1. Mullin AP, Gokhale A, Moreno-De-Luca A, Sanyal S, Waddington JL, et al. Neurodevelopmental disorders: mechanisms and boundary definitions from genomes, interactomes and proteomes. Transl Psychiatry. 2013; 3(12): e329.
2. Sowa M, Meulenbroek R. Effects of physical exercise on autism spectrum disorders: A meta-analysis. Res Autism Spectr Disord. 2012; 6(1): 46–57.
3. Silverman JL, Thurm A, Ethridge SB, Soller MM, Petkova SP, Abel T, et al. Reconsidering animal models used to study autism spectrum disorder: Current state and optimizing future. Genes Brain Behav. 2022; 21(5): e12803.
4. Casey AF, Quenneville-Himbeault G, Normore A, Davis H, Martell SG. A therapeutic skating intervention for children with autism spectrum disorder. Pediatr Phys Ther. 2015; 27(2): 170–7.
5. Posar A, Visconti P. Early motor signs in autism spectrum disorder. Children (Basel). 2022; 9(2): 294.
6. Kindregan D, Gallagher L, Gormley J. Gait deviations in children with autism spectrum disorders: a review. Autism Res Treat. 2015; 741480.
7. Glumbić N, Đorđević M, Brojčin B. Digital inclusion of individuals with autism spectrum disorder. Cham: Springer; 2022.
8. Leeflang L. Een onderzoek naar de effectiviteit van welbevindentherapie bij cliënten met een Posttraumatische stressstoornis [Thesis]. Enschede: University of Twente; 2016.
9. Fournier KA, Hass CJ, Naik SK, Lodha N, Cauraugh JH. Motor coordination in autism spectrum disorders: a synthesis and meta-analysis. J Autism Dev Disord. 2010; 40(10): 1227–40.
10. Sedaghati P, Alghosi M, Hosseini F. The effect of fatigue on postural control in individuals with multiple sclerosis: a systematic review. BMC Neurol. 2023; 23(1):409.
11. Zhong T, Liu H, Li Y, Qi J. Correlates of Physical Activity of Children and Adolescents with Autism Spectrum Disorder in Low-and Middle-Income Countries: A Systematic Review of Cross-Sectional Studies. Int J Environ Res Public Health. 2022; 19(23): 16301.
12. Foroushani N, Ameri E, Hemayattalab R. Relationship between executive function/attention and motor skills by mediation of anthropometric indicators in preschoolers. Int J Sport Stud. 2016; 6(2): 109–15.
13. Nazary Sharif H, Daneshmandi H, Norasteh AA, Aboutalebi S. Postural profile in children with autism. J Mazandaran Univ Med Sci. 2016; 26(143): 71–9. [In Persian].
14. Salar S, Daneshmandi H, Karimizadeh Ardakani M, Nazari Sharif H. The relationship of core strength with static and dynamic balance in children with autism. Ann Appl Sport Sci. 2014; 2(4): 33–42.
15. Salar S, Daneshmandi H, Panaghi L, Karimizadeh Ardekani M, Nazari Sharif H. The investigation of the relationship between core endurance with static and dynamic balance in children with autism spectrum disorder. Int J Sport Stud. 2015; 5(1): 48–56.
16. Salar S, Daneshmandi H. Relationship between lumbar-pelvic function and static and dynamic balance in children with autism spectrum disorders. Sci J Rehabil Med. 2017; 6(2): 168–79. [In Persian].
17. Salar S, Haegele JA, Daneshmandi H. Iranian Parents’ Perceptions on Physical Activity for Their Children with Autism Spectrum Disorder during the COVID-19 Pandemic. Phys Treat-Spec Phys Ther J. 2022; 12(1): 23–30.
18. Salar S, Daneshmandi H, J Lieberman L, Kashi A, Shafiee S. Physical activity levels in Iranian children and adolescents with autism spectrum disorder. Sport Sci Health Res. 2021; 13(2): 187–96. [In Persian].
