Evidence map›Paper›PMID 32219099›Full record

ReviewFrontiers in molecular biosciences2020

Saif N Haify, Teresa Botta-Orfila, Renate K Hukema, Gian Gaetano Tartaglia

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in molecular biosciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

6 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Regulation of Bone Morphogenetic Protein Receptor Type II Expression byInternational journal of molecular sciences · 2024
    Article
  3. Article
  4. Article
  5. Prodromal Markers of Upper Limb Deficits inMovement disorders clinical practice · 2020
    Article
  6. 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

4 authors at 4 institutions in 3 countries.

Saif N HaifyDepartment of Clinical Genetics, Erasmus MC, Rotterdam, Netherlands.
Teresa Botta-OrfilaBiological Fluids Bank of the Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.
Renate K HukemaDepartment of Clinical Genetics, Erasmus MC, Rotterdam, Netherlands.
Gian Gaetano TartagliaCentre for Genomic Regulation (CRG), The Barcelona Institute for Science and Technology, Barcelona, Spain.
Consorci Institut D'Investigacions Biomediques August Pi I Sunyer · ESErasmus MC · NLErasmus University Rotterdam · NLInstitució Catalana de Recerca i Estudis Avançats · ES

Funding

Wellcome Trust
6 · The paper itself

Abstract

Fragile X-associated tremor/ataxia syndrome (FXTAS) is a late-onset neurodegenerative monogenetic disorder affecting carriers of premutation (PM) forms of the

Indexed as

computational modelingFragile X associated tremor ataxia syndrome (FXTAS)mouse modelprotein networkRNA

Identifiers

PMID32219099
PMCPMC7078329
OpenAlexW3010992727

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.