Evidence map›Paper›PMID 26022165›Full record

ReviewPediatric clinics of North America2015

Diagnosis and management of autism spectrum disorder in the era of genomics: rare disorders can pave the way for targeted treatments.

Elizabeth Baker, Shafali Spurling Jeste

Abstract readReview
In one paragraph

Review in Pediatric clinics of North America, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

11 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
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  7. Review
  8. [Research advances in the role of vitamin D in autism spectrum disorders].Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2016
    Review
  9. Review
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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

2 authors.

Elizabeth BakerDepartment of Psychiatry and Biobehavioral Sciences, Semel Institute for Neuroscience and Human Behavior, David Geffen School of Medicine, UCLA, 760 Westwood Plaza, Los Angeles, CA 90095, USA.
Shafali Spurling JesteDepartment of Psychiatry and Biobehavioral Sciences, Semel Institute for Neuroscience and Human Behavior, David Geffen School of Medicine, UCLA, 760 Westwood Plaza, Los Angeles, CA 90095, USA. Electronic address: sjeste@mednet.ucla.edu.

Funding

Neural Predictors of Language Function After Intervention in Children with AutismK23MH094517 · NIMH · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI JESTE, SHAFALI SPURLING · 2011 to 2015
$906k
NCRR NIH HHS L40 RR024973NIMH NIH HHS K23 MH094517
6 · The paper itself

Abstract

Although the diagnosis of autism spectrum disorder (ASD) is based on behavioral signs and symptoms, the evaluation of a child with ASD has become increasingly focused on the identification of the genetic etiology of the disorder. In this review, we begin with a clinical overview of ASD, highlighting the heterogeneity of the disorder. We then discuss the genetics of ASD and present updated guidelines on genetic testing. We then consider the insights gained from the identification of both single gene disorders and rare variants, with regard to clinical phenomenology and potential treatment targets.

Indexed as

GenomicsChildChild Development Disorders, PervasiveGene DosageGenetic TestingGenotypeHumansPhenotypePractice Guidelines as TopicRare DiseasesAutism spectrum disordersChromosomal microarrayCopy number variantsGeneticsNeurodevelopmental disordersWhole-exome sequencing

Identifiers

PMID26022165
PMCPMC4449456

What OpenQuestion holds

Textmetadata
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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.