Evidence map›Paper›PMID 35844270›Full record

ArticleMovement disorders clinical practice2022

A Novel Co-existence of Spinocerebellar Ataxia 1 and Spinocerebellar Ataxia 2 Mutations in Indian Patients.

Pooja Sharma, Akhilesh K Sonakar, Vinay Goel, Ajay Garg, Achal K Srivastava, Mohammed Faruq

Open access · bronzeAbstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Movement disorders clinical practice, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 64% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Movement Disorders in Hereditary Cerebellar Ataxia.Movement disorders clinical practice · 2025
    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

6 authors at 2 institutions in 1 country.

Pooja SharmaGenomics and Molecular Medicine, CSIR-Institute of Genomics and Integrative Biology (CSIR-IGIB), Mall Road Delhi India.
Akhilesh K SonakarNeurology Department, Neuroscience Centre All India Institute of Medical Sciences New Delhi India.
Vinay GoelNeuroradiology Department, Neuroscience Centre All India Institute of Medical Sciences New Delhi India.
Ajay GargNeuroradiology Department, Neuroscience Centre All India Institute of Medical Sciences New Delhi India.
Achal K SrivastavaNeurology Department, Neuroscience Centre All India Institute of Medical Sciences New Delhi India.ORCID https://orcid.org/0000-0002-4590-7947
Mohammed FaruqGenomics and Molecular Medicine, CSIR-Institute of Genomics and Integrative Biology (CSIR-IGIB), Mall Road Delhi India.
All India Institute of Medical Sciences · INInstitute of Genomics and Integrative Biology · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Spinocerebellar ataxia 1 (SCA1) and SCA2 are dominantly inherited ataxias caused due to CAG expansion mutation in Cases: Here, we report a novel co-occurrence of SCA1 and SCA2 mutations in two unrelated patients. Case-1 was observed to carry Conclusion: These cases highlight the probabilistic interactive outcome of two unrelated genetic events towards a converging phenotype.

Indexed as

SCASCA and IndiaSCA combinatorial mutationsspino cerebellar ataxiastwo‐in‐one mutations

Identifiers

PMID35844270
PMCPMC9274345
OpenAlexW4224300818

What OpenQuestion holds

Textmetadata
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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.