19. Hashemian M, Daneshmandi H, Kashi A. Effect of Corrective Games and Physical Exercise Packages on Motor Skills of Children With Autism Spectrum Disorder. Iran Rehabil J. 2025; 23(2): 191–200.
20. Aminikhah B, Daneshmandi H. The effect of six weeks corrective virtual game on balance and orientation in children with autism: A Randomized Controlled Study. J Res Sport Rehabil. 2024; 11(22): 47–59. [In Persian].
21. Deitz JC, Kartin D, Kopp K. Review of the Bruininks-Oseretsky test of motor proficiency, (BOT-2). Phys Occup Ther Pediatr 2007; 27(4): 87-102.
22. Ayhan F, Konopka G. Genomics of autism spectrum disorder: approach to therapy. F1000Res 2018; 7: 627.
23. Loke YJ, Hannan AJ, Craig JM. The role of epigenetic change in autism spectrum disorders. Front Neurol 2015; 6: 107.
24. Antaki D, Guevara J, Maihofer AX, Klein M, Gujral M, et al. A phenotypic spectrum of autism is attributable to the combined effects of rare variants, polygenic risk and sex. Nat Genet 2022; 54(9): 1284-92.
25. Jiang R, Huang W, Qiu X, Chen J, Luo R, et al. Unveiling promising drug targets for autism spectrum disorder: insights from genetics, transcriptomics, and proteomics. Brief Bioinform. 2024; 25(4): bbae353.
26. Moyses-Oliveira M, Yadav R, Erdin S, Talkowski ME. New gene discoveries highlight functional convergence in autism and related neurodevelopmental disorders. Curr Opin Genet Dev. 2020; 65: 195-206.
27. Dell’Osso L, Bonelli C, Giovannoni F, Poli F, Anastasio L, et al. Available Treatments for Autism Spectrum Disorder: From Old Strategies to New Options. Pharmaceuticals (Basel). 2025; 18(3): 324.
28. Huguet G, Ey E, Bourgeron T. The genetic landscapes of autism spectrum disorders. Annu Rev Genomics Hum Genet. 2013; 14: 191-213.
29. Bourgeron T. From the genetic architecture to synaptic plasticity in autism spectrum disorder. Nat Rev Neurosci. 20.
30. Grove J, Ripke S, Als TD, Mattheisen M, Walters RK, et al. Identification of common genetic risk variants for autism spectrum disorder. Nat Genet. 2019; 51(3): 431-44.
31. Fu JM, Satterstrom FK, Peng M, Brand H, Collins RL, et al. Rare coding variation provides insight into the genetic architecture and phenotypic context of autism. Nat Genet. 2022; 54(9): 1320-31.
32. Rylaarsdam L, Guemez-Gamboa A. Genetic causes and modifiers of autism spectrum disorder. Front Cell Neurosci. 2019;
13: 365.
33. Wawszczak-Kasza M, Rachuna J, Madej Ł, Lewitowicz W, Lewitowicz P, et al. Familial Molecular Burden in Autism Spectrum Disorder: A Next-Generation Sequencing Study of Polish Affected Families. Int J Mol Sci 2025; 26(19): 9672.
34. Selvanayagam T, Hoang N, Sarikaya E, Howe J, Russell C, et al. Clinical utility of genome sequencing in autism: illustrative examples from a genomic research study. J Med Genet 2025; 62(6): 413-21.
35. Kim SW, An JY. Advancing precision diagnosis in autism: Insights from large-scale genomic studies. Mol Cells 2025: 100248.
36. Litman A, Sauerwald N, Green Snyder L, Foss-Feig J, Park CY, et al. Decomposition of phenotypic heterogeneity in autism reveals underlying genetic programs. Nat Genet 2025; 57(7): 1611-9.
37. La Monica I, Di Iorio MR, Sica A, Rufino F, Sotira C, et al. Autism Spectrum Disorder: Genetic Mechanisms and Inheritance Patterns. Genes 2025; 16(5): 478.
