Imputation-based analysis of association studies: candidate regions and quantitative traits (Q30833155)

11 August 2017

Imputation-based analysis of association studies: candidate regions and quantitative traits (English)

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11 August 2017

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1

Bertrand Servin

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11 August 2017

Matthew Stephens

2

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11 August 2017

30 May 2007

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11 August 2017

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11 August 2017

3

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11 August 2017

7

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11 August 2017

e114

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Creative Commons Attribution 4.0 International

11 August 2017

start time

27 July 2007

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

Nova2 interacts with a cis-acting polymorphism to influence the proportions of drug-responsive splice variants of SCN1A.

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A flexible Bayesian framework for modeling haplotype association with disease, allowing for dominance effects of the underlying causative variants

21 June 2018

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A fast and flexible statistical model for large-scale population genotype data: applications to inferring missing genotypes and haplotypic phase

21 June 2018

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A comparison of phasing algorithms for trios and unrelated individuals

21 June 2018

1 reference

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Genetic variation in the HSD17B1 gene and risk of prostate cancer

21 June 2018

1 reference

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A haplotype map of the human genome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1934390

Genetic predictors of the maximum doses patients receive during clinical use of the anti-epileptic drugs carbamazepine and phenytoin

21 June 2018

1 reference

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Accounting for decay of linkage disequilibrium in haplotype inference and missing-data imputation

21 June 2018

1 reference

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Low LDL cholesterol in individuals of African descent resulting from frequent nonsense mutations in PCSK9.

21 June 2018

1 reference

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Coalescent-based association mapping and fine mapping of complex trait loci

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1934390

Identifying candidate causal variants responsible for altered activity of the ABCB1 multidrug resistance gene

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1934390

Modeling linkage disequilibrium and identifying recombination hotspots using single-nucleotide polymorphism data

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1934390

Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibrium

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1934390

Selection and evaluation of tagging SNPs in the neuronal-sodium-channel gene SCN1A: implications for linkage-disequilibrium gene mapping

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1934390

A New Statistical Method for Haplotype Reconstruction from Population Data

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1934390

Multipoint quantitative-trait linkage analysis in general pedigrees

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1934390

msHOT: modifying Hudson's ms simulator to incorporate crossover and gene conversion hotspots.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1934390

Imputation methods to improve inference in SNP association studies.

25 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1934390

Testing untyped alleles (TUNA)-applications to genome-wide association studies.

25 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1934390

A Bayesian toolkit for genetic association studies.

25 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1934390

Imputation and variable selection in linear regression models with missing covariates

25 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1934390

Bayesian association-based fine mapping in small chromosomal segments.

25 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1934390

Detecting disease associations due to linkage disequilibrium using haplotype tags: a class of tests and the determinants of statistical power

25 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1934390

An invariant form for the prior probability in estimation problems

25 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17676998

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PGEN.0030114

1 reference

11 August 2017

1 reference

PMC publication ID

1934390

11 August 2017

PubMed publication ID

17676998

1 reference

PMC publication ID

1934390