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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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IDDM2/insulin VNTR modifies risk conferred by IDDM1/HLA for development of type 1 diabetes and associated autoimmunity

Diabetologia, 2003-05, Vol.46 (5), p.712-720

2003

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Identification of the sources of error in allele frequency estimations from pooled DNA indicates an optimal experimental design

Annals of human genetics, 2002-11, Vol.66 (5‐6), p.393-405

2002

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Case/pseudocontrol analysis in genetic association studies: A unified framework for detection of genotype and haplotype associations, gene-gene and gene-environment interactions, and parent-of-origin effects

Genetic epidemiology, 2004-04, Vol.26 (3), p.167-185

2004

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Haplotype tagging for the identification of common disease genes

Nature genetics, 2001-10, Vol.29 (2), p.233-237

2001

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Cost-effective analysis of candidate genes using htSNPs: a staged approach

Genes and immunity, 2004-06, Vol.5 (4), p.301-305

2004

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Genetic determinants of statin-induced low-density lipoprotein cholesterol reduction: the Justification for the Use of Statins in Prevention: an Intervention Trial Evaluating Rosuvastatin (JUPITER) trial

Circulation. Cardiovascular genetics, 2012-04, Vol.5 (2), p.257

2012

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Evaluation of single nucleotide polymorphism typing with invader on PCR amplicons and its automation

Genome research, 2000-03, Vol.10 (3), p.330

2000

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Lack of association between SLCO1B1 polymorphisms and clinical myalgia following rosuvastatin therapy

The American heart journal, 2013-06, Vol.165 (6), p.1008-1014

2013

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Identification of the sources of error in allele frequency estimations from pooled DNA indicates an optimal experimental design

Annals of human genetics, 2002-11, Vol.66 (5-6), p.393-405

2002

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Genome-wide association studies: theoretical and practical concerns

Nature reviews. Genetics, 2005-02, Vol.6 (2), p.109-118

2005

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Pharmacogenetic determinants of statin-induced reductions in C-reactive protein

Circulation. Cardiovascular genetics, 2012-02, Vol.5 (1), p.58

2012

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Differential Genetic Effects on Statin-Induced Changes Across Low-Density Lipoprotein-Related Measures

Circulation. Cardiovascular genetics, 2015-10, Vol.8 (5), p.688

2015

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Replication of an Association Between the Lymphoid Tyrosine Phosphatase Locus (LYP/PTPN22) With Type 1 Diabetes, and Evidence for Its Role as a General Autoimmunity Locus

Diabetes (New York, N.Y.), 2004-11, Vol.53 (11), p.3020-3023

2004

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Maternal-Fetal Interactions and Birth Order Influence Insulin Variable Number of Tandem Repeats Allele Class Associations with Head Size at Birth and Childhood Weight Gain

Diabetes (New York, N.Y.), 2004-04, Vol.53 (4), p.1128-1133

2004

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Optimizing the power of genome-wide association studies by using publicly available reference samples to expand the control group

Genetic epidemiology, 2010-05, Vol.34 (4), p.319-326

2010

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Interstitial lung disease in gefitinib-treated Japanese patients with non-small-cell lung cancer: genome-wide analysis of genetic data

Pharmacogenomics, 2011-07, Vol.12 (7), p.965-975

2011

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SNP allele frequency estimation in DNA pools and variance components analysis

BioTechniques, 2004-05, Vol.36 (5), p.840-845

2004

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Haplotype Tag Single Nucleotide Polymorphism Analysis of the Human Orthologues of the Rat Type 1 Diabetes Genes Ian4 (Lyp/Iddm1) and Cblb

Diabetes (New York, N.Y.), 2004-02, Vol.53 (2), p.505-509

2004

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Analysis of the Type 2 Diabetes-Associated Single Nucleotide Polymorphisms in the Genes IRS1, KCNJ11, and PPARG2 in Type 1 Diabetes

Diabetes (New York, N.Y.), 2004-03, Vol.53 (3), p.870-873

2004

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Comparison of population‐ and family‐based methods for genetic association analysis in the presence of interacting loci

Genetic epidemiology, 2005-07, Vol.29 (1), p.51-67

2005

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Lack of association of the Ala(45)Thr polymorphism and other common variants of the NeuroD gene with type 1 diabetes

Diabetes (New York, N.Y.), 2004-04, Vol.53 (4), p.1158

2004

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Association Analysis of the Lymphocyte-Specific Protein Tyrosine Kinase (LCK) Gene in Type 1 Diabetes

Diabetes (New York, N.Y.), 2004-09, Vol.53 (9), p.2479-2482

2004

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The genetics of type 1 diabetes

Barratt, B J

2004

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Common polymorphism in H19 associated with birthweight and cord blood IGF-II levels in humans

BMC genetics, 2005-05, Vol.6, p.22

2005

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

IDDM2/insulin VNTR modifies risk conferred by IDDM1/HLA for development of type 1 diabetes and associated autoimmunity

Identification of the sources of error in allele frequency estimations from pooled DNA indicates an optimal experimental design

Case/pseudocontrol analysis in genetic association studies: A unified framework for detection of genotype and haplotype associations, gene-gene and gene-environment interactions, and parent-of-origin effects

Haplotype tagging for the identification of common disease genes

Cost-effective analysis of candidate genes using htSNPs: a staged approach

Genetic determinants of statin-induced low-density lipoprotein cholesterol reduction: the Justification for the Use of Statins in Prevention: an Intervention Trial Evaluating Rosuvastatin (JUPITER) trial

Evaluation of single nucleotide polymorphism typing with invader on PCR amplicons and its automation

Lack of association between SLCO1B1 polymorphisms and clinical myalgia following rosuvastatin therapy

Identification of the sources of error in allele frequency estimations from pooled DNA indicates an optimal experimental design

Genome-wide association studies: theoretical and practical concerns

Pharmacogenetic determinants of statin-induced reductions in C-reactive protein

Differential Genetic Effects on Statin-Induced Changes Across Low-Density Lipoprotein-Related Measures

Replication of an Association Between the Lymphoid Tyrosine Phosphatase Locus (LYP/PTPN22) With Type 1 Diabetes, and Evidence for Its Role as a General Autoimmunity Locus

Maternal-Fetal Interactions and Birth Order Influence Insulin Variable Number of Tandem Repeats Allele Class Associations with Head Size at Birth and Childhood Weight Gain

Optimizing the power of genome-wide association studies by using publicly available reference samples to expand the control group

Interstitial lung disease in gefitinib-treated Japanese patients with non-small-cell lung cancer: genome-wide analysis of genetic data

SNP allele frequency estimation in DNA pools and variance components analysis

Haplotype Tag Single Nucleotide Polymorphism Analysis of the Human Orthologues of the Rat Type 1 Diabetes Genes Ian4 (Lyp/Iddm1) and Cblb

Analysis of the Type 2 Diabetes-Associated Single Nucleotide Polymorphisms in the Genes IRS1, KCNJ11, and PPARG2 in Type 1 Diabetes

Comparison of population‐ and family‐based methods for genetic association analysis in the presence of interacting loci

Lack of association of the Ala(45)Thr polymorphism and other common variants of the NeuroD gene with type 1 diabetes

Association Analysis of the Lymphocyte-Specific Protein Tyrosine Kinase (LCK) Gene in Type 1 Diabetes

The genetics of type 1 diabetes

Common polymorphism in H19 associated with birthweight and cord blood IGF-II levels in humans

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