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Rare and common variants: twenty arguments
scientific article published on February 2011
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scholarly article
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Europe PubMed Central
PubMed ID
22251874
retrieved
8 August 2017
title
Rare and common variants: twenty arguments
(English)
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stated in
Europe PubMed Central
PubMed ID
22251874
retrieved
8 August 2017
author name string
Greg Gibson
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
22251874
retrieved
8 August 2017
publication date
1 February 2011
1 reference
stated in
Europe PubMed Central
PubMed ID
22251874
retrieved
8 August 2017
published in
Nature Reviews Genetics
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stated in
Europe PubMed Central
PubMed ID
22251874
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8 August 2017
volume
13
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stated in
Europe PubMed Central
PubMed ID
22251874
retrieved
8 August 2017
page(s)
135-145
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stated in
Europe PubMed Central
PubMed ID
22251874
retrieved
8 August 2017
issue
2
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stated in
Europe PubMed Central
PubMed ID
22251874
retrieved
8 August 2017
exact match
https://scigraph.springernature.com/pub.10.1038/nrg3118
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12 July 2018
A HapMap harvest of insights into the genetics of common disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4408201
retrieved
12 July 2018
Genome-wide association analysis identifies 20 loci that influence adult height
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4408201
retrieved
12 July 2018
Heritability in the genomics era — concepts and misconceptions
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4408201
retrieved
12 July 2018
Genomic selection.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4408201
retrieved
12 July 2018
A systematic genetic assessment of 1,433 sequence variants of unknown clinical significance in the BRCA1 and BRCA2 breast cancer-predisposition genes
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4408201
retrieved
12 July 2018
Endophenotypes in the genetic analyses of mental disorders.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4408201
retrieved
12 July 2018
Probing genetic overlap among complex human phenotypes.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4408201
retrieved
12 July 2018
Copy-number variation and association studies of human disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4408201
retrieved
12 July 2018
Phenotypic plasticity and the epigenetics of human disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4408201
retrieved
12 July 2018
Joint estimates of quantitative trait locus effect and frequency using synthetic recombinant populations of Drosophila melanogaster.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4408201
retrieved
12 July 2018
Insights on pathogenesis of type 2 diabetes from MODY genetics
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4408201
retrieved
12 July 2018
Strong association of de novo copy number mutations with autism
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4408201
retrieved
12 July 2018
Most rare missense alleles are deleterious in humans: implications for complex disease and association studies
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4408201
retrieved
12 July 2018
Schizophrenia: a common disease caused by multiple rare alleles
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4408201
retrieved
12 July 2018
The evolutionary significance of cis-regulatory mutations
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4408201
retrieved
12 July 2018
Modifier genes and sickle cell anemia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4408201
retrieved
12 July 2018
A systematic review of the prevalence of schizophrenia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4408201
retrieved
12 July 2018
Uncovering cryptic genetic variation.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4408201
retrieved
12 July 2018
Theoretical basis of the Beavis effect.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4408201
retrieved
12 July 2018
Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4408201
retrieved
12 July 2018
The allelic architecture of human disease genes: common disease-common variant... or not?
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4408201
retrieved
12 July 2018
Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4408201
retrieved
12 July 2018
Systematic genetic analysis with ordered arrays of yeast deletion mutants
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4408201
retrieved
12 July 2018
The genetic architecture of quantitative traits
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4408201
retrieved
12 July 2018
On the allelic spectrum of human disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4408201
retrieved
12 July 2018
Advancing paternal age and the risk of schizophrenia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4408201
retrieved
12 July 2018
Deficiency mapping of quantitative trait loci affecting longevity in Drosophila melanogaster
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4408201
retrieved
12 July 2018
Fisher, Medawar, Hamilton and the evolution of aging
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4408201
retrieved
12 July 2018
Genome partitioning and whole-genome analysis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4408201
retrieved
12 July 2018
Distinct types of diffuse large B-cell lymphoma identified by gene expression profiling
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4408201
retrieved
12 July 2018
Characterization of single-nucleotide polymorphisms in coding regions of human genes
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4408201
retrieved
12 July 2018
Synthetic lethality and semi-lethality among functionally related mutants of Drosophila melanfgaster
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4408201
retrieved
12 July 2018
The control of flux
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4408201
retrieved
12 July 2018
Evolutionary quantitative genetics: how little do we know?
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4408201
retrieved
12 July 2018
Linkage strategies for genetically complex traits. I. Multilocus models
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4408201
retrieved
12 July 2018
The Heritability Hang-Up
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4408201
retrieved
12 July 2018
The LDL receptor locus and the genetics of familial hypercholesterolemia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4408201
retrieved
12 July 2018
Uncovering the total heritability explained by all true susceptibility variants in a genome-wide association study
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4408201
retrieved
26 September 2018
Clinical profile of diabetes in the young seen between 1992 and 2009 at a specialist diabetes centre in south India.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4408201
retrieved
26 September 2018
A family-based study of common polygenic variation and risk of schizophrenia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4408201
retrieved
26 September 2018
Hints of hidden heritability in GWAS.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4408201
retrieved
26 September 2018
Contribution of genetics and environment to craniofacial anthropometric phenotypes in Belgian nuclear families.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4408201
retrieved
26 September 2018
The Human Gene Mutation Database: 2008 update
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4408201
retrieved
26 September 2018
Systematic mapping of genetic interactions in Caenorhabditis elegans identifies common modifiers of diverse signaling pathways
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4408201
retrieved
26 September 2018
The new genomics: global views of biology
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/22251874
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1038/NRG3118
1 reference
stated in
Europe PubMed Central
PubMed ID
22251874
retrieved
8 August 2017
Dimensions Publication ID
1001779725
0 references
PMCID
4408201
1 reference
stated in
Europe PubMed Central
PubMed ID
22251874
retrieved
8 August 2017
PubMed ID
22251874
1 reference
stated in
Europe PubMed Central
PubMed ID
22251874
retrieved
8 August 2017
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