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UnknownGenome-wide association analysis for chronic venous disease identifies EFEMP1 and KCNH8 as susceptibility loci.
Not available
S-EPMC5379489 | biostudies-literature
UnknownStructural variation of chromosomes in autism spectrum disorder.
Not available
S-EPMC2426913 | biostudies-literature
UnknownDisruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disability.
Not available
S-EPMC2987731 | biostudies-literature
UnknownCommon breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2.
Not available
S-EPMC3326552 | biostudies-literature
UnknownCommon variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers.
Not available
S-EPMC3733139 | biostudies-literature
UnknownCommon variants at the 19p13.1 and ZNF365 loci are associated with ER subtypes of breast cancer and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers.
Not available
S-EPMC3319317 | biostudies-literature
UnknownCommon variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers.
Not available
S-EPMC3496151 | biostudies-literature
UnknownOvarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers.
Not available
S-EPMC3458423 | biostudies-literature
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