||common in complete genomics
||Genome-wide association study identifies susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33
[PMID 22009367] Susceptibility Loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21, and 9q33.3 in a cohort of caucasian women
[PMID 22081247] Family-based analysis of susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3
[PMID 22504079] Association of polycystic ovary syndrome susceptibility single nucleotide polymorphism rs2479106 and PCOS in Caucasian patients with PCOS or hirsutism as referral diagnosis.
[PMID 22547425] Variants in DENND1A Are Associated with Polycystic Ovary Syndrome in Women of European Ancestry.
[PMID 23208300] Genotype-phenotype correlations of PCOS susceptibility SNPs identified by GWAS in a large cohort of Han Chinese women
[PMID 22902918] Variants in DENND1A and LHCGR are associated with endometrioid adenocarcinoma
[PMID 29727258] Association study between variants in LHCGR DENND1A and THADA with preeclampsia risk in Han Chinese populations.