Evidence map›Paper›PMID 33564152›Full record

ArticleGenetics in medicine : official journal of the American College of Medical Genetics2021

Correspondence on "Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment" by Roux et al.

Joohyun Park, Natalie Deininger, Maren Rautenberg, Carsten Saft, Florian Harmuth, Marc Sturm, Olaf Riess, Ludger Schöls, Matthis Synofzik, Tobias B Haack

Open access · hybridAbstract readLetterComment
PubMed Full text at PMC Publisher
In one paragraph

Article in Genetics in medicine : official journal of the American College of Medical Genetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 53% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Genetic Dominant Variants inInternational journal of molecular sciences · 2021
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 1 country.

Joohyun ParkInstitute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany. joohyun.park@med.uni-tuebingen.de.
Natalie DeiningerInstitute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.
Maren RautenbergInstitute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.
Carsten SaftDepartment of Neurology, Huntington Centre NRW, Ruhr-University Bochum, St. Josef-Hospital, Bochum, Germany.
Florian HarmuthInstitute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.
Marc SturmInstitute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.
Olaf RiessInstitute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.
Ludger SchölsCentre for Rare Diseases, University of Tübingen, Tübingen, Germany.
Matthis SynofzikDepartment of Neurodegenerative Diseases, Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany.
Tobias B HaackInstitute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.
University of Tübingen · DEGerman Center for Neurodegenerative Diseases · DERuhr University Bochum · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Cerebellar AtaxiaCognitive DysfunctionNervous System DiseasesAtaxiaHumansUbiquitin-Protein LigasesSTUB1 protein, humanUbiquitin-Protein Ligases

Identifiers

PMID33564152
PMCPMC8187144
OpenAlexW3127246767

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.