Evidence map›Paper›PMID 37323959›Full record

ArticleBasic and clinical neuroscience

Repetitive Suicidal Behaviors in a Case With a New Mutation of Wolfram Syndrome: A Jump From the Gene to the Behavior.

Fatemeh Sadat Mirfazeli, Fatemeh Mohebi, Amin Jahanbakhshi, Omid Aryani, Mostafa Almasi-Dooghaee

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

Article in Basic and clinical neuroscience. 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
–field-weighted citation impact, top 87% 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. 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

5 authors at 1 institution in 1 country.

Fatemeh Sadat MirfazeliMental Health Research Center, Psychosocial Health Research Institute, Iran University of Medical Sciences, Tehran, Iran.ORCID https://orcid.org/0000-0001-8361-8639
Fatemeh MohebiDepartment of Psychiatry, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Amin JahanbakhshiSkull Base Research Center, Department of Neurosurgery, Rasool Akram Hospital, Iran University of Medical Sciences, Tehran, Iran.
Omid AryaniEndocrinology and Metabolism Research Institute, Tehran University of Medical Sciences, Tehran, Iran.
Mostafa Almasi-DooghaeeDepartment of Neurology, Firoozgar Hospital, Iran University of Medical Sciences, Tehran, Iran.ORCID https://orcid.org/0000-0002-3244-1615
Iran University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Wolfram syndrome (WS) is a rare autosomal recessive neurodegenerative disease with variable symptoms, including neuropsychiatric manifestations. A 26-year-old man was reported with classic symptoms of WS and repetitive psychiatric hospitalizations and at least 16 suicidal attempts. The genetic study demonstrated a novel homozygous stop-codon mutation on the WFS1 gene. This special type of mutation may be related to repetitive suicidal behaviors in this case of WS. Psychological support should be a routine practice in patients with WS.

Indexed as

GeneMutationSuicidal behaviorWFS1 geneWolfram syndrome

Identifiers

PMID37323959
PMCPMC10262289
OpenAlexW3208698483

What OpenQuestion holds

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LicenceCC BY-NC
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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.