Evidence map›Paper›PMID 36002662›Full record

ArticleEuropean journal of human genetics : EJHG2022

Spectrum of movement disorders and motor abnormalities in adults with a 22q11.2 microdeletion: Comment on the literature and retrospective study of 92 adults.

Erik Boot, Connie Marras, Anne S Bassett

Open access · bronzeAbstract read
In one paragraph

Article in European journal of human genetics : EJHG, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 31% 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

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. 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

3 authors at 2 institutions in 2 countries.

Erik BootThe Dalglish Family 22q Clinic, University Health Network, Toronto, Ontario, Canada. erik.boot@sheerenloo.nl.ORCID http://orcid.org/0000-0002-0593-1539
Connie MarrasThe Edmond J. Safra Program in Parkinson's Disease and the Morton and Gloria Shulman Movement Disorders Clinic, Toronto Western Hospital and University of Toronto, Toronto, Ontario, Canada.
Anne S BassettThe Dalglish Family 22q Clinic, University Health Network, Toronto, Ontario, Canada.ORCID http://orcid.org/0000-0002-0681-7279
University Health Network · CAUniversity of Toronto · CA

Funding

CIHR MOP111238CIHR MOP 97800CIHR PJT-148924CIHR PJT–169161
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

DiGeorge SyndromeMovement DisordersAdultChromosome DeletionChromosomes, Human, Pair 22HumansRetrospective Studies

Identifiers

PMID36002662
PMCPMC9712387
OpenAlexW4293001229

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.