Identification and Characterization of Genetic Components in Autism Spectrum Disorders 2020
The Identification of the Genetic Components of Autism Spectrum Disorders 2020 will be a useful resource for laboratory and clinical scientists, translational-based researchers, primary healthcare providers and physicians, psychologists/psychiatrists, neurologists, developmental pediatricians, clini...
保存先:
| フォーマット: | Online |
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| 言語: | 英語 |
| 出版事項: |
MDPI - Multidisciplinary Digital Publishing Institute
2022
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| 主題: | |
| オンライン･アクセス: | ONIX_20220506_9783036536118_113 |
| タグ: |
タグなし, このレコードへの初めてのタグを付けませんか!
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| _version_ | 1869520543734038528 |
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| collection | Directory of Open Access Books |
| description | The Identification of the Genetic Components of Autism Spectrum Disorders 2020 will be a useful resource for laboratory and clinical scientists, translational-based researchers, primary healthcare providers and physicians, psychologists/psychiatrists, neurologists, developmental pediatricians, clinical geneticists, teachers, special educators, and caregivers involved with individuals who have autism spectrum disorders (ASD), with the goal to translate information directly to the clinical, education and home settings. Other professionals, students at all levels, and families who are interested in this important neurodevelopmental disorder will find this textbook of value by obtaining a better awareness of the causes, testing, and understanding of genetic components leading to autism, and research that may open avenues for treatment with new approaches. This textbook includes nine chapters divided into three sections (clinical, genetics, other) written by experts in the field dedicated to genetics research and clinical care, description, and treatment by generating reviews for ASD and related disorders. These chapters include information on discoveries, risk factors, causation, diagnosis, treatment, and phenotyping with characterization of genomic or genetic factors and the environment, as genetics play an important role in up to 90% of individuals with autism via over 800 currently recognized genes. |
| format | Online |
| id | doab-20.500.12854ir-81047 |
| institution | Directory of Open Access Books |
| language | eng |
| publishDate | 2022 |
| publishDateRange | 2022 |
| publishDateSort | 2022 |
| publisher | MDPI - Multidisciplinary Digital Publishing Institute |
| publisherStr | MDPI - Multidisciplinary Digital Publishing Institute |
| record_format | ojs |
| spelling | doab-20.500.12854ir-810472024-03-28T03:31:09Z Identification and Characterization of Genetic Components in Autism Spectrum Disorders 2020 Butler, Merlin G. autism ASD genetics heterogeneity syndromes assessment medications treatment causes autism spectrum disorders (ASDs) proteomics metabolomics interactomics disease biomarkers clinical decision support systems (CDSSs) phenotypic subgroups stratified by ASD severity simplex families DNA methylation subgroup-associated genes and biological functions Broader Autism Phenotype genetic autism spectrum disorder multiplex family genetic factors epigenetic factors environmental factors pervasive developmental disorder post-synaptic density CNV SNP gene fusion CACNA1C CaV1.2 short QT syndrome dental enamel defect bioinformatics human genetics pharmacogenomics 15q11.2 BP1-BP2 deletion Burnside-Butler syndrome clinical findings cognition neuropsychiatric behavior development genomic characterization exome sequencing protein–protein interaction 22q13.3 duplication auditory steady-state response ASSR SHANK3 biomarker auditory event-related potential ERP autism spectrum disorders intellectual disabilities thema EDItEUR::G Reference, Information and Interdisciplinary subjects::GP Research and information: general thema EDItEUR::P Mathematics and Science::PS Biology, life sciences thema EDItEUR::P Mathematics and Science::PS Biology, life sciences::PSA Life sciences: general issues::PSAK Genetics (non-medical) The Identification of the Genetic Components of Autism Spectrum Disorders 2020 will be a useful resource for laboratory and clinical scientists, translational-based researchers, primary healthcare providers and physicians, psychologists/psychiatrists, neurologists, developmental pediatricians, clinical geneticists, teachers, special educators, and caregivers involved with individuals who have autism spectrum disorders (ASD), with the goal to translate information directly to the clinical, education and home settings. Other professionals, students at all levels, and families who are interested in this important neurodevelopmental disorder will find this textbook of value by obtaining a better awareness of the causes, testing, and understanding of genetic components leading to autism, and research that may open avenues for treatment with new approaches. This textbook includes nine chapters divided into three sections (clinical, genetics, other) written by experts in the field dedicated to genetics research and clinical care, description, and treatment by generating reviews for ASD and related disorders. These chapters include information on discoveries, risk factors, causation, diagnosis, treatment, and phenotyping with characterization of genomic or genetic factors and the environment, as genetics play an important role in up to 90% of individuals with autism via over 800 currently recognized genes. 2022-05-06T11:24:24Z 2022-05-06T11:24:24Z 2022 book ONIX_20220506_9783036536118_113 9783036536118 9783036536125 https://directory.doabooks.org/handle/20.500.12854/81047 eng image/jpeg Attribution 4.0 International https://mdpi.com/books/pdfview/book/5389 https://mdpi.com/books/pdfview/book/5389 MDPI - Multidisciplinary Digital Publishing Institute 10.3390/books978-3-0365-3612-5 10.3390/books978-3-0365-3612-5 46cabcaa-dd94-4bfe-87b4-55023c1b36d0 9783036536118 9783036536125 204 Basel open access |
