A coding variant in RARG confers susceptibility to anthracycline-induced cardiotoxicity in childhood cancer

F Aminkeng, AP Bhavsar, H Visscher, SR Rassekh… - Nature …, 2015 - nature.com
Anthracyclines are used in over 50% of childhood cancer treatment protocols, but their
clinical usefulness is limited by anthracycline-induced cardiotoxicity (ACT) manifesting as …

Pharmacogenomic prediction of anthracycline-induced cardiotoxicity in children

H Visscher, CJD Ross, SR Rassekh… - Journal of clinical …, 2012 - ascopubs.org
Purpose Anthracycline-induced cardiotoxicity (ACT) is a serious adverse drug reaction
limiting anthracycline use and causing substantial morbidity and mortality. Our aim was to …

Genetic variants in TPMT and COMT are associated with hearing loss in children receiving cisplatin chemotherapy

CJD Ross, H Katzov-Eckert, MP Dubé, B Brooks… - Nature …, 2009 - nature.com
Cisplatin is a widely used and effective chemotherapeutic agent, although its use is
restricted by the high incidence of irreversible ototoxicity associated with it. In children …

Validation of variants in SLC28A3 and UGT1A6 as genetic markers predictive of anthracycline‐induced cardiotoxicity in children

H Visscher, CJD Ross, SR Rassekh… - Pediatric blood & …, 2013 - Wiley Online Library
Background. The use of anthracyclines as effective antineoplastic drugs is limited by the
occurrence of cardiotoxicity. Multiple genetic variants predictive of anthracycline‐induced …

Genetic Variants in SLC22A17 and SLC22A7 are Associated With Anthracycline-Induced Cardiotoxicity in Children

H Visscher, SR Rassekh, GS Sandor… - …, 2015 - Taylor & Francis
Aim: To identify novel variants associated with anthracycline-induced cardiotoxicity and to
assess these in a genotype-guided risk prediction model. Patients & methods: Two cohorts …

HLA‐A* 31: 01 and HLA‐B* 15: 02 as genetic markers for carbamazepine hypersensitivity in children

U Amstutz, CJD Ross… - Clinical …, 2013 - Wiley Online Library
The occurrence of hypersensitivity reactions including rare but life‐threatening Stevens–
Johnson syndrome (SJS) and drug‐induced hypersensitivity syndrome (HSS) limits the use …

Replication of TPMT and ABCC3 Genetic Variants Highly Associated With Cisplatin‐Induced Hearing Loss in Children

K Pussegoda, CJ Ross, H Visscher… - Clinical …, 2013 - Wiley Online Library
Cisplatin is a widely used chemotherapeutic agent for the treatment of solid tumors. A
serious complication of cisplatin treatment is permanent hearing loss. The aim of this study …

Pharmacogenomics strategies to optimize treatments for multiple sclerosis: insights from clinical research

I Grossman, V Knappertz, D Laifenfeld, C Ross… - Progress in …, 2017 - Elsevier
Multiple sclerosis (MS) is a chronic, progressive, disabling disorder characterized by
immune-mediated demyelination, inflammation, and neurodegenerative tissue damage in …

Genetic ancestry plays a central role in population pharmacogenomics

HC Yang, CW Chen, YT Lin, SK Chu - Communications biology, 2021 - nature.com
Recent studies have pointed out the essential role of genetic ancestry in population
pharmacogenetics. In this study, we analyzed the whole-genome sequencing data from The …

Heterogeneity in the distribution of 159 drug-response related SNPs in world populations and their genetic relatedness

T Ahsan, NJ Urmi, AA Sajib - PLoS One, 2020 - journals.plos.org
Interethnic variability in drug response arises from genetic differences associated with drug
metabolism, action and transport. These genetic variations can affect drug efficacy as well as …