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Identification and Characterization of Genetic Components in Autism Spectrum Disorders 2019
Identification and Characterization of Genetic Components in Autism Spectrum Disorders 2019
Autore Butler Merlin G
Pubbl/distr/stampa Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022
Descrizione fisica 1 online resource (256 p.)
Soggetto topico Biology, life sciences
Genetics (non-medical)
Research & information: general
Soggetto non controllato 15q11.2 BP1-BP2 microdeletion (Burnside-Butler syndrome)
15q11.2 BP1-BP2 microdeletion (Burnside-Butler) syndrome
AMPA receptors
AmplideX
animal model
ASD
autism
autism candidate genes
autism spectrum disorder
Autism spectrum disorder
autism spectrum disorders
autism spectrum disorders (ASD)
biological networks
BMI
Body mass index
cancer
case-control association analysis
collapsin response mediator protein 4
CYFIP1
cytokine
data integration
developmental delays
DNA methylation
epigenetics
expression profile
fragile X syndrome
gene expression
genetics
genomics
guanine nucleotide exchange factor
gut
gut-brain interaction
heterogeneity reduction
IL-6
imprinting
intellectual disability
leaky gut
magnesium transporters and supplementation
maternal immune activation
mice
microbiome
microRNA- interactions
molecular functions and processes
monocyte
mosaicism
motor delays
MS-QMA
multi-omics
nanostring
network diffusion
neurodevelopmental disorder
NIPA1
NIPA2
NMDA receptors
Obesity
overlapping genes and gene profiling
Overweight
parent-of-origin effects
pediatrics
Phelan McDermid Syndrome
phenotype-genotype correlation
phenotypes and diseases
postnatal VPA injection
potential treatment options
Prader-Willi and Angelman syndromes
ProSAP2
quantitative traits
RNA toxicity
SAM
sex different phenotypes
SHANK
stratification by trait severity
STRING-protein-protein interaction
super-pathways
synaptic plasticity
synaptotagmin-like protein 4 (SYTL4)
SYTL4-protein structure
T cell cytokine
trained immunity
transmembrane protein 187 (TMEM187)
TUBGCP5 genes
whole-exome sequencing
β-glucan
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910566483203321
Butler Merlin G  
Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Identification and Characterization of Genetic Components in Autism Spectrum Disorders 2020
Identification and Characterization of Genetic Components in Autism Spectrum Disorders 2020
Autore Butler Merlin G
Pubbl/distr/stampa Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022
Descrizione fisica 1 online resource (204 p.)
Soggetto topico Biology, life sciences
Genetics (non-medical)
Research & information: general
Soggetto non controllato 15q11.2 BP1-BP2 deletion
22q13.3 duplication
ASD
assessment
ASSR
auditory event-related potential
auditory steady-state response
autism
autism spectrum disorder
autism spectrum disorders
autism spectrum disorders (ASDs)
bioinformatics
biomarker
Broader Autism Phenotype
Burnside-Butler syndrome
CACNA1C
causes
CaV1.2
clinical decision support systems (CDSSs)
clinical findings
CNV
cognition
dental enamel defect
disease biomarkers
DNA methylation
environmental factors
epigenetic factors
ERP
exome sequencing
gene fusion
genetic
genetic factors
genetics
genomic characterization
heterogeneity
human genetics
intellectual disabilities
interactomics
medications
metabolomics
multiplex family
neuropsychiatric behavior development
pervasive developmental disorder
pharmacogenomics
phenotypic subgroups stratified by ASD severity
post-synaptic density
protein-protein interaction
proteomics
SHANK3
short QT syndrome
simplex families
SNP
subgroup-associated genes and biological functions
syndromes
treatment
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910566463603321
Butler Merlin G  
Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui