(Q31037165)

17 August 2017

FINEMAP: efficient variable selection using summary data from genome-wide association studies (English)

1 reference

genome-wide association study

17 August 2017

0 references

author

Veikko Salomaa

4

0 references

Samuli Ripatti

5

object named as

Samuli Ripatti

0 references

Matti Pirinen

object named as

Matti Pirinen

6

0 references

Aki S Havulinna

3

object named as

Aki S Havulinna

1 reference

17 August 2017

Christian Benner

1

1 reference

PMCID

4866522

17 August 2017

Chris C A Spencer

2

1 reference

PMCID

4866522

17 August 2017

language of work or name

English

0 references

publication date

14 January 2016

1 reference

17 August 2017

1 reference

17 August 2017

32

1 reference

17 August 2017

10

1 reference

17 August 2017

1493-1501

1 reference

Creative Commons Attribution-NonCommercial 4.0 International

17 August 2017

start time

12 October 2016

1 reference

April 2023 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

Leveraging Functional-Annotation Data in Trans-ethnic Fine-Mapping Studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4866522

Dissection of a Complex Disease Susceptibility Region Using a Bayesian Stochastic Search Approach to Fine 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=4866522

The impact of low-frequency and rare variants on lipid levels

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4866522

Fine Mapping Causal Variants with an Approximate Bayesian Method Using Marginal Test Statistics

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4866522

Integrating functional data to prioritize causal variants in statistical fine-mapping studies

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4866522

Defining the role of common variation in the genomic and biological architecture of adult human height

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4866522

Identifying causal variants at loci with multiple signals of association

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4866522

Fast and accurate imputation of summary statistics enhances evidence of functional enrichment

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4866522

Systematic evaluation of coding variation identifies a candidate causal variant in TM6SF2 influencing total cholesterol and myocardial infarction risk

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4866522

GUESS-ing polygenic associations with multiple phenotypes using a GPU-based evolutionary stochastic search algorithm

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4866522

Bayesian refinement of association signals for 14 loci in 3 common diseases

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4866522

GCTA: a tool for genome-wide complex trait analysis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4866522

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4866522

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4866522

The C-514T polymorphism in the human hepatic lipase gene promoter diminishes its activity.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4866522

An Introduction to MCMC for Machine Learning

21 June 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTW018

Forty-year trends in cardiovascular risk factors in Finland

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTW018

Stochastic Relaxation, Gibbs Distributions, and the Bayesian Restoration of Images

21 January 2018

2 references

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTW018

21 January 2018

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4866522

Monte Carlo sampling methods using Markov chains and their applications

25 November 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTW018

DIST: direct imputation of summary statistics for unmeasured SNPs

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTW018

Equation of State Calculations by Fast Computing Machines

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTW018

Evolutionary stochastic search for Bayesian model exploration

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTW018

Efficient computation with a linear mixed model on large-scale data sets with applications to genetic studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTW018

Molecular characterization of human hepatic lipase deficiency. In vitro expression of two naturally occurring mutations

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26773131

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1093/BIOINFORMATICS/BTW018

1 reference

journals/bioinformatics/BennerSHSRP16

17 August 2017

1 reference

DBLP Dataset 2021-01-02

28 January 2021

1 reference

17 August 2017

1 reference

PMCID

4866522