Dr. Cooney is on Doximity
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Office
301 University Blvd Route 0359
Galveston, TX 77555Phone+1 409-772-3466Fax+1 409-772-9595- Is this information wrong?
Summary
- Dr. Erin Cooney is an associate professor in the Division of Medical Genetics and Metabolism at the University of Texas Medical Branch (UTMB). Dr. Cooney’s clinical focus is on medical genetics and the inborn errors of metabolism. She is a consultant for the Texas Newborn Screening Program and advocates on a national level for improved metabolic practices through the Society for Inherited Metabolic Disorders Public Policy Committee. She also serves as the UTMB faculty supervisor for prenatal genetics and has a special interest in medical education.
Dr. Cooney holds undergraduate degrees in Biochemistry and Molecular Genetic Technology from the University of Texas at Austin and the University of Texas at MD Anderson Cancer Center, respectively. She received her doctoral degree from the University of Texas Health Science Center in Houston and completed Pediatrics and Medical Genetics and Genomics residencies as well as a clinical fellowship in Medical Biochemical Genetics at Baylor College of Medicine (affiliated with Texas Children's Hospital in Houston, Texas). Dr. Cooney is triple boarded with certifications in the following: (1) Pediatrics; (2) Medical Genetics and Genomics; and (3) Medical Biochemical Genetics.
Dr. Cooney was recipient of the Shire / American College of Medical Genetics Training Award. In 2017, she was named Resident of the Year by the Baylor Department of Molecular and Human Genetics. In 2021, she was honored with the Early Career Pediatric Educator Award for Excellence in Student Education by the UTMB Department of Pediatrics.
She is a fellow of the American Academy of Pediatrics, Texas Pediatric Society, American College of Medical Genetics and Genomics, and the Society for Inherited Metabolic Disorders.
Clinical Expertise
- Marfan syndrome, Down syndrome, Dyslipidemia, Skeletal dysplasias, Inborn errors of metabolism, Newborn screening, Peroxisomal disorders, Monogenic hearing loss, Neonatal hypotonia
Education & Training
- Baylor College of MedicineFellowship, Medical Biochemical Genetics, 2017 - 2018
- Baylor College of MedicineResidency, Pediatrics/Medical Genetics and Genomics, 2012 - 2017
- McGovern Medical School at UTHealthClass of 2012
Certifications & Licensure
- TX State Medical License 2016 - 2024
- American Board of Medical Genetics and Genomics Clinical Genetics
- American Board of Medical Genetics and Genomics Medical Biochemical Genetics
- American Board of Pediatrics Pediatrics
- American Board of Medical Genetics and Genomics Clinical Genetics and Genomics
Awards, Honors, & Recognition
- Lillian L. Lockhart, MD Endowed Professorship in Genetics UTMB, 2023-2024
- 2021 Early Career Pediatric Educator Award for Excellence in Student Education University of Texas Medical Branch, Department of Pediatrics, 2021
- SHIRE-ACMG Training Award ACMG, 2017
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Publications & Presentations
PubMed
- Outcomes in 14 live births resulting from Pegvaliase-treated pregnancies in PKU-affected females.Bier, C., Dickey, K., Bibb, B., Crutcher, A., Sponberg, R., Chang, R., Boyer, M., Davis-Keppen, L., Matthes, C., Tharp, M., Vice, D., Cooney, E., Morand, M., Ray, J., ...> ;Molecular Genetics and Metabolism. 2024 Mar 1
- Variants in the WDR44 WD40-repeat domain cause a spectrum of ciliopathy by impairing ciliogenesis initiation.Accogli, A., Shakya, S., Yang, T., Insinna, C., Kim, S., Bell, D., Butov, K., Severino, M., Niceta, M., Scala, M., Lee, H., Yoo, T., Stauffer, J., Zhao, H., Fiorillo, ...> ;Nature Communications. 2024 Jan 8
- 1 citationsGABRG1 variant as a potential novel cause of epileptic encephalopathy, hypotonia, and global developmental delay.Aaron Williams, Erin Cooney, Gabrielle Segal, Swetha Narayanan, Megan Morand, Satish Agadi> ;American Journal of Medical Genetics. Part A. 2022 Dec 1
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Journal Articles
- Novel abdomino-pelvic anomalies in Kagami-Ogata syndromeKelly Lamiman, Vasilis Mavratsas, Tanvi Gupta, Erin Cooney, Toy G. Lee, Claire Cummins, Brendan Gorman, Jonathan Gerber, Ravi Radhakrishnan, Journal of Pediatric Surgery Case Reports, 2021
Press Mentions
- Making Muscles with the Most Expensive Drug in the WorldFebruary 4th, 2021
Committees
- member, SIMD Public Policy Committee 2020 - Present
- Member, ECI Genetics Webinar Series Committee 2018 - Present
Professional Memberships
- Fellow
- American College of Medical Genetics & Genomics - ACMGFellow
- Society for Inherited Metabolic DisordersFellow
- Texas Pediatric SocietyMember
Hospital Affiliations
- University of Texas Medical BranchGalveston, Texas
External Links
- UTMB Providerhttps://doctors.utmbhealth.com/providersearch/default/?id=047852
- UTMB Geneticshttps://www.utmb.edu/pedi/academic-divisions/genetics
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