Genome-wide association study identifies a maternal copy-number deletion in PSG11 enriched among preeclampsia patients
Published 2012 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Genome-wide association study identifies a maternal copy-number deletion in PSG11 enriched among preeclampsia patients
Authors
Keywords
-
Journal
BMC Pregnancy and Childbirth
Volume 12, Issue 1, Pages -
Publisher
Springer Nature
Online
2012-06-29
DOI
10.1186/1471-2393-12-61
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- The genetics of pre-eclampsia and other hypertensive disorders of pregnancy
- (2011) Paula J. Williams et al. BEST PRACTICE & RESEARCH CLINICAL OBSTETRICS & GYNAECOLOGY
- Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism
- (2011) Stephan J. Sanders et al. NEURON
- Rare Copy Number Deletions Predict Individual Variation in Intelligence
- (2011) Ronald A. Yeo et al. PLoS One
- Mutations in Complement Regulatory Proteins Predispose to Preeclampsia: A Genetic Analysis of the PROMISSE Cohort
- (2011) Jane E. Salmon et al. PLOS MEDICINE
- Structural Variation in the Human Genome and its Role in Disease
- (2010) Paweł Stankiewicz et al. Annual Review of Medicine
- The clinical context of copy number variation in the human genome
- (2010) Charles Lee et al. EXPERT REVIEWS IN MOLECULAR MEDICINE
- Novel common copy number variation for early onset extreme obesity on chromosome 11q11 identified by a genome-wide analysis
- (2010) Ivonne Jarick et al. HUMAN MOLECULAR GENETICS
- The Effect of Algorithms on Copy Number Variant Detection
- (2010) Debby W. Tsuang et al. PLoS One
- Population Analysis of Large Copy Number Variants and Hotspots of Human Genetic Disease
- (2009) Andy Itsara et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Copy Number Variation in Human Health, Disease, and Evolution
- (2009) Feng Zhang et al. Annual Review of Genomics and Human Genetics
- Gene copy number variation and common human disease
- (2009) M Fanciulli et al. CLINICAL GENETICS
- High-resolution mapping and analysis of copy number variations in the human genome: A data resource for clinical and research applications
- (2009) T. H. Shaikh et al. GENOME RESEARCH
- Origins and functional impact of copy number variation in the human genome
- (2009) Donald F. Conrad et al. NATURE
- On the analysis of copy-number variations in genome-wide association studies: a translation of the family-based association test
- (2008) Iuliana Ionita-Laza et al. GENETIC EPIDEMIOLOGY
- Genes and the preeclampsia syndrome
- (2008) Sabine Mütze et al. JOURNAL OF PERINATAL MEDICINE
- Rare chromosomal deletions and duplications increase risk of schizophrenia
- (2008) Jennifer L. Stone et al. NATURE
- Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs
- (2008) Joshua M Korn et al. NATURE GENETICS
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started