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Office
2785 Gulf Fwy S
Ste 2.200
League City, TX 77573Phone+1 888-886-2543Fax+1 409-772-3680
Summary
- Dr. Erin Cooney is an Associate Professor in the Division of Medical Genetics and Metabolism. Her clinical focus is on medical genetics and the inborn errors of metabolism. She is the Medical Director for UTMB Biochemical Genetics and Newborn Screening, and Genetics of Autism Clinic; and Medical Supervisor for UTMB Prenatal Genetics. Dr. Cooney is a consultant for the Texas Newborn Screening Program and advocates on a national level through the Society for Inherited Metabolic Disorders Public Policy Committee.
Dr. Cooney has a special interest in medical education. She works with trainees of all levels including medical and physician assistant students through the UTMB School of Medicine; genetic counseling students as adjunct faculty through the UT Health Houston Graduate School of Biomedical Sciences; UTMB pediatric residents; and UTMB maternal fetal medicine fellows.
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 Clinical Genetics & Genomics residencies as well as a clinical fellowship in Medical Biochemical Genetics at Baylor College of Medicine (affiliated with Texas Children's Hospital). Dr. Cooney is triple boarded with certifications in the following: (1) Pediatrics; (2) Clinical Genetics & Genomics; and (3) Medical Biochemical Genetics.
Dr. Cooney was recipient of the American College of Medical Genetics Foundation Training Award and Resident of the Year by the Baylor Department of Molecular and Human Genetics in 2017. In 2021, she was honored with the UTMB Early Career Pediatric Educator Award for Excellence in Student Education. In 2024, she was honored with the first ever UTMB Lillian L. Lockhart, MD Endowed Professorship in Genetics.
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 - 2026
- 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
- 47 citationsNovel EED mutation in patient with Weaver syndromeErin Cooney, Weimin Bi, Alan E Schlesinger, Sherry S. Vinson, Lorraine Potocki
American Journal of Medical Genetics. Part A. 2017-02-01 - 45 citationsAnalyses of SLC13A5-epilepsy patients reveal perturbations of TCA cycleMatthew N. Bainbridge, Erin Cooney, Marcus J. Miller, Adam D. Kennedy, Jacob Wulff
Molecular Genetics and Metabolism. 2017-08-01 - 74 citationsMutations in PURA Cause Profound Neonatal Hypotonia, Seizures, and Encephalopathy in 5q31.3 Microdeletion SyndromeSeema R. Lalani, Jing Zhang, Christian P. Schaaf, Chester W. Brown, Pilar L. Magoulas
American Journal of Human Genetics. 2014-11-06
Journal Articles
- Variants in the WDR44 WD40-repeat domain cause a spectrum of ciliopathy by impairing ciliogenesis initiationAccogli A, Shakya S, Yang T, Insinna C, Kim SY, Bell D, Butov KR, Severino M, Niceta M, Scala M, Lee HS, Yoo T, Stauffer J, Zhao H, Fiorillo C, Pedemonte M, Diana MC, ..., Nature Communications, 1/2024
- 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
Grant Support
- Texas Department of State Health Services Pilot Newborn Screen ProgramTexas Department of State Health Services2024–2029
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
External Links
- UTMB Providerhttps://doctors.utmbhealth.com/providersearch/default/?id=047852
- UTMB Geneticshttps://www.utmb.edu/pedi/academic-divisions/genetics
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