology, 2019-10, Vol.114 (1), p.S1584-S1585

2019

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Genomic Microsatellite Signatures Identify Germline Mismatch Repair Deficiency and Risk of Cancer Onset

Journal of clinical oncology, 2023-02, Vol.41 (4), p.766-777

2023

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Abstract P056: Germline cancer susceptibility gene testing in unselected patients with soft tissue sarcoma: a multi-center prospective study

Cancer prevention research (Philadelphia, Pa.), 2023-01, Vol.16 (1_Supplement), p.P056-P056

2023

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Improving the referral rate of universal genetic counseling for pancreatic ductal adenocarcinoma (PDAC) at the Cleveland Clinic Taussig Cancer Center: A quality improvement project

Journal of clinical oncology, 2020-10, Vol.38 (29_suppl), p.196-196

2020

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S3382 Juvenile Polyposis Syndrome & Inflammatory Bowel Disease: Balancing the Risk of Malignancy

The American journal of gastroenterology, 2020-10, Vol.115 (1), p.S1758-S1758

2020

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S1305 Cancer Surveillance in Peutz Jeghers Syndrome

The American journal of gastroenterology, 2020-10, Vol.115 (1), p.S655-S655

2020

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S0205 Association of Cancer With Comorbid Inflammatory Diseases in Lynch Syndrome and Lynch-Like Syndrome Individuals

The American journal of gastroenterology, 2020-10, Vol.115 (1), p.S68-S68

2020

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Defining Phenotypes and Cancer Risk in Hyperplastic Polyposis Syndrome

Diseases of the colon & rectum, 2011-02, Vol.54 (2), p.164-170

2011

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The prevalence of hereditary hemorrhagic telangiectasia in Juvenile Polyposis syndrome patients with SMAD4 mutations

Hereditary cancer in clinical practice, 2011-03, Vol.9 (Suppl 1), p.O5-O5

2011

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High risk clinic for hereditary colorectal neoplasia: a focus for patient care and an opportunity for clinical research

Hereditary cancer in clinical practice, 2010-05, Vol.8 (Suppl 1), p.P10-P10

2010

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WWP1 Gain-of-Function Inactivation of PTEN in Cancer Predisposition

Natural history of colonic polyposis in young patients with familial adenomatous polyposis

The Second Allele: A Key to Understanding the Timing of Sporadic and Hereditary Colorectal Tumorigenesis

Web-Based Model for Predicting Time to Surgery in Young Patients with Familial Adenomatous Polyposis: An Internally Validated Study

S620 Clinically Actionable Findings on Surveillance EGD in Asymptomatic Patients With Lynch Syndrome

Compound heterozygous MSH3 germline variants and associated tumor somatic DNA mismatch repair dysfunction

Proximal colon cancers and the serrated pathway: a systematic analysis of precursor histology and BRAF mutation status

Hereditary colorectal cancer syndromes and genetic testing

Lynch syndrome screening in newly diagnosed colorectal cancer in general pathology practice: From the revised Bethesda guidelines to a universal approach

Malignancy risk in individuals with familial adenomatous polyposis receiving biologics and immunomodulators

A Multi-Institutional Cohort of Therapy-Associated Polyposis in Childhood and Young Adulthood Cancer Survivors

Primer on Hereditary Cancer Predisposition Genes Included Within Somatic Next-Generation Sequencing Panels

SMAD4 mutation and the combined syndrome of juvenile polyposis syndrome and hereditary haemorrhagic telangiectasia

Diagnosis of “Tumor Lynch” syndrome: implications for clinical management

The impact of clinical decision making in a molecular tumor board at a tertiary care center

2894 The Gastrointestinal Phenotype of Cowden’s Syndrome and Effects of Surveillance

Genomic Microsatellite Signatures Identify Germline Mismatch Repair Deficiency and Risk of Cancer Onset

Abstract P056: Germline cancer susceptibility gene testing in unselected patients with soft tissue sarcoma: a multi-center prospective study

Improving the referral rate of universal genetic counseling for pancreatic ductal adenocarcinoma (PDAC) at the Cleveland Clinic Taussig Cancer Center: A quality improvement project

S3382 Juvenile Polyposis Syndrome & Inflammatory Bowel Disease: Balancing the Risk of Malignancy

S1305 Cancer Surveillance in Peutz Jeghers Syndrome

S0205 Association of Cancer With Comorbid Inflammatory Diseases in Lynch Syndrome and Lynch-Like Syndrome Individuals

Defining Phenotypes and Cancer Risk in Hyperplastic Polyposis Syndrome

The prevalence of hereditary hemorrhagic telangiectasia in Juvenile Polyposis syndrome patients with SMAD4 mutations

High risk clinic for hereditary colorectal neoplasia: a focus for patient care and an opportunity for clinical research

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