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Journal of Personalized Medicine|November 27, 2021
Association between Genetic Variants and Cisplatin-Induced Nephrotoxicity: A Genome-Wide Approach and Validation StudyZulfan Zazuli, Corine de Jong, Wei Xu, et al.
Pediatric Blood & Cancer|March 27, 2026
Novel Genetic Risk Factor Identified for L-Asparaginase-Induced Pancreatitis in Pediatric Patients With CancerEdward J Raack, Wan-Chun Chang, Miguel Cordova-Delgado, et al.
The Journal of Experimental Medicine|July 31, 2025
ASXL1 deficiency causes epigenetic dysfunction, combined immunodeficiency, and EBV-associated lymphomaMaggie P Fu, Mehul Sharma, Pariya Yousefi, et al.
Neurology|December 31, 2017
Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patientsMark McCormack, Hongsheng Gui, Andrés Ingason, et al.
NPJ Precision Oncology|July 15, 2021
TCERG1L allelic variation is associated with cisplatin-induced hearing loss in childhood cancer, a PanCareLIFE studyA J M Meijer, F A Diepstraten, T Langer, et al.
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