- Residency - UT Southwestern/Children's Medical Center (2014-2018), Neurodevelopmental Disabilities
- Residency - UT Southwestern/Children's Medical Center (2012-2014), Pediatrics
- Medical School - UT Health Science Center at Houston (2008-2012)


Kimberly Goodspeed, M.D.
- Dedman Family Scholar in Clinical Care
- Pediatric Neurology
- Autism
- Rare genetic developmental disorders in children

Biography
Kimberly Goodspeed, M.D., is an Assistant Professor in the Departments of Pediatrics, Neurology, and Psychiatry and a Dedman Family Scholar in Clinical Care at UT Southwestern Medical Center. She is a child neurologist and neurodevelopmental specialist who cares for children and young adults with autism spectrum disorder and intellectual disability. She has particular expertise in rare genetic developmental disorders in children, including Angelman syndrome, Pitt-Hopkins syndrome, SLC6A1-related disorders, Phelan-McDermid Syndrome, and Rett syndrome.
Dr. Goodspeed earned her medical degree at the UT Health Science Center at Houston and completed residencies in pediatrics and neurodevelopmental disabilities at UT Southwestern.
Board certified in pediatrics, neurology, and neurodevelopmental disabilities, she joined the UT Southwestern faculty in 2018.
Among her other roles at UT Southwestern, Dr. Goodspeed serves on the Neurodevelopmental Disabilities Program Evaluation Committee, the Neurodevelopmental Disabilities Clinical Competencies Committee, and the Child Neurology and Neurodevelopmental Disabilities Residency Interview Committee.
Her research seeks to better understand rare genetic developmental disorders in children and the genetic causes of developmental delays in children with autism spectrum disorder and intellectual disability. She partners with basic scientists to help develop novel treatments, such as gene therapy, for these conditions.
Dr. Goodspeed is a member of several professional associations, including the American Academy of Neurology, the American Society of Gene and Cell Therapy, and the Child Neurology Society. She serves as an ad hoc reviewer for many journals, among them the Journal of Child Neurology, the Journal of Inherited Metabolic Disease, and Developmental Medicine and Child Neurology.
She is the author or co-author of numerous research articles, case reports, and book chapters, including a recent contribution to Autism Spectrum Disorders: Clinical Considerations.
In 2021, Dr. Goodspeed was rated one of Dallas’ Best Pediatric Specialists by D Magazine.
Education & Training
Professional Associations & Affiliations
- American Academy of Neurology
- American Neurological Association
- American Society of Gene and Cell Therapy
- Child Neurology Society
- Dallas Pediatric Society
- Gold Humanism Honor Society
Honors & Awards
- D Magazine Best Doctor 2022
- D Magazine Best Pediatric Specialist 2020-2021
- Dedman Family Scholar in Clinical Care 2020, UT Southwestern
- NeuroNEXT Early Stage Investigator Award 2019, UT Southwestern
- Swim with the Sharks finalist 2018, UT Southwestern Center for Translational Medicine
- Research Scholar 2016, American Neurological Association
- Research Scholar 2016, Rare Disease Clinical Research Network Scholar
- Pediatric Intern of the Year 2013, UT Southwestern
- Merck Manual Award 2012, UT Health Science Center at Houston Medical School
- Medical Student of the Year 2011, Texas Medical Association
Books & Publications
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Books
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Autism Spectrum Disorders: Clinical Considerations in The Molecular and Genetic Basis of Neurological and Psychiatric Disease, 6th Ed.
Goodspeed K, Haffner D, Golla S, Morris MA, Evans P (2019), San Diego, Academic Press
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Autism Spectrum Disorders: Clinical Considerations in The Molecular and Genetic Basis of Neurological and Psychiatric Disease, 6th Ed.
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Publications
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Current knowledge of SLC6A1-related neurodevelopmental disorders.
Goodspeed K, Pérez-Palma E, Iqbal S, Cooper D, Scimemi A, Johannesen KM, Stefanski A, Demarest S, Helbig KL, Kang J, Shaffo FC, Prentice B, Brownstein CA, Lim B, Helbig I, De Los Reyes E, McKnight D, Crunelli V, Campbell AJ, Møller RS, Freed A, Lal D, Brain communications 2020 2 2 fcaa170 -
Bringing everyone to the table - findings from the 2018 Phelan-McDermid Syndrome Foundation International Conference.
Goodspeed K, Bliss G, Linnehan D, Orphanet journal of rare diseases 2020 06 15 1 152 -
Pitt-Hopkins Syndrome: A Unique Case Study.
Tan A, Goodspeed K, Edgar VB Journal of the International Neuropsychological Society : JINS 2018 Oct 24 9 995-1002 -
Pitt-Hopkins Syndrome: A Review of Current Literature, Clinical Approach, and 23-Patient Case Series.
Goodspeed K, Newsom C, Morris MA, Powell C, Evans P, Golla S Journal of child neurology 2018 Mar 33 3 233-244 -
Analysis of recent shared ancestry in a familial cohort identifies coding and noncoding autism spectrum disorder variants.
Tuncay IO, Parmalee NL, Khalil R, Kaur K, Kumar A, Jimale M, Howe JL, Goodspeed K, Evans P, Alzghoul L, Xing C, Scherer SW, Chahrour MH, NPJ genomic medicine 2022 Feb 7 1 13 -
Optical coherence tomography features in brothers with aspartylglucosaminuria.
Goodspeed K, Harder L, Hughes S, Conger D, Taravella J, Gray SJ, Minassian B Annals of clinical and translational neurology 2018 Dec 5 12 1622-1626
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Current knowledge of SLC6A1-related neurodevelopmental disorders.
Research
- Phelan-McDermid syndrome
- Pitt-Hopkins syndrome
- Rare genetic developmental disorders in children
- Rett syndrome
- SLC6A1-related disorders
Clinical Focus
- Autism
- Rare genetic developmental disorders in children
- Angelman syndrome
- DDX3X encephalopathy
- Phelan-McDermid Syndrome
- Pitt-Hopkins syndrome
- Rett Syndrome
- SLC6A1-related disorders