(Q35225238)

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Allelic heterogeneity and more detailed analyses of known loci explain additional phenotypic variation and reveal complex patterns of association

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scholarly article

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Europe PubMed Central

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7 August 2017

Allelic heterogeneity and more detailed analyses of known loci explain additional phenotypic variation and reveal complex patterns of association (English)

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Europe PubMed Central

PubMed publication ID

7 August 2017

object named as

Anna Murray

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object named as

Timothy M Frayling

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Michael N Weedon

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Michael N Weedon

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13

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Luigi Ferrucci

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7 August 2017

Andrew Singleton

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Andrew B Singleton

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7 August 2017

Hanieh Yaghootkar

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Hanieh Yaghootkar

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7 August 2017

Stefania Bandinelli

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Stefania Bandinelli

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7 August 2017

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Jack M Guralnik

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7 August 2017

Dena G. Hernandez

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Dena G Hernandez

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7 August 2017

Lorna W Harries

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Lorna W Harries

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ORCID Public Data File 2021

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object named as

Michael A Nalls

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7 August 2017

1

object named as

Andrew R Wood

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7 August 2017

J Raphael Gibbs

5

object named as

J Raphael Gibbs

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7 August 2017

15

object named as

David Melzer

1 reference

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7 August 2017

7

object named as

Sean Chong

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7 August 2017

author name string

Matthew Moore

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7 August 2017

publication date

28 July 2011

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7 August 2017

Human Molecular Genetics

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7 August 2017

20

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7 August 2017

20

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Europe PubMed Central

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7 August 2017

4082-4092

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Europe PubMed Central

PubMed publication ID

7 August 2017

The architecture of gene regulatory variation across multiple human tissues: the MuTHER study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3177649

13 July 2018

MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3177649

13 July 2018

Fine-mapping at three loci known to affect fetal hemoglobin levels explains additional genetic variation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3177649

13 July 2018

Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21.

1 reference

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13 July 2018

A map of human genome variation from population-scale sequencing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3177649

13 July 2018

Hundreds of variants clustered in genomic loci and biological pathways affect human height

1 reference

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13 July 2018

Abundant quantitative trait loci exist for DNA methylation and gene expression in human brain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3177649

13 July 2018

Rare variants create synthetic genome-wide associations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3177649

13 July 2018

A re-annotation pipeline for Illumina BeadArrays: improving the interpretation of gene expression data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3177649

13 July 2018

Global patterns of cis variation in human cells revealed by high-density allelic expression analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3177649

13 July 2018

Common regulatory variation impacts gene expression in a cell type-dependent manner

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3177649

13 July 2018

Rare variants of IFIH1, a gene implicated in antiviral responses, protect against type 1 diabetes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3177649

13 July 2018

A genome-wide association study identifies protein quantitative trait loci (pQTLs)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3177649

13 July 2018

Likelihood-based association analysis for nuclear families and unrelated subjects with missing genotype data

1 reference

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13 July 2018

A genome-wide association study of global gene expression

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3177649

13 July 2018

Population genomics of human gene expression

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3177649

13 July 2018

Subsystems contributing to the decline in ability to walk: bridging the gap between epidemiology and geriatric practice in the InCHIANTI study.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3177649

13 July 2018

A survey of genetic human cortical gene expression

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3177649

8 December 2018

Identifiers

10.1093/HMG/DDR328

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

ResearchGate publication ID

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