Evidence map›Paper›PMID 28232783›Full record

ArticleMolecular syndromology2017

Complex Mosaic Ring Chromosome 11 Associated with Hemizygous Loss of 8.6 Mb of 11q24.2qter in Atypical Jacobsen Syndrome.

Alexandra Galvão Gomes, Carlos H Paiva Grangeiro, Luiz R Silva, Flávia G Oliveira-Gennaro, Ciro S Pereira, Tatiana M Joaquim, Rodrigo A Panepucci, Jeremy A Squire, Lucia Martelli

Open access · bronzeAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Molecular syndromology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
9.6field-weighted citation impact, top 2% 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

2 citing papers in PubMed, 36 citations in OpenAlex.

  1. Review
  2. 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 3 institutions in 1 country.

Alexandra Galvão GomesDepartment of Genetics, University of São Paulo (USP), Brazil.
Carlos H Paiva GrangeiroDepartment of Genetics, University of São Paulo (USP), Brazil; Department of Division of Clinical Genetics, Clinical Hospital of Ribeirão Preto, Ribeirão Preto, Brazil.
Luiz R SilvaDepartment of Pediatric Clinic, Federal University of Uberlândia, Minas Gerais, Brazil.
Flávia G Oliveira-GennaroDepartment of Genetics, University of São Paulo (USP), Brazil.
Ciro S PereiraDepartment of Center of Biotechnology and Cell Therapy, São Rafael Hospital, Salvador, Brazil.
Tatiana M JoaquimDepartment of Genetics, University of São Paulo (USP), Brazil.
Rodrigo A PanepucciDepartment of Center for Cell-Based Therapy and Regional Blood Center, University of São Paulo (USP), Brazil.
Jeremy A SquireDepartment of Genetics, University of São Paulo (USP), Brazil; Department of Pathology and Forensic Medicine, University of São Paulo (USP), Brazil.
Lucia MartelliDepartment of Genetics, University of São Paulo (USP), Brazil; Department of Division of Clinical Genetics, Clinical Hospital of Ribeirão Preto, Ribeirão Preto, Brazil.
Hospital São Rafael · BRUniversidade de São Paulo · BRUniversidade Federal de Uberlândia · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Jacobsen syndrome (JBS) is a contiguous gene deletion syndrome involving terminal chromosome 11q. The haploinsufficiency of multiple genes contributes to the overall clinical phenotype, which can include the variant Paris-Trousseau syndrome, a transient thrombocytopenia related to

Indexed as

Comparative genomic hybridizationDeletion 11qFLI1Jacobsen syndromeRing chromosomeThrombocytopenia Paris-Trousseau type

Identifiers

PMID28232783
PMCPMC5260599
OpenAlexW2553986252

What OpenQuestion holds

Textmetadata
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.