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Blood Cancer Journal|March 29, 2025
Carfilzomib prescribing patterns and outcomes for relapsed or refractory multiple myeloma: a real-world analysisSharlene Dong, Rahul Banerjee, Adeel M Khan, et al.
Plos Genetics|June 7, 2008
Genetic identification of a network of factors that functionally interact with the nucleosome remodeling ATPase ISWIGiosalba Burgio, Gaspare La Rocca, Anna Sala, et al.
Scientific Reports|July 25, 2018
Topical Curcumin Nanocarriers are Neuroprotective in Eye DiseaseBenjamin M Davis, Milena Pahlitzsch, Li Guo, et al.
American Journal of Medical Genetics. Part A|January 12, 2026
Binder Phenotype: Evaluating the Utility and Influence of Genetic Results on Parental Decision Making in Antenatally Diagnosed CasesShivangini Gupta, Dhanashree Kanago, Preetha Tilak, et al.
Nature Communications|February 9, 2021
Biallelic loss of BCMA as a resistance mechanism to CAR T cell therapy in a patient with multiple myelomaMehmet Kemal Samur, Mariateresa Fulciniti, Anil Aktas Samur, et al.
American Journal of Hematology|December 6, 2019
Increased mitochondrial apoptotic priming with targeted therapy predicts clinical response to re-induction chemotherapyJacqueline S Garcia, Shruti Bhatt, Geoffrey Fell, et al.
Biorxiv : the Preprint Server for Biology|June 12, 2026
Distinct Proteasomal Pathways Drive Oncogenic PPM1D ActivationNi Yan, Deumaya Shrestha, Cameron Schluter, et al.
European Journal of Medical Genetics|February 21, 2023
Proband only exome sequencing in 403 Indian children with neurodevelopmental disorders: Diagnostic yield, utility and challenges in a resource-limited settingRayabarapu Pranav Chand, Wankhede Vinit, Varsha Vaidya, et al.
Cureus|June 21, 2023
Epidemiology, Trends, Utilization Disparities, and Outcomes of Catheter Ablation and Its Association With Coronary Vasospasm Amongst Patients With Non-valvular Atrial Fibrillation: A Nationwide Burden of Last DecadeSiva Naga S Yarrarapu, Parth Shah, Beshoy Iskander, et al.
Leukemia|November 18, 2025
Putative multiple myeloma susceptibility genes identified by exome sequencing of 347 familial and early-onset casesMaroulio Pertesi, Delphine Demangel, Abhishek Niroula, et al.
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