Identification and Characterization of Genetic Components in Autism Spectrum Disorders 2019

The Identification of the Genetic Components of Autism Spectrum Disorders 2019 will serve as a resource for laboratory and clinical scientists as well as translational-based researchers, primary healthcare providers or physicians, psychologists/psychiatrists, neurologists, developmental pediatrician...

Full description

Saved in:
Bibliographic Details
Sonstige:
Year of Publication:2022
Language:English
Physical Description:1 electronic resource (256 p.)
Tags: Add Tag
No Tags, Be the first to tag this record!
id 993545370904498
ctrlnum (CKB)5680000000037548
(oapen)https://directory.doabooks.org/handle/20.500.12854/81036
(EXLCZ)995680000000037548
collection bib_alma
record_format marc
spelling Butler, Merlin G. edt
Identification and Characterization of Genetic Components in Autism Spectrum Disorders 2019
Basel MDPI - Multidisciplinary Digital Publishing Institute 2022
1 electronic resource (256 p.)
text txt rdacontent
computer c rdamedia
online resource cr rdacarrier
The Identification of the Genetic Components of Autism Spectrum Disorders 2019 will serve as a resource for laboratory and clinical scientists as well as translational-based researchers, primary healthcare providers or physicians, psychologists/psychiatrists, neurologists, developmental pediatricians, clinical geneticists, and other healthcare providers, teachers, caregivers and students involved in autism spectrum disorders (ASD) with the goal to translate information directly to the clinic, education and home setting. Other professionals, students and families might find this textbook of value based on better awareness, causes and understanding of genetic components leading to autism and open avenues for treatment. Genetics play a role with up to 90% of autism, with over 800 currently recognized genes contributing to causes, clinical presentation, treatment, and counseling of family members. This textbook includes 13 chapters divided into three sections (clinical, genetics, other) written by experts in the field dedicated to research and clinical care, description, treatment and generating relevant reviews for ASD and related disorders impacting gene expression, profiling, and pathways. Identification of potential risk factors will be discussed, including obesity, microbiota, malignancy, and the immune system, as well as their direct or indirect contribution to ASD treatment and causation.
English
Research & information: general bicssc
Biology, life sciences bicssc
Genetics (non-medical) bicssc
autism spectrum disorders (ASD)
cancer
overlapping genes and gene profiling
super-pathways
phenotypes and diseases
molecular functions and processes
15q11.2 BP1-BP2 microdeletion (Burnside-Butler) syndrome
imprinting
parent-of-origin effects
phenotype-genotype correlation
autism
developmental delays
motor delays
microbiome
gut
ProSAP2
Phelan McDermid Syndrome
gut–brain interaction
leaky gut
IL-6
SHANK
collapsin response mediator protein 4
autism spectrum disorder
neurodevelopmental disorder
whole-exome sequencing
animal model
sex different phenotypes
15q11.2 BP1–BP2 microdeletion (Burnside–Butler syndrome)
NIPA1
NIPA2
CYFIP1
TUBGCP5 genes
Prader–Willi and Angelman syndromes
magnesium transporters and supplementation
potential treatment options
intellectual disability
AMPA receptors
NMDA receptors
guanine nucleotide exchange factor
synaptic plasticity
Autism spectrum disorder
ASD
Obesity
Overweight
Body mass index
BMI
autism candidate genes
synaptotagmin-like protein 4 (SYTL4)
transmembrane protein 187 (TMEM187)
SYTL4-protein structure
STRING-protein-protein interaction
expression profile
microRNA- interactions
autism spectrum disorders
biological networks
genomics
multi-omics
network diffusion
data integration
genetics
quantitative traits
stratification by trait severity
heterogeneity reduction
case-control association analysis
fragile X syndrome
RNA toxicity
DNA methylation
mosaicism
pediatrics
MS-QMA
AmplideX
cytokine
monocyte
β-glucan
T cell cytokine
trained immunity
maternal immune activation
epigenetics
mice
postnatal VPA injection
SAM
gene expression
nanostring
3-0365-3609-4
3-0365-3610-8
Butler, Merlin G. oth
language English
format eBook
author2 Butler, Merlin G.
