Evidence map›Paper›PMID 25410672›Full record

ArticleWorld journal of pediatrics : WJP2015

Cytogenetic analysis of chromosomal abnormalities in Sri Lankan children.

Sharmila Thillainathan, Nirmala D Sirisena, Kariyawasam W J C Kariyawasam, Rohan W Jayasekara, Vajira H W Dissanayake

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Article in World journal of pediatrics : WJP, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

8 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Genetics and genomic medicine in Sri Lanka.Molecular genetics & genomic medicine · 2019
    Review
  4. Article
  5. Cytogenetic Analysis for Suspected Chromosomal Abnormalities; A Five Years Experience.Journal of clinical and diagnostic research : JCDR · 2016
    Article
  6. Correspondence.World journal of pediatrics : WJP · 2016
    Article
  7. Article
  8. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Sharmila Thillainathan, Colombo, Sri Lanka.
Nirmala D Sirisena, Colombo, Sri Lanka.
Kariyawasam W J C Kariyawasam, Colombo, Sri Lanka.
Rohan W Jayasekara, Colombo, Sri Lanka.
Vajira H W Dissanayake, Colombo, Sri Lanka. vajirahwd@hotmail.com.
University of Colombo · LK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCytogenetic analysis is a valuable investigation in the diagnostic work up of children with suspected chromosomal disorders. The objective of this study was to describe the prevalence of various types of chromosomal abnormalities in Sri Lankan children undergoing cytogenetic analysis.

methodsCytogenetic reports of 1554 consecutive children with suspected chromosomal disorders who underwent karyotyping in two genetic centers in Sri Lanka from January 2006 to December 2011 were reviewed retrospectively.

resultsA total of 1548 children were successfully karyotyped. Abnormal karyotypes were found in 783 (50.6%) children. Numerical and structural abnormalities accounted for 90.8% and 9.2%, respectively. Down syndrome was the commonest aneuploidy identified. Other various autosomal and sex chromosomal aneuploidies as well as micro-deletion syndromes were also detected.

conclusionsThe prevalence of chromosomal abnormalities in Sri Lankan children undergoing cytogenetic analysis for suspected chromosomal disorders was relatively higher than that in Caucasian and other Asian populations.

Indexed as

Cytogenetic AnalysisChildChild, PreschoolChromosome AberrationsFemaleHumansInfantInfant, NewbornKaryotypingMalePrevalenceRetrospective StudiesSri Lankaaneuploidychromosome aberrationscytogenetic analysiskaryotypes

Identifiers

PMID25410672
OpenAlexW2043353608

What OpenQuestion holds

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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.