- American Academy of Pediatrics (1986)
- Child Neurology Society (1992)
- American Academy of Neurology (1992)
- Fragile X National Foundation (2012)
Patricia Evans, M.D., Ph.D.
- Pediatric Neurology
- General Neurology
Biography
Patricia Evans, M.D., Ph.D., serves as the Director of the Neurodevelopmental Disabilities program at UT Southwestern Medical Center at Dallas, which includes an ACGME-accredited, 4 year core residency in Neurodevelopmental Disabilities. Dr. Evans received her MD from Texas Tech University School of Medicine, and completed her pediatric training at Texas Tech University Health Science Center; her Adult and Pediatric Neurology training at UT Southwestern School of Medicine; and her fellowship in Cognitive Development through the NIH at Johns Hopkins School of Medicine. Dr. Evans received her Ph.D. in research psychology through Walden University. She completed the Palatucci Fellowship in Advocacy (AAN); and was formerly the chair of the Ethics Section for the AAN. She carries board certification in Pediatrics (ABP), Neurology with Special Qualification in Pediatric Neurology (AAN), and Neurodevelopmental Disabilities (AAN). She is a fellow of the American Academy of Neurology and the American Academy of Pediatrics; she is a member of the Child Neurology Society (CNS). Special research interests include Fragile X Syndrome; Autism Spectrum Disorder across the lifespan; and neuroethics in the pediatric setting, particularly in the context of end-of-life decision making. Dr. Evans has authored a textbook on Autism Spectrum Disorder; as well as several book chapters on autism as well as ethics.
Education & Training
- Residency - Texas Tech University Health Sciences Center (1983-1986), Pediatrics
- Residency - UT Southwestern Medical Center (1992-1995), Pediatric Neurology
- Fellowship - Johns Hopkins University School of Medicine (1995-1996), Neurology
- Fellowship - Wake Forest University School of Medicine (2004-2004), Pediatric Neurology
- Fellowship - Albert Einstein College of Medicine/Jacobi Medical Center (1994-1994), Autism Spectrum Disorders
- Fellowship - Wake Forest University School of Medicine (1993-1993), Epilepsy
- Medical School - Texas Tech University School of Medicine (1979-1983)
- Other Post Graduate Training - Walden University (2013-2014), Research Psychology
Professional Associations & Affiliations
Honors & Awards
- Outstanding Neurologist of Dallas, D Magazine (2002, 2012)
- America's Top Pediatricians 2004-2006, Consumers Research Council of America
- Donald Palatucci Fellowship for Patient Advocacy 2005
- Fellow of the American Academy of Neurology 2007
- Neurology-on-the-Hill Spokesperson for the 2008 Leadership Development Program 2008, American Academy of Neurology
- Best Pediatric Specialists 2013-2014, D Magazine
Books & Publications
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Books
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End-of-life-Care for the Neurologically Impaired Child. in In William, McGuire, Rizzo, eds. Practical Ethics in Clinical Neurology. American Academy of Neurology.
Evans, Patricia (2012), Philadelphia, PA:, Lippincott, Wilkins and Williams, -
Evans P. Informed Assent and Refusal for Children and Adolescents. in In William, McGuire, Rizzo, eds. Practical Ethics in Clinical Neurology. American Academy of Neurology,
Evans, Patricia (2012), Philadelphia, PA, Lippincott, Wilkins and Williams -
Clinical Guide to Autistic Spectrum Disorders for Primary Care Practitioners.
Evans, Patricia; Morris, Mary Ann (2010), Philadelphia, PA:, Lippincott, Wilkins and Williams -
Practicing Inclusivity for Children with Special Needs. in In Water, L, ed. Why, O God? A Biblical Theology of Suffering and Disability.
Evans, Patricia (2011), Wheaton, IL., Good News and Crossways Publishers
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End-of-life-Care for the Neurologically Impaired Child. in In William, McGuire, Rizzo, eds. Practical Ethics in Clinical Neurology. American Academy of Neurology.
