Walker McKinney, PhD
| Title | Clinical Psychologist |
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| Institution | Children's Mercy Kansas City |
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| Department | Developmental and Behavioral Health |
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| Address | 2401 Gillham Rd Kansas City MO 64108
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ORCID
.gif) | 0000-0001-5281-3749  |
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| vCard | Download vCard |
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| Title | Assistant Professor |
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| Institution | University of Missouri-Kansas City |
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| Department | Pediatrics |
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Biography | Northwestern University, Evanston, IL | BS | 2017 | Psychology, Communication Sciences and Disorders | | University of Kansas, Lawrence, KS | PhD | 2023 | Clinical Child Psychology | | Nationwide Children's Hospital, Columbus, OH | Internship | 2023 | Intellectual/Developmental Disabilities | | Cincinnati Children’s Hospital Medical Center, Cincinnati, OH | Fellowship | 2025 | Fragile X Syndrome Research, Treatment, and Evaluation |
Overview Research Dr. McKinney is a clinical psychologist at Children’s Mercy Kansas City in the Division of Developmental and Behavioral Health and an Assistant Professor in the Department of Pediatrics at the University of Missouri-Kansas City School of Medicine. He completed his clinical residency at Nationwide Children's Hospital and his research fellowship at Cincinnati Children's Hospital Medical Center. Dr. McKinney's research focuses on treatment development for individuals with neurodevelopmental disabilities. He is also interested in identifying social-environmental drivers of phenotypic differences in individuals with neurogenetic conditions such as Fragile X syndrome, Prader-Willi syndrome, and Angelman syndrome.
1568503 (Walker McKinney)May 1, 2026 - Oct 31, 2027 Foundation for Prader-Willi Research Adapting a Group Intervention for Emotion Dysregulation in Prader-Willi Syndrome Role Description: The goal of this study is to help teens with Prader-Willi Syndrome (PWS) and their families learn practical strategies for managing issues like irritability, meltdowns, and anxiety. The main objective of the study is to adapt current Regulating Together materials to create an outpatient group program for emotion dysregulation in Prader-Willi Syndrome (PWS) that will improve psychosocial outcomes for youth with PWS. Role: Principal Investigator |
| KL2TR002367 (Walker McKinney)Jul 1, 2026 - Jun 30, 2028 NIH/NCATS Adapting a group intervention for emotion dysregulation in autism and intellectual disability Role Description: The goal of this study is to help children with autism and a co-occurring intellectual disability and their families learn practical strategies for managing issues like irritability, aggression, and other challenging behaviors. The main objective of this study is:To adapt current Regulating Together materials to create an outpatient group program for emotion dysregulation in autism and co-occurring intellectual disability (ASD + ID) that will improve psychosocial outcomes for youth with ASD + ID. Role: Principal Investigator |
Bibliography
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Shafer RL, Wang J, Qu H, Simpson JP, Terza M, Shirley DJ, McKinney WS, Pulver S, Orlando AM, Romero RA, Karmakar B, Mosconi MW, Wang Z. Gait variability development in autistic individuals across childhood and adulthood. Res Sq. 2026 May 07. PMID: 42147152.
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Shin YS, Wang J, Pulver SL, Orlando AM, Romero RA, Cuomo CR, Lauzan IV, Dentry T, Shirley DJ, Christensen D, Unruh KE, Stevens CJ, McKinney WS, Mosconi MW, Vaillancourt DE, Wang Z, Coombes SA. Neuroanatomical patterns of dementia risk in autism spectrum disorder. Front Aging Neurosci. 2026; 18:1771822. PMID: 42006949.
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Blackburn AD, McKinney W, Birnschein AM, Esbensen AJ, McKinley S, Rosselot H, Hoffman EK, Erickson C, Shaffer R. Adapting a Behavioral Intervention for Caregivers of Children with Down Syndrome or Fragile X Syndrome: A Pilot Study of RUBI-DD. Behav Sci (Basel). 2026 Mar 22; 16(3). PMID: 41898133.
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McKinney WS, Nelson M, Shaffer RC, Dominick KC, Erickson CA, Schmitt LM. Brief Report: Differences Between Stanford-Binet Abbreviated and Full-Scale Estimates of IQ in Fragile X Syndrome Vary Across Development. J Autism Dev Disord. 2025 Oct 23. PMID: 41128961.
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McKinney WS, Corsmeier A, Dapore A, Gross C, Dominick KC, Erickson CA, Schmitt LM. Beyond the Fragile X protein: neighborhood characteristics explain individual differences in IQ and adaptive behaviors of Fragile X syndrome. Front Psychiatry. 2025; 16:1636987. PMID: 41048907.
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Christensen D, Shin YS, Wang J, Cuomo CR, Dentry T, Gemmell HM, Pulver SL, Orlando AM, McKinney WS, Stevens CJ, Unruh KE, Karmakar B, Coombes SA, Mosconi MW, Wang Z. Subcortical brain volume variations in autistic individuals across the lifespan. Mol Autism. 2025 Sep 01; 16(1):46. PMID: 40887620.
