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Office
1201 W La Veta Ave
Orange, CA 92868Phone+1 877-734-6618Fax+1 626-413-3663
Summary
- I am a neurogeneticist at UC Irvine medical center. I am board certified in general neurology, medical genetics, and medical biochemical genetics. My interests include rare disease diagnosis, neurogenetic and neurometabolic conditions, and adult inborn metabolic diseases. My aim is to provide a medical home for adults with neurogenetic and metabolic conditions and increase access to precision therapy. In my spare time, I enjoy trying new foods, playing with my dog, and traveling with my family.
Education & Training
- National Institutes of Health Clinical CenterFellowship, Medical Genetics and Genomics, 2020 - 2021
- NIH Clinical CenterMedical Genetics, 2021
- Johns Hopkins University School of MedicineFellowship, Clinical Biochemical Genetics, 2018 - 2020
- National Institutes of Health Clinical CenterFellowship, Medical Genetics and Genomics, 2018 - 2020
- University of ChicagoChief Residency, Neurology, 2017 - 2018
- University of Chicago Medical CenterFellowship, General Internal Medicine and Clinical Medical Ethics, 2017 - 2018
- University of ChicagoResidency, Neurology, 2014 - 2018
- Duke University School of MedicineClass of 2014
- University of California, BerkeleyBA, Biochemistry and molecular biology, Cum Laude, 2006 - 2009
Certifications & Licensure
- CA State Medical License 2022 - 2026
- DC State Medical License 2018 - 2022
- VA State Medical License 2018 - 2019
- IL State Medical License 2017 - 2018
- American Board of Medical Genetics and Genomics Medical Biochemical Genetics
- American Board of Psychiatry and Neurology Neurology
- American Board of Medical Genetics and Genomics Clinical Genetics and Genomics
Publications & Presentations
PubMed
- Considerations for reporting variants in novel candidate genes identified during clinical genomic testing.Jessica X Chong, Seth I Berger, Samantha Baxter, Erica Smith, Changrui Xiao
Genetics in Medicine. 2024-10-01 - 61 citationsFunctional Genomic Analyses of Mendelian and Sporadic Disease Identify Impaired eIF2α Signaling as a Generalizable Mechanism for DystoniaJoseph E. Rittiner, Zachary F. Caffall, Ricardo Hernández-Martínez, Sydney M. Sanderson, James L. Pearson
Neuron. 2016-12-21 - 4 citationsDe novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndrome.Yuyang Chen, Ruebena Dawes, Hyung Chul Kim, Alicia Ljungdahl, Sarah L Stenton
Nature. 2024-08-01
Professional Memberships
- Member
- American College of Medical GeneticsFellow
- Society for Inborn Errors of MetabolismMember
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