Evidence map›Paper›PMID 31405222›Full record

ArticleInternational journal of molecular sciences2019

Significantly Elevated

Michael Field, Tracy Dudding-Byth, Marta Arpone, Emma K Baker, Solange M Aliaga, Carolyn Rogers, Chriselle Hickerton, David Francis, Dean G Phelan, Elizabeth E Palmer and 5 more

Open access · goldAbstract readCase Reports
In one paragraph

Article in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

11 citing papers in PubMed, 16 citations in OpenAlex.

  1. In Utero Alcohol and Unsuitable Home Environmental Exposure Combined withInternational journal of molecular sciences · 2025
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  7. X Chromosome Inactivation Timing is Not eFrontiers in genetics · 2022
    Article
  8. Ethnicity has a multiplex impact upon the risk of a full mutation expansion among female heterozygotes for FMR1 premutation.Genetics in medicine : official journal of the American College of Medical Genetics · 2021
    Article
  9. Article
  10. Article
  11. 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

15 authors at 2 institutions in 1 country.

Michael FieldGenetics of Learning Disability Service, Hunter Genetics, Waratah, NSW 2298, Australia.
Tracy Dudding-BythGenetics of Learning Disability Service, Hunter Genetics, Waratah, NSW 2298, Australia.
Marta ArponeDiagnosis and Development, Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, VIC 3052, Australia.
Emma K BakerDiagnosis and Development, Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, VIC 3052, Australia.ORCID 0000-0003-1165-0490
Solange M AliagaDiagnosis and Development, Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, VIC 3052, Australia.
Carolyn RogersGenetics of Learning Disability Service, Hunter Genetics, Waratah, NSW 2298, Australia.
Chriselle HickertonDiagnosis and Development, Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, VIC 3052, Australia.
David FrancisVictorian Clinical Genetics Services, Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, VIC 3052, Australia.
Dean G PhelanVictorian Clinical Genetics Services, Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, VIC 3052, Australia.
Elizabeth E PalmerGenetics of Learning Disability Service, Hunter Genetics, Waratah, NSW 2298, Australia.
David J AmorDiagnosis and Development, Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, VIC 3052, Australia.
Howard SlaterDiagnosis and Development, Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, VIC 3052, Australia.
Lesley BrethertonDiagnosis and Development, Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, VIC 3052, Australia.
Ling LingDiagnosis and Development, Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, VIC 3052, Australia.
David E GodlerDiagnosis and Development, Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, VIC 3052, Australia. david.godler@mcri.edu.au.ORCID 0000-0002-6405-269X
Royal Children's Hospital · AUHunter Genetics · AU

Funding

Financial Markets Foundation for Children 2017-361Medical Research Future Fund 1141334National Health and Medical Research Council 1049299National Health and Medical Research Council 1103389
6 · The paper itself

Abstract

Although fragile X syndrome (FXS) is caused by a hypermethylated full mutation (FM) expansion with ≥200 cytosine-guanine-guanine (CGG) repeats, and a decrease in

Indexed as

AllelesAutistic DisorderChild, PreschoolDNA MethylationFragile X Messenger Ribonucleoprotein 1Fragile X SyndromeHumansMaleMosaicismMutationRNA, MessengerSiblingsUp-RegulationFMR1 protein, humanFragile X Messenger Ribonucleoprotein 1RNA, MessengerAmplideXautismDNA methylationfragile X syndromemosaicismMS-QMApediatricsRNA toxicity

Identifiers

PMID31405222
PMCPMC6721168
OpenAlexW2967227613

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.