38. Wang T, Zhao PA, Eichler EE. Rare variants and the oligogenic architecture of autism. Trends Genet. 2022; 38(9): 895-903.
39. Jeste SS, Geschwind DH. Disentangling the heterogeneity of autism spectrum disorder through genetic findings. Nat Rev Neurol. 2014; 10(2): 74-81.
40. Gaugler T, Klei L, Sanders SJ, Bodea CA, Goldberg AP, et al. Most genetic risk for autism resides with common variation. Nat Genet. 2014; 46(8): 881-5.
41. Nygren G, Cederlund M, Sandberg E, Gillstedt F, Arvidsson T, et al. The prevalence of autism spectrum disorders in toddlers: a population study of 2-year-old Swedish children. J Autism Dev Disord. 2012; 42(7): 1491-7.
42. De Rubeis S, He X, Goldberg AP, Poultney CS, Samocha K, et al. Synaptic, transcriptional and chromatin genes disrupted in autism. Nature. 2014; 515(7526): 209-15.
43. Sanders SJ, He X, Willsey AJ, Ercan-Sencicek AG, Samocha KE, et al. Insights into autism spectrum disorder genomic architecture and biology from 71 risk loci. Neuron. 2015; 87(6): 1215-33.
44. Sestan N. Lost in translation: traversing the complex path from genomics to therapeutics in autism spectrum disorder. Neuron. 2018; 100(2): 406-23.
45. Cirnigliaro M, Chang TS, Arteaga SA, Pérez-Cano L, Ruzzo EK, et al. The contributions of rare inherited and polygenic risk to ASD in multiplex families. Proc Natl Acad Sci U S A 2023; 120(31): e2215632120.
46. Khundrakpam B, Vainik U, Gong J, Al-Sharif N, Bhutani N, et al. Neural correlates of polygenic risk score for autism spectrum disorders in general population. Brain Commun 2020; 2(2): fcaa092.
47. Mohammad S, Gentreau M, Dubol M, Rukh G, Mwinyi J, et al. Association of polygenic scores for autism with volumetric MRI phenotypes in cerebellum and brainstem in adults. Mol Autism 2024; 15(1): 34.
48. Li D, Choque-Olsson N, Jiao H, Norgren N, Jonsson U, et al. The influence of common polygenic risk and gene sets on social skills group training response in autism spectrum disorder. NPJ Genom Med 2020; 5(1): 45.
49. Chawner SJ, Doherty JL, Anney RJ, Antshel KM, Bearden CE, et al. A genetics-first approach to dissecting the heterogeneity of autism: phenotypic comparison of autism risk copy number variants. Am J Psychiatry 2021; 178(1): 77-86.
50. Bernier R, Hudac CM, Chen Q, Zeng C, Wallace AS, et al. Developmental trajectories for young children with 16p11.2 copy number variation. Am J Med Genet B Neuropsychiatr Genet 2017; 174(4): 367-80.
51. Kubota T, Mochizuki K. Epigenetic effect of environmental factors on autism spectrum disorders. Int J Environ Res Public Health. 2016; 13(5): 504.
52. Gregory SG, Connelly JJ, Towers AJ, Johnson J, Biscocho D, et al. Genomic and epigenetic evidence for oxytocin receptor deficiency in autism. BMC Med 2009; 7(1): 62.
53. Wang SE, Jiang Y-H. Epigenetic epidemiology of autism and other neurodevelopmental disorders. In: Karmodiya K, editor. Epigenetic Epidemiology. New York: Springer; 2022. p. 405-26.
54. Ladd-Acosta C, Fallin MD. The role of epigenetics in genetic and environmental epidemiology. Epigenomics 2016; 8(2):
271-83.
