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Emre Ertürk; Ümit Isik; Evrim Aktepe – International Journal of Developmental Disabilities, 2024
Introduction: A number of recent studies have brought attention to the involvement of dietary salt and blood sodium levels in the etiopathogenesis of autism. In our study, by comparing the blood sodium levels of children with autism spectrum disease (ASD) and healthy children, we aimed to shed light on the etiopathogenesis of ASD. Method: We…
Descriptors: Foreign Countries, Autism Spectrum Disorders, Children, Adolescents
Al-Mamari, Watfa; Idris, Ahmed B.; Al-Thihli, Khalid; Abdulrahim, Reem; Jalees, Saquib; Al-Jabri, Muna; Gabr, Ahlam; Al Murshedi, Fathiya; Al Kindy, Adila; Al-Hadabi, Intisar; Bruwer, Zandrè; Islam, M. Mazharul; Alsayegh, Abeer – International Journal of Developmental Disabilities, 2023
This study aimed to systematically assess the impact of clinical and demographic variables on the diagnostic yield of Whole Exome Sequencing (WES) when applied to children with Autism Spectrum Disorder (ASD) from a consanguineous population. Ninety-seven children were included in the analysis, 63% were male and 37% were females. 77.3% had a…
Descriptors: Autism Spectrum Disorders, Genetics, Children, Etiology
Yitik Tonkaz, Gülsüm; Esin, Ibrahim Selçuk; Turan, Bahadir; Uslu, Hakan; Dursun, Onur Burak – Journal of Autism and Developmental Disorders, 2023
Leaky gut hypothesis is one of the well-known theory which tries to explain etiology of Autism Spectrum Disorder (ASD). Unfortunately there is still a gap of evidence to investigate the corner points of the hypothesis. The aim of this study was to investigate the determinants of leaky gut in children with ASD, their siblings and healthy controls.…
Descriptors: Human Body, Physical Health, Etiology, Autism Spectrum Disorders
Panahi, Yasin; Salasar Moghaddam, Fahimeh; Babaei, Khadijeh; Eftekhar, Mohammad; Shervin Badv, Reza; Eskandari, Mohammad Reza; Vafaee-Shahi, Mohammad; Pezeshk, Hamid; Pedram, Mehrdad – Journal of Autism and Developmental Disorders, 2023
Autism spectrum disorders (ASD) are strikingly more prevalent in males, but the molecular mechanisms responsible for ASD sex-differential risk are poorly understood. Abnormally shorter telomeres have been associated with autism. Examination of relative telomere lengths (RTL) among non-syndromic male (N = 14) and female (N = 10) children with…
Descriptors: Autism Spectrum Disorders, Gender Differences, Symptoms (Individual Disorders), Children
Serdar Karatoprak; Sadettin Burak Acikel; Abdulbaki Akyildiz; Fatma Coskun; Fatma Hümeyra Yerlikaya – International Journal of Developmental Disabilities, 2024
Background: Autism Spectrum Disorder (ASD) is a neurodevelopmental disorder, the etiology of which has not been clearly determined yet. There is increasing evidence that synaptic and dendritic changes are involved in the etiology of ASD. The aim of this study is to determine whether serum Thrombospondin-1 and Thrombospondin-2 differ between ASD…
Descriptors: Children, Autism Spectrum Disorders, Etiology, Metabolism
Vicedo, Marga; Ilerbaig, Juan – Journal of Autism and Developmental Disorders, 2021
This paper examines the genesis of Leo Kanner's 1943 seminal paper on autism. It shows that describing children as autistic or lacking affective contact with people was not new by this time. But Kanner's proposal that infantile autism constituted a hitherto unidentified condition that was inborn and different from childhood schizophrenia was new.…
Descriptors: Autism, Etiology, Children, History
Brief Report: Neuroimaging Endophenotypes of Social Robotic Applications in Autism Spectrum Disorder
Cerasa, Antonio; Ruta, Liliana; Marino, Flavia; Biamonti, Giuseppe; Pioggia, Giovanni – Journal of Autism and Developmental Disorders, 2021
A plethora of neuroimaging studies have focused on the discovery of potential neuroendophenotypes useful to understand the etiopathogenesis of autism and predict treatment response. Social robotics has recently been proposed as an effective tool to strengthen the current treatments in children with autism. However, the high clinical heterogeneity…
Descriptors: Neurology, Diagnostic Tests, Genetics, Robotics
Blessed Sheriff; Kwame Sakyi; Esther K. Malm; Celeste Zabel; Prince G. Owusu; Leonie-Akofio Sowah; Adote Anum – International Journal of Developmental Disabilities, 2024
