Evidence map›Paper›PMID 28933790›Full record

ArticleGenetics in medicine : official journal of the American College of Medical Genetics2017

Is it time to retire fragile X testing as a first-tier test for developmental delay, intellectual disability, and autism spectrum disorder?

Sureni V Mullegama, Steven D Klein, Dzung C Nguyen, Arang Kim, Rebecca Signer, Michelle Fox, Naghmeh Dorrani, Andrea Hendershot, Rebecca Mardach, Robert Suddath and 7 more

Abstract readComment
PubMed Publisher
In one paragraph

Article in Genetics in medicine : official journal of the American College of Medical Genetics, 2017. 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
–field-weighted citation impact
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.

  1. Article
  2. Article
  3. Screening forBioMed research international · 2021
    Article
  4. Review
  5. Re-evaluating the first-tier status of fragile X testing in neurodevelopmental disorders.Genetics in medicine : official journal of the American College of Medical Genetics · 2020
    Article
  6. Response to Metcalfe et al.Genetics in medicine : official journal of the American College of Medical Genetics · 2018
    Article
  7. Response to Hartley et al. and Mullegama et al.Genetics in medicine : official journal of the American College of Medical Genetics · 2017
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors.

Sureni V MullegamaDepartment of Pathology and Laboratory Medicine, David Geffen School of Medicine, University of California-Los Angeles, Los Angeles, California, USA.
Steven D KleinDepartment of Human Genetics, David Geffen School of Medicine, University of California-Los Angeles, Los Angeles, California, USA.
Dzung C NguyenDepartment of Human Genetics, David Geffen School of Medicine, University of California-Los Angeles, Los Angeles, California, USA.
Arang KimDepartment of Pediatrics, David Geffen School of Medicine, University of California-Los Angeles, Los Angeles, California, USA.
Rebecca SignerDepartment of Pediatrics, David Geffen School of Medicine, University of California-Los Angeles, Los Angeles, California, USA.
Michelle FoxDepartment of Pediatrics, David Geffen School of Medicine, University of California-Los Angeles, Los Angeles, California, USA.
Naghmeh DorraniDepartment of Pediatrics, David Geffen School of Medicine, University of California-Los Angeles, Los Angeles, California, USA.
Andrea HendershotCalifornia Cryobank, Los Angeles, California, USA.
Rebecca MardachDepartment of Pediatrics and MIND Institute, University of California-Davis, Davis, California USA.
Robert SuddathDepartment of Child and Adolescent Psychiatry, Resnick Neuropsychiatric Hospital, University of California-Los Angeles, Los Angeles, California, USA.
Katrina DippleSeattle Children's Hospital and Division of Genetic Medicine, Department of Pediatrics, University of Washington, Seattle, Washington, USA.
Eric VilainDepartment of Human Genetics, David Geffen School of Medicine, University of California-Los Angeles, Los Angeles, California, USA.
Derek A WongDepartment of Pediatrics, David Geffen School of Medicine, University of California-Los Angeles, Los Angeles, California, USA.
Joshua L DeignanDepartment of Pathology and Laboratory Medicine, David Geffen School of Medicine, University of California-Los Angeles, Los Angeles, California, USA.
Stephen D CederbaumDepartment of Human Genetics, David Geffen School of Medicine, University of California-Los Angeles, Los Angeles, California, USA.
Wayne W GrodyDepartment of Pathology and Laboratory Medicine, David Geffen School of Medicine, University of California-Los Angeles, Los Angeles, California, USA.
Julian A Martinez-AgostoDepartment of Human Genetics, David Geffen School of Medicine, University of California-Los Angeles, Los Angeles, California, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Autism Spectrum DisorderIntellectual DisabilityChildDevelopmental DisabilitiesFragile X SyndromeHumans

Identifiers

PMID28933790

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.