(Q34271719)

1 August 2017

title

Genome-wide association studies: hypothesis-"free" or "engaged"? (English)

1 reference

genome-wide association study

1 August 2017

main subject

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author name string

Georgios D Kitsios

series ordinal

1

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1 August 2017

Elias Zintzaras

series ordinal

2

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1 August 2017

publication date

29 July 2009

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1 August 2017

published in

Translational Research

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1 August 2017

volume

154

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1 August 2017

issue

4

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1 August 2017

page(s)

161-164

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Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

1 August 2017

cites work

1 reference

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6 July 2018

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The genetic signatures of noncoding RNAs

6 July 2018

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Common genetic variation and human traits

6 July 2018

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Genomewide association studies and human disease

6 July 2018

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Deletion polymorphism upstream of IRGM associated with altered IRGM expression and Crohn's disease

6 July 2018

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Six new loci associated with body mass index highlight a neuronal influence on body weight regulation

6 July 2018

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Gene-environment interaction in genome-wide association studies

6 July 2018

1 reference

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Genome-wide association studies: potential next steps on a genetic journey

6 July 2018

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Integrated detection and population-genetic analysis of SNPs and copy number variation

6 July 2018

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Expectations and challenges stemming from genome-wide association studies

6 July 2018

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Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data

6 July 2018

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Future impact of integrated high-throughput methylome analyses on human health and disease

6 July 2018

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From Darwin's finches to canaries in the coal mine--mining the genome for new biology

6 July 2018

1 reference

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Common and rare variants in multifactorial susceptibility to common diseases

6 July 2018

1 reference

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A HapMap harvest of insights into the genetics of common disease

6 July 2018

1 reference

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Genome-wide association studies for complex traits: consensus, uncertainty and challenges

6 July 2018

1 reference

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Rare independent mutations in renal salt handling genes contribute to blood pressure variation

6 July 2018

1 reference

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How to interpret a genome-wide association study

6 July 2018

1 reference

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The genetic basis of complex traits: rare variants or "common gene, common disease"?

6 July 2018

1 reference

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Copy number variants and common disorders: filling the gaps and exploring complexity in genome-wide association studies

6 July 2018

1 reference

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Copy-number variation and association studies of human disease

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2971665

Genome-wide association studies for common diseases and complex traits

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2971665

Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

6 July 2018

1 reference

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Genetic dissection of diseases: design and methods

6 July 2018

1 reference

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Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease

6 July 2018

1 reference

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Epistasis: what it means, what it doesn't mean, and statistical methods to detect it in humans

6 July 2018

1 reference

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On the allelic spectrum of human disease

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2971665

Genetic risk prediction--are we there yet?

6 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1016%2FJ.TRSL.2009.07.001

The hypothesis is there is no hypothesis. The Microarray Meeting, Scottsdale, Arizona, USA, 22-25 September 1999

7 January 2021

1 reference

Crossref

https://api.crossref.org/works/10.1016%2FJ.TRSL.2009.07.001

10.1016/J.TRSL.2009.07.001

7 January 2021

Identifiers

DOI

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1 August 2017

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1 August 2017

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