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The support of human genetic evidence for approved drug indications

Nature genetics, 2015-08, Vol.47 (8), p.856-860

2015

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Genome-wide strategies for detecting multiple loci that influence complex diseases

Nature genetics, 2005-04, Vol.37 (4), p.413-417

2005

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Population stratification and spurious allelic association

The Lancet (British edition), 2003-02, Vol.361 (9357), p.598-604

2003

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The effects of human population structure on large genetic association studies

Nature genetics, 2004-05, Vol.36 (5), p.512-517

2004

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Merlin-rapid analysis of dense genetic maps using sparse gene flow trees

Nature genetics, 2002-01, Vol.30 (1), p.97-101

2002

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Association study designs for complex diseases

Nature reviews. Genetics, 2001-02, Vol.2 (2), p.91-99

2001

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The complex interplay among factors that influence allelic association

Nature reviews. Genetics, 2004-02, Vol.5 (2), p.89-100

2004

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Measures of human population structure show heterogeneity among genomic regions

Genome research, 2005-11, Vol.15 (11), p.1468-1476

2005

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A General Test of Association for Quantitative Traits in Nuclear Families

American journal of human genetics, 2000-01, Vol.66 (1), p.279-292

2000

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Using haplotype blocks to map human complex trait loci

Trends in genetics, 2003-03, Vol.19 (3), p.135-140

2003

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Efficient selective screening of haplotype tag SNPs

Bioinformatics, 2003-01, Vol.19 (2), p.287-288

2003

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Guidelines for Genotyping in Genomewide Linkage Studies: Single-Nucleotide–Polymorphism Maps Versus Microsatellite Maps

American journal of human genetics, 2004-10, Vol.75 (4), p.687-692

2004

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A High-Resolution Linkage-Disequilibrium Map of the Human Major Histocompatibility Complex and First Generation of Tag Single-Nucleotide Polymorphisms

American journal of human genetics, 2005-04, Vol.76 (4), p.634-646

2005

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Genome-wide pharmacogenetic investigation of a hepatic adverse event without clinical signs of immunopathology suggests an underlying immune pathogenesis

The pharmacogenomics journal, 2008-06, Vol.8 (3), p.186-195

2008

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GRR: graphical representation of relationship errors

Bioinformatics, 2001-08, Vol.17 (8), p.742-743

2001

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Linkage Disequilibrium Mapping via Cladistic Analysis of Single-Nucleotide Polymorphism Haplotypes

American journal of human genetics, 2004-07, Vol.75 (1), p.35-43

2004

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A 77-Kilobase Region of Chromosome 6p22.2 Is Associated with Dyslexia in Families From the United Kingdom and From the United States

American journal of human genetics, 2004-12, Vol.75 (6), p.1046-1058

2004

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What makes a good case-control study? Design issues for complex traits such as endometriosis

Human reproduction (Oxford), 2002-06, Vol.17 (6), p.1415-1423

2002

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A Comparison of Linkage Disequilibrium Patterns and Estimated Population Recombination Rates across Multiple Populations

American journal of human genetics, 2005-04, Vol.76 (4), p.681-687

2005

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Inflammatory bowel disease is associated with a TNF polymorphism that affects an interaction between the OCT1 and NF-κB transcription factors

Human molecular genetics, 2002-05, Vol.11 (11), p.1281-1289

2002

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A first-generation linkage disequilibrium map of human chromosome 22

Nature (London), 2002-08, Vol.418 (6897), p.544-548

2002

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The impact of SNP density on fine-scale patterns of linkage disequilibrium

Human molecular genetics, 2004-03, Vol.13 (6), p.577-588

2004

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Extent and Distribution of Linkage Disequilibrium in Three Genomic Regions

American journal of human genetics, 2001-01, Vol.68 (1), p.191-197

2001

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An evaluation of HapMap sample size and tagging SNP performance in large-scale empirical and simulated data sets

Nature genetics, 2005-12, Vol.37 (12), p.1320-1322

2005

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The Interleukin 1 Gene Cluster Contains a Major Susceptibility Locus for Ankylosing Spondylitis

American journal of human genetics, 2004-10, Vol.75 (4), p.587-595

2004

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The support of human genetic evidence for approved drug indications

Genome-wide strategies for detecting multiple loci that influence complex diseases

Population stratification and spurious allelic association

The effects of human population structure on large genetic association studies

Merlin-rapid analysis of dense genetic maps using sparse gene flow trees

Association study designs for complex diseases

The complex interplay among factors that influence allelic association

Measures of human population structure show heterogeneity among genomic regions

A General Test of Association for Quantitative Traits in Nuclear Families

Using haplotype blocks to map human complex trait loci

Efficient selective screening of haplotype tag SNPs

Guidelines for Genotyping in Genomewide Linkage Studies: Single-Nucleotide–Polymorphism Maps Versus Microsatellite Maps

A High-Resolution Linkage-Disequilibrium Map of the Human Major Histocompatibility Complex and First Generation of Tag Single-Nucleotide Polymorphisms

Genome-wide pharmacogenetic investigation of a hepatic adverse event without clinical signs of immunopathology suggests an underlying immune pathogenesis

GRR: graphical representation of relationship errors

Linkage Disequilibrium Mapping via Cladistic Analysis of Single-Nucleotide Polymorphism Haplotypes

A 77-Kilobase Region of Chromosome 6p22.2 Is Associated with Dyslexia in Families From the United Kingdom and From the United States

What makes a good case-control study? Design issues for complex traits such as endometriosis

A Comparison of Linkage Disequilibrium Patterns and Estimated Population Recombination Rates across Multiple Populations

Inflammatory bowel disease is associated with a TNF polymorphism that affects an interaction between the OCT1 and NF-κB transcription factors

A first-generation linkage disequilibrium map of human chromosome 22

The impact of SNP density on fine-scale patterns of linkage disequilibrium

Extent and Distribution of Linkage Disequilibrium in Three Genomic Regions

An evaluation of HapMap sample size and tagging SNP performance in large-scale empirical and simulated data sets

The Interleukin 1 Gene Cluster Contains a Major Susceptibility Locus for Ankylosing Spondylitis

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