| spellingShingle | autism ASD genetics heterogeneity syndromes assessment medications treatment causes autism spectrum disorders (ASDs) proteomics metabolomics interactomics disease biomarkers clinical decision support systems (CDSSs) phenotypic subgroups stratified by ASD severity simplex families DNA methylation subgroup-associated genes and biological functions Broader Autism Phenotype genetic autism spectrum disorder multiplex family genetic factors epigenetic factors environmental factors pervasive developmental disorder post-synaptic density CNV SNP gene fusion CACNA1C CaV1.2 short QT syndrome dental enamel defect bioinformatics human genetics pharmacogenomics 15q11.2 BP1-BP2 deletion Burnside-Butler syndrome clinical findings cognition neuropsychiatric behavior development genomic characterization exome sequencing protein–protein interaction 22q13.3 duplication auditory steady-state response ASSR SHANK3 biomarker auditory event-related potential ERP autism spectrum disorders intellectual disabilities thema EDItEUR::G Reference, Information and Interdisciplinary subjects::GP Research and information: general thema EDItEUR::P Mathematics and Science::PS Biology, life sciences thema EDItEUR::P Mathematics and Science::PS Biology, life sciences::PSA Life sciences: general issues::PSAK Genetics (non-medical) Identification and Characterization of Genetic Components in Autism Spectrum Disorders 2020 |
| title | Identification and Characterization of Genetic Components in Autism Spectrum Disorders 2020 |
| title_full | Identification and Characterization of Genetic Components in Autism Spectrum Disorders 2020 |
| title_fullStr | Identification and Characterization of Genetic Components in Autism Spectrum Disorders 2020 |
| title_full_unstemmed | Identification and Characterization of Genetic Components in Autism Spectrum Disorders 2020 |
| title_short | Identification and Characterization of Genetic Components in Autism Spectrum Disorders 2020 |
| title_sort | identification and characterization of genetic components in autism spectrum disorders 2020 |
| topic | autism ASD genetics heterogeneity syndromes assessment medications treatment causes autism spectrum disorders (ASDs) proteomics metabolomics interactomics disease biomarkers clinical decision support systems (CDSSs) phenotypic subgroups stratified by ASD severity simplex families DNA methylation subgroup-associated genes and biological functions Broader Autism Phenotype genetic autism spectrum disorder multiplex family genetic factors epigenetic factors environmental factors pervasive developmental disorder post-synaptic density CNV SNP gene fusion CACNA1C CaV1.2 short QT syndrome dental enamel defect bioinformatics human genetics pharmacogenomics 15q11.2 BP1-BP2 deletion Burnside-Butler syndrome clinical findings cognition neuropsychiatric behavior development genomic characterization exome sequencing protein–protein interaction 22q13.3 duplication auditory steady-state response ASSR SHANK3 biomarker auditory event-related potential ERP autism spectrum disorders intellectual disabilities thema EDItEUR::G Reference, Information and Interdisciplinary subjects::GP Research and information: general thema EDItEUR::P Mathematics and Science::PS Biology, life sciences thema EDItEUR::P Mathematics and Science::PS Biology, life sciences::PSA Life sciences: general issues::PSAK Genetics (non-medical) |
| topic_facet | autism ASD genetics heterogeneity syndromes assessment medications treatment causes autism spectrum disorders (ASDs) proteomics metabolomics interactomics disease biomarkers clinical decision support systems (CDSSs) phenotypic subgroups stratified by ASD severity simplex families DNA methylation subgroup-associated genes and biological functions Broader Autism Phenotype genetic autism spectrum disorder multiplex family genetic factors epigenetic factors environmental factors pervasive developmental disorder post-synaptic density CNV SNP gene fusion CACNA1C CaV1.2 short QT syndrome dental enamel defect bioinformatics human genetics pharmacogenomics 15q11.2 BP1-BP2 deletion Burnside-Butler syndrome clinical findings cognition neuropsychiatric behavior development genomic characterization exome sequencing protein–protein interaction 22q13.3 duplication auditory steady-state response ASSR SHANK3 biomarker auditory event-related potential ERP autism spectrum disorders intellectual disabilities thema EDItEUR::G Reference, Information and Interdisciplinary subjects::GP Research and information: general thema EDItEUR::P Mathematics and Science::PS Biology, life sciences thema EDItEUR::P Mathematics and Science::PS Biology, life sciences::PSA Life sciences: general issues::PSAK Genetics (non-medical) |
| url | ONIX_20220506_9783036536118_113 |