Gregory Enns
Academic Appointments
- Associate Professor - Med Center Line, Pediatrics - Medical Genetics
- Member, Child Health Research Institute
Key Documents
Contact Information
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Clinical Offices
Medicine Specialties Clinic 730 Welch Rd 2nd Floor Palo Alto, CA 94304 Tel Work (650) 723-6858 Fax (650) 498-4555Practices at Stanford Hospital and Clinics and Lucile Packard Children's Hospital
- Academic Offices
Personal Information Email Tel (650) 498-5798 Tel (650) 723-6858Not for medical emergencies or patient use
Professional Overview
Clinical Focus
- Clinical Genetics
- Biochemical Genetics
- Mitochondrial Diseases
Professional Education
| Board Certification: | Clinical Genetics, American Board of Medical Genetics (1999) |
| Board Certification: | Clinical Biochemical Genetics, American Board of Medical Genetics (1999) |
| Fellowship: | UCSF Medical Center CA (1998) |
| Residency: | Children's Hospital of Los Angeles CA (1995) |
| Board Certification: | General Pediatrics, American Board of Pediatrics (1994) |
Postdoctoral Advisees
Graduate & Fellowship Program Affiliations
Industry Relationships
Stanford is committed to ethical and transparent interactions with our industry partners. It is our policy to disclose payments of $5,000 or more, equity valued at $5,000 or more in a publicly traded company, or any equity in a privately held company, to physicians and scientists employed by Stanford University from companies or other commercial entities with which they interact as part of their professional activities. View Full Information
| Consulting: | Barnes & Thornburg, LLP , County of San Joaquin , Dummit, Buchholz & Trapp , LeBeau Thelen LLP , Zurick American Insurance Co. |
Scientific Focus
Current Research Interests
Research interests include novel means of diagnosing and treating mitochondrial disorders, with an emphasis on antioxidant therapy, lysosomal disorders, and newborn screening by tandem mass spectrometry. Current pursuits include the analysis of glutathione and antioxidant status in patients who have mitochondrial disorders and the development of new techniques for diagnosing these conditions.
Clinical Trials
Publications
- Initial experience in the treatment of inherited mitochondrial disease with EPI-743. Mol Genet Metab. 2012; (1): 91-102
- High-quality DNA sequence capture of 524 disease candidate genes. Proc Natl Acad Sci U S A. 2011; (16): 6549-54
- Leigh syndrome caused by a novel m.4296G>A mutation in mitochondrial tRNA isoleucine. Mitochondrion. 2011
- Inherited disorders affecting mitochondrial function are associated with glutathione deficiency and hypocitrullinemia. Proc Natl Acad Sci U S A. 2009; (10): 3941-5
- Mapping gene associations in human mitochondria using clinical disease phenotypes. PLoS Comput Biol. 2009; (4): e1000374
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