Mia Wadelius
Professor at Department of Medical Sciences; Clinical pharmacogenomics and osteoporosis
- Telephone:
- +46 18 611 49 45
- Fax:
- +46 18 611 37 03
- E-mail:
- Mia.Wadelius@medsci.uu.se
- Visiting address:
- Akademiska sjukhuset, ingång 61
- Postal address:
- Akademiska sjukhuset, ingång 61
751 85 Uppsala

Publications
Recent publications
Genome-wide association study of myocarditis and pericarditis following COVID-19 vaccination
Part of npj Vaccines, 2025
- DOI for Genome-wide association study of myocarditis and pericarditis following COVID-19 vaccination
- Download full text (pdf) of Genome-wide association study of myocarditis and pericarditis following COVID-19 vaccination
Part of Critical reviews in oncology/hematology, 2025
- DOI for Pharmacogenomics in pediatric oncology patients with solid tumors related to chemotherapy-induced toxicity: A systematic review
- Download full text (pdf) of Pharmacogenomics in pediatric oncology patients with solid tumors related to chemotherapy-induced toxicity: A systematic review
Genome-wide association study of direct oral anticoagulants and their relation to bleeding
Part of European Journal of Clinical Pharmacology, p. 771-783, 2025
- DOI for Genome-wide association study of direct oral anticoagulants and their relation to bleeding
- Download full text (pdf) of Genome-wide association study of direct oral anticoagulants and their relation to bleeding
Whole genome case-control study of central nervous system toxicity due to antimicrobial drugs
Part of PLOS ONE, 2024
- DOI for Whole genome case-control study of central nervous system toxicity due to antimicrobial drugs
- Download full text (pdf) of Whole genome case-control study of central nervous system toxicity due to antimicrobial drugs
Part of Genes, Chromosomes and Cancer, 2024
- DOI for Precision Diagnostics in Myeloid Malignancies: Development and Validation of a National Capture‐Based Gene Panel
- Download full text (pdf) of Precision Diagnostics in Myeloid Malignancies: Development and Validation of a National Capture‐Based Gene Panel
All publications
Articles in journal
Genome-wide association study of myocarditis and pericarditis following COVID-19 vaccination
Part of npj Vaccines, 2025
- DOI for Genome-wide association study of myocarditis and pericarditis following COVID-19 vaccination
- Download full text (pdf) of Genome-wide association study of myocarditis and pericarditis following COVID-19 vaccination
Genome-wide association study of direct oral anticoagulants and their relation to bleeding
Part of European Journal of Clinical Pharmacology, p. 771-783, 2025
- DOI for Genome-wide association study of direct oral anticoagulants and their relation to bleeding
- Download full text (pdf) of Genome-wide association study of direct oral anticoagulants and their relation to bleeding
Whole genome case-control study of central nervous system toxicity due to antimicrobial drugs
Part of PLOS ONE, 2024
- DOI for Whole genome case-control study of central nervous system toxicity due to antimicrobial drugs
- Download full text (pdf) of Whole genome case-control study of central nervous system toxicity due to antimicrobial drugs
Part of Genes, Chromosomes and Cancer, 2024
- DOI for Precision Diagnostics in Myeloid Malignancies: Development and Validation of a National Capture‐Based Gene Panel
- Download full text (pdf) of Precision Diagnostics in Myeloid Malignancies: Development and Validation of a National Capture‐Based Gene Panel
Autoantibodies to protein S may explain rare cases of coagulopathy following COVID-19 vaccination
Part of Scientific Reports, 2024
- DOI for Autoantibodies to protein S may explain rare cases of coagulopathy following COVID-19 vaccination
- Download full text (pdf) of Autoantibodies to protein S may explain rare cases of coagulopathy following COVID-19 vaccination
Part of Journal of Bone and Mineral Research, p. 1315-1326, 2024
- DOI for Gene-based association analysis of a large patient cohort provides insights into genetics of atypical femur fractures
- Download full text (pdf) of Gene-based association analysis of a large patient cohort provides insights into genetics of atypical femur fractures
Autoantibodies to protein S may explain rare cases of coagulopathy following COVID-19 vaccination
Part of Scientific Reports, 2024
No link between type I interferon autoantibody positivity and adverse reactions to COVID-19 vaccines
