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Mia Wadelius

Showing results (71-80 of 92) with videos related to

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Genes, Chromosomes & Cancer|July 20, 2024
Precision Diagnostics in Myeloid Malignancies: Development and Validation of a National Capture-Based Gene PanelChristina Orsmark-Pietras, Anna Lyander, Claes Ladenvall, et al.
Pharmacogenomics|July 7, 2010
A systematic review of cost-effectiveness analyses of pharmacogenetic-guided dosing in treatment with coumarin derivativesTalitha I Verhoef, William K Redekop, Josep Darba, et al.
Blood|March 6, 2010
Warfarin pharmacogenetics: a single VKORC1 polymorphism is predictive of dose across 3 racial groupsNita A Limdi, Mia Wadelius, Larisa Cavallari, et al.
The New England Journal of Medicine|November 21, 2013
A randomized trial of genotype-guided dosing of acenocoumarol and phenprocoumonTalitha I Verhoef, Georgia Ragia, Anthonius de Boer, et al.
Pharmacogenomics|April 2, 2026
The 8th European Society of Pharmacogenomics and Personalized Therapy (ESPT) congressRon H N van Schaik, Jesse J Swen, Adrián Llerena, et al.
Clinical Pharmacology and Therapeutics|February 13, 2022
The Clinical Pharmacogenetics Implementation Consortium Guideline for SLCO1B1, ABCG2, and CYP2C9 genotypes and Statin-Associated Musculoskeletal SymptomsRhonda M Cooper-DeHoff, Mikko Niemi, Laura B Ramsey, et al.
Nature Genetics|July 18, 2018
Common variation near IRF6 is associated with IFN-β-induced liver injury in multiple sclerosisKaarina Kowalec, Galen E B Wright, Britt I Drögemöller, et al.
Clinical Pharmacology and Therapeutics|June 5, 2020
Exome Sequencing Reveals Common and Rare Variants in F5 Associated With ACE Inhibitor and Angiotensin Receptor Blocker-Induced AngioedemaCyrielle Maroteau, Moneeza Kalhan Siddiqui, Abirami Veluchamy, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|August 10, 2024
Gene-based association analysis of a large patient cohort provides insights into genetics of atypical femur fracturesWei Zhou, Joel Ås, Catherine Shore-Lorenti, et al.
European Heart Journal|October 12, 2017
A common missense variant of LILRB5 is associated with statin intolerance and myalgiaMoneeza K Siddiqui, Cyrielle Maroteau, Abirami Veluchamy, et al.
Pageof 10

Showing results (71-80 of 92) with videos related to

Sort By:
Pageof 10
Genes, Chromosomes & Cancer|July 20, 2024
Precision Diagnostics in Myeloid Malignancies: Development and Validation of a National Capture-Based Gene PanelChristina Orsmark-Pietras, Anna Lyander, Claes Ladenvall, et al.
Pharmacogenomics|July 7, 2010
A systematic review of cost-effectiveness analyses of pharmacogenetic-guided dosing in treatment with coumarin derivativesTalitha I Verhoef, William K Redekop, Josep Darba, et al.
Blood|March 6, 2010
Warfarin pharmacogenetics: a single VKORC1 polymorphism is predictive of dose across 3 racial groupsNita A Limdi, Mia Wadelius, Larisa Cavallari, et al.
The New England Journal of Medicine|November 21, 2013
A randomized trial of genotype-guided dosing of acenocoumarol and phenprocoumonTalitha I Verhoef, Georgia Ragia, Anthonius de Boer, et al.
Pharmacogenomics|April 2, 2026
The 8th European Society of Pharmacogenomics and Personalized Therapy (ESPT) congressRon H N van Schaik, Jesse J Swen, Adrián Llerena, et al.
Clinical Pharmacology and Therapeutics|February 13, 2022
The Clinical Pharmacogenetics Implementation Consortium Guideline for SLCO1B1, ABCG2, and CYP2C9 genotypes and Statin-Associated Musculoskeletal SymptomsRhonda M Cooper-DeHoff, Mikko Niemi, Laura B Ramsey, et al.
Nature Genetics|July 18, 2018
Common variation near IRF6 is associated with IFN-β-induced liver injury in multiple sclerosisKaarina Kowalec, Galen E B Wright, Britt I Drögemöller, et al.
Clinical Pharmacology and Therapeutics|June 5, 2020
Exome Sequencing Reveals Common and Rare Variants in F5 Associated With ACE Inhibitor and Angiotensin Receptor Blocker-Induced AngioedemaCyrielle Maroteau, Moneeza Kalhan Siddiqui, Abirami Veluchamy, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|August 10, 2024
Gene-based association analysis of a large patient cohort provides insights into genetics of atypical femur fracturesWei Zhou, Joel Ås, Catherine Shore-Lorenti, et al.
European Heart Journal|October 12, 2017
A common missense variant of LILRB5 is associated with statin intolerance and myalgiaMoneeza K Siddiqui, Cyrielle Maroteau, Abirami Veluchamy, et al.
Pageof 10