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Recommendations for Clinical CYP2D6 Genotyping Allele Selection: A Joint Consensus Recommendation of the Association for Molecular Pathology, College of American Pathologists, Dutch Pharmacogenetics Working Group of the Royal Dutch Pharmacists Association, and the European Society for Pharmacogenomics and Personalized Therapy

The Journal of molecular diagnostics : JMD, 2021-09, Vol.23 (9), p.1047-1064

2021

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Cytochrome P450 Oxidoreductase (POR) Associated with Severe Paclitaxel-Induced Peripheral Neuropathy in Patients of European Ancestry from ECOG-ACRIN E5103

Clinical cancer research, 2023-07, Vol.29 (13), p.2494

2023

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Recommendations for Clinical Warfarin Genotyping Allele Selection: A Report of the Association for Molecular Pathology and the College of American Pathologists

The Journal of molecular diagnostics : JMD, 2020-07, Vol.22 (7), p.847-859

2020

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Life-Threatening Docetaxel Toxicity in a Patient With Reduced-Function CYP3A Variants: A Case Report

Frontiers in oncology, 2022-01, Vol.11, p.809527

2022

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TPMT and NUDT15 Genotyping Recommendations: A Joint Consensus Recommendation of the Association for Molecular Pathology, Clinical Pharmacogenetics Implementation Consortium, College of American Pathologists, Dutch Pharmacogenetics Working Group of the Royal Dutch Pharmacists Association, European Society for Pharmacogenomics and Personalized Therapy, and Pharmacogenomics Knowledgebase

The Journal of molecular diagnostics : JMD, 2022-10, Vol.24 (10), p.1051-1063

2022

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CYP3A4 and CYP3A5 Genotyping Recommendations: A Joint Consensus Recommendation of the Association for Molecular Pathology, Clinical Pharmacogenetics Implementation Consortium, College of American Pathologists, Dutch Pharmacogenetics Working Group of the Royal Dutch Pharmacists Association, European Society for Pharmacogenomics and Personalized Therapy, and Pharmacogenomics Knowledgebase

The Journal of molecular diagnostics : JMD, 2023-09, Vol.25 (9), p.619-629

2023

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PharmVar Tutorial on CYP2D6 Structural Variation Testing and Recommendations on Reporting

Clinical pharmacology and therapeutics, 2023-12, Vol.114 (6), p.1220-1237

2023

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Analytical Validation of a Computational Method for Pharmacogenetic Genotyping from Clinical Whole Exome Sequencing

The Journal of molecular diagnostics : JMD, 2022-06, Vol.24 (6), p.576-585

2022

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Computational pharmacogenotype extraction from clinical next-generation sequencing

Frontiers in oncology, 2023-07, Vol.13, p.1199741-1199741

2023

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Characterization of Reference Materials for CYP3A4 and CYP3A5: A (GeT-RM) Collaborative Project

The Journal of molecular diagnostics : JMD, 2023-09, Vol.25 (9), p.655-664

2023

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Pharmacokinetic modeling of R and S‐Methadone and their metabolites to study the effects of various covariates in post‐operative children

CPT: pharmacometrics and systems pharmacology, 2021-10, Vol.10 (10), p.1183-1194

2021

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Metformin pharmacogenomics: a genome-wide association study to identify genetic and epigenetic biomarkers involved in metformin anticancer response using human lymphoblastoid cell lines

Human molecular genetics, 2016-11, Vol.25 (21), p.4819-4834

2016

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P237: A de novo gain-of-function ANO5 variant in a patient with anoctaminopathy5-related muscular dystrophy challenges the skeletal/muscular phenotype dichotomy into question

Genetics in Medicine Open, 2023, Vol.1 (1), p.100265, Article 100265

2023

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Association of QT interval-prolonging drugs with clinical trial eligibility in patients with advanced cancer

Frontiers in cardiovascular medicine, 2022-12, Vol.9, p.894623

2022

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P535: The undiagnosed rare disease clinic program of Indiana University: Lessons learned from the first 100 patients enrolled (Phase-I pilot)

Genetics in Medicine Open, 2024, Vol.2, p.101434, Article 101434

2024

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The novel function of tumor protein D54 in regulating pyruvate dehydrogenase and metformin cytotoxicity in breast cancer

