Christopher W. Bartlett
Neuroscience · The Ohio State University
Publications
99
Citations
3,388
Est. group size
~4
Recurring co-author estimate
Active years
26
Publishing since 2001
Christopher W. Bartlett studies the genetics underlying autism spectrum disorder, language and reading disorders, and related neurodevelopmental conditions, often examining how genetic risk factors overlap between conditions like autism and ADHD. His work combines genetic analysis with statistical and computational methods (such as natural language processing and data harmonization techniques) to study these conditions across large study cohorts. This research could interest students wanting to work at the intersection of genetics, developmental disorders, and quantitative/computational methods.
Publication output has fluctuated over the past decade, with a notable peak in 2022, a gap in 2024, and a resurgence in 2025-2026, suggesting an active but variable publication pace rather than steady linear growth.
Generated by claude-sonnet-5 from public bibliographic data · Jul 20, 2026
- Narrow Versus Broad Phenotype Definitions Affect Genetic Analysis of Language More than Other Broad Autism Phenotype Traits
Genes · 2026
- Development of a rule-based natural language processing algorithm to extract sleep information in pediatric primary care patients with a sleep diagnosis
SLEEP Advances · 2026
- EE523 Human Metapneumovirus (hMPV): Systematic Literature Review of Economic and Humanistic Disease Burden in Adults
Value in Health · 2025
- A Latent Trait-based Measure as a Data Harmonization and Missing Data Solution Applied to the Environmental Influences on Child Health Outcomes Cohort
Epidemiology · 2025
- Narrow Versus Broad Phenotype Definitions Affect Genetic Analysis of Language More Than Other Broad Autism Phenotype Traits
Research Square · 2025
- Rosetta: A Method for Integration of Genetically Informative Studies of Reading Comprehension Development
Scientific Studies of Reading · 2025
- Structural Variations Contribute to the Genetic Etiology of Autism Spectrum Disorder and Language Impairments
International Journal of Molecular Sciences · 2023
- Common genetic risk factors in ASD and ADHD co-occurring families
Human Genetics · 2022
- MicroRNA and MicroRNA-Target Variants Associated with Autism Spectrum Disorder and Related Disorders
Genes · 2022
- Early considerations of genetics in aphasia rehabilitation: a narrative review
Aphasiology · 2022
- Common Genetic Risk Factors in ASD and ADHD Co-occurring Families
medRxiv · 2022
- Predicting with Confidence: A Case-Based Reasoning Framework for Predicting Survival in Breast Cancer
Proceedings of the ... International Florida Artificial Intelligence Research Society Conference · 2021
- Understanding developmental language disorder - the Helsinki longitudinal SLI study (HelSLI): a study protocol
BMC Psychology · 2018
- Applied Predictive Modeling of Coronary Microvascular Disease using Coronary Doppler and Cardiac Echocardiography
The FASEB Journal · 2018
- Behavioral and Molecular Genetics of Reading-Related AM and FM Detection Thresholds
Behavior Genetics · 2016
- Figshare×5
- Genes×3
- npj Health Systems×2
- Journal of the American Medical Informatics Association×2
- bioRxiv (Cold Spring Harbor Laboratory)×2
- Bridgette Kelleher
Neuroscience · Purdue University West Lafayette
- Carolyn E. B. McCormick
Neuroscience · Purdue University West Lafayette
- Kevin G. Stephenson
Neuroscience · The Ohio State University
- Soo Youn Kim
Neuroscience · The Ohio State University
- Wei Siong Neo
Neuroscience · Purdue University West Lafayette
This profile was generated automatically from public scholarly data (OpenAlex). Group size and activity levels are estimates derived from co-authorship patterns.
Last updated Jul 19, 2026.
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