Part of NPJ VACCINES, 2024
- DOI for No link between type I interferon autoantibody positivity and adverse reactions to COVID-19 vaccines
- Download full text (pdf) of No link between type I interferon autoantibody positivity and adverse reactions to COVID-19 vaccines
Meta-analysis of ACE inhibitor-induced angioedema identifies novel risk locus
Part of Journal of Allergy and Clinical Immunology, p. 1073-1082, 2024
Identification of risk factors for adverse drug reactions in a pharmacovigilance database
Part of Pharmacoepidemiology and Drug Safety, 2024
Whole genome case-control study of central nervous system toxicity due to antimicrobial drugs
Part of PLOS ONE, 2024
- DOI for Whole genome case-control study of central nervous system toxicity due to antimicrobial drugs
- Download full text (pdf) of Whole genome case-control study of central nervous system toxicity due to antimicrobial drugs
Identification of risk factors for adverse drug reactions in a pharmacovigilance database
Part of Pharmacoepidemiology and Drug Safety, p. 1431-1438, 2023
- DOI for Identification of risk factors for adverse drug reactions in a pharmacovigilance database
- Download full text (pdf) of Identification of risk factors for adverse drug reactions in a pharmacovigilance database
Narcolepsy risk loci outline role of T cell autoimmunity and infectious triggers in narcolepsy
Part of Nature Communications, 2023
- DOI for Narcolepsy risk loci outline role of T cell autoimmunity and infectious triggers in narcolepsy
- Download full text (pdf) of Narcolepsy risk loci outline role of T cell autoimmunity and infectious triggers in narcolepsy
Part of Pharmacogenomics (London), p. 813-820, 2022
- DOI for Genome-wide association study of liver enzyme elevation in an extended cohort of rheumatoid arthritis patients starting low-dose methotrexate
- Download full text (pdf) of Genome-wide association study of liver enzyme elevation in an extended cohort of rheumatoid arthritis patients starting low-dose methotrexate
HLA variants associated with azathioprine-induced pancreatitis in patients with Crohn's disease
Part of Clinical and Translational Science, p. 1249-1256, 2022
- DOI for HLA variants associated with azathioprine-induced pancreatitis in patients with Crohn's disease
- Download full text (pdf) of HLA variants associated with azathioprine-induced pancreatitis in patients with Crohn's disease
Part of Frontiers in Genetics, 2022
- DOI for Genetic determinants of apixaban plasma levels and their relationship to bleeding and thromboembolic events
- Download full text (pdf) of Genetic determinants of apixaban plasma levels and their relationship to bleeding and thromboembolic events
Implementing precision medicine in a regionally organized healthcare system in Sweden.
Part of Nature Medicine, p. 1980-1982, 2022
Part of Frontiers in Genetics, 2022
- DOI for Molecular Genetic Screening in Patients With ACE Inhibitor/Angiotensin Receptor Blocker-Induced Angioedema to Explore the Role of Hereditary Angioedema Genes
- Download full text (pdf) of Molecular Genetic Screening in Patients With ACE Inhibitor/Angiotensin Receptor Blocker-Induced Angioedema to Explore the Role of Hereditary Angioedema Genes
Part of Clinical Pharmacology and Therapeutics, p. 1007-1021, 2022
Part of Pharmacogenomics (London), p. 973-982, 2021
- DOI for Genome-wide association study of liver enzyme elevation in rheumatoid arthritis patients starting methotrexate
- Download full text (pdf) of Genome-wide association study of liver enzyme elevation in rheumatoid arthritis patients starting methotrexate
Part of Journal of the American College of Cardiology, p. 696-709, 2021
Pharmacogenetics of angiotensin-converting enzyme inhibitor-induced angioedema
Part of Pharmacogenomics (London), p. 319-321, 2021
Part of Läkartidningen, 2021
Part of Clinical Pharmacology and Therapeutics, p. 662-676, 2021
Part of Clinical Pharmacology and Therapeutics, p. 1125-1135, 2021
- DOI for Genetic Risk Factors in Drug-Induced Liver Injury Due to Isoniazid-Containing Antituberculosis Drug Regimens
- Download full text (pdf) of Genetic Risk Factors in Drug-Induced Liver Injury Due to Isoniazid-Containing Antituberculosis Drug Regimens
Part of The Pharmacogenomics Journal, p. 770-783, 2020
- DOI for Genome-wide association study of angioedema induced by angiotensin-converting enzyme inhibitor and angiotensin receptor blocker treatment.