Cancer & metabolism, 2019-01, Vol.7 (1), p.1-15, Article 1

2019

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Clinical Opportunities for Germline Pharmacogenetics and Management of Drug-Drug Interactions in Patients With Advanced Solid Cancers

JCO precision oncology, 2022-02, Vol.6, p.e2100312

2022

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Lambda waves and occipital generators

Clinical EEG and neuroscience, 2013-10, Vol.44 (4), p.307

2013

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ASCPT News

Clinical pharmacology and therapeutics, 2021-02, Vol.109 (2), p.285-289

2021

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eP373: Analytical validation of a computational method for pharmacogenetic genotyping from clinical exome sequencing

Genetics in medicine, 2022-03, Vol.24 (3), p.S234-S235

2022

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Abstract P1-08-02: Cytochrome P450 reductase gene , POR, associated with paclitaxel induced peripheral neuropathy in patients of European ancestry from the adjuvant breast cancer trial, ECOG-ACRIN E5103

Cancer research (Chicago, Ill.), 2022-02, Vol.82 (4_Supplement), p.P1-P1-08-02

2022

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CYP3A4 and CYP3A5 Genotyping Recommendations

The Journal of molecular diagnostics : JMD, 2023-09, Vol.25 (9), p.619-629

2023

Link zum Volltext

Verfügbarkeit prüfen

Characterization of Reference Materials for CYP3A4 and CYP3A5

The Journal of molecular diagnostics : JMD, 2023-09, Vol.25 (9), p.655-664

2023

Link zum Volltext

Verfügbarkeit prüfen

Recommendations for Clinical CYP2D6 Genotyping Allele Selection

The Journal of molecular diagnostics : JMD, 2021-09, Vol.23 (9), p.1047-1064

2021

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Metformin Pharmacogenomics: Functional Genomics of CDC25b and TPD54 Regulation of Metformin Anticancer Response in Breast Cancer

Ly, Reynold

2018

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Cytochrome P450 Oxidoreductase (POR) Associated with Severe Paclitaxel-Induced Peripheral Neuropathy in Patients of European Ancestry from ECOG-ACRIN E5103

Recommendations for Clinical Warfarin Genotyping Allele Selection: A Report of the Association for Molecular Pathology and the College of American Pathologists

Life-Threatening Docetaxel Toxicity in a Patient With Reduced-Function CYP3A Variants: A Case Report

PharmVar Tutorial on CYP2D6 Structural Variation Testing and Recommendations on Reporting

Analytical Validation of a Computational Method for Pharmacogenetic Genotyping from Clinical Whole Exome Sequencing

Computational pharmacogenotype extraction from clinical next-generation sequencing

Characterization of Reference Materials for CYP3A4 and CYP3A5: A (GeT-RM) Collaborative Project

Pharmacokinetic modeling of R and S‐Methadone and their metabolites to study the effects of various covariates in post‐operative children

Metformin pharmacogenomics: a genome-wide association study to identify genetic and epigenetic biomarkers involved in metformin anticancer response using human lymphoblastoid cell lines

P237: A de novo gain-of-function ANO5 variant in a patient with anoctaminopathy5-related muscular dystrophy challenges the skeletal/muscular phenotype dichotomy into question

Association of QT interval-prolonging drugs with clinical trial eligibility in patients with advanced cancer

P535: The undiagnosed rare disease clinic program of Indiana University: Lessons learned from the first 100 patients enrolled (Phase-I pilot)

The novel function of tumor protein D54 in regulating pyruvate dehydrogenase and metformin cytotoxicity in breast cancer

Clinical Opportunities for Germline Pharmacogenetics and Management of Drug-Drug Interactions in Patients With Advanced Solid Cancers

Lambda waves and occipital generators

ASCPT News

eP373: Analytical validation of a computational method for pharmacogenetic genotyping from clinical exome sequencing

Abstract P1-08-02: Cytochrome P450 reductase gene , POR, associated with paclitaxel induced peripheral neuropathy in patients of European ancestry from the adjuvant breast cancer trial, ECOG-ACRIN E5103

CYP3A4 and CYP3A5 Genotyping Recommendations

Characterization of Reference Materials for CYP3A4 and CYP3A5

Recommendations for Clinical CYP2D6 Genotyping Allele Selection

Metformin Pharmacogenomics: Functional Genomics of CDC25b and TPD54 Regulation of Metformin Anticancer Response in Breast Cancer

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