Evidence map›Paper›PMID 11897815›Full record

ArticleJournal of medical genetics2002

Organisation of the pericentromeric region of chromosome 15: at least four partial gene copies are amplified in patients with a proximal duplication of 15q.

J A Fantes, S K Mewborn, C M Lese, J Hedrick, R L Brown, V Dyomin, R S K Chaganti, S L Christian, D H Ledbetter

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In one paragraph

Article in Journal of medical genetics, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
4.2field-weighted citation impact, top 6% 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

9 citing papers in PubMed, 82 citations in OpenAlex.

  1. Article
  2. Article
  3. The interstitial duplication 15q11.2-q13 syndrome includes autism, mild facial anomalies and a characteristic EEG signature.Autism research : official journal of the International Society for Autism Research · 2013
    Article
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  5. 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

9 authors at 3 institutions in 2 countries.

J A FantesDepartment of Human Genetics, University of Chicago, Chicago, IL 60637, USA.
S K Mewborn
C M Lese
J Hedrick
R L Brown
V Dyomin
R S K Chaganti
S L Christian
D H Ledbetter
University of Chicago · USMemorial Sloan Kettering Cancer Center · USUniversity of Edinburgh · GB

Funding

GVL TO REDUCE AML RELAPSE AFTER MURINE ALLOGENEIC BMTR01CA072669 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI BLAZAR, BRUCE R · 1997 to 2017
$4.9M
MECHANISMS AND CONSEQUENCES OF CHROMOSOMAL ABNORMALITIESR01HD036111 · NICHD · UNIVERSITY OF CHICAGO · PI LEDBETTER, DAVID H. · 1998 to 2002
$961k
NCI NIH HHS CA72669NICHD NIH HHS HD36111
6 · The paper itself

Abstract

Clinical cytogenetic laboratories frequently identify an apparent duplication of proximal 15q that does not involve probes within the PWS/AS critical region and is not associated with any consistent phenotype. Previous mapping data placed several pseudogenes, NF1, IgH D/V, and GABRA5 in the pericentromeric region of proximal 15q. Recent studies have shown that these pseudogene sequences have increased copy numbers in subjects with apparent duplications of proximal 15q. To determine the extent of variation in a control population, we analysed NF1 and IgH D pseudogene copy number in interphase nuclei from 20 cytogenetically normal subjects by FISH. Both loci are polymorphic in controls, ranging from 1-4 signals for NF1 and 1-3 signals for IgH D. Eight subjects with apparent duplications, examined by the same method, showed significantly increased NF1 copy number (5-10 signals). IgH D copy number was also increased in 6/8 of these patients (4-9 signals). We identified a fourth pseudogene, BCL8A, which maps to the pericentromeric region and is coamplified along with the NF1 sequences. Interphase FISH ordering experiments show that IgH D lies closest to the centromere, while BCL8A is the most distal locus in this pseudogene array; the total size of the amplicon is estimated at approximately 1 Mb. The duplicated chromosome was inherited from either sex parent, indicating no parent of origin effect, and no consistent phenotype was present. FISH analysis with one or more of these probes is therefore useful in discriminating polymorphic amplification of proximal pseudogene sequences from clinically significant duplications of 15q.

Indexed as

Gene DuplicationAdultAutistic DisorderCentromereChildChild, PreschoolChromosomes, Human, Pair 15FemaleGene DosageGene OrderGenes, DuplicateGenes, Neurofibromatosis 1HumansImmunoglobulin DIn Situ Hybridization, FluorescenceIntellectual DisabilityImmunoglobulin DNBEAP1 protein, humanNeoplasm Proteins

Identifiers

PMID11897815
PMCPMC1735052
OpenAlexW2137464415

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Registered trials

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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.