Dr. Christopher W. Bartlett received his PhD in computation neuroscience from Rutgers University and his Masters in Health Administration (MHA) from the University Cincinnati. After a post-doctoral fellowship at the University of Iowa, Dr. Bartlett joined The Ohio State University (OSU) and Nationwide Children's Hospital (NCH) as faculty. He is currently Professor of Pediatrics and Biomedical Informatics at OSU and Principal Investigator with the Institute of Genomic Medicine at NCH. Most recently, Dr. Bartlett was appointed Associate Chief Data Science Officer for biomedical informatics at NCH. Funded by the Wexner Medical Center and the Clinical and Translational Science Institute (CTSI), a CSTA partnership between OSU, The Ohio State University Wexner Medical Center, and NCH, Drs. Bartlett and co-PI Timothy Huerta are developing an OSU/Nationwide clinical data enclave for research.
Recent Publications
- Petrill, SA, Klamer, BG, Buyske, S, Willcutt, EG, Gruen, JR, Francis, DJ, Flax, JF, Brzustowicz, LM, Bartlett, CW. The Rosetta Phenotype Harmonization Method Facilitates Finding a Relationship Quantitative Trait Locus for a Complex Cognitive Trait. Genes (Basel) 2023; 14 (9): . PubMed PMID:37761888 PubMed Central PMC10531321.
- Alibutud, R, Hansali, S, Cao, X, Zhou, A, Mahaganapathy, V, Azaro, M, Gwin, C, Wilson, S, Buyske, S, Bartlett, CW et al.. Structural Variations Contribute to the Genetic Etiology of Autism Spectrum Disorder and Language Impairments. Int J Mol Sci 2023; 24 (17): . PubMed PMID:37686052 PubMed Central PMC10487745.
- Harnish, SM, Diedrichs, VA, Bartlett, CW. EARLY CONSIDERATIONS OF GENETICS IN APHASIA REHABILITATION: A NARRATIVE REVIEW. Aphasiology 2023; 37 (6): 835-853. PubMed PMID:37346093 PubMed Central PMC10281715.
- Bartlett, CW, Bossenbroek, J, Ueyama, Y, McCallinhart, P, Peters, OA, Santillan, DA, Santillan, MK, Trask, AJ, Ray, WC. Invasive or More Direct Measurements Can Provide an Objective Early-Stopping Ceiling for Training Deep Neural Networks on Non-invasive or Less-Direct Biomedical Data. SN Comput Sci 2023; 4 (2): 161. PubMed PMID:36647373 PubMed Central PMC9836982.
- Quinney, SK, Bies, RR, Grannis, SJ, Bartlett, CW, Mendonca, E, Rogerson, CM, Backes, CH, Shah, DK, Tillman, EM, Costantine, MM et al.. The MPRINT Hub Data, Model, Knowledge and Research Coordination Center: Bridging the gap in maternal-pediatric therapeutics research through data integration and pharmacometrics. Pharmacotherapy 2023; 43 (5): 391-402. PubMed PMID:36625779 PubMed Central PMC10192201.
- Zhou, A, Cao, X, Mahaganapathy, V, Azaro, M, Gwin, C, Wilson, S, Buyske, S, Bartlett, CW, Flax, JF, Brzustowicz, LM et al.. Common genetic risk factors in ASD and ADHD co-occurring families. Hum Genet 2023; 142 (2): 217-230. PubMed PMID:36251081 PubMed Central PMC10177627.
- Wong, A, Zhou, A, Cao, X, Mahaganapathy, V, Azaro, M, Gwin, C, Wilson, S, Buyske, S, Bartlett, CW, Flax, JF et al.. MicroRNA and MicroRNA-Target Variants Associated with Autism Spectrum Disorder and Related Disorders. Genes (Basel) 2022; 13 (8): . PubMed PMID:35893067 PubMed Central PMC9329941.
- Bossenbroek, J, Ueyama, Y, McCallinhart, PE, Bartlett, CW, Ray, WC, Trask, AJ. Improvement of automated analysis of coronary Doppler echocardiograms. Sci Rep 2022; 12 (1): 7490. PubMed PMID:35523823 PubMed Central PMC9076637.
- Pavlek, LR, Vudatala, S, Bartlett, CW, Buhimschi, IA, Buhimschi, CS, Rogers, LK. MiR-29b is associated with perinatal inflammation in extremely preterm infants. Pediatr Res 2021; 89 (4): 889-893. PubMed PMID:32386397 PubMed Central PMC7649129.
- Bartlett, CW, Klamer, BG, Buyske, S, Petrill, SA, Ray, WC. Forming Big Datasets through Latent Class Concatenation of Imperfectly Matched Databases Features. Genes (Basel) 2019; 10 (9): . PubMed PMID:31546899 PubMed Central PMC6771148.
