ChristinaT.LamMD(she/her)
Medical Genetics • Seattle, WAClinical Genetics, Medical Biochemical Genetics, Pediatric Medical Genetics
Medical Biochemical Geneticist
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Office
4800 Sand Point Way NE
MS Mb8632
Seattle, WA 98105Phone+1 206-987-5230Fax+1 206-987-5329
Summary
- Dr. Christina Lam is a specialist in Medical Genetics based in Seattle, WA, with subspecialties in Clinical Genetics, Medical Biochemical Genetics, and Pediatric Medical Genetics. She completed her education and training at institutions including UCLA and the National Institutes of Health. Currently, she serves as the Medical Director of Biochemical Genetics at Seattle Children's Hospital and holds a position as an Associate Professor at the University of Washington School of Medicine. Her extensive research includes publications in prominent journals such as the American Journal of Human Genetics and Genetics in Medicine, with notable works on biochemical genetic disorders. Dr. Lam is also involved in clinical trials focused on congenital disorders of glycosylation.
Education & Training
National Institutes of Health Clinical CenterFellowship, Medical Biochemical Genetics, 2012 - 2013
Cedars-Sinai Medical Center/Harbor/UCLAResidency, Pediatrics/Medical Genetics and Genomics, 2007 - 2012
UCLA David Geffen School of Medicine/UCLA Medical CenterResidency, Pediatrics, 2007 - 2010
David Geffen School of Medicine at UCLAClass of 2007
Certifications & Licensure
MT State Medical License 2021 - 2027
AK State Medical License 2022 - 2026
CA State Medical License 2009 - 2025
WA State Medical License 2016 - 2025
American Board of Medical Genetics and Genomics Medical Biochemical Genetics- American Board of Medical Genetics and Genomics Clinical Genetics and Genomics
Clinical Trials
- Clinical and Basic Investigations Into Known and Suspected Congenital Disorders of Glycosylation Start of enrollment: 2014 Mar 07
- Natural History Study Protocol in PMM2-CDG (CDG-Ia) Start of enrollment: 2018 Jan 08
- Acetazolamide Efficacy in Ataxia in PMM2-CDG Start of enrollment: 2021 Mar 17
Publications & Presentations
PubMed
- 10 citationsExpanding the Phenotype, Genotype and Biochemical Knowledge of ALG3‐CDGHind Alsharhan, Bobby G. Ng, Earnest James Paul Daniel, Jennifer Friedman, Eniko K. Pivnick
Journal of Inherited Metabolic Disease. 2021-02-13 - 25 citationsUrine oligosaccharide screening by MALDI-TOF for the identification of NGLY1 deficiencyPatricia L. Hall, Christina Lam, John J. Alexander, Ghazia Asif, Gerard T. Berry
Molecular Genetics and Metabolism. 2018-05-01 - 128 citationsDe Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual DisabilitySébastien Küry, Geeske M. van Woerden, Thomas Besnard, Martina Proietti Onori, Xenia Latypova
American Journal of Human Genetics. 2017-11-02
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