Hereditary bladder cancer.
Publication year
2008Author(s)
Source
Scandinavian Journal of Urology and Nephrology-Supplementum, 2008, 218, (2008), pp. 110-5ISSN
Publication type
Article / Letter to editor
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Organization
Urology
Health Evidence
Former Organization
Epidemiology, Biostatistics & HTA
Journal title
Scandinavian Journal of Urology and Nephrology-Supplementum
Volume
vol. 2008
Issue
iss. 218
Page start
p. 110
Page end
p. 5
Subject
NCEBP 1: Molecular epidemiology; ONCOL 1: Hereditary cancer and cancer-related syndromes; ONCOL 3: Translational research; ONCOL 5: Aetiology, screening and detection; UMCN 1.2: Molecular diagnosis, prognosis and monitoringAbstract
First degree relatives of patients with bladder cancer have a two-fold increased risk of bladder cancer but high-risk bladder cancer families are extremely rare. There is no clear Mendelian inheritance pattern that can explain the increased familial risk. This makes classical linkage studies for the mapping of susceptibility genes impossible. The disease is probably caused by a combination of exposure to exogenous carcinogens and a large number of susceptibility genes with modest effects. Genome-wide association studies are better suited to identify these genes. Three such studies are currently underway and are expected to report their results in 2008.
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- Academic publications [242839]
- Electronic publications [129660]
- Faculty of Medical Sciences [92293]
- Open Access publications [104240]
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