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

Volumn 77, Issue 4, 2013, Pages 277-287

  Zhao, Linlu ^a,b   Bracken, Michael B ^a,b   DeWan, Andrew T ^a,b  

^a YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b YALE UNIVERSITY   (United States)

Author keywords

Copy number variant; Genome wide association study; Microarray analysis; Pre eclampsia; Single nucleotide polymorphism

Indexed keywords

ADVERSE OUTCOME; ARTICLE; CASE CONTROL STUDY; COHORT ANALYSIS; CONTROLLED STUDY; COPY NUMBER VARIATION; ETHNIC GROUP; FEMALE; GENETIC ASSOCIATION; GENOTYPE; HUMAN; HYPERGLYCEMIA; MAJOR CLINICAL STUDY; MATERNAL HYPERTENSION; MULTICENTER STUDY; PREECLAMPSIA; PREGNANCY OUTCOME; PRIORITY JOURNAL; PROSPECTIVE STUDY; SINGLE NUCLEOTIDE POLYMORPHISM; CLINICAL TRIAL; GENETIC PREDISPOSITION; GENETICS; PHENOTYPE; PRE-ECLAMPSIA; PREGNANCY;

CASE-CONTROL STUDIES; DNA COPY NUMBER VARIATIONS; ETHNIC GROUPS; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENOME-WIDE ASSOCIATION STUDY; GENOTYPE; HUMANS; HYPERGLYCEMIA; PHENOTYPE; POLYMORPHISM, SINGLE NUCLEOTIDE; PRE-ECLAMPSIA; PREGNANCY; PREGNANCY OUTCOME; PROSPECTIVE STUDIES;

EID: 84883147479     PISSN: 00034800     EISSN: 14691809     Source Type: Journal    
DOI: 10.1111/ahg.12021     Document Type: Article

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