ReviewNeuromolecular medicine2002
Autism: in search of susceptibility genes.
Review in Neuromolecular medicine, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 2 of them syntheses that pooled it.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
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.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
18 citing papers in PubMed, 2 syntheses or guidelines pooled it.
- Association of Allelic Variants of the Reelin Gene with Autistic Spectrum Disorder: A Systematic Review and Meta-Analysis of Candidate Gene Association Studies.International journal of environmental research and public health · 2020Pooled it
- Autism.BMJ clinical evidence · 2010Pooled it
- Mapping the Autistic Advantage from the Accounts of Adults Diagnosed with Autism: A Qualitative Study.Autism in adulthood · 2019Article
- Genetic Causes and Modifiers of Autism Spectrum Disorder.Frontiers in cellular neuroscience · 2019Review
- Selective patient and public involvement: The promise and perils of pharmaceutical intervention for autism.Health expectations : an international journal of public participation in health care and health policy · 2018Article
- Autism and metabolic cytopathy.The open neuroimaging journal · 2011Article
- A high-density SNP genome-wide linkage scan in a large autism extended pedigree.Molecular psychiatry · 2009Article
- Electrophysiological signatures: magnetoencephalographic studies of the neural correlates of language impairment in autism spectrum disorders.International journal of psychophysiology : official journal of the International Organization of Psychophysiology · 2008Review
- De novo balanced translocation t (7;16) (p22.1; p11.2) associated with autistic disorder.Journal of biomedicine & biotechnology · 2008Article
- Candidate-gene screening and association analysis at the autism-susceptibility locus on chromosome 16p: evidence of association at GRIN2A and ABAT.American journal of human genetics · 2005Article
- Autism research: lessons from the past and prospects for the future.Journal of autism and developmental disorders · 2005Review
- Analysis of IMGSAC autism susceptibility loci: evidence for sex limited and parent of origin specific effects.Journal of medical genetics · 2005Article
- Proteomic studies identified a single nucleotide polymorphism in glyoxalase I as autism susceptibility factor.American journal of medical genetics. Part A · 2004Article
- Autism as a disorder of neural information processing: directions for research and targets for therapy.Molecular psychiatry · 2004Review
- Conducting genetic epidemiology studies of autism spectrum disorders: issues in matching.Journal of autism and developmental disorders · 2004Review
- Neuropsychiatric symptoms of fragile X syndrome: pathophysiology and pharmacotherapy.CNS drugs · 2004Review
- Screening of nine candidate genes for autism on chromosome 2q reveals rare nonsynonymous variants in the cAMP-GEFII gene.Molecular psychiatry · 2003Article
- Analysis of reelin as a candidate gene for autism.Molecular psychiatry · 2003Article
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.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Autism is a neurodevelopmental disorder of unknown etiology. There is convincing data for the involvement of genetic factors in the development of autism, and the absence of any consistent evidence for an environmental, neuroanatomical, or biochemical cause has led to an increasing number of genetic studies to determine the basis of this complex disorder. The results of recent genetic linkage and candidate gene studies are reviewed in relation to the challenge of clinical and genetic heterogeneity, and prospects for the future of genetic research in autism are considered.
Indexed as
Identifiers
12230302What OpenQuestion holds
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.