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McKinney WS, Tadevich LJ, Schmitt LM, Horn PS, Ruberg JR, White SW, Reisinger DL, Burkett KW, Sarawgi S, Kang S, Shaffer RC. Study protocol for a randomized controlled trial of Regulating Together (RT), a group therapy for emotion dysregulation in school-age autistic youth and their caregivers. BMC Psychol. 2025 Apr 24; 13(1):436. PMID: 40275407.
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Norris JE, De Stefano LA, McKinney WS, Schmitt LM, Miyakoshi M, Gross C, Piloto S, Heald B, Pedapati EV, Erickson CA, Sweeney JA, Ethridge LE. Auditory steady-state response deficits in Fragile X Syndrome implicate deficits in stimulus representation maintenance and GABAergic modulation. medRxiv. 2025 Jan 31. PMID: 39973986.
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McKinney WS, Schmitt LM, De Stefano LA, Ethridge L, Norris JE, Horn PS, Dauterman S, Rosselot H, Pedapati EV, Reisinger DL, Dominick KC, Shaffer RC, Chin D, Friedman NR, Hong M, Sweeney JA, Erickson C. Results from a Double-Blind, Randomized, Placebo-Controlled, Single-Dose, Crossover Trial of Lovastatin or Minocycline in Fragile X Syndrome. J Child Adolesc Psychopharmacol. 2025 May; 35(4):211-221. PMID: 39651602.
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McKinney WS, Williford DN, Abbeduto L, Schmitt LM. The impact of social-environmental factors on IQ in syndromic intellectual developmental disabilities. J Clin Transl Sci. 2024; 8(1):e59. PMID: 38655457.
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Unruh KE, Bartolotti JV, McKinney WS, Schmitt LM, Sweeney JA, Mosconi MW. Functional connectivity of cortical-cerebellar networks in relation to sensorimotor behavior and clinical features in autism spectrum disorder. Cereb Cortex. 2023 07 05; 33(14):8990-9002. PMID: 37246152.
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McKinney WS, Kelly SE, Unruh KE, Shafer RL, Sweeney JA, Styner M, Mosconi MW. Corrigendum: Cerebellar volumes and sensorimotor behavior in autism spectrum disorder. Front Integr Neurosci. 2022; 16:1020980. PMID: 36159091.
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McKinney WS, Kelly SE, Unruh KE, Shafer RL, Sweeney JA, Styner M, Mosconi MW. Cerebellar Volumes and Sensorimotor Behavior in Autism Spectrum Disorder. Front Integr Neurosci. 2022; 16:821109. PMID: 35592866.
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Lepping RJ, McKinney WS, Magnon GC, Keedy SK, Wang Z, Coombes SA, Vaillancourt DE, Sweeney JA, Mosconi MW. Visuomotor brain network activation and functional connectivity among individuals with autism spectrum disorder. Hum Brain Mapp. 2022 Feb 01; 43(2):844-859. PMID: 34716740.
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Unruh KE, McKinney WS, Bojanek EK, Fleming KK, Sweeney JA, Mosconi MW. Initial action output and feedback-guided motor behaviors in autism spectrum disorder. Mol Autism. 2021 Jul 10; 12(1):52. PMID: 34246292.
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Wang Z, Lane C, Terza M, Khemani P, Lui S, McKinney WS, Mosconi MW. Upper and Lower Limb Movement Kinematics in Aging FMR1 Gene Premutation Carriers. Brain Sci. 2020 Dec 24; 11(1). PMID: 33374331.
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McKinney WS, Bartolotti J, Khemani P, Wang JY, Hagerman RJ, Mosconi MW. Cerebellar-cortical function and connectivity during sensorimotor behavior in aging FMR1 gene premutation carriers. Neuroimage Clin. 2020; 27:102332. PMID: 32711390.
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McKinney WS, Wang Z, Kelly S, Khemani P, Lui S, White SP, Mosconi MW. Precision Sensorimotor Control in Aging FMR1 Gene Premutation Carriers. Front Integr Neurosci. 2019; 13:56. PMID: 31632248.
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Nayar K, McKinney W, Hogan AL, Martin GE, La Valle C, Sharp K, Berry-Kravis E, Norton ES, Gordon PC, Losh M. Language processing skills linked to FMR1 variation: A study of gaze-language coordination during rapid automatized naming among women with the FMR1 premutation. PLoS One. 2019; 14(7):e0219924. PMID: 31348790.
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Park SH, Wang Z, McKinney W, Khemani P, Lui S, Christou EA, Mosconi MW. Functional motor control deficits in older FMR1 premutation carriers. Exp Brain Res. 2019 Sep; 237(9):2269-2278. PMID: 31161414.
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Nayar K, Gordon PC, Martin GE, Hogan AL, La Valle C, McKinney W, Lee M, Norton ES, Losh M. Links between looking and speaking in autism and first-degree relatives: insights into the expression of genetic liability to autism. Mol Autism. 2018; 9:51. PMID: 30338047.
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| Year | Publications |
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| 2018 | 1 | | 2019 | 3 | | 2020 | 2 | | 2021 | 2 | | 2022 | 2 | | 2023 | 1 | | 2024 | 2 | | 2025 | 5 | | 2026 | 3 |
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