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Human Genome Epidemiology, 2nd EditionBuilding the evidence for using genetic information to improve health and prevent disease$
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Muin Khoury, Sara Bedrosian, Marta Gwinn, Julian Higgins, John Ioannidis, and Julian Little

Print publication date: 2009

Print ISBN-13: 9780195398441

Published to Oxford Scholarship Online: May 2010

DOI: 10.1093/acprof:oso/9780195398441.001.0001

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PRINTED FROM OXFORD SCHOLARSHIP ONLINE (www.oxfordscholarship.com). (c) Copyright Oxford University Press, 2019. All Rights Reserved. Under the terms of the licence agreement, an individual user may print out a PDF of a single chapter of a monograph in OSO for personal use (for details see www.oxfordscholarship.com/page/privacy-policy).date: 17 July 2019

Bladder cancer

Bladder cancer

Chapter:
(p.299) 15 Bladder cancer
Source:
Human Genome Epidemiology, 2nd Edition
Author(s):

Jonine D. Figueroa

Montserrat Garcia-Closas

Nathaniel Rothman

Publisher:
Oxford University Press
DOI:10.1093/acprof:oso/9780195398441.003.0015

A literature search was performed using the HuGE Navigator with the term “bladder cancer” and PubMed searches with the terms “ bladder cancer polymorphisms” and “bladder cancer risk variants” through September, 2008 for the purpose of performing systematic meta-analysis. Publications that did not have controls that were related to outcomes other than bladder cancer risk (e.g. survival), or were performed in special populations (e.g. non-smokers), were excluded. From this search, 32 SNPs reported on in three or more studies were identified, and this chapter summarizes the current evidence for the role of common genetic variation in the etiology of the bladder.

Keywords:   genetic variants, genetic variations, human disease, genome-wide studies, bladder cancer, cancer risk

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