C. Ukaegbu

发表

Cancer Susceptibility Gene Mutations in Individuals With Colorectal Cancer.

Hajime Uno, Deborah Schrag, John Kidd, 2017, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Characterizing germline APC and MUTYH variants in Ashkenazi Jews compared to other individuals

H. Uno, S. Syngal, F. Kastrinos, 2020, Familial Cancer.

Clinical Factors Associated With Gastric Cancer in Individuals with Lynch Syndrome.

G. Parmigiani, S. Syngal, F. Kastrinos, 2020, Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association.

Comparison of Colorectal and Endometrial Microsatellite Instability Tumor Analysis and Premm5 Risk Assessment for Predicting Pathogenic Germline Variants on Multigene Panel Testing.

H. Uno, S. Syngal, C. S. Furniss, 2020, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Implementing Systematic Genetic Counseling and Multigene Germline Testing for Individuals With Pancreatic Cancer.

H. Uno, B. Wolpin, S. Syngal, 2021, JCO oncology practice.

Literacy-adapted, electronic family history assessment for genetics referral in primary care: patient user insights from qualitative interviews

Kathleen F. Mittendorf, K. Goddard, B. Wilfond, 2022, Hereditary cancer in clinical practice.

A validation of models for prediction of pathogenic variants in mismatch repair genes.

Aung Ko Win, G. Parmigiani, H. Uno, 2022, Genetics in medicine : official journal of the American College of Medical Genetics.

Linda S. Lee, M. Goggins, A. Chak, 2021, Pancreatology.

Familial burden and other clinical factors associated with various types of cancer in individuals with Lynch syndrome.

H. Uno, S. Syngal, M. Yurgelun, 2021, Gastroenterology.

Clinical Factors Associated with Urinary Tract Cancer in Individuals with Lynch Syndrome

H. Uno, S. Syngal, F. Kastrinos, 2019, Cancer Epidemiology, Biomarkers & Prevention.

Novel Models of Genetic Education and Testing for Pancreatic Cancer Interception: Preliminary Results from the GENERATE Study

Pamela E. Constantinou, Catherine C. Lafferty, H. Uno, 2021, Cancer Prevention Research.

Therapy-associated polyposis – a novel form of acquired gastrointestinal polyposis

J. Hornick, E. Brown, A. Chittenden, 2014 .

Development and Validation of the PREMMplus Model for Multigene Hereditary Cancer Risk Assessment

H. Uno, J. Garber, S. Syngal, 2022, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Mutational signature profiling classifies subtypes of clinically different mismatch-repair-deficient tumours with a differential immunogenic response potential

Joanna A Gibson, E. Stoffel, J. Sweasy, 2021, British Journal of Cancer.

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

J. Church, Z. Stadler, E. Stoffel, 2020, Cancer Prevention Research.

Risk of Pancreatic Cancer Among Individuals With Pathogenic Variants in the ATM Gene.

R. Hruban, A. Klein, F. Hsu, 2021, JAMA oncology.

Phenotypic Differences in Juvenile Polyposis Syndrome With or Without a Disease-causing SMAD4/BMPR1A Variant

S. Plon, Z. Stadler, R. Brand, 2020, Cancer Prevention Research.

Mutations in RABL3 alter KRAS prenylation and are associated with hereditary pancreatic cancer

Carol L. Williams, J. Rosenfeld, G. Getz, 2019, Nature Genetics.

Adaptation and early implementation of the PREdiction model for gene mutations (PREMM5™) for lynch syndrome risk assessment in a diverse population

Kathleen F. Mittendorf, Marian J. Gilmore, K. Goddard, 2021, Familial Cancer.

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

Ewout W Steyerberg, Hajime Uno, Deborah Schrag, 2017, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

A prospective prostate cancer screening programme for men with pathogenic variants in mismatch repair genes (IMPACT): initial results from an international prospective study

R. Eeles, Z. Kote-Jarai, F. Hamdy, 2021, The Lancet. Oncology.

Mutation spectrum and risk of colorectal cancer in African American families with Lynch syndrome.

Aung Ko Win, O. Olopade, P. Newcomb, 2015, Gastroenterology.

Therapy-associated polyposis as a late sequela of cancer treatment.

S. Syngal, J. Hornick, A. Chittenden, 2014, Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association.

Kathleen F. Mittendorf, Charisma L. Jenkins, Marian J. Gilmore, 2022, Genetics in medicine : official journal of the American College of Medical Genetics.

Clinical Implications of Pathogenic Germline Variants in Small Intestine Neuroendocrine Tumors (SI-NETs)

J. Garber, Shan Yang, S. Syngal, 2021, JCO precision oncology.

Improving cascade genetic testing for families with inherited pancreatic cancer (PDAC) risk: The GENetic Education, Risk Assessment and TEsting (GENERATE) study.

S. Lippman, A. Maitra, A. Klein, 2019, Journal of Clinical Oncology.

MyLynch: A Patient-Facing Clinical Decision Support Tool for Genetically-Guided Personalized Medicine in Lynch Syndrome

G. Parmigiani, T. Bickmore, J. Stopfer, 2023, Cancers.