PLINK: a tool set for whole-genome association and population-based linkage analyses (Q24677407)

7

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Mark Joseph Daly

10

object named as

Mark J Daly

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Pamela Sklar

8

object named as

Pamela Sklar

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Benjamin M. Neale

2

object named as

Benjamin Neale

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author name string

Kathe Todd-Brown

3

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Lori Thomas

4

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Manuel A R Ferreira

5

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David Bender

6

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Paul I W de Bakker

9

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Pak C Sham

American Journal of Human Genetics

11

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language of work or name

English

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publication date

September 2007

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published in

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volume

81

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issue

3

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page(s)

559-75

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cites work

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Mapping of sudden infant death with dysgenesis of the testes syndrome (SIDDT) by a SNP genome scan and identification of TSPYL loss of function

7 April 2017

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Are rare variants responsible for susceptibility to complex diseases?

7 April 2017

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Inference of population structure using multilocus genotype data

7 April 2017

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Long homozygous chromosomal segments in reference families from the centre d'Etude du polymorphisme humain

7 April 2017

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A sibship test for linkage in the presence of association: the sib transmission/disequilibrium test

7 April 2017

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The transmission/disequilibrium test: history, subdivision, and admixture

7 April 2017

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Assessing the impact of population stratification on genetic association studies

7 April 2017

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A comprehensive review of genetic association studies

7 April 2017

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Principal components analysis corrects for stratification in genome-wide association studies

7 April 2017

1 reference

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Haploview: analysis and visualization of LD and haplotype maps

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950838

Genome screening by searching for shared segments: mapping a gene for benign recurrent intrahepatic cholestasis

7 April 2017

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Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels

7 April 2017

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Genomic control for association studies

7 April 2017

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The future of genetic studies of complex human diseases

7 April 2017

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Population structure, differential bias and genomic control in a large-scale, case-control association study

7 April 2017

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A fine-scale map of recombination rates and hotspots across the human genome

7 April 2017

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Genome-wide association studies for common diseases and complex traits

7 April 2017

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On the allelic spectrum of human disease

7 April 2017

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Genetic dissection of complex traits

7 April 2017

1 reference

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A fine-scale linkage-disequilibrium measure based on length of haplotype sharing

7 April 2017

1 reference

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Parental phenotypes in family-based association analysis

28 September 2017

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Maximum-likelihood estimation of relatedness.

28 September 2017

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Trimming, weighting, and grouping SNPs in human case-control association studies

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950838

A general test of association for quantitative traits in nuclear families

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950838

Combined linkage and association sib-pair analysis for quantitative traits

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950838

Permutation tests for multiple loci affecting a quantitative character

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950838

Construction of multilocus genetic linkage maps in humans

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950838

Ascertainment Through Family History of Disease Often Decreases the Power of Family-based Association Studies

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950838

Implications of small effect sizes of individual genetic variants on the design and interpretation of genetic association studies of complex diseases.

28 November 2018

1 reference

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Evaluating and improving power in whole-genome association studies using fixed marker sets.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950838

Properties of structured association approaches to detecting population stratification.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950838

Perspectives of identity by descent (IBD) mapping in founder populations

28 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17701901

12 December 2020

inferred from PubMed ID database lookup

Detecting population stratification using a panel of single nucleotide polymorphisms

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17701901

12 December 2020

inferred from PubMed ID database lookup

Haplotype sharing analysis using mantel statistics

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17701901

12 December 2020

inferred from PubMed ID database lookup

Sequential Monte Carlo p-values

1 reference

Crossref

https://api.crossref.org/works/10.1086%2F519795

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1086/519795

1 reference

1 reference

1 reference

PubMed publication ID

17701901

1 reference