CDKN2A Germline Rare Coding Variants and Risk of Pancreatic Cancer in Minority Populations-Reference-Cited by-同舟云学术

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CDKN2A Germline Rare Coding Variants and Risk of Pancreatic Cancer in Minority Populations

Published:2018-07-23 Issue:11 Volume:27 Page:1364-1370
ISSN:1055-9965
Container-title:Cancer Epidemiology Biomarkers & Prevention
language:en
Short-container-title:Cancer Epidemiol Biomarkers Prev

Author:

McWilliams Robert R.,Wieben Eric D.,Chaffee Kari G.^ORCID,Antwi Samuel O.,Raskin Leon^ORCID,Olopade Olufunmilayo I.,Li Donghui^ORCID,Highsmith W. Edward,Colon-Otero Gerardo,Khanna Lauren G.,Permuth Jennifer B.^ORCID,Olson Janet E.,Frucht Harold,Genkinger Jeanine,Zheng Wei,Blot William J.,Wu Lang,Almada Luciana L.,Fernandez-Zapico Martin E.,Sicotte Hugues^ORCID,Pedersen Katrina S.,Petersen Gloria M.

Funder

NIH

Publisher

American Association for Cancer Research (AACR)

Subject

Oncology,Epidemiology

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1. Disparities in race, ethnicity, sex, and age inclusion in pancreatic cancer screening studies: a systematic review and meta-analysis;Gastrointestinal Endoscopy;2024-07

2. Understanding familial risk of pancreatic ductal adenocarcinoma;Familial Cancer;2024-04-12

3. Functional characterization of all CDKN2A missense variants and comparison to in silico models of pathogenicity;2024-02-19

4. Functional characterization of all CDKN2A missense variants and comparison to in silico models of pathogenicity;2024-02-19

5. Precursor lesions in familial and hereditary pancreatic cancer;Familial Cancer;2024-02-06

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