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Initial genome sequencing and analysis of multiple myeloma

Publication: Journal Article

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.

Publication: Journal Article

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.

Publication: Journal Article

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.

Publication: Journal Article

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.

Publication: Journal Article

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.

Publication: Journal Article

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.

Publication: Journal Article

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.

Publication: Journal Article

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).

Publication: Journal Article

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.

Publication: Journal Article

Andrade, Hope, Allen, Yorgan, Lipscombe, and JQ Pan. 2016. “A Rare Schizophrenia Risk Variant of CACNA1I Disrupts Ca V 3.3 Channel Activity”. Scientific Reports 6 (1): 1–13.