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Chapman, M. A., M. S. Lawrence, J. J. Keats, K. Cibulskis, C. Sougnez, A. C. Schinzel, C. L. Harview, et al. 2011. “Initial Genome Sequencing and Analysis of Multiple Myeloma”. Nature 471: 467-72.

Chapuy, B., M. G. Roemer, C. Stewart, Y. Tan, R. P. Abo, L. Zhang, A. J. Dunford, et al. 2016. “Targetable Genetic Features of Primary Testicular and Primary Central Nervous System Lymphomas”. Blood 127: 869-81.

Chattopadhyay, S., A. L. Stewart, S. Mukherjee, C. Huang, K. A. Hartwell, P. G. Miller, R. Subramanian, et al. 2015. “Niche-Based Screening in Multiple Myeloma Identifies a Kinesin-5 Inhibitor With Improved Selectivity over Hematopoietic Progenitors”. Cell Rep 10: 755-70.

Corsello, S. M., J. A. Bittker, Z. Liu, J. Gould, P. McCarren, J. E. Hirschman, S. E. Johnston, et al. 2017. “The Drug Repurposing Hub: A Next-Generation Drug Library and Information Resource”. Nat Med 23: 405-8.

Corsello, S. M., G. Roti, K. N. Ross, K. T. Chow, I. Galinsky, D. J. DeAngelo, R. M. Stone, A. L. Kung, T. R. Golub, and K. Stegmaier. 2009. “Identification of AML1-ETO Modulators by Chemical Genomics”. Blood 113: 6193-205.

Ding, Z., C. J. Wu, G. C. Chu, Y. Xiao, D. Ho, J. Zhang, S. R. Perry, et al. 2011. “SMAD4-Dependent Barrier Constrains Prostate Cancer Growth and Metastatic Progression”. Nature 470: 269-73.

Dulak, A. M., P. Stojanov, S. Peng, M. S. Lawrence, C. Fox, C. Stewart, S. Bandla, et al. 2013. “Exome and Whole-Genome Sequencing of Esophageal Adenocarcinoma Identifies Recurrent Driver Events and Mutational Complexity”. Nat Genet 45: 478-86.

Heyne, Henrike, David Baez-Nieto, Sumaiya Iqbal, Duncan Palmer, Andreas Brunklaus, Patrick May, Epi25 Collaborative, et al. 2020. “Predicting Functional Effects of Missense Variants in Voltage-Gated Sodium and Calcium Channels”. Science Translational Medicine 12 (556).

Ghoshal, Ayan, David Uygun, Lingling Yang, James McNally, Violeta Lopez-Huerta, Mario Arias-Garcia, David Baez-Nieto, et al. 2020. “Effects of a Patient-Derived de Novo Coding Alteration of CACNA1I in Mice Connect a Schizophrenia Risk Gene With Sleep Spindle Deficits”. Translational Psychiatry 10 (1): 1–12.