Identifying plausible genetic models based on association and linkage results: application to type 2 diabetes (Q36625794)

15 August 2017

Identifying plausible genetic models based on association and linkage results: application to type 2 diabetes (English)

1 reference

15 August 2017

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2

Michael Boehnke

1 reference

15 August 2017

4

Nancy J Cox

1 reference

15 August 2017

Weihua Guan

1

1 reference

PMCID

3578091

15 August 2017

Anna Pluzhnikov

series ordinal

3

1 reference

PMCID

3578091

15 August 2017

Laura J Scott

series ordinal

5

1 reference

15 August 2017

3 August 2012

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15 August 2017

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15 August 2017

36

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15 August 2017

8

1 reference

15 August 2017

820-828

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Estimating missing heritability for disease from genome-wide association studies

15 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3578091

Synthetic associations are unlikely to account for many common disease genome-wide association signals

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3578091

Synthetic associations created by rare variants do not explain most GWAS results

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3578091

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3578091

Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3578091

Interpretation of association signals and identification of causal variants from genome-wide association studies

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3578091

Genetic variants at 2q24 are associated with susceptibility to type 2 diabetes

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3578091

Rare variants create synthetic genome-wide associations

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3578091

New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3578091

Finding the missing heritability of complex diseases

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3578091

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3578091

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3578091

Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3578091

Meta-analysis of 23 type 2 diabetes linkage studies from the International Type 2 Diabetes Linkage Analysis Consortium

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3578091

Prediction of individual genetic risk to disease from genome-wide association studies

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3578091

Overcoming the winner's curse: estimating penetrance parameters from case-control data

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3578091

The allelic architecture of human disease genes: common disease-common variant... or not?

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3578091

On the allelic spectrum of human disease

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3578091

Linkage disequilibrium in humans: models and data

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3578091

Linkage strategies for genetically complex traits. II. The power of affected relative pairs

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3578091

Trend tests for case-control studies of genetic markers: power, sample size and robustness

30 September 2017

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FGEPI.21668

The information contained in multiple sibling pairs

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22865662

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1002/GEPI.21668

1 reference

15 August 2017

1 reference

15 August 2017

1 reference

PMCID

3578091