Results 201 to 210 of about 385,791 (336)

Intact Susceptibility to Visual Illusions in Autistic Individuals

open access: yesAutism Research, EarlyView.
ABSTRACT Altered sensory perception, a core characteristic of autism, has been attributed to attenuated use of stimuli context or prior information in perception. Reduced susceptibility to perceptual illusions was extensively used to support these accounts for autistic perception. However, empirical evidence has been inconsistent.
Yarden Mazuz   +2 more
wiley   +1 more source

AutoCaSc: Prioritizing candidate genes for neurodevelopmental disorders

open access: yesHuman Mutation, Volume 43, Issue 12, Page 1795-1807, December 2022., 2022
Abstract Routine exome sequencing (ES) in individuals with neurodevelopmental disorders (NDD) remains inconclusive in >50% of the cases. Research analysis of unsolved cases can identify novel candidate genes but is time‐consuming, subjective, and hard to compare between labs.
Johann Kaspar Lieberwirth   +5 more
wiley   +1 more source

Cochlear implant in patients with autistic spectrum disorder-a systematic review. [PDF]

open access: yesBraz J Otorhinolaryngol, 2021
Tavares FDS   +6 more
europepmc   +1 more source

Recognition of biological motion in children with autistic spectrum disorders [PDF]

open access: green, 2008
Carole Parron   +5 more
openalex   +1 more source

Investigation of a broad‐spectrum micronutrient formulation as a possible precipitant of pharmacokinetic micronutrient–drug interactions

open access: yesBritish Journal of Clinical Pharmacology, EarlyView.
Aims Daily broad‐spectrum micronutrients are being used by the general public and formulations are receiving research interest in mental health settings. Despite concerns about combining medicines and broad‐spectrum micronutrients in mental health care, there have not been any formal evaluations of potential interactions.
Bess M. Kew   +7 more
wiley   +1 more source

Mosaicism in tuberous sclerosis complex: Lowering the threshold for clinical reporting

open access: yesHuman Mutation, Volume 43, Issue 12, Page 1956-1969, December 2022., 2022
Abstract Tuberous sclerosis complex (TSC) is a multi‐system genetic disorder. Most patients have germline mutations in TSC1 or TSC2 but, 10%–15% patients do not have TSC1/TSC2 mutations detected on routine clinical genetic testing. We investigated the contribution of low‐level mosaic TSC1/TSC2 mutations in unsolved sporadic patients and families with ...
Zimeng Ye   +31 more
wiley   +1 more source

Error and feedback processing in children with ADHD and children with Autistic Spectrum Disorder: An EEG event-related potential study [PDF]

open access: green, 2008
Yvonne Groen   +5 more
openalex   +1 more source

Listening to Hong Kong children's perspectives through pretend play

open access: yesBritish Educational Research Journal, EarlyView.
Abstract Quality in early childhood education and care (ECEC) has become an increasing concern in recent years. The issue has been regularly discussed by different stakeholders. However, the rising concern regarding quality in ECEC has not seriously taken into account children's perspectives.
Suzannie K. Y. Leung
wiley   +1 more source

de novo variant calling identifies cancer mutation signatures in the 1000 Genomes Project

open access: yesHuman Mutation, Volume 43, Issue 12, Page 1979-1993, December 2022., 2022
Abstract Detection of de novo variants (DNVs) is critical for studies of disease‐related variation and mutation rates. To accelerate DNV calling, we developed a graphics processing units‐based workflow. We applied our workflow to whole‐genome sequencing data from three parent‐child sequenced cohorts including the Simons Simplex Collection (SSC), Simons
Jeffrey K. Ng   +16 more
wiley   +1 more source

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