- Download full text (pdf) of Genome-wide association study of angioedema induced by angiotensin-converting enzyme inhibitor and angiotensin receptor blocker treatment.
Part of Frontiers in Genetics, 2020
- DOI for High-Throughput Sequencing to Investigate Associations Between HLA Genes and Metamizole-Induced Agranulocytosis
- Download full text (pdf) of High-Throughput Sequencing to Investigate Associations Between HLA Genes and Metamizole-Induced Agranulocytosis
Part of Clinical Pharmacology and Therapeutics, p. 1195-1202, 2020
- DOI for Exome sequencing reveals common and rare variants in F5 associated with ACE inhibitor and angiotensin receptor blocker-induced angioedema
- Download full text (pdf) of Exome sequencing reveals common and rare variants in F5 associated with ACE inhibitor and angiotensin receptor blocker-induced angioedema
Genome-Wide Association Study of Metamizole-Induced Agranulocytosis in European Populations
Part of Genes, 2020
- DOI for Genome-Wide Association Study of Metamizole-Induced Agranulocytosis in European Populations
- Download full text (pdf) of Genome-Wide Association Study of Metamizole-Induced Agranulocytosis in European Populations
Part of The Pharmacogenomics Journal, p. 579-585, 2020
- DOI for SWEDEGENE: a Swedish nation-wide DNA sample collection for pharmacogenomic studies of serious adverse drug reactions
- Download full text (pdf) of SWEDEGENE: a Swedish nation-wide DNA sample collection for pharmacogenomic studies of serious adverse drug reactions
Part of Pharmacogenomics (London), p. 337-346, 2020
Part of INTERNATIONAL JOURNAL OF RHEUMATIC DISEASES, p. 1226-1232, 2019
- DOI for Methotrexate treatment in rheumatoid arthritis and elevated liver enzymes: A long-term follow-up of predictors, surveillance, and outcome in clinical practice
- Download full text (pdf) of Methotrexate treatment in rheumatoid arthritis and elevated liver enzymes: A long-term follow-up of predictors, surveillance, and outcome in clinical practice
A Missense Variant in PTPN22 is a Risk Factor for Drug-induced Liver Injury
Part of Gastroenterology, p. 1707-1716, 2019
Part of Clinical Pharmacology and Therapeutics, p. 245-253, 2019
Shared Genetic Risk Factors Across Carbamazepine-Induced Hypersensitivity Reactions
Part of Clinical Pharmacology and Therapeutics, p. 1028-1036, 2019
- DOI for Shared Genetic Risk Factors Across Carbamazepine-Induced Hypersensitivity Reactions
- Download full text (pdf) of Shared Genetic Risk Factors Across Carbamazepine-Induced Hypersensitivity Reactions
Part of PLOS ONE, 2019
- DOI for Pharmacogenomics of statin-related myopathy: Meta-analysis of rare variants from whole-exome sequencing
- Download full text (pdf) of Pharmacogenomics of statin-related myopathy: Meta-analysis of rare variants from whole-exome sequencing
Pandemrix-induced narcolepsy is associated with genes related to immunity and neuronal survival
Part of EBioMedicine, p. 595-604, 2019
- DOI for Pandemrix-induced narcolepsy is associated with genes related to immunity and neuronal survival
- Download full text (pdf) of Pandemrix-induced narcolepsy is associated with genes related to immunity and neuronal survival
A Genome-Wide Association Study of Bisphosphonate-Associated Atypical Femoral Fracture
Part of Calcified Tissue International, p. 51-67, 2019
- DOI for A Genome-Wide Association Study of Bisphosphonate-Associated Atypical Femoral Fracture
