(Q34153597)

31 July 2017

Founder population-specific HapMap panel increases power in GWA studies through improved imputation accuracy and CNV tagging (English)

1 reference

genome-wide association study

31 July 2017

0 references

1 reference

2

1 reference

31 July 2017

11

Samuli Ripatti

0 references

Ida Surakka

1

Ida Surakka

1 reference

31 July 2017

3

Verneri Anttila

0 references

Chris Barnes

Chris Barnes

5

0 references

Veikko Salomaa

7

Veikko Salomaa

1 reference

31 July 2017

9

Aarno Palotie

1 reference

31 July 2017

8

Mark Daly

1 reference

PubMed ID

20810666

31 July 2017

Leena Peltonen-Palotie

10

Leena Peltonen

1 reference

31 July 2017

4

Michael Inouye

1 reference

31 July 2017

Loukas Moutsianas

6

1 reference

31 July 2017

1 September 2010

1 reference

31 July 2017

8

0 references

published in

Genome Research

1 reference

31 July 2017

20

1 reference

31 July 2017

1344-1351

1 reference

31 July 2017

10

1 reference

Integrating common and rare genetic variation in diverse human populations

31 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2945183

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2945183

A flexible and accurate genotype imputation method for the next generation of genome-wide association studies

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2945183

The genome-wide patterns of variation expose significant substructure in a founder population

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2945183

A robust statistical method for case-control association testing with copy number variation

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2945183

Systematic assessment of copy number variant detection via genome-wide SNP genotyping

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2945183

Genome-wide association studies for complex traits: consensus, uncertainty and challenges

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2945183

A second generation human haplotype map of over 3.1 million SNPs

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2945183

PLINK: a tool set for whole-genome association and population-based linkage analyses

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2945183

A new multipoint method for genome-wide association studies by imputation of genotypes

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2945183

Global variation in copy number in the human genome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2945183

Linkage disequilibrium and heritability of copy-number polymorphisms within duplicated regions of the human genome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2945183

The International HapMap Project

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2945183

Molecular genetics of the Finnish disease heritage.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2945183

The Finnish population structure A genetic and genealogical study

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2945183

Unique disease heritage of the Dutch-German Mennonite population.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2945183

Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studies

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2945183

Common deletion polymorphisms in the human genome.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2945183

Linkage disequilibrium in isolated populations: Finland and a young sub-population of Kuusamo.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2945183

28 October 2018

Identifiers

DOI

10.1101/GR.106534.110

1 reference

31 July 2017

1 reference

31 July 2017

1 reference

PubMed ID

20810666