author_facet Butler, Merlin G.
author2_variant m g b mg mgb
author2_role Sonstige
title Identification and Characterization of Genetic Components in Autism Spectrum Disorders 2019
spellingShingle Identification and Characterization of Genetic Components in Autism Spectrum Disorders 2019
title_full Identification and Characterization of Genetic Components in Autism Spectrum Disorders 2019
title_fullStr Identification and Characterization of Genetic Components in Autism Spectrum Disorders 2019
title_full_unstemmed Identification and Characterization of Genetic Components in Autism Spectrum Disorders 2019
title_auth Identification and Characterization of Genetic Components in Autism Spectrum Disorders 2019
title_new Identification and Characterization of Genetic Components in Autism Spectrum Disorders 2019
title_sort identification and characterization of genetic components in autism spectrum disorders 2019
publisher MDPI - Multidisciplinary Digital Publishing Institute
publishDate 2022
physical 1 electronic resource (256 p.)
isbn 3-0365-3609-4
3-0365-3610-8
illustrated Not Illustrated
work_keys_str_mv AT butlermerling identificationandcharacterizationofgeneticcomponentsinautismspectrumdisorders2019
status_str n
ids_txt_mv (CKB)5680000000037548
(oapen)https://directory.doabooks.org/handle/20.500.12854/81036
(EXLCZ)995680000000037548
carrierType_str_mv cr
is_hierarchy_title Identification and Characterization of Genetic Components in Autism Spectrum Disorders 2019
author2_original_writing_str_mv noLinkedField
_version_ 1796651990698164224
fullrecord <?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>05418nam-a2201309z--4500</leader><controlfield tag="001">993545370904498</controlfield><controlfield tag="005">20231214133427.0</controlfield><controlfield tag="006">m o d </controlfield><controlfield tag="007">cr|mn|---annan</controlfield><controlfield tag="008">202205s2022 xx |||||o ||| 0|eng d</controlfield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(CKB)5680000000037548</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(oapen)https://directory.doabooks.org/handle/20.500.12854/81036</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(EXLCZ)995680000000037548</subfield></datafield><datafield tag="041" ind1="0" ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Butler, Merlin G.</subfield><subfield code="4">edt</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Identification and Characterization of Genetic Components in Autism Spectrum Disorders 2019</subfield></datafield><datafield tag="260" ind1=" " ind2=" "><subfield code="a">Basel</subfield><subfield code="b">MDPI - Multidisciplinary Digital Publishing Institute</subfield><subfield code="c">2022</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">1 electronic resource (256 p.)</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">computer</subfield><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">online resource</subfield><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">The Identification of the Genetic Components of Autism Spectrum Disorders 2019 will serve as a resource for laboratory and clinical scientists as well as translational-based researchers, primary healthcare providers or physicians, psychologists/psychiatrists, neurologists, developmental pediatricians, clinical geneticists, and other healthcare providers, teachers, caregivers and students involved in autism spectrum disorders (ASD) with the goal to translate information directly to the clinic, education and home setting. Other professionals, students and families might find this textbook of value based on better awareness, causes and understanding of genetic components leading to autism and open avenues for treatment. Genetics play a role with up to 90% of autism, with over 800 currently recognized genes contributing to causes, clinical presentation, treatment, and counseling of family members. This textbook includes 13 chapters divided into three sections (clinical, genetics, other) written by experts in the field dedicated to research and clinical care, description, treatment and generating relevant reviews for ASD and related disorders impacting gene expression, profiling, and pathways. Identification of potential risk factors will be discussed, including obesity, microbiota, malignancy, and the immune system, as well as their direct or indirect contribution to ASD treatment and causation.</subfield></datafield><datafield tag="546" ind1=" " ind2=" "><subfield code="a">English</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Research &amp; information: general</subfield><subfield code="2">bicssc</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Biology, life sciences</subfield><subfield code="2">bicssc</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Genetics (non-medical)</subfield><subfield code="2">bicssc</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">autism spectrum disorders (ASD)</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">cancer</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">overlapping genes and gene profiling</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">super-pathways</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">phenotypes and diseases</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">molecular functions and processes</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">15q11.2 BP1-BP2 microdeletion (Burnside-Butler) syndrome</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">imprinting</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">parent-of-origin effects</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">phenotype-genotype correlation</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">autism</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">developmental delays</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">motor delays</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">microbiome</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">gut</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">ProSAP2</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Phelan