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Chung Lee
Clinical Assistant Professor, Pediatrics - Medical Genetics
Print Profile
Email Profile
Bio
Bio
Publications
Clinical Focus
Clinical Genetics
Biochemical Genetics
Academic Appointments
Clinical Assistant Professor,
Pediatrics - Medical Genetics
Administrative Appointments
Program Director, Medical Biochemical Genetics Fellowship Program (2020 - Present)
Associate Program Director, Medical Biochemical Genetics Fellowship Program (2017 - 2020)
Honors & Awards
Phi Beta Kappa, Northwestern University (2001)
Summa cum laude, Northwestern University (2002)
Dr. Koch Memorial Scholarship Recipient, National PKU Alliance (2012)
Professional Education
Residency: Kaiser Permanente Northern California GME Programs (2011) CA
Internship: Kaiser Permanente Northern California GME Programs (2009) CA
Board Certification: American Board of Medical Genetics and Genomics, Clinical Biochemical Genetics (2015)
Board Certification: American Board of Medical Genetics and Genomics, Clinical Genetics (2013)
Fellowship: University of California, San Francisco (UCSF) (2014) CA
Residency: University of California, San Francisco (UCSF) (2013) CA
Board Certification: American Board of Pediatrics, Pediatrics (2011)
Medical Education: University of Illinois at Chicago (2008) IL
Contact
Academic
chunglee@stanford.edu
Clinical (Primary)
This is the primary clinic for this clinical provider. For additional clinical locations and information, please visit the link(s) listed below in the 'Additional Clinical Info' section.
Medical Genetics
730 Welch Rd
2nd Fl
Palo Alto CA 94304
Tel: (650) 721-5804
Fax: (650) 498-4555
Additional Clinical Info
Stanford Medicine Children's Health
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Publications (30)
All Publications
(30)
Journal Articles
(17)
Conference Proceedings
(11)
Profiles With Related Publications
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Jon Bernstein
Professor of Pediatrics (Genetics) and, by courtesy, of Genetics
Clinical Focus
Clinical Genetics and Genomics, Rare Diseases, Undiagnosed Diseases, Autism, Developmental Disorders, Craniofacial Conditions, Craniosynostosis, Cleft Lip, Cleft Palate
Research Interests
My research is focused on the diagnosis, discovery and delineation of rare genetic conditions with a focus on neurodevelopmental disorders. This work includes the application of novel computational methods and multi-omics profiling (whole genome sequencing, long-read DNA sequencing, RNA sequencing, methylomics, metabolomics). I additionally participate in an interdisciplinary project to develop induced pluripotent stem cell and assembloid models of genetic neurodevelopmental disorders.
154
Total Publications
close
Caroline Buckway
Clinical Professor, Pediatrics - Endocrinology and Diabetes
Clinical Focus
Pediatric Endocrinology, General pediatric endocrine disorders including growth, puberty, Turner syndrome, adrenal, thyroid, pituitary disorders, and late effects after cancer therapy
8
Total Publications
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Holly Cooper
Clinical Assistant Professor, Pediatrics - Endocrinology and Diabetes
Clinical Focus
Pediatric Diabetes, Pediatric Endocrinology, Cystic Fibrosis-Related Diabetes (CFRD) and Other Endocrine Disorders in Children with CF, Total Pancreatectomy with Islet Autotransplantation (TPIAT) in Children
4
Total Publications
close
Tina Cowan
Professor of Pathology (Clinical) and, by courtesy, of Pediatrics (Genetics)
Clinical Focus
Pathology and Laboratory Medicine, Pathology, Clinical Biochemical Genetics
Research Interests
screening and diagnosis of patients with inborn errors of metabolism, including newborn screening, development of new testing methods and genotype/phenotype correlations.
91
Total Publications
close
Gerald Crabtree
David Korn, MD, Professor of Pathology and Professor of Developmental Biology
Research Interests
Chromatin regulation and its roles in human cancer and the development of the nervous system. Engineering new methods for studying and controlling chromatin and epigenetic regulation in living cells.
265
Total Publications
close
Gregory Enns
Professor of Pediatrics (Genetics)
Clinical Focus
Biochemical Genetics, Mitochondrial Diseases, Medical Biochemical Genetics
Research Interests
mitochondrial genomics, lysosomal disorders, tandem-mass spectrometry newborn screening, and inborn errors of metabolism presentations and natural history
245
Total Publications
close
Paul Graham Fisher, MD
Beirne Family Professor of Pediatric Neuro-Oncology, Professor of Pediatrics and, by courtesy, of Neurosurgery and of Epidemiology and Population Health
Clinical Focus
Cancer > Neuro Oncology, Neurology - Child Neurology, Neuro-Oncology, Neurology
Research Interests
Clinical neuro-oncology: My research explores the epidemiology, natural history, and disease patterns of brain tumors and other cancers in childhood, as well as prospective clinical trials for treating these neoplasms. Research interests also include neurologic effects of cancer and its therapies.
286
Total Publications
close
Uta Francke
Professor of Genetics and of Pediatrics, Emerita
Clinical Focus
Neurogenetics, Clinical Genetics, Marfan syndrome, Williams syndrome, Heritable connective tissue disorders
Research Interests
Functional consequences and pathogenetic mechanisms of mutations and microdeletions in human neurogenetic syndromes and mouse models. Integration of genomic information into medical care.
565
Total Publications
close
Nathan Gamarra
Postdoctoral Scholar, Genetics
1
Total Publications
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Monica Grover
Clinical Associate Professor, Pediatrics - Endocrinology and Diabetes
Clinical Focus
Pediatric Endocrinology, Pediatric Bone health
29
Total Publications
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Hanmin Guo
Postdoctoral Scholar, Psychiatry
8
Total Publications
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Joachim Hallmayer
Professor of Psychiatry and Behavioral Sciences (Child and Adolescent Psychiatry and Child Development)
243
Total Publications
Publication Topics For This Person
Adolescent
Amino Acid Metabolism, Inborn Errors
Base Sequence
Biomarkers
Brain Diseases, Metabolic
Child, Preschool
Chromosomal Proteins, Non-Histone
Chromosomes, Human, Pair 22
Craniofacial Abnormalities
DNA, Complementary
DNA-Binding Proteins
Diagnosis, Differential
Exons
Gene Components
Genes, Dominant
Genetic Predisposition to Disease
Germ-Line Mutation
Glutaryl-CoA Dehydrogenase
Growth Disorders
Heart Septal Defects, Ventricular
Homozygote
Hydroxymethylglutaryl-CoA Synthase
Infant
Lipid Metabolism, Inborn Errors
Loss of Heterozygosity
Marfan Syndrome
Microfilament Proteins
Microsatellite Repeats
Models, Molecular
Molecular Sequence Data