- Download full text (pdf) of A Genome-Wide Association Study of Bisphosphonate-Associated Atypical Femoral Fracture
Part of Annals of the Rheumatic Diseases, p. 977-977, 2018
Clinical factors predicting drug-induced liver injury due to flucloxacillin
Part of Drug, Healthcare and Patient Safety, p. 95-101, 2018
- DOI for Clinical factors predicting drug-induced liver injury due to flucloxacillin
- Download full text (pdf) of Clinical factors predicting drug-induced liver injury due to flucloxacillin
Common variation near IRF6 is associated with IFN-beta-induced liver injury in multiple sclerosis
Part of Nature Genetics, p. 1081-+, 2018
Fusidic Acid: A Neglected Risk Factor for Statin-Associated Myopathy
Part of Clinical Medicine Insights, 2018
- DOI for Fusidic Acid: A Neglected Risk Factor for Statin-Associated Myopathy
- Download full text (pdf) of Fusidic Acid: A Neglected Risk Factor for Statin-Associated Myopathy
Sulfasalazine-Induced Agranulocytosis Is Associated With the Human Leukocyte Antigen Locus.
Part of Clinical Pharmacology and Therapeutics, p. 843-853, 2018
- DOI for Sulfasalazine-Induced Agranulocytosis Is Associated With the Human Leukocyte Antigen Locus.
- Download full text (pdf) of Sulfasalazine-Induced Agranulocytosis Is Associated With the Human Leukocyte Antigen Locus.
Assessment of 105 patients with angiotensin converting enzyme-inhibitor induced angioedema eva
Part of Allergy. European Journal of Allergy and Clinical Immunology, p. 415-415, 2018
Part of Basic & Clinical Pharmacology & Toxicology, p. 12-13, 2018
Part of Clinical Pharmacology and Therapeutics, 2018
Part of Hepatology, 2017
Part of Gastroenterology, p. 1078-1089, 2017
A common missense variant of LILRB5 is associated with statin intolerance and myalgia
Part of European Heart Journal, p. 3569-U31, 2017
- DOI for A common missense variant of LILRB5 is associated with statin intolerance and myalgia
- Download full text (pdf) of A common missense variant of LILRB5 is associated with statin intolerance and myalgia
Part of Genome Medicine, 2017
- DOI for Cohort-specific imputation of gene expression improves prediction of warfarin dose for African Americans
- Download full text (pdf) of Cohort-specific imputation of gene expression improves prediction of warfarin dose for African Americans
CKM Glu83Gly Is Associated With Blunted Creatine Kinase Variation, but Not With Myalgia
Part of Circulation, 2017
Preventivt arbete kan minska läkemedelsbiverkningar
Part of Läkartidningen, 2017
Whole exome sequencing in individuals with statin-induced myopathy
Part of Drug Safety, p. 1026-1026, 2017
Assessment of 105 Patients with Angiotensin Converting Enzyme-Inhibitor Induced Angioedema
Part of International Journal of Otolaryngology, 2017
- DOI for Assessment of 105 Patients with Angiotensin Converting Enzyme-Inhibitor Induced Angioedema
- Download full text (pdf) of Assessment of 105 Patients with Angiotensin Converting Enzyme-Inhibitor Induced Angioedema
Part of The Annals of Pharmacotherapy, p. 293-300, 2017
Part of Pharmacogenomics (London), p. 201-213, 2017
- DOI for Genetic variants associated with angiotensin-converting enzyme inhibitor-induced cough: a genome-wide association study in a Swedish population
- Download full text (pdf) of Genetic variants associated with angiotensin-converting enzyme inhibitor-induced cough: a genome-wide association study in a Swedish population
