Julie Law, M.D.
Health Sciences Assistant Clinical Professor
To see if Julie Law is accepting new patients, or for assistance finding a UC Davis doctor, please call 800-2-UCDAVIS (800-282-3284).
Locations and Contact
Philosophy of Care
I am honored to work with you and your child. As a doctor, I believe in building strong relationships based on trust, compassion, and truly getting to know my patients. I am here to listen to your concerns so that we can work together. My goal is to help you feel empowered to support your child's growth and long-term success.
Clinical Interests
Dr. Law is a developmental and behavioral pediatrician specializing in the care of children and adolescents with a variety of neurodevelopmental conditions including developmental delay, autism, attention deficit hyperactivity disorder (ADHD), anxiety, learning disabilities, Fetal Alcohol Spectrum Disorder (FASD), intellectual disability, and genetic conditions. She has a special clinical interest in FASD.
Research/Academic Interests
Dr. Law's research focuses on improving knowledge and medical care for FASD through collaborative partnerships.
Division
Child Development and Behavior
Undergraduate School
B.S., Science, Portland State University, 2006
Undergraduate School
B.S., Architecture, University of Michigan, 2003
Medical School
M.D., Medicine, Oregon Health & Science University, 2010
Internship
Pediatrics, UC Davis Medical Center, 2010-2011
Residency
Pediatrics, UC Davis Medical Center, 2011-2013
Fellowship
Developmental-Behavioral Pediatrics, UC Davis MIND Institute, 2023-2026
People’s Choice Award, UC Davis MIND Institute, 2025,
Fellow Scholarship Grant Award, UC Davis Department of Pediatrics, 2025,
Community Access to Child Health (CATCH) Implementation Grant, American Academy of Pediatrics, 2024,
Winarni, T. I., Aishworiya, R., Culpepper, H., Zafarullah, M., Mendoza, G., Wilaisakditipakorn, T. J., Likhitweerawong, N., Law, J., Hagerman, R., & Tassone, F. (2025). In Utero Alcohol and Unsuitable Home Environmental Exposure Combined with FMR1 Full Mutation Allele Cause Severe Fragile X Syndrome Phenotypes. International Journal of Molecular Sciences, 26(7), 2840. https://doi.org/10.3390/ijms26072840