Genome‐Wide Association Study of Pre‐Eclampsia Detects Novel Maternal Single Nucleotide Polymorphisms and Copy‐Number Variants in Subsets of the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) Study Cohort
Zhao L, Bracken MB, DeWan AT. Genome‐Wide Association Study of Pre‐Eclampsia Detects Novel Maternal Single Nucleotide Polymorphisms and Copy‐Number Variants in Subsets of the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) Study Cohort. Annals Of Human Genetics 2013, 77: 277-287. PMID: 23551011, PMCID: PMC3740040, DOI: 10.1111/ahg.12021.Peer-Reviewed Original ResearchConceptsCopy number variantsSingle nucleotide polymorphismsAssociation studiesGenome-wide SNP dataMaternal single nucleotide polymorphismsGenome-wide association studiesTop single nucleotide polymorphismsNucleotide polymorphismsWide association studyEuropean ancestry subjectsCandidate genetic variantsSNP dataBeadChip microarrayGenetic variantsCase-control datasetEuropean ancestryCandidate copy-number variantsIllumina Human610-QuadCNV findingsPolymorphismVariants