Part of Oral Diseases, p. 477-483, 2017
Part of Multiple Sclerosis Journal, p. 834-836, 2016
Novel regulatory variant detected on the VKORC1 haplotype that is associated with warfarin dose
Part of Pharmacogenomics (London), p. 1305-1314, 2016
- DOI for Novel regulatory variant detected on the VKORC1 haplotype that is associated with warfarin dose
- Download full text (pdf) of Novel regulatory variant detected on the VKORC1 haplotype that is associated with warfarin dose
Part of Pharmacogenomics (London), p. 1425-1439, 2016
- DOI for Genetic determinants of warfarin maintenance dose and time in therapeutic treatment range: a RE-LY genomics substudy
- Download full text (pdf) of Genetic determinants of warfarin maintenance dose and time in therapeutic treatment range: a RE-LY genomics substudy
Cost-effectiveness of pharmacogenetic-guided dosing of warfarin in the United Kingdom and Sweden
Part of The Pharmacogenomics Journal, p. 478-484, 2016
Part of The Lancet Diabetes and Endocrinology, p. 507-516, 2016
Part of BMC Medical Informatics and Decision Making, 2015
- DOI for A Bayesian decision support tool for efficient dose individualization of warfarin in adults and children
- Download full text (pdf) of A Bayesian decision support tool for efficient dose individualization of warfarin in adults and children
Genome-wide association study of warfarin maintenance dose in a Brazilian sample
Part of Pharmacogenomics (London), p. 1253-1263, 2015
Part of Thrombosis Research, p. 69-75, 2015
Part of Journal of Clinical Oncology, p. 1031-1039, 2014
Part of Clinical Pharmacology and Therapeutics, p. 423-428, 2014
Genotype-Guided Dosing of Vitamin K Antagonists REPLY
Part of New England Journal of Medicine, p. 1764-1765, 2014
Patients Benefit From Genetics-Guided Coumarin Anticoagulant Therapy
Part of Clinical Pharmacology and Therapeutics, p. 15-17, 2014
Part of The Pharmacogenomics Journal, p. 424-431, 2014
Part of Current drug metabolism, p. 209-217, 2014
Waran doseras bättre efter genanalys
Part of Läkartidningen, p. 22-22, 2014
Warfarin pharmacogenetics: it matters if you're black or white
Part of Blood, p. 2171-2171, 2014
Characterising variability in warfarin dose requirements in children using modelling and simulation
Part of British Journal of Clinical Pharmacology, p. 158-169, 2013
A Randomized Trial of Genotype-Guided Dosing of Warfarin
Part of New England Journal of Medicine, p. 2294-2303, 2013
A Randomized Trial of Genotype-Guided Dosing of Acenocoumarol and Phenprocoumon
Part of New England Journal of Medicine, p. 2304-2312, 2013
Part of Circulation, p. 2710-2711, 2013
Part of European Journal of Clinical Pharmacology, p. 1275-1283, 2013
- DOI for Warfarin dose prediction in children using pharmacometric bridging: comparison with published pharmacogenetic dosing algorithms
- Download full text (pdf) of Warfarin dose prediction in children using pharmacometric bridging: comparison with published pharmacogenetic dosing algorithms
Genetic Determinants of Dabigatran Plasma Levels and Their Relation to Bleeding
Part of Circulation, p. 1404, 2013
Part of Clinical Pharmacology and Therapeutics, 2013
Part of The Lancet, p. 790-796, 2013
Part of Läkartidningen, p. 951-952, 2013
Part of Thrombosis and Haemostasis, p. 232-240, 2012
Part of Molecular Medicine, p. 1466-1472, 2012
