Gene variations in sex hormone pathways and the risk of testicular germ cell tumour: a case–parent triad study in a Norwegian–Swedish population
Author(s) -
Wenche Kristiansen,
Kristine Andreassen,
Robert Karlsson,
Elin L. Aschim,
Roy M. Bremnes,
O. Dahl,
Sophie D. Fosså,
Olbjørn Klepp,
Carl W. Langberg,
A. Solberg,
Steinar Tretli,
HansOlov Adami,
F. Wiklund,
Tom Grotmol,
Trine B. Haugen
Publication year - 2012
Publication title -
human reproduction
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.446
H-Index - 226
eISSN - 1460-2350
pISSN - 0268-1161
DOI - 10.1093/humrep/des075
Subject(s) - single nucleotide polymorphism , biology , genetics , oncology , odds ratio , case control study , population , medicine , gene , genotype , environmental health
Testicular germ cell tumour (TGCT) is the most common cancer in young men, and an imbalance between the estrogen and androgen levels in utero is hypothesized to influence TGCT risk. Thus, polymorphisms in genes involved in the action of sex hormones may contribute to variability in an individual's susceptibility to TGCT.
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