User profiles for S. Beighley
Steven BeighleyUniversity of Delaware Verified email at udel.edu Cited by 46 |
Comorbidity of physical and motor problems in children with autism
ML Matson, JL Matson, JS Beighley - Research in developmental …, 2011 - Elsevier
Autism and the related pervasive developmental disorders are a heavily researched group
of neurodevelopmental conditions. In addition to core symptoms, there are a number of other …
of neurodevelopmental conditions. In addition to core symptoms, there are a number of other …
[HTML][HTML] Genome sequencing identifies multiple deleterious variants in autism patients with more severe phenotypes
…, J Gerdts, TN Turner, MC Zody, JS Beighley… - Genetics in …, 2019 - Elsevier
… Then, candidate sites were chosen where the father’s genotype was 0/0, the mother’s
genotype was 0/0, and the child’s genotype was either 0/1 or 1/1. Finally, we applied allele count, …
genotype was 0/0, and the child’s genotype was either 0/1 or 1/1. Finally, we applied allele count, …
Food selectivity in children with and without an autism spectrum disorder: investigation of diagnosis and age.
JS Beighley, JL Matson, RD Rieske… - Research in …, 2013 - europepmc.org
Feeding problems are common in children with autism spectrum disorders (ASDs), with food
selectivity being the most frequently reported. Selectivity based on type and/or texture of …
selectivity being the most frequently reported. Selectivity based on type and/or texture of …
Information, meaning and animal communication
F Adams, SM Beighley - Animal communication theory …, 2013 - books.google.com
… Our perspective on animal signalling is consistent with Adams and Beighley’s argument
that it does not have linguistic properties. Nevertheless, some signals, like alarm calls, appear …
that it does not have linguistic properties. Nevertheless, some signals, like alarm calls, appear …
[PDF][PDF] Truncating variants in NAA15 are associated with variable levels of intellectual disability, autism spectrum disorder, and congenital anomalies
…, S Giusto, E Stracuzzi, C Romano, JS Beighley… - The American Journal of …, 2018 - cell.com
N-alpha-acetylation is a common co-translational protein modification that is essential for
normal cell function in humans. We previously identified the genetic basis of an X-linked …
normal cell function in humans. We previously identified the genetic basis of an X-linked …
Remembering: Does the emotional content of a photograph affect boundary extension?
… We reasoned that a 15 s duration would be less likely to undermine initiation of rumination
than would a briefer 5 s duration, and that studies that have presented images for 15 s each …
than would a briefer 5 s duration, and that studies that have presented images for 15 s each …
Developmental predictors of cognitive and adaptive outcomes in genetic subtypes of autism spectrum disorder
AB Arnett, JS Beighley, EC Kurtz‐Nelson… - Autism …, 2020 - Wiley Online Library
Approximately one‐fourth of autism spectrum disorder (ASD) cases are associated with a
disruptive genetic variant. Many of these ASD genotypes have been described previously, and …
disruptive genetic variant. Many of these ASD genotypes have been described previously, and …
Comparing challenging behavior in children diagnosed with autism spectrum disorders according to the DSM-IV-TR and the proposed DSM-5
Objective: The aim of the current study is to investigate challenging behavior in children who
may no longer meet criteria for an autism spectrum disorder (ASD) diagnosis according to …
may no longer meet criteria for an autism spectrum disorder (ASD) diagnosis according to …
The relationship between gender and age of first concern in toddlers with autism spectrum disorders
…, JL Matson, N Turygin, JS Beighley - Research in autism …, 2012 - Elsevier
The age at which parents first developed concerns over their child's development was
examined in 965 toddlers with autism spectrum disorders (ASD) and atypical development to …
examined in 965 toddlers with autism spectrum disorders (ASD) and atypical development to …
Clinical phenotypes of carriers of mutations in CHD8 or its conserved target genes
Background Variants disruptive to CHD8 (which codes for the protein CHD8 [chromodomain-helicase-DNA-binding
protein 8]) are among the most common mutations revealed by …
protein 8]) are among the most common mutations revealed by …