Warfarin dose prediction in children using pharmacogenetics information
Part of British Journal of Haematology, p. 106-109, 2012
Part of Pharmacogenetics & Genomics, p. 152-158, 2012
Part of Clinical Pharmacology and Therapeutics, p. 112-117, 2012
Pharmacogenomics and personalized medicine: the plunge into next-generation sequencing
Part of Genome Medicine, p. 78, 2011
Part of The Pharmacogenomics Journal, p. 61-71, 2011
Genotyping for CYP2C9 and VKORC1 alleles by a novel point of care assay with HyBeacon® probes
Part of Clinica Chimica Acta, p. 2063-2069, 2011
Part of Clinical Pharmacology and Therapeutics, p. 701-706, 2011
Part of Blood, p. 3827-3834, 2010
Part of Clinical Pharmacology and Therapeutics, p. 727-734, 2010
Part of Pharmacogenomics (London), p. 989-1002, 2010
Integration of genetic, clinical, and INR data to refine warfarin dosing
Part of Clinical Pharmacology and Therapeutics, p. 572-578, 2010
Part of PLoS genetics, 2009
The largest prospective warfarin-treated cohort supports genetic forecasting
Part of Blood, p. 784-792, 2009
Part of Clinical Chemistry, p. 804-812, 2009
POINT: Use of Pharmacogenetics in Guiding Treatment with Warfarin
Part of Clinical Chemistry, p. 709-711, 2009
Part of Pharmacogenomics (London), p. 1687-1695, 2009
Gene polymorphism influencing treatment response in psychotic patients in a naturalistic setting
Part of Journal of Psychiatric Research, p. 884-893, 2008
Warfarin-noscapine interaction: a series of four case reports
Part of The Annals of Pharmacotherapy, p. 448-450, 2008
Part of Journal of Thrombosis and Haemostasis, p. 1038-1040, 2008
Part of Human and Experimental Toxicology, p. 65-71, 2008
Part of Clinical Pharmacology and Therapeutics, p. 529-538, 2007
Placental transfer of quetiapine in relation to P-glycoprotein activity
Part of Journal of Psychopharmacology, p. 751-756, 2007
Association of warfarin dose with genes involved in its action and metabolism
Part of Human Genetics, p. 23-34, 2007
Possible fluconazole-fentanyl interaction: a case report
Part of European Journal of Clinical Pharmacology, p. 491-2, 2006
Common VKORC1 and GGCX polymorphisms associated with warfarin dose
Part of The Pharmacogenomics Journal, p. 262-70, 2005
Warfarin dose related to apolipoprotein E (APOE) genotype
Part of European Journal of Clinical Pharmacology, p. 381-8, 2005
Gamma-glutamyl carboxylase (GGCX) microsatellite and warfarin dosing
Part of Blood, p. 3673-4, 2005
Apolipoprotein E (APOE) and warfarin dosing in an Italian population
Part of European Journal of Clinical Pharmacology, p. 781-3, 2005
Functional role of P-glycoprotein in the human blood-placental barrier
Part of Clinical Pharmacology and Therapeutics, p. 123-31, 2005
CYP2D6 genotypes and depressive symptoms during late pregnancy and postpartum
Part of Nordic Journal of Psychiatry, p. 61-4, 2004
Part of BMC Blood Disorders, p. 5, 2004
Warfarin sensitivity related to CYP2C9, CYP3A5, ABCB1 (MDR1) and other factors
Part of The Pharmacogenomics Journal, p. 40-8, 2004
Gene expression of cytochrome P450 1B1 and 2D6 in leukocytes in human pregnancy
Part of Pharmacology and Toxicology, p. 295-9, 2003
Cytochrome P450 genotyping by multiplexed real-time DNA sequencing with Pyrosequencing TM technology
Part of Assay and drug development technologies, p. 49-59, 2002
5alfa-reductase 2 polymorphisms as risk factors in prostate cancer
Part of Pharmacogenetics, p. 307-12, 2002