Proper treatment of developmental disabilities requires health workers to have adequate knowledge of etiology and referral procedures. There is a dearth of research on knowledge of developmental disabilities among health workers in Ghana. The purpose of this study was to document knowledge about developmental disorders, causes, and referral…
Descriptors: Foreign Countries, Allied Health Personnel, Knowledge Level, Hospitals
Gallardo-Carrasco, Maria Carmen; Jiménez-Barbero, José Antonio; Bravo-Pastor, María del Mar; Martin-Castillo, David; Sánchez-Muñoz, María – Journal of Autism and Developmental Disorders, 2022
Vitamin and fatty acid deficiency in children diagnosed with autism has been linked to the etiology and course of the disease but the results have been inconsistent. In our work, we present a narrative review, which includes 20 observational studies that provide data on the blood levels of vitamin D, folate, or fatty acids of children diagnosed…
Descriptors: Biochemistry, Autism Spectrum Disorders, Meta Analysis, Comparative Analysis
Michaelides, Orestis; Luciano, Michelle – Journal of Speech, Language, and Hearing Research, 2023
Purpose: Reading and speech difficulties are common in childhood, yet it is not fully understood how much of their etiology is shared. This partly derives from methodological issues related to overlooking the potential co-occurrence between the two sets of difficulties. This study investigated the effects of five bioenvironmental predictors in a…
Descriptors: Predictor Variables, Reading Difficulties, Speech Impairments, Etiology
Valerie J. Pereira; Debbie Sell – International Journal of Language & Communication Disorders, 2024
Background: Speech in individuals with cleft lip and/or palate (CLP) is a complex myriad of presenting symptoms. It is uniquely associated with the structural difference of velopharyngeal insufficiency (VPI), together with a wide and heterogeneous range of other aetiologies which often co-occur. The nature of the speech sound disorder (SSD)…
Descriptors: Anatomy, Physiology, Labeling (of Persons), Congenital Impairments
Chin Yang Shapland; Ellen Verhoef; George Davey Smith; Simon E. Fisher; Brad Verhulst; Philip S. Dale; Beate St Pourcain – npj Science of Learning, 2021
Several abilities outside literacy proper are associated with reading and spelling, both phenotypically and genetically, though our knowledge of multivariate genomic covariance structures is incomplete. Here, we introduce structural models describing genetic and residual influences between traits to study multivariate links across measures of…
Descriptors: Multivariate Analysis, Genetics, Literacy, Language Skills
Dana Kamara; Theodore P. Beauchaine – Review Journal of Autism and Developmental Disorders, 2020
Sleep problems are common among children with neurodevelopmental disorders (NDDs). We review sleep disturbance in three major NDDs: autism spectrum disorder, Down syndrome, and fetal alcohol spectrum disorder (FASD). We review associations with functional impairment, discuss how patterns of sleep disturbance inform understanding of etiology, and…
Descriptors: Sleep, Infants, Children, Neurodevelopmental Disorders
Cann, Nicola – Child Care in Practice, 2023
Historically sleep was considered a passive activity, but research now strongly suggests that it is a time of neurological growth, where memories and skills are consolidated (Fallone et al., 2002). Good sleep is thought to influence cognitive, physical and emotional performance, and aid in effective emotional regulation (Alfano & Gamble,…
Descriptors: Autism Spectrum Disorders, Children, Adolescents, Sleep
Haghighatfard, Arvin; Yaghoubi asl, Elham; Bahadori, Rosita Azar; Aliabadian, Rojina; Farhadi, Mahdi; Mohammadpour, Fatemeh; Tabrizi, Zeinab – Autism & Developmental Language Impairments, 2022
Background and aims: Autism spectrum disorder (ASD) is a neurodevelopmental disorder characterized by language impairment, and challenges with social interaction, communication, and repetitive behaviors. Although genetics are a primary cause of ASD, the exact genes and molecular mechanisms involved in its pathogenesis are not completely clear. The…
Descriptors: Autism Spectrum Disorders, Executive Function, Genetic Disorders, Genetics