<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Canzian F</submitter><funding>Intramural NIH HHS</funding><funding>Medical Research Council</funding><funding>NCI NIH HHS</funding><pagination>3873-84</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2935856</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>19(19)</volume><pubmed_abstract>There is extensive evidence that increases in blood and tissue concentrations of steroid hormones and of insulin-like growth factor I (IGF-I) are associated with breast cancer risk. However, studies of common variation in genes involved in steroid hormone and IGF-I metabolism have yet to provide convincing evidence that such variants predict breast cancer risk. The Breast and Prostate Cancer Cohort Consortium (BPC3) is a collaboration of large US and European cohorts. We genotyped 1416 tagging single nucleotide polymorphisms (SNPs) in 37 steroid hormone metabolism genes and 24 IGF-I pathway genes in 6292 cases of breast cancer and 8135 controls, mostly Caucasian, postmenopausal women from the BPC3. We also imputed 3921 additional SNPs in the regions of interest. None of the SNPs tested was</pubmed_abstract><journal>Human molecular genetics</journal><pubmed_title>Comprehensive analysis of common genetic variation in 61 genes related to steroid hormone and insulin-like growth factor-I metabolism and breast cancer risk in the NCI breast and prostate cancer cohort consortium.</pubmed_title><pmcid>PMC2935856</pmcid><funding_grant_id>U01-CA98233</funding_grant_id><funding_grant_id>G0401527</funding_grant_id><funding_grant_id>U01-CA98758</funding_grant_id><funding_grant_id>U01-CA98710</funding_grant_id><funding_grant_id>U01-CA98216</funding_grant_id><pubmed_authors>Diver WR</pubmed_authors><pubmed_authors>Beckmann L</pubmed_authors><pubmed_authors>Berg CD</pubmed_authors><pubmed_authors>Setiawan VW</pubmed_authors><pubmed_authors>Feigelson HS</pubmed_authors><pubmed_authors>Buring J</pubmed_authors><pubmed_authors>Hankinson SE</pubmed_authors><pubmed_authors>Peeters PH</pubmed_authors><pubmed_authors>Kaaks R</pubmed_authors><pubmed_authors>Thomas G</pubmed_authors><pubmed_authors>Clavel-Chapelon F</pubmed_authors><pubmed_authors>Kolonel LN</pubmed_authors><pubmed_authors>Hunter DJ</pubmed_authors><pubmed_authors>Khaw KT</pubmed_authors><pubmed_authors>Trichopoulos D</pubmed_authors><pubmed_authors>Le Marchand L</pubmed_authors><pubmed_authors>Cox DG</pubmed_authors><pubmed_authors>Lund E</pubmed_authors><pubmed_authors>Tjonneland A</pubmed_authors><pubmed_authors>Isaacs C</pubmed_authors><pubmed_authors>Yeager M</pubmed_authors><pubmed_authors>Hoover RN</pubmed_authors><pubmed_authors>Thun MJ</pubmed_authors><pubmed_authors>Hallmans G</pubmed_authors><pubmed_authors>Husing A</pubmed_authors><pubmed_authors>Haiman CA</pubmed_authors><pubmed_authors>Riboli E</pubmed_authors><pubmed_authors>Chanock SJ</pubmed_authors><pubmed_authors>Overvad K</pubmed_authors><pubmed_authors>DeLancey JO</pubmed_authors><pubmed_authors>Ziegler RG</pubmed_authors><pubmed_authors>Tumino R</pubmed_authors><pubmed_authors>Blanche H</pubmed_authors><pubmed_authors>Pollak M</pubmed_authors><pubmed_authors>Stram DO</pubmed_authors><pubmed_authors>Panico S</pubmed_authors><pubmed_authors>Calle EE</pubmed_authors><pubmed_authors>Bingham S</pubmed_authors><pubmed_authors>Buys SS</pubmed_authors><pubmed_authors>Barricarte A</pubmed_authors><pubmed_authors>Henderson BE</pubmed_authors><pubmed_authors>Dorronsoro M</pubmed_authors><pubmed_authors>Dossus L</pubmed_authors><pubmed_authors>Kraft P</pubmed_authors><pubmed_authors>Canzian F</pubmed_authors></additional><is_claimable>false</is_claimable><name>Comprehensive analysis of common genetic variation in 61 genes related to steroid hormone and insulin-like growth factor-I metabolism and breast cancer risk in the NCI breast and prostate cancer cohort consortium.</name><description>There is extensive evidence that increases in blood and tissue concentrations of steroid hormones and of insulin-like growth factor I (IGF-I) are associated with breast cancer risk. However, studies of common variation in genes involved in steroid hormone and IGF-I metabolism have yet to provide convincing evidence that such variants predict breast cancer risk. The Breast and Prostate Cancer Cohort Consortium (BPC3) is a collaboration of large US and European cohorts. We genotyped 1416 tagging single nucleotide polymorphisms (SNPs) in 37 steroid hormone metabolism genes and 24 IGF-I pathway genes in 6292 cases of breast cancer and 8135 controls, mostly Caucasian, postmenopausal women from the BPC3. We also imputed 3921 additional SNPs in the regions of interest. None of the SNPs tested was</description><dates><release>2010-01-01T00:00:00Z</release><publication>2010 Oct</publication><modification>2026-05-01T05:03:17.862Z</modification><creation>2026-04-07T16:40:03.768Z</creation></dates><accession>S-EPMC2935856</accession><cross_references><pubmed>20634197</pubmed><doi>10.1093/hmg/ddq291</doi></cross_references></HashMap>