Brian C. Kavanaugh, Psy.D.
Affiliations: | 2015-2016 | Psychiatry and Human Behavior | Warren Alpert Medical School of Brown University, Providence, RI, United States |
| 2016- | Psychiatry and Human Behavior | Warren Alpert Medical School of Brown University, Providence, RI, United States |
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Parents
Sign in to add mentor| Eric Morrow | post-doc | 2015-2016 | Warren Alpert Medical School of Brown University | |
| (Instructor in Psychiatry at Warren Alpert Medical School of Brown University as of 2016) | ||||
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Publications
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| Kavanaugh BC, Elacio J, Best CR, et al. (2024) Christianson syndrome across the lifespan: genetic mutations and longitudinal study in children, adolescents, and adults. Journal of Medical Genetics |
| Kavanaugh BC, Elacio J, Best CR, et al. (2023) Christianson Syndrome across the Lifespan: An International Longitudinal Study in Children, Adolescents, and Adults. Medrxiv : the Preprint Server For Health Sciences |
| Kavanaugh BC, Gabert T, et al. (2021) Parental age and autism severity in the Rhode Island Consortium for Autism Research and Treatment (RI-CART) study. Autism Research : Official Journal of the International Society For Autism Research |
| Kavanaugh BC, Schremp CA, Jones RN, et al. (2021) Moderators of Age of Diagnosis in > 20,000 Females with Autism in Two Large US Studies. Journal of Autism and Developmental Disorders |
| Lizarraga SB, Ma L, Maguire AM, et al. (2021) Human neurons from Christianson syndrome iPSCs reveal mutation-specific responses to rescue strategies. Science Translational Medicine. 13 |
| Moreno-De-Luca D, Kavanaugh BC, Best CR, et al. (2020) Clinical Genetic Testing in Autism Spectrum Disorder in a Large Community-Based Population Sample. Jama Psychiatry |
| McCormick CEB, Kavanaugh BC, Sipsock D, et al. (2020) Autism Heterogeneity in a Densely Sampled U.S. Population: Results From the First 1,000 Participants in the RI-CART Study. Autism Research : Official Journal of the International Society For Autism Research |
| Ouyang Q, Kavanaugh BC, Joesch-Cohen L, et al. (2019) GPT2 mutations in autosomal recessive developmental disability: extending the clinical phenotype and population prevalence estimates. Human Genetics |
| Kavanaugh BC, Warren EB, Baytas O, et al. (2019) Longitudinal MRI findings in patient with SLC25A12 pathogenic variants inform disease progression and classification. American Journal of Medical Genetics. Part A |
| Pescosolido MF, Kavanaugh BC, Pochet N, et al. (2019) Complex Neurological Phenotype in Female Carriers of Mutations. Molecular Neuropsychiatry. 5: 98-108 |