Literature DB >> 26983421

The association between familial ASD diagnosis, autism symptomatology and developmental functioning in young children.

Jasper A Estabillo1, Johnny L Matson2, Xinrui Jiang2.   

Abstract

Few studies have directly compared individuals with and without a relative diagnosed with ASD on various domains. The present study aimed to examine the relationship between familial ASD diagnosis and the exhibition of ASD symptoms in young children with and without ASD diagnoses. Participants included 8353 children aged 17-37 months old and their families. They were divided into four groups based on individual and family diagnosis, then compared on autism symptomatology and developmental domains. No differences were found between ASD groups on overall scores and each of the factor domains, indicating no association between family ASD diagnosis and ASD symptomatology or developmental functioning. Disparate results were found for atypically developing groups with and without relatives diagnosed with ASD. Implications of these results are discussed.

Entities:  

Keywords:  Autism; Autism symptomatology; Broad autism phenotype; Concordance; Developmental functioning; Familial risk

Mesh:

Year:  2016        PMID: 26983421     DOI: 10.1007/s00787-016-0838-1

Source DB:  PubMed          Journal:  Eur Child Adolesc Psychiatry        ISSN: 1018-8827            Impact factor:   4.785


  37 in total

1.  Defining key features of the broad autism phenotype: a comparison across parents of multiple- and single-incidence autism families.

Authors:  Molly Losh; Debra Childress; Kristen Lam; Joseph Piven
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2008-06-05       Impact factor: 3.568

Review 2.  Genetic testing for autism spectrum disorders.

Authors:  Sarah C Bauer; Michael E Msall
Journal:  Dev Disabil Res Rev       Date:  2011

3.  Genetic heritability and shared environmental factors among twin pairs with autism.

Authors:  Joachim Hallmayer; Sue Cleveland; Andrea Torres; Jennifer Phillips; Brianne Cohen; Tiffany Torigoe; Janet Miller; Angie Fedele; Jack Collins; Karen Smith; Linda Lotspeich; Lisa A Croen; Sally Ozonoff; Clara Lajonchere; Judith K Grether; Neil Risch
Journal:  Arch Gen Psychiatry       Date:  2011-07-04

Review 4.  Disentangling the heterogeneity of autism spectrum disorder through genetic findings.

Authors:  Shafali S Jeste; Daniel H Geschwind
Journal:  Nat Rev Neurol       Date:  2014-01-28       Impact factor: 42.937

Review 5.  Intellectual disability and autism spectrum disorders: causal genes and molecular mechanisms.

Authors:  Anand K Srivastava; Charles E Schwartz
Journal:  Neurosci Biobehav Rev       Date:  2014-04-04       Impact factor: 8.989

Review 6.  Etiological heterogeneity in autism spectrum disorders: more than 100 genetic and genomic disorders and still counting.

Authors:  Catalina Betancur
Journal:  Brain Res       Date:  2010-12-01       Impact factor: 3.252

7.  Broader autism phenotype in mothers predicts social responsiveness in young children with autism spectrum disorders.

Authors:  Chiaki Hasegawa; Mitsuru Kikuchi; Yuko Yoshimura; Hirotoshi Hiraishi; Toshio Munesue; Hideo Nakatani; Haruhiro Higashida; Minoru Asada; Manabu Oi; Yoshio Minabe
Journal:  Psychiatry Clin Neurosci       Date:  2014-07-14       Impact factor: 5.188

8.  Defining the broader, medium and narrow autism phenotype among parents using the Autism Spectrum Quotient (AQ).

Authors:  Sally Wheelwright; Bonnie Auyeung; Carrie Allison; Simon Baron-Cohen
Journal:  Mol Autism       Date:  2010-06-17       Impact factor: 7.509

9.  Autism spectrum disorder severity reflects the average contribution of de novo and familial influences.

Authors:  Elise B Robinson; Kaitlin E Samocha; Jack A Kosmicki; Lauren McGrath; Benjamin M Neale; Roy H Perlis; Mark J Daly
Journal:  Proc Natl Acad Sci U S A       Date:  2014-10-06       Impact factor: 11.205

10.  Autism and the broad autism phenotype: familial patterns and intergenerational transmission.

Authors:  Noah J Sasson; Kristen Sl Lam; Morgan Parlier; Julie L Daniels; Joseph Piven
Journal:  J Neurodev Disord       Date:  2013-05-02       Impact factor: 4.025

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