Evidence map›Paper›PMID 33008014›Full record

ArticleBrain sciences2020

A Genotype-Phenotype Study of High-Resolution

Dejan B Budimirovic, Annette Schlageter, Stela Filipovic-Sadic, Dragana D Protic, Eran Bram, E Mark Mahone, Kimberly Nicholson, Kristen Culp, Kamyab Javanmardi, Jon Kemppainen and 10 more

Open access · goldAbstract read
In one paragraph

Article in Brain sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
10.4field-weighted citation impact, top 1% 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

56 citing papers in PubMed, 76 citations in OpenAlex.

  1. Effects of AFQ056 on language learning in fragile X syndrome.The Journal of clinical investigation · 2023
    Trial
  2. Trial
  3. Trial
  4. Profile of Behavioral Comorbidities in Children With Fragile X Syndrome.Journal of autism and developmental disorders · 2026
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. In Utero Alcohol and Unsuitable Home Environmental Exposure Combined withInternational journal of molecular sciences · 2025
    Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Epigenetic insights into Fragile X Syndrome.Frontiers in cell and developmental biology · 2024
    Review
  18. Sex Differences in Brain Disorders.International journal of molecular sciences · 2023
    Review
  19. Review
  20. Review
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

20 authors at 5 institutions in 2 countries.

Dejan B BudimirovicDepartments of Psychiatry and Neurogenetics, Fragile X Clinic, Kennedy Krieger Institute, Baltimore, MD 21205, USA.ORCID 0000-0001-7263-5134
Annette SchlageterAsuragen, Inc., Austin, TX 78744, USA.
Stela Filipovic-SadicAsuragen, Inc., Austin, TX 78744, USA.
Dragana D ProticDepartments of Psychiatry and Neurogenetics, Fragile X Clinic, Kennedy Krieger Institute, Baltimore, MD 21205, USA.
Eran BramAsuragen, Inc., Austin, TX 78744, USA.ORCID 0000-0002-7213-5321
E Mark MahoneDepartment of Neuropsychology, Kennedy Krieger Institute, Baltimore, MD 21205, USA.ORCID 0000-0002-5022-1499
Kimberly NicholsonAsuragen, Inc., Austin, TX 78744, USA.
Kristen CulpAsuragen, Inc., Austin, TX 78744, USA.
Kamyab JavanmardiAsuragen, Inc., Austin, TX 78744, USA.ORCID 0000-0002-6449-6709
Jon KemppainenAsuragen, Inc., Austin, TX 78744, USA.
Andrew HaddAsuragen, Inc., Austin, TX 78744, USA.
Kevin SharpDepartment of Pediatrics, Rush University Medical Center, Chicago, IL 60612, USA.
Tatyana AdayevInstitute for Basic Research in Developmental Disabilities, Staten Island, NY 10314, USA.
Giuseppe LaFauciInstitute for Basic Research in Developmental Disabilities, Staten Island, NY 10314, USA.
Carl DobkinInstitute for Basic Research in Developmental Disabilities, Staten Island, NY 10314, USA.
Lili ZhouDepartment of Pediatrics, Rush University Medical Center, Chicago, IL 60612, USA.
William Ted BrownInstitute for Basic Research in Developmental Disabilities, Staten Island, NY 10314, USA.
Elizabeth Berry-KravisDepartment of Pediatrics, Rush University Medical Center, Chicago, IL 60612, USA.
Walter E KaufmannDepartment of Human Genetics, Emory University School of Medicine, Atlanta, GA 30322, USA.
Gary J LathamAsuragen, Inc., Austin, TX 78744, USA.ORCID 0000-0002-9263-3475
Asuragen (United States) · USNew York State Office for People With Developmental Disabilities · USKennedy Krieger Institute · USRush University Medical Center · USBoston Children's Hospital · US

Funding

Development of a reliable and standardized molecular assay for fragile x proteinR43HD082900 · NICHD · ASURAGEN, INC. · PI LATHAM, GARY J · 2015 to 2015
$225k
NICHD NIH HHS R43 HD082900
6 · The paper itself

Abstract

Fragile X syndrome (FXS) is caused by silencing of the

Indexed as

autism spectrum disorderFMR1FMRPfragile X syndromePCR

Identifiers

PMID33008014
PMCPMC7601415
OpenAlexW3090730450

What Socratic 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 Socratic graph.