Are you Dr. Wangler?
Join over one million U.S. Physicians, Nurse Practitioners and PAs, already on Doximity.
- Gain access to free telehealth tools, such as our "call shielding" and one-way patient texting.
- Connect with colleagues in the same hospital or clinic.
You already have 51 invites waiting! - Read the latest clinical news, personalized to your specialty.
Office
1504 Taub Loop
Houston, TX 77030Phone+1 713-873-8890Fax+1 832-825-4294
Summary
- Dr. Michael Wangler, MD is a pediatrician in Houston, Texas. He is currently licensed to practice medicine in Texas. He is affiliated with Texas Children's Hospital and is an Assistant Professor at Baylor College of Medicine.
Education & Training
- Baylor College of MedicineResidency, Medical Genetics and Genomics, 2009 - 2011
- Baylor College of Medicine (Houston)Residency, Pediatrics, 2006 - 2009
- Baylor College of MedicineClass of 2006
Certifications & Licensure
- TX State Medical License 2009 - 2025
- American Board of Medical Genetics and Genomics Clinical Genetics and Genomics
Publications & Presentations
PubMed
- 24 citationsDe novo mutations in TOMM70, a receptor of the mitochondrial import translocase, cause neurological impairmentD. Dutta, Lauren C. Briere, Oguz Kanca, Paul C. Marcogliese, Melissa A. Walker
Human Molecular Genetics. 2020-06-03 - 26 citationsRecurrent arginine substitutions in the ACTG2 gene are the primary driver of disease burden and severity in visceral myopathyNurit Assia Batzir, Pranjali K Bhagwat, Austin Larson, Zeynep Coban Akdemir, Maciej Bagłaj
Human Mutation. 2020-03-01 - 51 citationsLoss-of-Function Variants in MYLK Cause Recessive Megacystis Microcolon Intestinal Hypoperistalsis Syndrome.Danny Halim, Erwin Brosens, Françoise Muller, Michael F. Wangler, Arthur L. Beaudet
American Journal of Human Genetics. 2017-07-06
Press Mentions
- Peroxisomal Biogenesis Disorder: New Link to Sugar MetabolismJune 22nd, 2017
- Genes Nardilysin and OGDHL Linked to Human Neurological ConditionsDecember 22nd, 2016
- Genetic Cause Identified for Previously Unrecognized Developmental DisorderDecember 22nd, 2016
- Join now to see all