55. Ziegler C, Dannlowski U, Bräuer D, Stevens S, Laeger I, et al. Oxytocin receptor gene methylation: converging multilevel evidence for a role in social anxiety. Neuropsychopharmacology 2015; 40(6): 1528-38.
56. Elagoz Yuksel M, Yuceturk B, Karatas OF, Ozen M, Dogangun B. The altered promoter methylation of oxytocin receptor gene in autism. J Neurogenet 2016; 30(3-4): 280-4.
57. Halepoto DM, Bashir S, Zeina R, Al-Ayadhi LY. Correlation between hedgehog (Hh) protein family and brain-derived neurotrophic factor (BDNF) in autism spectrum disorder (ASD). J Coll Physicians Surg Pak 2015; 25(12): 882-5.
58. Pan C-Y. Motor proficiency and physical fitness in adolescent males with and without autism spectrum disorders. Autism. 2014; 18(2): 156-65.
59. Staples KL, Reid G. Fundamental movement skills and autism spectrum disorders. J Autism Dev Disord. 2010; 40(2): 209-17.
60. Morrow Jr JR, Tucker JS, Jackson AW, Martin SB, Greenleaf CA, et al. Meeting physical activity guidelines and health-related fitness in youth. Am J Prev Med. 2013; 44(5): 439-44.
61. Winnick JP, Short FX. Conceptual framework for the Brockport physical fitness test. Adapt Phys Activ Q. 2005; 22(4):
323-32.
62. Salar S, Daneshmandi H. The effect of 8 weeks of core stability training program on lumbar-pelvic function in children with autism spectrum. Sport Sci Health Res 2016; 8(1): 67-81.
63. Zhang L, Zhang C, Yuan X, Ji Y. The impact of exercise interventions on core symptoms of 3-12-year-old children with autism spectrum disorder: a systematic review and network meta-analysis. Eur Child Adolesc Psychiatry 2025: 1-15.
64. Kou R, Li Z, Li M, Zhou R, Zhu F, et al. Comparative effectiveness of physical exercise interventions on sociability and communication in children and adolescents with autism: a systematic review and network meta-analysis. BMC Psychol 2024; 12(1): 712.
65. Wang S, Chen D, Yang Y, Zhu L, Xiong X, et al. Effectiveness of physical activity interventions for core symptoms of autism spectrum disorder: a systematic review and meta-analysis. Autism Res 2023; 16(9): 1811-24.
66. Lloyd M, MacDonald M, Lord C. Motor skills of toddlers with autism spectrum disorders. Autism. 2013; 17(2): 133-46.
67. Hildebrandt V, Chorus A, Stubbe J. Bewegen en Gezondheid 2008/2009. Leiden: TNO Kwaliteit van Leven; 2010.
68. Pitetti KH, Rendoff AD, Grover T, Beets MW. The efficacy of a 9-month treadmill walking program on the exercise capacity and weight reduction for adolescents with severe autism. J Autism Dev Disord. 2007; 37(6): 997-1006.
69. Pan C-Y. The efficacy of an aquatic program on physical fitness and aquatic skills in children with and without autism spectrum disorders. Res Autism Spectr Disord. 2011; 5(1): 657-65.
70. Petrus C, Adamson SR, Block L, Einarson SJ, Sharifnejad M, et al. Effects of exercise interventions on stereotypic behaviours in children with autism spectrum disorder. Physiother Can. 2008; 60(2): 134-45.
71. Radak Z, Taylor AW. Issues on trainability. Front Physiol 2022; 12: 790196.
72. Williams CJ, Williams MG, Eynon N, Ashton KJ, Little JP, et al. Genes to predict VO2max trainability: a systematic review. BMC Genomics. 2017; 18(Suppl 8): 831.
73. Caru M, Petrykey K, Drouin S, Beaulieu P, St-Onge P, et al. Identification of genetic association between cardiorespiratory fitness and the trainability genes in childhood acute lymphoblastic leukemia survivors. BMC Cancer. 2019; 19(1): 443.
