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Frontiers in Pharmacology|January 26, 2023
Genome-wide analyses of platinum-induced ototoxicity in childhood cancer patients: Results of GO-CAT and United Kingdom MAGIC consortiaEvelien G E Hurkmans, Marije J Klumpers, Cinzia Dello Russo, et al.
The European Respiratory Journal|December 11, 2020
Genome-wide association study of asthma exacerbations despite inhaled corticosteroid useNatalia Hernandez-Pacheco, Susanne J Vijverberg, Esther Herrera-Luis, et al.
Nature Medicine|January 19, 2023
The impact of the COVID-19 pandemic on cardiovascular disease prevention and managementCaroline E Dale, Rohan Takhar, Raymond Carragher, et al.
The Pharmacogenomics Journal|July 25, 2020
Correction: Pharmacogenomic associations of adverse drug reactions in asthma: systematic review and research prioritizationCharlotte King, Amanda McKenna, Niloufar Farzan, et al.
The Pharmacogenomics Journal|January 18, 2020
Pharmacogenomic associations of adverse drug reactions in asthma: systematic review and research prioritisationCharlotte King, Amanda McKenna, Niloufar Farzan, et al.
Journal of Hepatology|October 17, 2021
A genetic risk score and diabetes predict development of alcohol-related cirrhosis in drinkersJohn B Whitfield, Tae-Hwi Schwantes-An, Rebecca Darlay, et al.
Clinical Pharmacology and Therapeutics|June 24, 2025
Pharmacogenetic Implementation Studies-Lessons Learned From the PREPARE StudyHenk-Jan Guchelaar, Cathelijne H van der Wouden, Lisanne E N Manson, et al.
Hepatology Communications|May 10, 2024
A polygenic risk score for alcohol-associated cirrhosis among heavy drinkers with European ancestryTae-Hwi Schwantes-An, John B Whitfield, Guruprasad P Aithal, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology|January 31, 2019
Genome-wide association study of inhaled corticosteroid response in admixed children with asthmaNatalia Hernandez-Pacheco, Niloufar Farzan, Ben Francis, et al.
Plos One|June 27, 2019
Pharmacogenomics of statin-related myopathy: Meta-analysis of rare variants from whole-exome sequencingJames S Floyd, Katarzyna M Bloch, Jennifer A Brody, et al.
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