(Q37654985)

English

One thousand genomes imputation in the National Cancer Institute Breast and Prostate Cancer Cohort Consortium aggressive prostate cancer genome-wide association study

scientific article published on 19 December 2012

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

One thousand genomes imputation in the National Cancer Institute Breast and Prostate Cancer Cohort Consortium aggressive prostate cancer genome-wide association study (English)

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

genome-wide association study

0 references

1 reference

based on heuristic

inferred from title

prostate cancer

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based on heuristic

inferred from title

Mitchell Machiela

1

object named as

Mitchell J Machiela

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

Stephen Chanock

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object named as

Stephen J Chanock

1 reference

Europe PubMed Central

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21 August 2017

Christopher A. Haiman

7

object named as

Christopher A Haiman

1 reference

Europe PubMed Central

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21 August 2017

4

object named as

W Ryan Diver

1 reference

Europe PubMed Central

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21 August 2017

David J. Hunter

9

object named as

David J Hunter

1 reference

Europe PubMed Central

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21 August 2017

Victoria L. Stevens

5

object named as

Victoria L Stevens

1 reference

Europe PubMed Central

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21 August 2017

10

object named as

Peter Kraft

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Europe PubMed Central

21 August 2017

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author name string

Constance Chen

2

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Europe PubMed Central

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21 August 2017

Liming Liang

3

1 reference

Europe PubMed Central

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21 August 2017

Konstantinos K Tsilidis

6

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Europe PubMed Central

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21 August 2017

National Cancer Institute Breast and Prostate Cancer Cohort Consortium

11

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Europe PubMed Central

PMC publication ID

21 August 2017

publication date

19 December 2012

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Europe PubMed Central

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21 August 2017

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

73

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Europe PubMed Central

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21 August 2017

7

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Europe PubMed Central

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21 August 2017

677-689

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Europe PubMed Central

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21 August 2017

describes a project that uses

genome-wide association study

1 reference

based on heuristic

inferred from title

Characterizing linkage disequilibrium and evaluating imputation power of human genomic insertion-deletion polymorphisms

1 reference

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A genome-wide association study for coronary artery disease identifies a novel susceptibility locus in the major histocompatibility complex

1 reference

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Common variants at 11p13 are associated with susceptibility to tuberculosis

1 reference

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23 August 2017

1000 Genomes-based imputation identifies novel and refined associations for the Wellcome Trust Case Control Consortium phase 1 Data

1 reference

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23 August 2017

Performance of genotype imputations using data from the 1000 Genomes Project

1 reference

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23 August 2017

A genome-wide association study of COPD identifies a susceptibility locus on chromosome 19q13.

1 reference

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23 August 2017

Genomic risk profiling of ischemic stroke: results of an international genome-wide association meta-analysis

1 reference

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23 August 2017

A general framework for detecting disease associations with rare variants in sequencing studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3962143

23 August 2017

Genome-wide association study identifies new prostate cancer susceptibility loci

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3962143

23 August 2017

Rare-variant association testing for sequencing data with the sequence kernel association test

1 reference

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23 August 2017

Cancer statistics, 2011: the impact of eliminating socioeconomic and racial disparities on premature cancer deaths

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3962143

23 August 2017

Large-scale fine mapping of the HNF1B locus and prostate cancer risk

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3962143

23 August 2017

Fine mapping of a region of chromosome 11q13 reveals multiple independent loci associated with risk of prostate cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3962143

23 August 2017

Testing for an unusual distribution of rare variants

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3962143

23 August 2017

Efficient study design for next generation sequencing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3962143

23 August 2017

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=3962143

23 August 2017

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=3962143

23 August 2017

METAL: fast and efficient meta-analysis of genomewide association scans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3962143

23 August 2017

Pooled association tests for rare variants in exon-resequencing studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3962143

23 August 2017

Refining the prostate cancer genetic association within the JAZF1 gene on chromosome 7p15.2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3962143

23 August 2017

ProbABEL package for genome-wide association analysis of imputed data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3962143

23 August 2017

Identification of a new prostate cancer susceptibility locus on chromosome 8q24.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3962143

23 August 2017

Two independent prostate cancer risk-associated Loci at 11q13

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3962143

23 August 2017

Fine mapping and functional analysis of a common variant in MSMB on chromosome 10q11.2 associated with prostate cancer susceptibility

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3962143

23 August 2017

Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3962143

23 August 2017

A groupwise association test for rare mutations using a weighted sum statistic

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3962143

23 August 2017

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

1 reference

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23 August 2017

Population substructure and control selection in genome-wide association studies

1 reference

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Exhaustive screens for disease susceptibility loci incorporating statistical interaction of genotypes: a comparison of likelihood-ratio-based and Akaike and Bayesian information criteria-based methods

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3962143

23 August 2017

Study designs for genome-wide association studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3962143

23 August 2017

Rapid and accurate haplotype phasing and missing-data inference for whole-genome association studies by use of localized haplotype clustering

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3962143

23 August 2017

Coverage and power in genomewide association studies

1 reference

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23 August 2017

From genotypes to genes: doubling the sample size

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23 August 2017

Current status of genome-wide association studies in cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3962143

6 September 2017

Comparison of six statistics of genetic association regarding their ability to discriminate between causal variants and genetically linked markers

1 reference

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25 June 2018

A common variant associated with prostate cancer in European and African populations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3962143

25 June 2018

Prostate cancer incidence and mortality trends in 37 European countries: an overview.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3962143

1 September 2018

Multiple loci on 8q24 associated with prostate cancer susceptibility.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3962143

1 September 2018

Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study

1 reference

https://api.crossref.org/works/10.1002%2FPROS.22608

21 January 2018

A candidate gene approach to searching for low-penetrance breast and prostate cancer genes

1 reference

https://api.crossref.org/works/10.1002%2FPROS.22608

21 January 2018

Two variants on chromosome 17 confer prostate cancer risk and the one in TCF2 protects against type 2 diabetes

1 reference

https://api.crossref.org/works/10.1002%2FPROS.22608

21 January 2018

Evaluating the power to discriminate between highly correlated SNPs in genetic association studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/23255287

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Commentary on "identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array." Eeles RA, Olama AA, Benlloch S, Saunders EJ, Leongamornlert DA, Tymrakiewicz M, Ghoussaini M, Luccarini C, Dennis J, Jugurnauth-Lit

1 reference

https://pubmed.ncbi.nlm.nih.gov/23255287

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1002/PROS.22608

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

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