Evidence map›Paper›PMID 32074998›Full record

ReviewInternational journal of molecular sciences2020

PPP2R5D-Related Intellectual Disability and Neurodevelopmental Delay: A Review of the Current Understanding of the Genetics and Biochemical Basis of the Disorder.

Dayita Biswas, Whitney Cary, Jan A Nolta

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
5.9field-weighted citation impact, top 3% 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

29 citing papers in PubMed, 50 citations in OpenAlex.

  1. A Novel Missense Variant in the GeneBioMed research international · 2021
    Trial
  2. Article
  3. Jordan syndrome due toTranslational pediatrics · 2025
    Article
  4. Article
  5. Article
  6. Pediatric reports · 2024
    Article
  7. Article
  8. Thirteen New Patients ofChildren (Basel, Switzerland) · 2024
    Article
  9. Observational
  10. Article
  11. B56δ long-disordered arms form a dynamic PP2A regulation interface coupled with global allostery and Jordan's syndrome mutations.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Quantum-based modeling implies that bidentate ArgFrontiers in cell and developmental biology · 2023
    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

3 authors at 2 institutions in 1 country.

Dayita BiswasSPARK Program Scholar, Institute for Regenerative Cures, University of California, Sacramento, CA 95817, USA.
Whitney CaryStem Cell Program, UC Davis School of Medicine. The University of California, Sacramento, CA 95817, USA.
Jan A NoltaSPARK Program Scholar, Institute for Regenerative Cures, University of California, Sacramento, CA 95817, USA.
University of California, Davis · USCalifornia Institute for Regenerative Medicine · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Protein Phosphatase 2 Regulatory Subunit B' Delta (

Indexed as

AnimalsCell Cycle CheckpointsDevelopmental DisabilitiesDisease Models, AnimalHumansIntellectual DisabilityNeuronsPolymorphism, Single NucleotideProtein Phosphatase 2Protein SubunitsPPP2R5D protein, humanProtein Phosphatase 2Protein Subunitsautism spectrum disordersintellectual disabilityneurodevelopmental disabilitiesphosphatasePP2APPP2R5Dreviewseizures

Identifiers

PMID32074998
PMCPMC7072873
OpenAlexW3005541957

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.