Evidence map›Paper›PMID 33595806›Full record

ReviewCellular and molecular neurobiology2022

Association of SHANK Family with Neuropsychiatric Disorders: An Update on Genetic and Animal Model Discoveries.

Lily Wan, Du Liu, Wen-Biao Xiao, Bo-Xin Zhang, Xiao-Xin Yan, Zhao-Hui Luo, Bo Xiao

Open access · greenAbstract readReview
In one paragraph

Review in Cellular and molecular neurobiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.1field-weighted citation impact, top 27% 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

9 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
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  6. Gene×environment interactions in autism spectrum disorders.Current topics in developmental biology · 2023
    Review
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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 1 institution in 1 country.

Lily Wan *Department of Neurology, Xiangya Hospital, Central South University, Changsha, 410008, Hunan, China.
Du Liu *Department of Neurology, Xiangya Hospital, Central South University, Changsha, 410008, Hunan, China.
Wen-Biao XiaoDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, 410008, Hunan, China.
Bo-Xin ZhangDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, 410008, Hunan, China.
Xiao-Xin YanDepartment of Anatomy and Neurobiology, Central South University, Changsha, 410013, Hunan, China.
Zhao-Hui LuoDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, 410008, Hunan, China. luozhaohui_xy@126.com.ORCID http://orcid.org/0000-0001-7175-1141
Bo XiaoDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, 410008, Hunan, China. xiaobo_xy@126.com.
Central South University · CN

Funding

National Natural Science Foundation of China 81671299The Hunan Natural Science Foundation 2018JJ2648
6 · The paper itself

Abstract

The Shank family proteins are enriched at the postsynaptic density (PSD) of excitatory glutamatergic synapses. They serve as synaptic scaffolding proteins and appear to play a critical role in the formation, maintenance and functioning of synapse. Increasing evidence from genetic association and animal model studies indicates a connection of SHANK genes defects with the development of neuropsychiatric disorders. In this review, we first update the current understanding of the SHANK family genes and their encoded protein products. We then denote the literature relating their alterations to the risk of neuropsychiatric diseases. We further review evidence from animal models that provided molecular insights into the biological as well as pathogenic roles of Shank proteins in synapses, and the potential relationship to the development of abnormal neurobehavioral phenotypes.

Indexed as

Nerve Tissue ProteinsSynapsesAnimalsDisease Models, AnimalMutationNerve Tissue ProteinsAutismNeurodevelopmentNeuropsychiatric disordersSynaptic plasticitySynaptic transmission

Identifiers

PMID33595806
PMCPMC11421742
OpenAlexW3132605845

What OpenQuestion holds

Textmetadata
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.