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Publications
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Relationship Between Intellectual Disability and Behavioral Comorbidity in Children With Fragile X Syndrome
Author Collaboration FC, Kaufmann WE, Horn PS, Budimirovic DB, Harris HK, Lozano R, Morris SM, Frazier JA, Buchanan C, Lozano R, Uy RS, Gropman AL, Givler BA, Morris MA, Evans PA, Frye RE, Esler A, Harris HK, Lachiewicz AM, Picker JD, Feldman G, Erickson CA, Hessl D, Hagerman RJ, Delahunty CM, Reiss A, Lightbody A, Barbouth D, Budimirovic DB, Filipink RA, Tartaglia N, Schuster M, Kaufmann WE, Sherman SL, Talboy AL, Velinov M, Berry-Kravis E Journal of Autism and Developmental Disorders 2025 -
The genetic landscape of autism spectrum disorder in an ancestrally diverse cohort
Gogate A, Kaur K, Khalil R, Bashtawi M, Morris MA, Goodspeed K, Evans P, Chahrour MH npj Genomic Medicine 2024 Dec 9 -
Correction to: The genetic landscape of autism spectrum disorder in an ancestrally diverse cohort (npj Genomic Medicine, (2024), 9, 1, (62), 10.1038/s41525-024-00444-6)
Gogate A, Kaur K, Khalil R, Bashtawi M, Morris MA, Goodspeed K, Evans P, Chahrour MH npj Genomic Medicine 2024 Dec 9 -
Latent Class Analysis Identifies Distinctive Behavioral Subtypes in Children with Fragile X Syndrome
Author Collaboration FC, Kaufmann WE, Raspa M, Bann CM, Gable JM, Harris HK, Budimirovic DB, Lozano R, Berry-Kravis E, Velinov M, Talboy AL, Sherman SL, Kaufmann WE, Schuster M, Tartaglia N, Filipink RA, Barbouth D, Lightbody A, Reiss A, Delahunty CM, Hagerman RJ, Hessl D, Erickson CA, Feldman G, Picker JD, Lachiewicz AM, Harris HK, Esler A, Frye RE, Evans PA, Morris MA, Haas-Givler BA, Gropman AL, Uy RS, Buchanan C, Frazier JA, Morris SM Journal of Autism and Developmental Disorders 2024 Feb 54 725-737 -
Neurological evaluation and management of autism spectrum disorder
Goodspeed K, Haffner D, Golla S, Morris MA, Evans P 2024 Jan 1 391-414 -
Electroencephalographic (EEG) Biomarkers in Genetic Neurodevelopmental Disorders
Goodspeed K, Armstrong D, Dolce A, Evans P, Said R, Tsai P, Sirsi D Journal of child neurology 2023 May 38 466-477 -
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 Dec 7 -
Neurological evaluation and management of autism spectrum disorder
Goodspeed K, Haffner D, Golla S, Ann Morris M, Evans P 2020 Jan 333-347 -
Obstructive sleep apnea in children with autism
Tomkies A, Johnson RF, Shah G, Caraballo M, Evans P, Mitchell RB Journal of Clinical Sleep Medicine 2019 Oct 15 1469-1476 -
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 33 233-244 -
Xp11.22 deletions encompassing CENPVL1, CENPVL2, MAGED1 and GSPT2 as a cause of syndromic X-linked intellectual disability
Grau C, Starkovich M, Azamian MS, Xia F, Cheung SW, Evans P, Henderson A, Lalani SR, Scott DA PloS one 2017 Apr 12 -
Efficacy of Low-Dose Buspirone for Restricted and Repetitive Behavior in Young Children with Autism Spectrum Disorder: A Randomized Trial
Chugani DC, Chugani HT, Wiznitzer M, Parikh S, Evans PA, Hansen RL, Nass R, Janisse JJ, Dixon-Thomas P, Behen M, Rothermel R, Parker JS, Kumar A, Muzik O, Edwards DJ, Hirtz D Journal of Pediatrics 2016 Mar 170 45-53.e4 -
Metabolic and Genetic Causes of Autism
Golla S, Evans P 2014 Nov 209-217 -
Autism Spectrum Disorders: Clinical Considerations
Evans P, Golla S, Ann Morris M 2014 Nov 197-207 -
Thiamine deficiency secondary to anorexia nervosa: An uncommon cause of peripheral neuropathy and wernicke encephalopathy in adolescence
Renthal W, Marin-Valencia I, Evans PA Pediatric Neurology 2014 Jul 51 100-103 -
Phenotypic spectrum and genotype-phenotype correlations of NRXN1 exon deletions
Schaaf CP, Boone PM, Sampath S, Williams C, Bader PI, Mueller JM, Shchelochkov OA, Brown CW, Crawford HP, Phalen JA, Tartaglia NR, Evans P, Campbell WM, Chun-Hui Tsai A, Parsley L, Grayson SW, Scheuerle A, Luzzi CD, Thomas SK, Eng PA, Kang SH, Patel A, Stankiewicz P, Cheung SW European Journal of Human Genetics 2012 Dec 20 1240-1247 -
Small genomic rearrangements involving FMR1 support the importance of its gene dosage for normal neurocognitive function
Nagamani SC, Erez A, Probst FJ, Bader P, Evans P, Baker LA, Fang P, Bertin T, Hixson P, Stankiewicz P, Nelson D, Patel A, Cheung SW Neurogenetics 2012 Nov 13 333-339 -
Efficacy of Porcine Secretin in Children with Autism and Pervasive Developmental Disorder
Kern JK, Miller VS, Evans PA, Trivedi MH Journal of Autism and Developmental Disorders 2002 Jun 32 153-160
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Relationship Between Intellectual Disability and Behavioral Comorbidity in Children With Fragile X Syndrome
Research
- Down's Syndrome
- Autism Spectrum Disorders
- Fragile X
Clinical Focus
- General Neurology
Children's Medical Center of Dallas
1935 Medical District DriveDallas, Texas 75235 214-730-5437 Directions to Children's Medical Center of Dallas at Children's Medical Center of Dallas, Dallas