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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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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.257-264

2012

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Genome-wide association and Mendelian randomization study of NT-proBNP in patients with acute coronary syndrome

Human molecular genetics, 2016-04, Vol.25 (7), p.1447-1456

2016

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Molecular and genetic association of interleukin-6 in tacrine-induced hepatotoxicity

Pharmacogenetics and genomics, 2007-11, Vol.17 (11), p.961-972

2007

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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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Genome-wide association study evaluating lipoprotein-associated phospholipase A2 mass and activity at baseline and after rosuvastatin therapy

Circulation. Cardiovascular genetics, 2012-12, Vol.5 (6), p.676

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.688-695

2015

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Investigating the utility of combining Φ29 whole genome amplification and highly multiplexed single nucleotide polymorphism BeadArray™ genotyping

BMC biotechnology, 2004-07, Vol.4 (1), p.15-15, Article 15

2004

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Tacrine-induced liver damage: an analysis of 19 candidate genes

Pharmacogenetics and genomics, 2007-12, Vol.17 (12), p.1091-1100

2007

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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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Serious carbamazepine-induced hypersensitivity reactions associated with the HSP70 gene cluster

Pharmacogenetics and genomics, 2006-04, Vol.16 (4), p.287-296

2006

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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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Lack of Association of the Ala45Thr Polymorphism and Other Common Variants of the NeuroD Gene With Type 1 Diabetes

Diabetes (New York, N.Y.), 2004-04, Vol.53 (4), p.1158-1161

2004

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Development of an integrated genome informatics, data management and workflow infrastructure: a toolbox for the study of complex disease genetics

Human genomics, 2004-01, Vol.1 (2), p.98-109

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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Haplotype tagging for the identification of common disease genes

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

2001

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Gene mapping strategies for complex disease and drug response

Drug discovery today. Technologies, 2006, Vol.3 (2), p.131-136

2006

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Abstract P221: Genome-wide Association Study Evaluating Genetic Determinants of Rosuvastatin Effects on Lp-PLA 2 Mass and Activity

Circulation (New York, N.Y.), 2012-03, Vol.125 (suppl_10)

2012

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

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

2013

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Evaluation of the Effect of Interleukin 18 Associated Genetic Polymorphisms on Risk of Cardiovascular Events in Patients With Acute Coronary Syndrome

Circulation (New York, N.Y.), 2013, Vol.128 (22)

2013

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Are There Any Causal Relations Between Growth Differentiation Factor 15 and Outcomes in Patients With Acute Coronary Syndrome?: A Report From the Plato Gwas Study

Circulation (New York, N.Y.), 2013, Vol.128 (22)

2013

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Genome-Wide Association Study Evaluating Lipoprotein-Associated Phospholipase A 2 Mass and Activity at Baseline and After Rosuvastatin Therapy

Circulation. Cardiovascular genetics, 2012-12, Vol.5 (6), p.676-685

2012

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Lack of Association of the Ala^sup 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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The HapMap – A Haplotype Map of the Human Genome

Bioinformatics for Geneticists, 2007, p.33-58

2007

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Lack of association of the [Ala.sup.45]Thr polymorphism and other common variants of the Neurod gene with type 1 diabetes.(Brief Genetics Report)

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

2004

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Genome-wide association studies: theoretical and practical concerns

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

Genome-wide association and Mendelian randomization study of NT-proBNP in patients with acute coronary syndrome

Molecular and genetic association of interleukin-6 in tacrine-induced hepatotoxicity

SNP allele frequency estimation in DNA pools and variance components analysis

Genome-wide association study evaluating lipoprotein-associated phospholipase A2 mass and activity at baseline and after rosuvastatin therapy

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

Investigating the utility of combining Φ29 whole genome amplification and highly multiplexed single nucleotide polymorphism BeadArray™ genotyping

Tacrine-induced liver damage: an analysis of 19 candidate genes

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

Serious carbamazepine-induced hypersensitivity reactions associated with the HSP70 gene cluster

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

Lack of Association of the Ala45Thr Polymorphism and Other Common Variants of the NeuroD Gene With Type 1 Diabetes

Development of an integrated genome informatics, data management and workflow infrastructure: a toolbox for the study of complex disease genetics

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

Haplotype tagging for the identification of common disease genes

Gene mapping strategies for complex disease and drug response

Abstract P221: Genome-wide Association Study Evaluating Genetic Determinants of Rosuvastatin Effects on Lp-PLA 2 Mass and Activity

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

Evaluation of the Effect of Interleukin 18 Associated Genetic Polymorphisms on Risk of Cardiovascular Events in Patients With Acute Coronary Syndrome

Are There Any Causal Relations Between Growth Differentiation Factor 15 and Outcomes in Patients With Acute Coronary Syndrome?: A Report From the Plato Gwas Study

Genome-Wide Association Study Evaluating Lipoprotein-Associated Phospholipase A 2 Mass and Activity at Baseline and After Rosuvastatin Therapy

Lack of Association of the Ala^sup 45^Thr Polymorphism and Other Common Variants of the NeuroD Gene With Type 1 Diabetes

The HapMap – A Haplotype Map of the Human Genome

Lack of association of the [Ala.sup.45]Thr polymorphism and other common variants of the Neurod gene with type 1 diabetes.(Brief Genetics Report)

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