Overrepresentation of rare variants in a specific ethnic group may confuse interpretation of association analyses (Q34573373)

3 August 2017

title

Overrepresentation of rare variants in a specific ethnic group may confuse interpretation of association analyses (English)

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3 August 2017

Victor I Reus

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Carol A Mathews

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3 August 2017

Dianne Keen-Kim

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3 August 2017

Thomas L Lowe

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3 August 2017

Luis Diego Herrera

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3 August 2017

Cathy L Budman

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3 August 2017

Varda Gross-Tsur

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3 August 2017

Ann E Pulver

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3 August 2017

Ruth D Bruun

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3 August 2017

Gerald Erenberg

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3 August 2017

Allan Naarden

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3 August 2017

Chiara Sabatti

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3 August 2017

Nelson B Freimer

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3 August 2017

publication date

11 October 2006

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3 August 2017

published in

Human Molecular Genetics

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3 August 2017

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3 August 2017

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3 August 2017

page(s)

3324-3328

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Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease

3 August 2017

cites work

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https://api.crossref.org/works/10.1093%2FHMG%2FDDL408

Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

21 January 2018

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https://api.crossref.org/works/10.1093%2FHMG%2FDDL408

MEF2A sequence variants and coronary artery disease: a change of heart?

21 January 2018

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Genetics and epidemiology of Tourette syndrome

21 January 2018

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Sequence variants in SLITRK1 are associated with Tourette's syndrome

21 January 2018

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https://api.crossref.org/works/10.1093%2FHMG%2FDDL408

Functional SLITRK1 var321, varCDfs and SLC6A4 G56A variants and susceptibility to obsessive-compulsive disorder.

21 January 2018

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https://api.crossref.org/works/10.1093%2FHMG%2FDDL408

Assessing the impact of population stratification on genetic association studies

21 January 2018

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https://api.crossref.org/works/10.1093%2FHMG%2FDDL408

Demonstrating stratification in a European American population

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL408

Genomic control for association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL408

Detect and adjust for population stratification in population-based association study using genomic control markers: an application of Affymetrix Genechip Human Mapping 10K array.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL408

Ancestry-environment interactions and asthma risk among Puerto Ricans

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL408

Population structure, differential bias and genomic control in a large-scale, case-control association study

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL408

Mutation of MEF2A in an inherited disorder with features of coronary artery disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL408

Lack of MEF2A mutations in coronary artery disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL408

Statistical false positive or true disease pathway?

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL408

21 January 2018

Identifiers

DOI

10.1093/HMG/DDL408

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3 August 2017

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