Evidence map›Paper›PMID 34825060›Full record

ArticleNeurology. Genetics2021

A 3.9-Mb Deletion on 2p11.2 Comprising the

Raquel Baviera-Muñoz, Dolores Martínez-Rubio, Isabel Sastre-Bataller, Marina Campins-Romeu, Mireya Losada-López, Julia Pérez-García, Edurne Novella-Maestre, Irene Martínez-Torres, Carmen Espinós

Open access · goldAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Neurology. 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
0.5field-weighted citation impact, top 28% 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. Review
  2. Mutations, Genes, and Phenotypes Related to Movement Disorders and Ataxias.International journal of molecular sciences · 2022
    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

9 authors at 1 institution in 1 country.

Raquel Baviera-MuñozHealth Research Institute (R.B.-M.), Hospital Universitari i Politècnic La Fe; Unit of Rare Neurodegenerative Diseases (D.M.-R., C.E.), Centro de Investigación Príncipe Felipe (CIPF); Joint Units INCLIVA & IIS La Fe Rare Diseases (D.M.-R., C.E.); Movement Disorders Unit (I.S.-B., M.C.-R., M.L.-L., J.P.-G., I.M.-T.), Neurology Department, Hospital Universitari i Politècnic La Fe; Department of Genetics (E.N.-M.), Hospital Universitari i Politècnic La Fe; and Health Sciences Faculty, Universidad Internacional de Valencia (VIU) (E.N.-M.), Valencia, Spain.
Dolores Martínez-RubioHealth Research Institute (R.B.-M.), Hospital Universitari i Politècnic La Fe; Unit of Rare Neurodegenerative Diseases (D.M.-R., C.E.), Centro de Investigación Príncipe Felipe (CIPF); Joint Units INCLIVA & IIS La Fe Rare Diseases (D.M.-R., C.E.); Movement Disorders Unit (I.S.-B., M.C.-R., M.L.-L., J.P.-G., I.M.-T.), Neurology Department, Hospital Universitari i Politècnic La Fe; Department of Genetics (E.N.-M.), Hospital Universitari i Politècnic La Fe; and Health Sciences Faculty, Universidad Internacional de Valencia (VIU) (E.N.-M.), Valencia, Spain.
Isabel Sastre-BatallerHealth Research Institute (R.B.-M.), Hospital Universitari i Politècnic La Fe; Unit of Rare Neurodegenerative Diseases (D.M.-R., C.E.), Centro de Investigación Príncipe Felipe (CIPF); Joint Units INCLIVA & IIS La Fe Rare Diseases (D.M.-R., C.E.); Movement Disorders Unit (I.S.-B., M.C.-R., M.L.-L., J.P.-G., I.M.-T.), Neurology Department, Hospital Universitari i Politècnic La Fe; Department of Genetics (E.N.-M.), Hospital Universitari i Politècnic La Fe; and Health Sciences Faculty, Universidad Internacional de Valencia (VIU) (E.N.-M.), Valencia, Spain.
Marina Campins-RomeuHealth Research Institute (R.B.-M.), Hospital Universitari i Politècnic La Fe; Unit of Rare Neurodegenerative Diseases (D.M.-R., C.E.), Centro de Investigación Príncipe Felipe (CIPF); Joint Units INCLIVA & IIS La Fe Rare Diseases (D.M.-R., C.E.); Movement Disorders Unit (I.S.-B., M.C.-R., M.L.-L., J.P.-G., I.M.-T.), Neurology Department, Hospital Universitari i Politècnic La Fe; Department of Genetics (E.N.-M.), Hospital Universitari i Politècnic La Fe; and Health Sciences Faculty, Universidad Internacional de Valencia (VIU) (E.N.-M.), Valencia, Spain.
Mireya Losada-LópezHealth Research Institute (R.B.-M.), Hospital Universitari i Politècnic La Fe; Unit of Rare Neurodegenerative Diseases (D.M.-R., C.E.), Centro de Investigación Príncipe Felipe (CIPF); Joint Units INCLIVA & IIS La Fe Rare Diseases (D.M.-R., C.E.); Movement Disorders Unit (I.S.-B., M.C.-R., M.L.-L., J.P.-G., I.M.-T.), Neurology Department, Hospital Universitari i Politècnic La Fe; Department of Genetics (E.N.-M.), Hospital Universitari i Politècnic La Fe; and Health Sciences Faculty, Universidad Internacional de Valencia (VIU) (E.N.-M.), Valencia, Spain.
Julia Pérez-GarcíaHealth Research Institute (R.B.-M.), Hospital Universitari i Politècnic La Fe; Unit of Rare Neurodegenerative Diseases (D.M.-R., C.E.), Centro de Investigación Príncipe Felipe (CIPF); Joint Units INCLIVA & IIS La Fe Rare Diseases (D.M.-R., C.E.); Movement Disorders Unit (I.S.-B., M.C.-R., M.L.-L., J.P.-G., I.M.-T.), Neurology Department, Hospital Universitari i Politècnic La Fe; Department of Genetics (E.N.-M.), Hospital Universitari i Politècnic La Fe; and Health Sciences Faculty, Universidad Internacional de Valencia (VIU) (E.N.-M.), Valencia, Spain.
Edurne Novella-MaestreHealth Research Institute (R.B.-M.), Hospital Universitari i Politècnic La Fe; Unit of Rare Neurodegenerative Diseases (D.M.-R., C.E.), Centro de Investigación Príncipe Felipe (CIPF); Joint Units INCLIVA & IIS La Fe Rare Diseases (D.M.-R., C.E.); Movement Disorders Unit (I.S.-B., M.C.-R., M.L.-L., J.P.-G., I.M.-T.), Neurology Department, Hospital Universitari i Politècnic La Fe; Department of Genetics (E.N.-M.), Hospital Universitari i Politècnic La Fe; and Health Sciences Faculty, Universidad Internacional de Valencia (VIU) (E.N.-M.), Valencia, Spain.
Irene Martínez-TorresHealth Research Institute (R.B.-M.), Hospital Universitari i Politècnic La Fe; Unit of Rare Neurodegenerative Diseases (D.M.-R., C.E.), Centro de Investigación Príncipe Felipe (CIPF); Joint Units INCLIVA & IIS La Fe Rare Diseases (D.M.-R., C.E.); Movement Disorders Unit (I.S.-B., M.C.-R., M.L.-L., J.P.-G., I.M.-T.), Neurology Department, Hospital Universitari i Politècnic La Fe; Department of Genetics (E.N.-M.), Hospital Universitari i Politècnic La Fe; and Health Sciences Faculty, Universidad Internacional de Valencia (VIU) (E.N.-M.), Valencia, Spain.
Carmen EspinósHealth Research Institute (R.B.-M.), Hospital Universitari i Politècnic La Fe; Unit of Rare Neurodegenerative Diseases (D.M.-R., C.E.), Centro de Investigación Príncipe Felipe (CIPF); Joint Units INCLIVA & IIS La Fe Rare Diseases (D.M.-R., C.E.); Movement Disorders Unit (I.S.-B., M.C.-R., M.L.-L., J.P.-G., I.M.-T.), Neurology Department, Hospital Universitari i Politècnic La Fe; Department of Genetics (E.N.-M.), Hospital Universitari i Politècnic La Fe; and Health Sciences Faculty, Universidad Internacional de Valencia (VIU) (E.N.-M.), Valencia, Spain.ORCID 0000-0003-4435-1809
Hospital Universitari i Politècnic La Fe · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID34825060
PMCPMC8610491
OpenAlexW3216683193

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.