Evidence map›Paper›PMID 19877165›Full record

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

Identification of chromosome 7 inversion breakpoints in an autistic family narrows candidate region for autism susceptibility.

Holly N Cukier, David A Skaar, Melissa Y Rayner-Evans, Ioanna Konidari, Patrice L Whitehead, James M Jaworski, Michael L Cuccaro, Margaret A Pericak-Vance, John R Gilbert

Open access · greenAbstract read
In one paragraph

Article 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 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.8field-weighted citation impact, top 23% 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

7 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Striking a balance: PIPExploration of neuroprotective therapy · 2021
    Article
  5. Defective phosphoinositide metabolism in autism.Journal of neuroscience research · 2017
    Review
  6. Article
  7. 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

9 authors at 5 institutions in 1 country.

Holly N CukierJohn P. Hussman Institute for Human Genomics, University of Miami, Miami, Florida, USA.
David A Skaar
Melissa Y Rayner-Evans
Ioanna Konidari
Patrice L Whitehead
James M Jaworski
Michael L Cuccaro
Margaret A Pericak-Vance
John R Gilbert
Duke Medical Center · USDr. John T. Macdonald Foundation · USDuke University Hospital · USCenter for Human Genetics · USUniversity of Miami · US

Funding

USE OF DNA PROBE FOR CHOLINERGIC AND NON-CHOLINERGIC MG ANTIGENP01NS026630 · NINDS · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI PERICAK-VANCE, MARGARET A. · 1989 to 2009
$12.6M
NINDS NIH HHS 7P01 NS 26630-19NINDS NIH HHS P01 NS026630
6 · The paper itself

Abstract

Chromosomal breaks and rearrangements have been observed in conjunction with autism and autistic spectrum disorders. A chromosomal inversion has been previously reported in autistic siblings, spanning the region from approximately 7q22.1 to 7q31. This family is distinguished by having multiple individuals with autism and associated disabilities. The region containing the inversion has been strongly implicated in autism by multiple linkage studies, and has been particularly associated with language defects in autism as well as in other disorders with language components. Mapping of the inversion breakpoints by FISH has localized the inversion to the region spanning approximately 99-108.75 Mb of chromosome 7. The proximal breakpoint has the potential to disrupt either the coding sequence or regulatory regions of a number of cytochrome P450 genes while the distal region falls in a relative gene desert. Copy number variant analysis of the breakpoint regions detected no duplication or deletion that could clearly be associated with disease status. Association analysis in our autism data set using single nucleotide polymorphisms located near the breakpoints showed no significant association with proximal breakpoint markers, but has identified markers near the distal breakpoint ( approximately 108-110 Mb) with significant associations to autism. The chromosomal abnormality in this family strengthens the case for an autism susceptibility gene in the chromosome 7q22-31 region and targets a candidate region for further investigation.

Indexed as

Autistic DisorderChildChild, PreschoolChromosome InversionChromosomes, Human, Pair 7Comparative Genomic HybridizationDNA Copy Number VariationsFamilyFemaleFollow-Up StudiesGenetic MarkersGenetic Predisposition to DiseaseHumansIn Situ Hybridization, FluorescenceMaleOligonucleotide Array Sequence AnalysisGenetic Markers

Identifiers

PMID19877165
PMCPMC4441209
OpenAlexW2110473432

What OpenQuestion holds

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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.