ArticleJournal of human genetics2006
Sibling risk of pervasive developmental disorder estimated by means of an epidemiologic survey in Nagoya, Japan.
Article in Journal of human genetics, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
32 citing papers in PubMed, 117 citations in OpenAlex.
- Receiving de novo genetic diagnoses for autism with intellectual disability: parents' views of impacts on families' reproductive decisions.Journal of community genetics · 2024Article
- Can the "female protective effect" liability threshold model explain sex differences in autism spectrum disorder?Neuron · 2022Review
- Modelling Autism Spectrum Disorder (ASD) and Attention-Deficit/Hyperactivity Disorder (ADHD) Using Mice and Zebrafish.International journal of molecular sciences · 2022Review
- A Systematic Review of the Link Between Autism Spectrum Disorder and Acetaminophen: A Mystery to Resolve.Cureus · 2022Review
- Modeling dopamine dysfunction in autism spectrum disorder: From invertebrates to vertebrates.Neuroscience and biobehavioral reviews · 2022Review
- Using the tools of genetic epidemiology to understand sex differences in neuropsychiatric disorders.Genes, brain, and behavior · 2020Review
- Vasopressin in the Amelioration of Social Functioning in Autism Spectrum Disorder.Journal of clinical medicine · 2019Review
- Autism risk classification using placental chorionic surface vascular network features.BMC medical informatics and decision making · 2017Article
- Pleiotropic Mechanisms Indicated for Sex Differences in Autism.PLoS genetics · 2016Article
- Stoppage in Autism Spectrum Disorders.Journal of autism and developmental disorders · 2015Article
- Neuroimaging endophenotypes in autism spectrum disorder.CNS spectrums · 2015Review
- Selective Serotonin Reuptake Inhibitor Use during Pregnancy and the Risk of Autism Spectrum Disorders: A Review.Journal of pediatric genetics · 2015Review
- Sex/gender differences and autism: setting the scene for future research.Journal of the American Academy of Child and Adolescent Psychiatry · 2015Review
- The familial risk of autism.JAMA · 2014Article
- Investigation of maternal genotype effects in autism by genome-wide association.Autism research : official journal of the International Society for Autism Research · 2014Article
- Recurrence of autism spectrum disorders in full- and half-siblings and trends over time: a population-based cohort study.JAMA pediatrics · 2013Article
- Beyond autism: a baby siblings research consortium study of high-risk children at three years of age.Journal of the American Academy of Child and Adolescent Psychiatry · 2013Article
- Sex differences in children with autism spectrum disorder identified within a high-risk infant cohort.Journal of autism and developmental disorders · 2012Article
- Relation between early motor delay and later communication delay in infants at risk for autism.Infant behavior & development · 2012Article
- The Study to Explore Early Development (SEED): a multisite epidemiologic study of autism by the Centers for Autism and Developmental Disabilities Research and Epidemiology (CADDRE) network.Journal of autism and developmental disorders · 2012Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Broad-spectrum autism, referred to as pervasive developmental disorder (PDD), may be associated with genetic factors. We examined 241 siblings in 269 Japanese families with affected children. The sibling incidence of PDD was 10.0% whereas the prevalence of PDD in the general population in the same geographic region was 2.1%. Both of these rates are higher than those reported previously, probably because of the expanded clinical criteria applied. The prevalence in males of the general population was 3.3% and that in females was 0.82%. The sibling incidences were 7.7 and 20.0% for families in which the probands were male and female, respectively. Because the reversed sex ratios correspond to the general rule for a multifactorial threshold model, we suggest that most PDD cases result from the cumulative effects of multiple factors (mostly genetic). The sibling incidences were 0 and 10.9% for families in which the proband had low and normal birth-weight, respectively, suggesting the risk is lower in families with low-birth-weight probands.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.