Evidence map›Paper›PMID 35405628›Full record

ReviewCurrent opinion in neurobiology2022

Endosomal trafficking in schizophrenia.

Melissa Plooster, Patrick Brennwald, Stephanie L Gupton

Open access · greenAbstract readReview
In one paragraph

Review in Current opinion in neurobiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.4field-weighted citation impact, top 22% 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

10 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Late Endosome Transport by RILP-RAB7A Promotes Dendrite Arborization Independently of Degradation.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
    Article
  3. Article
  4. Late endosome transport by RILP-RAB7A promotes dendrite arborization.bioRxiv : the preprint server for biology · 2025
    Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Genetic and Epigenetic Regulation of Brain Organoids.Frontiers in cell and developmental biology · 2022
    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

3 authors at 1 institution in 1 country.

Melissa PloosterDepartment of Cell Biology & Physiology, University of North Carolina at Chapel Hill, United States. Electronic address: mplooster14@gmail.com.
Patrick BrennwaldDepartment of Cell Biology & Physiology, University of North Carolina at Chapel Hill, United States.
Stephanie L GuptonDepartment of Cell Biology & Physiology, University of North Carolina at Chapel Hill, United States. Electronic address: sgupton@email.unc.edu.
University of North Carolina at Chapel Hill · US

Funding

REGULATION OF EXOCYTOSIS BY A RHO GTPPASER01GM054712 · NIGMS · WEILL MEDICAL COLLEGE OF CORNELL UNIV · PI PATRICK J BRENNWALD · 1998 to 2026
$9.5M
Undergraduate Research: Coordinated Cytoskeletal Dynamics and Membrane Remodeling in Cellular Shape ChangeR35GM135160 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Stephanie Gupton · 2020 to 2026
$3.3M
Exocytosis fuels plasma membrane expansion in developing neuronsR01NS112326 · NINDS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI GUPTON, STEPHANIE · 2019 to 2023
$2.1M
Training in Mechanistic, Interdisciplinary Studies of Biological SystemsT32GM119999 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI RAMSDEN, DALE A · 2017 to 2021
$1.2M
Determining the localization and function of schizophrenia-linked protein tSNARE1bF31MH116576 · NIMH · UNIV OF NORTH CAROLINA CHAPEL HILL · PI PLOOSTER, MELISSA · 2018 to 2020
$100k
NIGMS NIH HHS R01 GM054712NIGMS NIH HHS R35 GM135160NIGMS NIH HHS T32 GM119999NIMH NIH HHS F31 MH116576NINDS NIH HHS R01 NS112326
6 · The paper itself

Abstract

Schizophrenia is a severe and heritable neuropsychiatric disorder, which arises due to a combination of common genetic variation, rare loss of function variation, and copy number variation. Functional genomic evidence has been used to identify candidate genes affected by this variation, which revealed biological pathways that may be disrupted in schizophrenia. Understanding the contributions of these pathways are critical next steps in understanding schizophrenia pathogenesis. A number of genes involved in endocytosis are implicated in schizophrenia. In this review, we explore the history of endosomal trafficking in schizophrenia and highlight new endosomal candidate genes. We explore the function of these candidate genes and hypothesize how their dysfunction may contribute to schizophrenia.

Indexed as

SchizophreniaDNA Copy Number VariationsEndocytosisEndosomesGenetic Predisposition to DiseaseGenomicsHumans

Identifiers

PMID35405628
PMCPMC9167700
OpenAlexW4223422779

What OpenQuestion holds

Textmetadata
LicenceTDM
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.