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Dr. Gregory Enns, MBChB, MD
Dr. Gregory Enns, MBChB, MD
Professor , Stanford University School of Medicine
Bachelor of Medicine and Surgery, University of Glasgow
Dr. Gregory M. Enns has over 33 years of experience in the field of Pediatric Medical Genetics. He earned his BA in Biology from Pomona College, his Diploma in Medical Science from the University of St. Andrews, and his MBChB from the University of Glasgow. After completing his internship and residency in Pediatrics at Children’s Hospital of Los Angeles, he went on to complete a fellowship in Medical Genetics at the University of California, San Francisco. Today, this expert is board certified in Clinical Biochemical Genetics and Clinical Genetics and Genomics. Formerly, this expert held roles as an Assistant Professor of Pediatrics at Stanford University and as Associate Program Director of the Medical Genetics Residency Training Program at Stanford University School of Medicine. Currently, he is the Associate Program Director of the Medical Biochemical Genetics Fellowship Program and he works as the Medical Director of the Inherited Metabolic Disease. He is a Physician in the General Genetics Clinic at Stanford Children's Health and the Director of the Biochemical Genetics Program.
g*********@******.edu
(650) ***-****
Palo Alto, California
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Radar Metrics At A Glance
Expert Witness Activity
63
Plaintiff Cases
16
Defense Cases
41
Expert Challenges
16
Deposition Transcripts
14
Publications
208
Media & News
320
Social Media Mentions
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Expert Witness Activity
Radar found 68 records
Case Name | Role | Filed Date |
|---|---|---|
Carla A. Turner, M.D., et al. v. Tara D. Clark Newberry, et al. | Expert Witness | 2023-09-26 |
In re: Gregory Enns, M.D. | Other | 2022-04-12 |
Nicole Kilpatrick v. Medical Faculty Associates, Inc., et al. | Expert Witness | 2020-07-28 |
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Litigation Analytics
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Publications
Radar found 208 records
Title | Type |
|---|---|
High prevalence of hepatic fibrosis in liver tissue from individuals with argininosuccinate lyase deficiency | Journal Article |
Reply | Letter |
Profound Neonatal Lactic Acidosis and Renal Tubulopathy in a Patient with Glycogen Storage Disease Type IXa2? 2 Secondary To a De Novo Pathogenic Variant in PHKA2 | Case Report |
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Media & News
Radar found 320 records
Title | Description |
|---|---|
Pediatric endocrinology and inborn errors of metabolism | Lysosomal Disorders / Gregory M. Enns, Robert D. Steiner, Tina M. Cowan ; Purine and Pyrimidine Metabolism / William L. Nyhan. -- Part 10: Neurotransmitter ... |
Human Genome Epidemiology Literature Finder|Home | Apr 8, 2024 -- Molecular genetics and metabolism 2023 8 140 (3): 107668. May Flowers, Alexa Dickson, Marcus J Miller, Elaine Spector, Gregory Mark Enns ... |
ASL expression in ALDH1A1+ neurons in the ... - ICH GCP | Feb 14, 2024 -- ... Gregory Enns, Renata C Gallagher, Andrea ... Part 2: the evolving clinical phenotype. ... Identification of novel risk loci, causal insights, and ... |
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Depositions & Transcripts
Radar found 14 records
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Education
Institution | Degree Type |
|---|---|
University of Glasgow | Bachelor of Medicine and Surgery |
University of St Andrews | Diploma |
Pomona College | Bachelor of Arts |
Work History
Title | Employer |
|---|---|
Professor | Stanford University School of Medicine |
Associate Program Director | Stanford University School of Medicine |
Program Director | Stanford University School of Medicine |
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