McDermid Syndrome</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">gut–brain interaction</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">leaky gut</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">IL-6</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">SHANK</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">collapsin response mediator protein 4</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">autism spectrum disorder</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">neurodevelopmental disorder</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">whole-exome sequencing</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">animal model</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">sex different phenotypes</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">15q11.2 BP1–BP2 microdeletion (Burnside–Butler syndrome)</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">NIPA1</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">NIPA2</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">CYFIP1</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">TUBGCP5 genes</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Prader–Willi and Angelman syndromes</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">magnesium transporters and supplementation</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">potential treatment options</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">intellectual disability</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">AMPA receptors</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">NMDA receptors</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">guanine nucleotide exchange factor</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">synaptic plasticity</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Autism spectrum disorder</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">ASD</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Obesity</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Overweight</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Body mass index</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">BMI</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">autism candidate genes</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">synaptotagmin-like protein 4 (SYTL4)</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">transmembrane protein 187 (TMEM187)</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">SYTL4-protein structure</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">STRING-protein-protein interaction</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">expression profile</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">microRNA- interactions</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">autism spectrum disorders</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">biological networks</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">genomics</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">multi-omics</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">network diffusion</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">data integration</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">genetics</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">quantitative traits</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">stratification by trait severity</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">heterogeneity reduction</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">case-control association analysis</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">fragile X syndrome</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">RNA toxicity</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">DNA methylation</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">mosaicism</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">pediatrics</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">MS-QMA</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">AmplideX</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">cytokine</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">monocyte</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">β-glucan</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">T cell cytokine</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">trained immunity</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">maternal immune activation</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">epigenetics</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">mice</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">postnatal VPA injection</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">SAM</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">gene expression</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">nanostring</subfield></datafield><datafield tag="776" ind1=" " ind2=" "><subfield code="z">3-0365-3609-4</subfield></datafield><datafield tag="776" ind1=" " ind2=" "><subfield code="z">3-0365-3610-8</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Butler, Merlin G.</subfield><subfield code="4">oth</subfield></datafield><datafield tag="906" ind1=" " ind2=" "><subfield code="a">BOOK</subfield></datafield><datafield tag="ADM" ind1=" " ind2=" "><subfield code="b">2023-12-15 05:53:45 Europe/Vienna</subfield><subfield code="f">system</subfield><subfield code="c">marc21</subfield><subfield code="a">2022-05-14 21:41:54 Europe/Vienna</subfield><subfield code="g">false</subfield></datafield><datafield tag="AVE" ind1=" " ind2=" "><subfield code="i">DOAB Directory of Open Access Books</subfield><subfield code="P">DOAB Directory of Open Access Books</subfield><subfield code="x">https://eu02.alma.exlibrisgroup.com/view/uresolver/43ACC_OEAW/openurl?u.ignore_date_coverage=true&amp;portfolio_pid=5337903860004498&amp;Force_direct=true</subfield><subfield code="Z">5337903860004498</subfield><subfield code="b">Available</subfield><subfield code="8">5337903860004498</subfield></datafield></record></collection>