Evidence map›Paper›PMID 37511534›Full record

ArticleInternational journal of molecular sciences2023

Whole Genome Sequencing Revealed Inherited Rare Oligogenic Variants Contributing to Schizophrenia and Major Depressive Disorder in Two Families.

I-Hang Chung, Yu-Shu Huang, Ting-Hsuan Fang, Chia-Hsiang Chen

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 73% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

4 authors at 2 institutions in 1 country.

I-Hang ChungDepartment of Psychiatry, Chang Gung Memorial Hospital-Linkou, Taoyuan 333, Taiwan.
Yu-Shu HuangDepartment of Psychiatry, Chang Gung Memorial Hospital-Linkou, Taoyuan 333, Taiwan.ORCID 0000-0002-4015-5942
Ting-Hsuan FangDepartment of Psychiatry, Chang Gung Memorial Hospital-Linkou, Taoyuan 333, Taiwan.
Chia-Hsiang ChenDepartment of Psychiatry, Chang Gung Memorial Hospital-Linkou, Taoyuan 333, Taiwan.ORCID 0000-0002-8232-2403
Chang Gung Memorial Hospital · TWChang Gung University · TW

Funding

Linkou Chang Gung Memorial Hospital CORPG3J0311Linkou Chang Gung Memorial Hospital CORPG3J0312Linkou Chang Gung Memorial Hospital CORPG3J0313Ministry of Science and Technology, Taiwan MOST 107-2314-B-182-057-MY2
6 · The paper itself

Abstract

Schizophrenia and affective disorder are two major complex mental disorders with high heritability. Evidence shows that rare variants with significant clinical impacts contribute to the genetic liability of these two disorders. Also, rare variants associated with schizophrenia and affective disorders are highly personalized; each patient may carry different variants. We used whole genome sequencing analysis to study the genetic basis of two families with schizophrenia and major depressive disorder. We did not detect de novo, autosomal dominant, or recessive pathogenic or likely pathogenic variants associated with psychiatric disorders in these two families. Nevertheless, we identified multiple rare inherited variants with unknown significance in the probands. In family 1, with singleton schizophrenia, we detected four rare variants in genes implicated in schizophrenia, including p.Arg1627Trp of

Indexed as

Major Depressive DisorderSchizophreniaGenetic Predisposition to DiseaseHumansSiblingsToll-Like Receptor 4Whole Genome SequencingToll-Like Receptor 4geneticsheritabilitymajor depressionoligogenicrare mutationsschizophrenia

Identifiers

PMID37511534
PMCPMC10380944
OpenAlexW4385172474

What OpenQuestion holds

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Registered trials

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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.