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Exploring the unknown: assumptions about allelic architecture and strategies for susceptibility variant discovery
scientific article published on 03 July 2009
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scholarly article
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Europe PubMed Central
PMCID
2717392
retrieved
20 August 2017
review article
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Europe PubMed Central
title
Exploring the unknown: assumptions about allelic architecture and strategies for susceptibility variant discovery
(English)
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Europe PubMed Central
PMCID
2717392
retrieved
20 August 2017
author
Mark McCarthy
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Mark I McCarthy
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English
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publication date
3 July 2009
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Europe PubMed Central
PMCID
2717392
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20 August 2017
published in
Genome Medicine
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Europe PubMed Central
PMCID
2717392
retrieved
20 August 2017
volume
1
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Europe PubMed Central
PMCID
2717392
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20 August 2017
page(s)
66
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Europe PubMed Central
PMCID
2717392
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20 August 2017
issue
7
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Europe PubMed Central
PMCID
2717392
retrieved
20 August 2017
exact match
https://scigraph.springernature.com/pub.10.1186/gm66
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cites work
Common vs. rare allele hypotheses for complex diseases
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2717392
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Potential etiologic and functional implications of genome-wide association loci for human diseases and traits
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PubMed Central
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1 reference
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https://pubmed.ncbi.nlm.nih.gov/19591663
retrieved
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Identifiers
DOI
10.1186/GM66
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Europe PubMed Central
PMCID
2717392
retrieved
20 August 2017
Dimensions Publication ID
1015897813
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release_m3vtboy4cnb4rfqdndod4l67li
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PMCID
2717392
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Europe PubMed Central
PMCID
2717392
retrieved
20 August 2017
PubMed ID
19591663
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Europe PubMed Central
PMCID
2717392
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20 August 2017
ResearchGate publication ID
26660621
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