Autism
What's New
Last Posted: Mar 23, 2024
- Genomic analysis of 116 autism families strengthens known risk genes and highlights promising candidates
M Viggiano et al, NPJ Genomic Medicine, March 22, 2024 - Experiences and concerns of parents of children with a 16p11.2 deletion or duplication diagnosis: a reflexive thematic analysis.
Charlotte E Butter et al. BMC Psychol 2024 12(1) 137 - De novo copy number variations in candidate genomic regions in patients of severe autism spectrum disorder in Vietnam.
Hoa Thi Phuong Bui et al. PLoS One 2024 19(3) e0290936 - What do parents of nonverbal and minimally verbal autistic children think about genomic autism research?
Kathryn Asbury et al. Autism 2024 13623613231213431 - Enhancing ASD detection accuracy: a combined approach of machine learning and deep learning models with natural language processing.
Sergio Rubio-Martín et al. Health Inf Sci Syst 2024 12(1) 20 - SPARKing New Insight Into Autism Across the Lifespan.
Khemika K Sudnawa et al. Am J Intellect Dev Disabil 2024 129(2) 91-95 - Parental Perspectives on Early Life Screening and Genetic Testing for ASD: A Systematic Review.
Katerina Dounavi et al. J Autism Dev Disord 2024 - Provider-reported experiences, barriers, and perspectives on genetic testing as part of autism diagnosis.
Amy Wang et al. PLoS One 2024 19(2) e0296942 - Impact of Receiving Genetic Diagnoses on Parents' Perceptions of Their Children with Autism and Intellectual Disability.
Robert Klitzman et al. J Autism Dev Disord 2023 - Improving care for rare genetic neurodevelopmental disorders: a systematic review and critical appraisal of clinical practice guidelines using AGREE II.
Mirthe J Klein Haneveld et al. Genet Med 2024 101071 - Autism Spectrum Disorder Detection by Hybrid Convolutional Recurrent Neural Networks from Structural and Resting State Functional MRI Images.
Emel Koc et al. Autism Res Treat 2023 20234136087 - An Umbrella Review of the Fusion of fMRI and AI in Autism.
Daniele Giansanti et al. Diagnostics (Basel) 2023 13(23) - Development of a Novel Telemedicine Tool to Reduce Disparities Related to the Identification of Preschool Children with Autism.
Liliana Wagner et al. J Autism Dev Disord 2023 - Molecular Diagnostic Yield of Exome Sequencing in Patients With Congenital Hydrocephalus: A Systematic Review and Meta-Analysis.
Ana B W Greenberg et al. JAMA Netw Open 2023 6(11) e2343384 - Whole genome analysis of rare deleterious variants adds further evidence to BRSK2 and other risk genes in Autism Spectrum Disorder.
Elena Bacchelli et al. Res Sq 2023 - Comparison of three bioinformatics tools in the detection of ASD candidate variants from whole exome sequencing data.
Apurba Shil et al. Sci Rep 2023 13(1) 18853 - Factors Associated With Underutilization of Genetic Testing in Autism Spectrum Disorders.
Nicolas J Abreu et al. Pediatr Neurol 2023 15017-23 - Postpartum and non-postpartum depression: a population-based matched case-control study comparing polygenic risk scores for severe mental disorders.
Trine Munk-Olsen et al. Transl Psychiatry 2023 13(1) 346 - [Differential diagnosis of autism spectrum disorder and global developmental delay based on machine learning and Children Neuropsychological and Behavioral Scale].
Gang Zhou et al. Zhongguo Dang Dai Er Ke Za Zhi 2023 25(10) 1028-1033 - Genetic counseling clinic model expansion: Impact on access for general genetics clinic.
Rachel Doberstein et al. J Genet Couns 2023
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About RCH PHGKB
Reproductive and Child Health PHGKB is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other materials that address the translation of genomic and other precision health discoveries into improved health care and prevention related to reproductive and child Health...more
Content Summary
Common RCH Related Topics
- Attention Deficit/Hyperactivity Disorder
- Autism
- Birth Defects
- Carrier Testing
- Cerebral Palsy
- Congenital heart defects
- Pregnancy loss
- Developmental Disabilities
- Gestational Diabetes
- Hearing loss
- Neural tube defects
- Infant Mortality
- Infertility
- Learning disability
- Newborn Screening
- Preeclampsia
- Prematurity
- Prenatal Testing
- Stillbirth
- Sudden Infant Death Syndrome
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
- Page last updated:Mar 27, 2024
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