74. Chomistek AK, Chasman DI, Cook NR, Rimm EB, Lee I-M. Physical activity, genes for physical fitness, and risk of coronary heart disease. Med Sci Sports Exerc. 2013; 45(4): 691-7.
75. Bouchard C, Sarzynski MA, Rice TK, Kraus WE, Church TS, et al. Genomic predictors of the maximal O2 uptake response to standardized exercise training programs. J Appl Physiol. 2011; 110(5): 1160-70.
76. Rico-Sanz J, Rankinen T, Joanisse DR, Leon AS, Skinner JS, et al. Familial resemblance for muscle phenotypes in the HERITAGE Family Study. Med Sci Sports Exerc. 2003; 35(8): 1360-6.
77. Mann TN, Lamberts RP, Lambert MI. High responders and low responders: factors associated with individual variation in response to standardized training. Sports Med. 2014; 44(8): 1113-24.
78. Bouchard C, Antunes-Correa LM, Ashley EA, Franklin N, Hwang PM, et al. Personalized preventive medicine: genetics and the response to regular exercise in preventive interventions. Prog Cardiovasc Dis. 2015; 57(4): 337-46.
79. Hasin Y, Seldin M, Lusis A. Multi-omics approaches to disease. Genome Biol 2017; 18(1): 83.
80. Zhuang H, Liang Z, Ma G, Qureshi A, Ran X, et al. Autism spectrum disorder: pathogenesis, biomarker, and intervention therapy. MedComm 2024; 5(3): e497.
81. Matoba N, Liang D, Sun H, Aygün N, McAfee JC, et al. Common genetic risk variants identified in the SPARK cohort support DDHD2 as a candidate risk gene for autism. Transl Psychiatry. 2020; 10(1): 265.
82. Eynon B, North KN, Britton SL, Ashley EA, Klissouras V, et al. Performance and Adaptation to Training. Med Sport Sci 2016; 61: 55-67.
83. Thomaes T, Thomis M, Onkelinx S, Fagard R, Matthijs G, et al. A genetic predisposition score for muscular endophenotypes predicts the increase in aerobic power after training: the CAREGENE study. BMC Genet. 2011; 12(1): 84.
84. Do Rhee K, Wang Y, Ten Hoeve J, Stiles L, Nguyen TTT, et al. Ciliary neurotrophic factor-mediated neuroprotection involves enhanced glycolysis and anabolism in degenerating mouse retinas. Nat Commun. 2022; 13(1): 7037.
85. Subramanian M, Timmerman CK, Schwartz JL, Pham DL, Meffert MK, et al. Characterizing autism spectrum disorders by key biochemical pathways. Front Neurosci. 2015; 9: 313.
86. Zhang L, Ou J, Xu X, Peng Y, Guo H, et al. AMPD1 functional variants associated with autism in Han Chinese population. Eur Arch Psychiatry Clin Neurosci. 2015; 265(6): 511-7.
87. Rico-Sanz J, Rankinen T, Joanisse DR, Leon AS, Skinner JS, et al. Cardiorespiratory responses to exercise and the C34T AMPD1 gene polymorphism in the HERITAGE family study. Med Sci Sports Exerc. 2003; 35(5): S377.
88. Karege F, Méary A, Perroud N, Jamain S, Leboyer M, et al. Genetic overlap between schizophrenia and bipolar disorder: a study with AKT1 gene variants and clinical phenotypes. Schizophr Res 2012; 135(1-3): 8-14.
89. Karege F, Perroud N, Schürhoff F, Meary A, Marillier G, et al. Association of AKT1 gene variants and protein expression in both schizophrenia and bipolar disorder. Genes Brain Behav 2010; 9(5): 503-11.
90. Onore C, Yang H, Van de Water J, Ashwood P. Dynamic Akt/mTOR signaling in children with autism spectrum disorder. Front Pediatr 2017; 5: 43.
