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The challenges, advantages and future of phenome‐wide association studies

Immunology, 2014-02, Vol.141 (2), p.157-165

Hebbring, Scott J.

2014

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The phenotypic legacy of admixture between modern humans and Neandertals

Science (American Association for the Advancement of Science), 2016-02, Vol.351 (6274), p.737-741

2016

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Mining Retrospective Data for Virtual Prospective Drug Repurposing: L-DOPA and Age-related Macular Degeneration

The American journal of medicine, 2016-03, Vol.129 (3), p.292-298

2016

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Application of clinical text data for phenome-wide association studies (PheWASs)

Bioinformatics (Oxford, England), 2015-06, Vol.31 (12), p.1981-1987

2015

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An independently validated, portable algorithm for the rapid identification of COPD patients using electronic health records

Scientific reports, 2021-10, Vol.11 (1), p.19959-19959, Article 19959

2021

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Medical Records-Based Genetic Studies of the Complement System

Journal of the American Society of Nephrology, 2021-08, Vol.32 (8), p.2031-2047

2021

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Assessment of the current status of real-world pharmacogenomic testing: informed consent, patient education, and related practices

Frontiers in pharmacology, 2024-02, Vol.15, p.1355412-1355412

2024

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Phenome-wide association study maps new diseases to the human major histocompatibility complex region

Journal of medical genetics, 2016-10, Vol.53 (10), p.681-689

2016

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Phenome-wide association studies (PheWASs) for functional variants

European journal of human genetics : EJHG, 2015-04, Vol.23 (4), p.523-529

2015

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Estimating the efficacy of pharmacogenomics over a lifetime

Frontiers in medicine, 2023, Vol.10, p.1006743-1006743

2023

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Opportunities for drug repositioning from phenome-wide association studies

Nature biotechnology, 2015-04, Vol.33 (4), p.342-345

2015

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Identifying genetically driven clinical phenotypes using linear mixed models

Nature communications, 2016-04, Vol.7 (1), p.11433-11433, Article 11433

2016

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The impact of glucocorticoid polymorphisms on markers of neonatal respiratory disease after antenatal betamethasone administration

American journal of obstetrics and gynecology, 2013-03, Vol.208 (3), p.215.e1-215.e6

2013

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Evaluation of Genetic Variations in the Androgen and Estrogen Metabolic Pathways as Risk Factors for Sporadic and Familial Prostate Cancer

Cancer epidemiology, biomarkers & prevention, 2007-05, Vol.16 (5), p.969-978

2007

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Use of an Electronic Medical Record to Create the Marshfield Clinic Twin/Multiple Birth Cohort

Genetic epidemiology, 2014-12, Vol.38 (8), p.692-698

2014

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E-Pedigrees: a large-scale automatic family pedigree prediction application

Bioinformatics (Oxford, England), 2021-11, Vol.37 (21), p.3966-3968

2021

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Phenome-wide scanning identifies multiple diseases and disease severity phenotypes associated with HLA variants

Science translational medicine, 2017-05, Vol.9 (389)

2017

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The impact of drug metabolizing enzyme polymorphisms on outcomes after antenatal corticosteroid use

American journal of obstetrics and gynecology, 2012-05, Vol.206 (5), p.447.e17-447.e24

2012

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Glutathione S-Transferase T1 and M1: Gene Sequence Variation and Functional Genomics

Clinical cancer research, 2007-12, Vol.13 (23), p.7207-7216

2007

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Polymorphisms in Mitochondrial Genes and Prostate Cancer Risk

Cancer epidemiology, biomarkers & prevention, 2008-12, Vol.17 (12), p.3558-3566

2008

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Kidney failure in Bardet–Biedl syndrome

Clinical genetics, 2022-04, Vol.101 (4), p.429-441

2022

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The Decay of Disease Association with Declining Linkage Disequilibrium: A Fine Mapping Theorem

Frontiers in genetics, 2016-12, Vol.7, p.217-217

2016

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Copy number variation and cytidine analogue cytotoxicity: a genome-wide association approach

BMC genomics, 2010-06, Vol.11 (1), p.357-357, Article 357

2010

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Ancestry-specific polygenic scores and SNP heritability of 25(OH)D in African- and European-ancestry populations

Human genetics, 2019-10, Vol.138 (10), p.1155-1169

2019

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The challenges, advantages and future of phenome‐wide association studies

The phenotypic legacy of admixture between modern humans and Neandertals

Mining Retrospective Data for Virtual Prospective Drug Repurposing: L-DOPA and Age-related Macular Degeneration

Application of clinical text data for phenome-wide association studies (PheWASs)

An independently validated, portable algorithm for the rapid identification of COPD patients using electronic health records

Medical Records-Based Genetic Studies of the Complement System

Assessment of the current status of real-world pharmacogenomic testing: informed consent, patient education, and related practices

Phenome-wide association study maps new diseases to the human major histocompatibility complex region

Phenome-wide association studies (PheWASs) for functional variants

Estimating the efficacy of pharmacogenomics over a lifetime

Opportunities for drug repositioning from phenome-wide association studies

Identifying genetically driven clinical phenotypes using linear mixed models

The impact of glucocorticoid polymorphisms on markers of neonatal respiratory disease after antenatal betamethasone administration

Evaluation of Genetic Variations in the Androgen and Estrogen Metabolic Pathways as Risk Factors for Sporadic and Familial Prostate Cancer

Use of an Electronic Medical Record to Create the Marshfield Clinic Twin/Multiple Birth Cohort

E-Pedigrees: a large-scale automatic family pedigree prediction application

Phenome-wide scanning identifies multiple diseases and disease severity phenotypes associated with HLA variants

The impact of drug metabolizing enzyme polymorphisms on outcomes after antenatal corticosteroid use

Glutathione S-Transferase T1 and M1: Gene Sequence Variation and Functional Genomics

Polymorphisms in Mitochondrial Genes and Prostate Cancer Risk

Kidney failure in Bardet–Biedl syndrome

The Decay of Disease Association with Declining Linkage Disequilibrium: A Fine Mapping Theorem

Copy number variation and cytidine analogue cytotoxicity: a genome-wide association approach

Ancestry-specific polygenic scores and SNP heritability of 25(OH)D in African- and European-ancestry populations

Quantifying the phenome‐wide disease burden of obesity using electronic health records and genomics

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