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Maury, Eduardo A., Maxwell A. Sherman, Giulio Genovese, Thomas G. Gilgenast, Prashanth Rajarajan, Erin Flaherty, Schahram Akbarian, et al. 2023. “Schizophrenia-Associated Somatic Copy Number Variants from 12,834 Cases Reveal Contribution to Risk and Recurrent, Isoform-Specific NRXN1 Disruptions”. Cell Genomics 3 (8).

Choudhury*, Sangita, August Yue Huang*, Kim, Zhou, Morillo, EA Maury, JW Tsai, et al. 2022. “Somatic Mutations in Single Human Cardiomyocytes Reveal Age-Associated DNA Damage and Widespread Genotoxicity”. Nature Aging 2 (8): 714-25.

Zhao, Boxun, Jill A. Madden, Jasmine Lin, Gerard T. Berry, Monica H. Wojcik, Xuefang Zhao, Harrison Brand, Michael Talkowski, Eunjung Alice Lee**, and Pankaj B. Agrawal**. 2022. “A Neurodevelopmental Disorder Caused by a Novel de Novo SVA Insertion in Exon 13 of the SRCAP Gene.”. European Journal of Human Genetics 30 (9): 1083-87.

Bourseguin, Julie, Wen Cheng, Emily Talbot, Liana Hardy, Jenny Lai, Ailsa Jeffries, Michael Lodato, Eunjung Alice Lee, and Svetlana Khoronenkova. 2022. “Persistent DNA Damage Associated With ATM Kinase Deficiency Promotes Microglial Dysfunction”. Nucleic Acids Research 50 (5): 2700-2718.