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 (Q28943265)

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English	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	scientific journal article

Statements

scholarly article

1 reference

14 March 2017

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 (English)

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14 March 2017

genome-wide association study

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based on heuristic

inferred from title

single-nucleotide polymorphism

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pregnancy outcome

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author name string

Linlu Zhao

1

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14 March 2017

Michael B. Bracken

2

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14 March 2017

Andrew T. DeWan

3

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14 March 2017

language of work or name

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publication date

1 July 2013

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14 March 2017

Annals of Human Genetics

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14 March 2017

77

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14 March 2017

277–287

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14 March 2017

4

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14 March 2017

describes a project that uses

genome-wide association study

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The role of inflammatory pathway genetic variation on maternal metabolic phenotypes during pregnancy

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16 March 2017

PLINK: a tool set for whole-genome association and population-based linkage analyses

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16 March 2017

Global variation in copy number in the human genome

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Principal components analysis corrects for stratification in genome-wide association studies

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16 March 2017

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16 March 2017

Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

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23 March 2017

LocusZoom: regional visualization of genome-wide association scan results

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7 April 2017

PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data

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7 April 2017

Genome-wide association study identifies a maternal copy-number deletion in PSG11 enriched among preeclampsia patients

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3 June 2018

The effect of algorithms on copy number variant detection

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3 June 2018

New approaches to population stratification in genome-wide association studies

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3 June 2018

Structural variation in the human genome and its role in disease

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QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data

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3 June 2018

Problems of reporting genetic associations with complex outcomes

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3 June 2018

Fetal and maternal contributions to risk of pre-eclampsia: population based study

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3 June 2018

The indicence of severe pre-eclampsia amongst mothers and mothers-in-law of pre-eclamptics and controls.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3740040

3 June 2018

Genetic and familial predisposition to eclampsia and pre-eclampsia in a defined population.

1 reference

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3 June 2018

Maternal ethnicity, paternal ethnicity, and parental ethnic discordance: predictors of preeclampsia.

1 reference

https://api.crossref.org/works/10.1111%2FAHG.12021

21 January 2018

The Hyperglycemia and Adverse Pregnancy Outcome (HAPO) Study

1 reference

https://api.crossref.org/works/10.1111%2FAHG.12021

21 January 2018

Menstrual and reproductive factors for salivary gland cancer risk in women

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21 January 2018

Maternal and fetal genetic factors account for most of familial aggregation of preeclampsia: A population-based Swedish cohort study

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21 January 2018

The classification and diagnosis of the hypertensive disorders of pregnancy: statement from the International Society for the Study of Hypertension in Pregnancy (ISSHP).

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26 November 2018

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Smoking Cessation and Mortality Trends among 118,000 Californians, 1960–1997

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