Dr. Michael Francis Wangler M.D.
Pediatrician
6701 Fannin St Houston TX, 77030About
Dr. Michael Wangler is a pediatrician practicing in Houston, TX. Dr. Wangler is a doctor who specializes in the health care of children. As a pedicatrician, Dr. Wangler diagnoses and treats infections, injuries, diseases and other disorders in children. Pediatricians typically work with infants, children, teenagers and young adults up to age 21. They practice medical care as well as preventative health care. Dr. Wangler can oversee and manage the physical, mental and emotional health of their patients.
Education and Training
Baylor College of Medicine 2009
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Fibrochondrogenesis results from mutations in the COL11A1 type XI collagen gene.
- Antioxidant proteins TSA and PAG interact synergistically with Presenilin to modulate Notch signaling in Drosophila.
- A drosophila genetic resource of mutants to study mechanisms underlying human genetic diseases.
- Fruit flies in biomedical research.
- A homozygous mutation in identified by whole-exome sequencing ending a diagnostic odyssey.
- Dataset for a case report of a homozygous PEX16 F332del mutation.
- Missense variants in the middle domain of DNM1L in cases of infantile encephalopathy alter peroxisomes and mitochondria when assayed in Drosophila.
- Diagnosis of a mild peroxisomal phenotype with next-generation sequencing.
- A Syndromic Neurodevelopmental Disorder Caused by De Novo Variants in EBF3.
- Loss of Nardilysin, a Mitochondrial Co-chaperone for α-Ketoglutarate Dehydrogenase, Promotes mTORC1 Activation and Neurodegeneration.
- A Recurrent De Novo Variant in NACC1 Causes a Syndrome Characterized by Infantile Epilepsy, Cataracts, and Profound Developmental Delay.
- MARRVEL: Integration of Human and Model Organism Genetic Resources to Facilitate Functional Annotation of the Human Genome.
- Loss-of-Function Variants in MYLK Cause Recessive Megacystis Microcolon Intestinal Hypoperistalsis Syndrome.
- Clinically severe CACNA1A alleles affect synaptic function and neurodegeneration differentially.
Treatments
- Birth Defects
Fellowships
- Baylor College of Medicine, Molecular & Human Genetics 2011
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