91. Levitt P, Campbell DB. The genetic and neurobiologic compass points toward common signaling dysfunctions in autism spectrum disorders. J Clin Invest 2009; 119(4): 747-54.
92. Hughes HK, Rowland ME, Onore CE, Rogers S, Ciernia AV, et al. Dysregulated gene expression associated with inflammatory and translation pathways in activated monocytes from children with autism spectrum disorder. Transl Psychiatry. 2022; 12(1): 39.
93. Jenkins NT, McKenzie JA, Damcott CM, Witkowski S, Hagberg JM. Endurance exercise training effects on body fatness, VO2max, HDL-C subfractions, and glucose tolerance are influenced by a PLIN haplotype in older Caucasians. J Appl Physiol. 2010; 108(3): 498-506.
94. Pirkmajer S, Chibalin AV. Na, K-ATPase regulation in skeletal muscle. Am J Physiol Endocrinol Metab 2016; 311(1): E1-E31.
95. Ukkola O, Joanisse DR, Tremblay A, Bouchard C. Na+-K+-ATPase α2-gene and skeletal muscle characteristics in response to long-term overfeeding. J Appl Physiol. 2003; 94(5): 1870-4.
96. Foraker J, Millard SP, Leong L, Thomson Z, Chen S, et al. The APOE gene is differentially methylated in Alzheimer’s disease. J Alzheimers Dis. 2015; 48(3): 745-55.
97. Ashley-Koch AE, Jaworski J, Mei H, Ritchie MD, Skaar DA, et al. Investigation of potential gene-gene interactions between APOE and RELN contributing to autism risk. Psychiatr Genet. 2007; 17(4): 221-6.
98. Hu Z, Yang Y, Zhao Y, Yu H, Ying X, et al. APOE hypermethylation is associated with autism spectrum disorder in a Chinese population. Exp Ther Med. 2018; 15(6): 4749-54.
99. Soraya GV, Fitrah YA, Bintang AK, Akbar M, Jannah AR, et al. Elucidating the role of APOE ε4 gene variants in the Clinical Manifestation of Parkinson’s Disease. Front Aging Neurosci 2025; 17: 1632480.
100. Yu B, Chen W, Wang R, Qi Q, Li K, et al. Association of apolipoprotein E polymorphism with maximal oxygen uptake after exercise training: a study of Chinese young adult. Lipids Health Dis. 2014; 13(1): 40.
101. Yan MH, Wang X, Zhu X. Mitochondrial defects and oxidative stress in Alzheimer disease and Parkinson disease. Free Radic Biol Med 2013; 62: 90-101.
102. Onkelinx S, Cornelissen V, Defoor J, Matthijs G, Thomaes T, et al. The CAREGENE study: genetic variants of the endothelium and aerobic power in patients with coronary artery disease. Acta Cardiol. 2011; 66(4): 407-14.
103. Rossignol D, Frye R. Mitochondrial dysfunction in autism spectrum disorders: a systematic review and meta-analysis. Mol Psychiatry 2012; 17(3): 290-314.
104. Frye RE, editor. Mitochondrial dysfunction in autism spectrum disorder: unique abnormalities and targeted treatments. St. Louis: Elsevier; 2020.
105. Singh K, Singh IN, Diggins E, Connors SL, Karim MA, et al. Developmental regression and mitochondrial function in children with autism. Ann Clin Transl Neurol. 2020; 7(5): 683-94.
106. Bjørklund G, Meguid NA, El-Bana MA, Tinkov AA, Saad K, et al. Oxidative stress in autism spectrum disorder. Mol Neurobiol. 2020;57(5):2314-32.
107. Wallace DC. Mitochondrial genetic medicine. Nat Genet 2018; 50(12): 1642-9.
108. Vellers HL, Verhein KC, Burkholder AB, Lee J, Kim Y, et al. Association between mitochondrial DNA sequence variants and VO2 max trainability. Med Sci Sports Exerc. 2020; 52(11): 2303-11.