Evidence map›Paper›PMID 34064836›Full record

ArticleBrain sciences2021

Final Exon Frameshift Biallelic

Reham Khalaf-Nazzal, James Fasham, Nishanka Ubeyratna, David J Evans, Joseph S Leslie, Thomas T Warner, Fida' Al-Hijawi, Shurouq Alshaer, Wisam Baker, Peter D Turnpenny and 2 more

Open access · goldAbstract read
In one paragraph

Article in Brain sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 38% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
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

12 authors at 4 institutions in 2 countries.

Reham Khalaf-NazzalBiomedical Sciences Department, Faculty of Medicine, Arab American University of Palestine, Jenin P227, Palestine.
James FashamCollege of Medicine and Health, RILD Wellcome Wolfson Centre, University of Exeter, Royal Devon & Exeter NHS Foundation Trust, Barrack Road, Exeter EX2 5DW, UK.ORCID 0000-0002-7614-9202
Nishanka UbeyratnaCollege of Medicine and Health, RILD Wellcome Wolfson Centre, University of Exeter, Royal Devon & Exeter NHS Foundation Trust, Barrack Road, Exeter EX2 5DW, UK.
David J EvansExeter Genomics Laboratory, Royal Devon & Exeter NHS Foundation Trust, Exeter EX2 5DW, UK.
Joseph S LeslieCollege of Medicine and Health, RILD Wellcome Wolfson Centre, University of Exeter, Royal Devon & Exeter NHS Foundation Trust, Barrack Road, Exeter EX2 5DW, UK.
Thomas T WarnerReta Lila Weston Institute, UCL Queen Square Institute of Neurology, 1 Wakefield Street, London WC1N 1PJ, UK.
Fida' Al-HijawiPaediatrics' Community Outpatient Clinics, Palestinian Ministry of Health, Jenin P200, Palestine.
Shurouq AlshaerFaculty of Graduate Studies, Arab American University, Ramallah P622, Palestine.
Wisam BakerPaediatrics Department, Dr. Khalil Suleiman Government Hospital, Jenin P200, Palestine.
Peter D TurnpennyCollege of Medicine and Health, RILD Wellcome Wolfson Centre, University of Exeter, Royal Devon & Exeter NHS Foundation Trust, Barrack Road, Exeter EX2 5DW, UK.
Emma L BapleCollege of Medicine and Health, RILD Wellcome Wolfson Centre, University of Exeter, Royal Devon & Exeter NHS Foundation Trust, Barrack Road, Exeter EX2 5DW, UK.
Andrew H CrosbyCollege of Medicine and Health, RILD Wellcome Wolfson Centre, University of Exeter, Royal Devon & Exeter NHS Foundation Trust, Barrack Road, Exeter EX2 5DW, UK.
University of Exeter · GBArab American University · PSNational Hospital for Neurology and Neurosurgery · GBRoyal Devon & Exeter NHS Foundation Trust · GB

Funding

Medical Research Council G1001931Medical Research Council G1002279Medical Research Council MC_PC_15047Medical Research Council MC_PC_15054Medical Research Council MC_PC_18047Medical Research Council MR/L023784/2Wellcome Trust 220600/Z/20/Z
6 · The paper itself

Abstract

The hereditary spastic paraplegias (HSPs) are a large clinically heterogeneous group of genetic disorders classified as 'pure' when the cardinal feature of progressive lower limb spasticity and weakness occurs in isolation and 'complex' when associated with other clinical signs. Here, we identify a homozygous frameshift alteration occurring in the last coding exon of the protein tyrosine phosphatase type 23 (

Indexed as

ESCRThereditary spastic paraplegiaHSPprotein tyrosine phosphatasePTPN23

Identifiers

PMID34064836
PMCPMC8151426
OpenAlexW3163747709

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.