AJ Waters, T Brendler-Spaeth, D Smith, V Offord… - Nature Genetics, 2024 - nature.com
Many variants that we inherit from our parents or acquire de novo or somatically are rare, limiting the precision with which we can associate them with disease. We performed …
MR Baker, AS Lee, AM Rajadhyaksha - Channels, 2023 - Taylor & Francis
Recent human genetic studies have linked a variety of genetic variants in the CACNA1C and CACNA1D genes to neuropsychiatric and neurodevelopmental disorders. This is not …
M Malara, AK Lutz, B Incearap, HF Bauer… - Cellular and Molecular …, 2022 - Springer
Mutations or deletions of the SHANK3 gene are causative for Phelan–McDermid syndrome (PMDS), a syndromic form of autism spectrum disorders (ASDs). We analyzed Shank3Δ11 …
H Zhong, R Xiao, R Ruan, H Liu, X Li, Y Cai, J Zhao… - …, 2020 - Springer
Abstract Rationale Autism spectrum disorders (ASDs) are highly prevalent neurodevelopmental disorders characterized by deficits in social communication and …
The developing central nervous system is highly sensitive to nutrient changes during the perinatal period, emphasising the potential impact of alterations of maternal diet on offspring …
Background Extracellular signal-regulated kinase (ERK/MAPK) pathway in the brain is hypothesized to be a critical convergent node in the development of autism spectrum …
The current study was conducted to examine an innovative method for synthesizing gold nanoparticles (AuNPs) from an aqueous sweet granadilla (Passiflora ligularis Juss) P …
N Cheng, E Pagtalunan, A Abushaibah, J Naidu… - Scientific reports, 2020 - nature.com
Human social cognition relies heavily on the processing of various visual cues, such as eye contact and facial expressions. Atypical visual perception and integration have been …
Ketogenic diet (KD) is a high-fat and low-carbohydrate therapy for medically intractable epilepsy, and its applications in other neurological conditions, including those occurring in …