Polymorphisms of NAT2 in relation to sulphasalazine-induced agranulocytosis
Part of Pharmacogenetics, p. 35-41, 2000
Prostate cancer associated with CYP17 genotype
Part of Pharmacogenetics, p. 635-9, 1999
Polymorphisms in NAT2, CYP2D6, CYP2C19 and GSTP1 and their association with prostate cancer
Part of Pharmacogenetics, p. 333-40, 1999
Part of Journal of Medical Genetics, p. 758-60, 1997
Induction of CYP2D6 in pregnancy
Part of Clinical Pharmacology and Therapeutics, p. 400-7, 1997
Lamotrigine and toxic epidermal necrolysis
Part of The Lancet, p. 1041, 1996
Articles, review/survey
Part of Critical reviews in oncology/hematology, 2025
- DOI for Pharmacogenomics in pediatric oncology patients with solid tumors related to chemotherapy-induced toxicity: A systematic review
- Download full text (pdf) of Pharmacogenomics in pediatric oncology patients with solid tumors related to chemotherapy-induced toxicity: A systematic review
Technological readiness and implementation of genomic-driven precision medicine for complex diseases
Part of Journal of Internal Medicine, p. 602-620, 2021
- DOI for Technological readiness and implementation of genomic-driven precision medicine for complex diseases
- Download full text (pdf) of Technological readiness and implementation of genomic-driven precision medicine for complex diseases
Part of Läkartidningen, 2021
Part of The Pharmacogenomics Journal, p. 306-319, 2020
Part of Clinical Pharmacology and Therapeutics, p. 397-404, 2017
- DOI for Clinical Pharmacogenetics Implementation Consortium (CPIC) Guideline for Pharmacogenetics-Guided Warfarin Dosing: 2017 Update
- Download full text (pdf) of Clinical Pharmacogenetics Implementation Consortium (CPIC) Guideline for Pharmacogenetics-Guided Warfarin Dosing: 2017 Update
Part of Cardiovascular Therapeutics, p. 297-307, 2016
Oral anticoagulation: a critique of recent advances and controversies
Part of TIPS - Trends in Pharmacological Sciences, p. 153-163, 2015
Part of Clinical Pharmacology and Therapeutics, p. 477-481, 2014
- DOI for Phenotype Standardization of Angioedema in the Head and Neck Region Caused by Agents Acting on the Angiotensin System
- Download full text (pdf) of Phenotype Standardization of Angioedema in the Head and Neck Region Caused by Agents Acting on the Angiotensin System
Phenotype Standardization for Statin-Induced Myotoxicity
Part of Clinical Pharmacology and Therapeutics, p. 470-476, 2014
- DOI for Phenotype Standardization for Statin-Induced Myotoxicity
- Download full text (pdf) of Phenotype Standardization for Statin-Induced Myotoxicity
Part of Expert Opinion on Drug Safety, p. 1305-1317, 2014
Pharmacogenetics-based warfarin dosing in children
Part of Pharmacogenomics (London), p. 361-374, 2014
Part of Pharmacogenomics (London), p. 1405-1417, 2012
Prediction of warfarin dose: why, when and how?
Part of Pharmacogenomics (London), p. 429-440, 2012
Part of Pharmacogenomics (London), p. 113-124, 2011
Part of Clinical Pharmacology and Therapeutics, p. 625-629, 2011
Pharmacogenetics of warfarin: current status and future challenges
Part of The Pharmacogenomics Journal, p. 99-111, 2007
Chapters in book
Part of Tietz Textbook of Laboratory Medicine, 7th Edition, Elsevier, 2022
Part of Tietz Fundamentals of Clinical Chemistry, 8th edition, Elsevier, 2018
Part of Tietz Textbook of Clinical Chemistry and Molecular Diagnostics, 6th edition, Elsevier, 2017