Rebecca Wilson, PsyD
Professor of Clinical Practice, Pediatrics-Developmental Pediatrics

Professional Titles

• Chair of Psychology

Teaching

Publications

• Early communication
• Nienke Bouw, Hanna Swaab, Nicole Tartaglia, Rebecca L Wilson, Kim Van der Velde , Sophie van Rijn. Early symptoms of autism spectrum disorder (ASD) in 1-8 year old children with sex chromosome trisomies (XXX, XXY, XYY), and the predictive value of joint attention Eur Child Adolesc Psychiatry . 2022 Sep 15. doi: 10.1007/s00787-022-02070-y
• Society for Developmental Behavioral Pediatrics, Research Symposium: Integrating Multiple Research Approaches to Advance Neurodevelopmental and Medical Care for Sex Chromosome Aneuploidies a. Authors: Nicole Tartaglia, Rebecca Wilson, Laura Pyle, Shanlee Davis, Jennifer Janusz, Talia Thompson, SDBP, Denver October 2022
• Society for Developmental Behavioral Pediatrics Informatics-based Intervention to Improve Documentation Efficiency Jack Dempsey, Abigail Angulo, Rebecca Wilson, Lisa Hayutin, Elizabeth Bennett, SDBP, Denver October 2022
• Society for Developmental Behavioral Pediatrics. Improving access to diagnosis and management of autism by increasing community provider comfort: a combined model of community of practice ECHO and second level screening tool for autism. Rebecca Wilson, Ann Reynolds, Richard Boles, Sandra Friedman. SDBP, Denver, October 2022
• Klinefelter Synposium: The eXtraordinarY Babies Study: Early Social Communication Skills in Infants with Sex Chromosome Trisomy (SCT). Stephanie K. Takamatsu, Talia Thomson, The eXtraordinarY Kids Study Team, Judith Ross, Nicole Tartaglia, and Rebecca Wilson, Leiden, Sept 2022
• Thompson, T., Davis, S., Janusz, J., Frith, E., Pyle,L., Howell, S., Boada, R., Wilson, R., and Tartaglia, T. "Supporting Students with Sex Chromosome Aneuploidies in Educational Settings." (2021).
• Thompson T, Howell S, Davis S, Wilson R, Janusz J, Boada R, Pyle L, Tartaglia N. Current survey of early childhood intervention services in infants and young children with sex chromosome aneuploidies. Am J Med Genet C Semin Med Genet. 2020 Jun;184(2):414-427. PubMed PMID: 32449585
• Tartaglia N, Howell S, Davis S, Kowal K, Tanda T, Brown M, Boada C, Alston A, Crawford L, Thompson T, van Rijn S, Wilson R, Janusz J, Ross J. Early neurodevelopmental and medical profile in children with sex chromosome trisomies: Background for the prospective eXtraordinarY babies study to identify early risk factors and targets for intervention. Am J Med Genet C Semin Med Genet. 2020 Jun;184(2):428-443. PubMed PMID: 32506668
• Wigby K, Cordeiro L, Wilson R, Angkustsiri K, Simon TJ, Tartaglia N. Adaptive functioning in children and adolescents with Trisomy X: An exploratory analysis. Am J Med Genet C Semin Med Genet. 2020 Jun;184(2):456-468. PubMed PMID: 32548885
• Villagomez AN, Muñoz FM, Peterson RL, Colbert AM, Gladstone M, MacDonald B, Wilson R, Fairlie L, Gerner GJ, Patterson J, Boghossian NS, Burton VJ, Cortés M, Katikaneni LD, Larson JCG, Angulo AS, Joshi J, Nesin M, Padula MA, Kochhar S, Connery AK. Neurodevelopmental delay: Case definition & guidelines for data collection, analysis, and presentation of immunization safety data. Vaccine. 2019 Dec 10;37(52):7623-7641. PubMed PMID: 31783983
• Tartaglia NR, Wilson R, Miller JS, Rafalko J, Cordeiro L, Davis S, Hessl D, Ross J. Autism Spectrum Disorder in Males with Sex Chromosome Aneuploidy: XXY/Klinefelter Syndrome, XYY, and XXYY. J Dev Behav Pediatr. 2017 Apr;38(3):197-207. PubMed PMID: 28333849
• Wigby K, D'Epagnier C, Howell S, Reicks A, Wilson R, Cordeiro L, Tartaglia N. Expanding the phenotype of Triple X syndrome: A comparison of prenatal versus postnatal diagnosis. Am J Med Genet A. 2016 Nov;170(11):2870-2881. PubMed PMID: 27644018
• Davis S, Howell S, Wilson R, Tanda T, Ross J, Zeitler P, Tartaglia N. Advances in the Interdisciplinary Care of Children with Klinefelter Syndrome. Adv Pediatr. 2016 Aug;63(1):15-46. PubMed PMID: 27426894
• Tartaglia N, Howell S, Wilson R, Janusz J, Boada R, Martin S, Frazier JB, Pfeiffer M, Regan K, McSwegin S, Zeitler P. The eXtraordinarY Kids Clinic: an interdisciplinary model of care for children and adolescents with sex chromosome aneuploidy. J Multidiscip Healthc. 2015;8:323-34. PubMed PMID: 26229481
• Pickler L, Wilson R, Tsai AC. Revisiting recombinant 8 syndrome. Am J Med Genet A. 2011 Aug;155A(8):1923-9. PubMed PMID: 21739594
• Tartaglia NR, Howell S, Sutherland A, Wilson R, Wilson L. A review of trisomy X (47,XXX). Orphanet J Rare Dis. 2010 May 11;5:8. PubMed PMID: 20459843
• Tartaglia N, Cordeiro L, Howell S, Wilson R, Janusz J. The spectrum of the behavioral phenotype in boys and adolescents 47,XXY (Klinefelter syndrome). Pediatr Endocrinol Rev. 2010 Dec;8 Suppl 1:151-9. PubMed PMID: 21217607
• Grigsby J, Brega AG, Leehey MA, Goodrich GK, Jacquemont S, Loesch DZ, Cogswell JB, Epstein J, Wilson R, Jardini T, Gould E, Bennett RE, Hessl D, Cohen S, Cook K, Tassone F, Hagerman PJ, Hagerman RJ. Impairment of executive cognitive functioning in males with fragile X-associated tremor/ataxia syndrome. Mov Disord. 2007 Apr 15;22(5):645-50. PubMed PMID: 17266074
• Grigsby J, Brega AG, Jacquemont S, Loesch DZ, Leehey MA, Goodrich GK, Hagerman RJ, Epstein J, Wilson R, Cogswell JB, Jardini T, Tassone F, Hagerman PJ. Impairment in the cognitive functioning of men with fragile X-associated tremor/ataxia syndrome (FXTAS). J Neurol Sci. 2006 Oct 25;248(1-2):227-33. PubMed PMID: 16780889
• Grigsby J, Leehey MA, Jacquemont S, Brunberg JA, Hagerman RJ, Wilson R, Epstein JH, Greco CM, Tassone F, Hagerman PJ. Cognitive impairment in a 65-year-old male with the fragile X-associated tremor-ataxia syndrome (FXTAS). Cogn Behav Neurol. 2006 Sep;19(3):165-71. PubMed PMID: 16957495