Evidence map›Paper›PMID 20029829›Full record

ReviewAutism research : official journal of the International Society for Autism Research2009

Autism spectrum and obsessive-compulsive disorders: OC behaviors, phenotypes and genetics.

Suma Jacob, Angeli Landeros-Weisenberger, James F Leckman

Abstract readReview
In one paragraph

Review in Autism research : official journal of the International Society for Autism Research, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 3 pooled it
3.4field-weighted citation impact, top 8% of its field
1 · What the graph read from 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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

38 citing papers in PubMed, 3 syntheses or guidelines pooled it, 86 citations in OpenAlex.

  1. Pooled it
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  18. Family Accommodation in Autism Spectrum Disorder.Journal of autism and developmental disorders · 2019
    Article
  19. Article
  20. Activation of Serotonin 5-HTFrontiers in molecular neuroscience · 2018
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 1 country.

Suma JacobDepartment of Psychiatry, University of Illinois School, Chicago, Illinois 60612, USA. sjacob@psych.uic.edu
Angeli Landeros-Weisenberger
James F Leckman
Yale University · USUniversity of Illinois Chicago · US

Funding

TRAINING PROGRAM IN CHILDHOOD NEUROPSYCHIATRIC DISORDERST32MH018268 · NIMH · YALE UNIVERSITY · PI Michael H Bloch, MICHAEL J CROWLEY · 1985 to 2026
$11.0M
PROGRAM FOR MINORITY RESEARCH TRAINING IN PSYCHIATRY (PMT32MH019126 · NIMH · AMERICAN PSYCHIATRIC INST FOR RES &EDUC · PI REGIER, DARREL A · 1989 to 2009
$5.3M
Autism: neuropeptide hormones and potential pathway genesK23MH082121 · NIMH · UNIVERSITY OF ILLINOIS AT CHICAGO · PI JACOB, SUMA · 2008 to 2012
$981k
Treatment of Tourette's Syndrome & Obsessive-Compulsive DisorderK05MH076273 · NIMH · YALE UNIVERSITY · PI LECKMAN, JAMES F · 2006 to 2010
$642k
NIMH NIH HHS K05 MH076273NIMH NIH HHS K05MH076273NIMH NIH HHS K23 MH082121NIMH NIH HHS K23MH082121NIMH NIH HHS L40 MH072451NIMH NIH HHS T32 MH018268NIMH NIH HHS T32 MH019126NIMH NIH HHS T32 MH 19126
6 · The paper itself

Abstract

Autism spectrum disorders (ASDs) are a phenotypically and etiologically heterogeneous set of disorders that include obsessive-compulsive behaviors (OCB) that partially overlap with symptoms associated with obsessive-compulsive disorder (OCD). The OCB seen in ASD vary depending on the individual's mental and chronological age as well as the etiology of their ASD. Although progress has been made in the measurement of the OCB associated with ASD, more work is needed including the potential identification of heritable endophenotypes. Likewise, important progress toward the understanding of genetic influences in ASD has been made by greater refinement of relevant phenotypes using a broad range of study designs, including twin and family-genetic studies, parametric and nonparametric linkage analyses, as well as candidate gene studies and the study of rare genetic variants. These genetic analyses could lead to the refinement of the OCB phenotypes as larger samples are studied and specific associations are replicated. Like ASD, OCB are likely to prove to be multidimensional and polygenic. Some of the vulnerability genes may prove to be generalist genes influencing the phenotypic expression of both ASD and OCD while others will be specific to subcomponents of the ASD phenotype. In order to discover molecular and genetic mechanisms, collaborative approaches need to generate shared samples, resources, novel genomic technologies, as well as more refined phenotypes and innovative statistical approaches. There is a growing need to identify the range of molecular pathways involved in OCB related to ASD in order to develop novel treatment interventions.

Indexed as

GenotypePhenotypeAnimalsChildChild Development Disorders, PervasiveChild, PreschoolComorbidityDiagnosis, DifferentialDisease Models, AnimalDiseases in TwinsGenetic Association StudiesGenetic Predisposition to DiseaseHumansInfantIntellectual DisabilityInterview, Psychological

Identifiers

PMID20029829
PMCPMC3974607
OpenAlexW2051979710

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.