Evidence map›Paper›PMID 34631954›Full record

ArticleMovement disorders clinical practice2021

A Novel Homozygous

Rauan Kaiyrzhanov, Maha S Zaki, Reza Maroofian, Natalia Dominik, Aboulfazl Rad, Barbara Vona, Henry Houlden

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

Article in Movement disorders clinical practice, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.3field-weighted citation impact, top 48% 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, 5 citations in OpenAlex.

  1. Update on Genetic Chorea.Current neurology and neuroscience reports · 2026
    Review
  2. Psychiatric Disorders and Apathy in Mixed Movement Disorders Linked to ADCY5 (MxMD-ADCY5).Movement disorders : official journal of the Movement Disorder Society · 2026
    Article
  3. Article
  4. Article
  5. Scoping Review on ADCY5-Related Movement Disorders.Movement disorders clinical practice · 2023
    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

7 authors at 3 institutions in 3 countries.

Rauan KaiyrzhanovDepartment of Neuromuscular Disorders University College London, Institute of Neurology London United Kingdom.
Maha S ZakiHuman Genetics and Genome Research Division, Clinical Genetics Department National Research Centre Cairo Egypt.
Reza MaroofianDepartment of Neuromuscular Disorders University College London, Institute of Neurology London United Kingdom.
Natalia DominikDepartment of Neuromuscular Disorders University College London, Institute of Neurology London United Kingdom.
Aboulfazl RadDepartment of Otolaryngology-Head & Neck Surgery Tübingen Hearing Research Centre, Eberhard Karls University Tübingen Tübingen Germany.
Barbara VonaDepartment of Otolaryngology-Head & Neck Surgery Tübingen Hearing Research Centre, Eberhard Karls University Tübingen Tübingen Germany.
Henry HouldenDepartment of Neuromuscular Disorders University College London, Institute of Neurology London United Kingdom.
University College London · GBUniversity of Tübingen · DENational Research Centre · EG

Funding

Medical Research Council G0601943Medical Research Council MR/S005021/1Medical Research Council MR/S01165X/1
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

ADCY5autosomal recessivedystoniamovement disordersneurodevelopmental disorder

Identifiers

PMID34631954
PMCPMC8485619
OpenAlexW3185121091

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.