Evidence map›Paper›PMID 26949739›Full record

ArticleCell systems2015

Identification of Human Neuronal Protein Complexes Reveals Biochemical Activities and Convergent Mechanisms of Action in Autism Spectrum Disorders.

Jingjing Li, Zhihai Ma, Minyi Shi, Ramy H Malty, Hiroyuki Aoki, Zoran Minic, Sadhna Phanse, Ke Jin, Dennis P Wall, Zhaolei Zhang and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell systems, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

34 citing papers in PubMed, 51 citations in OpenAlex.

  1. The Recycling Endosomal (NaActa physiologica (Oxford, England) · 2026
    Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. DYRK1A roles in human neural progenitors.Frontiers in neuroscience · 2025
    Article
  8. Article
  9. Article
  10. HGG advances · 2023
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Ankyrins and neurological disease.Current opinion in neurobiology · 2021
    Review
  17. Article
  18. Article
  19. Review
  20. 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

14 authors at 3 institutions in 2 countries.

Jingjing LiDepartment of Genetics, Stanford Center for Genomics and Personalized Medicine, Stanford, California, 94305 USA.
Zhihai MaDepartment of Genetics, Stanford Center for Genomics and Personalized Medicine, Stanford, California, 94305 USA.
Minyi ShiDepartment of Genetics, Stanford Center for Genomics and Personalized Medicine, Stanford, California, 94305 USA.
Ramy H MaltyDepartment of Biochemistry, Research and Innovation Centre, University of Regina, Regina, Saskatchewan S4S 0A2, Canada.
Hiroyuki AokiDepartment of Biochemistry, Research and Innovation Centre, University of Regina, Regina, Saskatchewan S4S 0A2, Canada.
Zoran MinicDepartment of Biochemistry, Research and Innovation Centre, University of Regina, Regina, Saskatchewan S4S 0A2, Canada.
Sadhna PhanseDepartment of Biochemistry, Research and Innovation Centre, University of Regina, Regina, Saskatchewan S4S 0A2, Canada.
Ke JinDepartment of Biochemistry, Research and Innovation Centre, University of Regina, Regina, Saskatchewan S4S 0A2, Canada; Banting and Best Department of Medical Research, Terrence Donnelly Center for Cellular and Biomolecular Research, University of Toronto, Toronto, Ontario M5S 3E1, Canada.
Dennis P WallDepartment of Psychiatry & Behavioral Sciences, Stanford University School of Medicine, Stanford, California, 94305 USA; Department of Pediatrics, Stanford, California, 94305 USA.
Zhaolei ZhangBanting and Best Department of Medical Research, Terrence Donnelly Center for Cellular and Biomolecular Research, University of Toronto, Toronto, Ontario M5S 3E1, Canada.
Alexander E UrbanDepartment of Genetics, Stanford Center for Genomics and Personalized Medicine, Stanford, California, 94305 USA; Department of Psychiatry & Behavioral Sciences, Stanford University School of Medicine, Stanford, California, 94305 USA.
Joachim HallmayerDepartment of Psychiatry & Behavioral Sciences, Stanford University School of Medicine, Stanford, California, 94305 USA.
Mohan BabuDepartment of Biochemistry, Research and Innovation Centre, University of Regina, Regina, Saskatchewan S4S 0A2, Canada.
Michael SnyderDepartment of Genetics, Stanford Center for Genomics and Personalized Medicine, Stanford, California, 94305 USA.
Stanford University · USUniversity of Regina · CAUniversity of Toronto · CA

Funding

Genomic and epigenomic effects of large CNV in neurons from iPSCDP2MH100010 · NIMH · STANFORD UNIVERSITY · PI URBAN, ALEXANDER ECKEHART · 2012 to 2012
$2.4M
Supplement to: PHYSICAL AND FUNCTIONAL SYSTEMS ANALYSIS OF MAMMALIAN MITOCHONDRIAR01GM106019 · NIGMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI BABU, MOHAN, NUNNARI, JODI M. · 2013 to 2016
$954k
NIGMS NIH HHS R01 GM106019NIMH NIH HHS DP2 MH100010
6 · The paper itself

Abstract

The prevalence of autism spectrum disorders (ASDs) is rapidly growing, yet its molecular basis is poorly understood. We used a systems approach in which ASD candidate genes were mapped onto the ubiquitous human protein complexes and the resulting complexes were characterized. The studies revealed the role of histone deacetylases (HDAC1/2) in regulating the expression of ASD orthologs in the embryonic mouse brain. Proteome-wide screens for the co-complexed subunits with HDAC1 and six other key ASD proteins in neuronal cells revealed a protein interaction network, which displayed preferential expression in fetal brain development, exhibited increased deleterious mutations in ASD cases, and were strongly regulated by FMRP and MECP2 causal for Fragile X and Rett syndromes, respectively. Overall, our study reveals molecular components in ASD, suggests a shared mechanism between the syndromic and idiopathic forms of ASDs, and provides a systems framework for analyzing complex human diseases.

Identifiers

PMID26949739
PMCPMC4776331
OpenAlexW2176254324

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.