Evidence map›Paper›PMID 35159210›Full record

ArticleCells2022

Neurodevelopmental Syndrome with Intellectual Disability, Speech Impairment, and Quadrupedia Is Associated with Glutamate Receptor Delta 2 Gene Defect.

Anastasia P Grigorenko, Maria S Protasova, Alexandra A Lisenkova, Denis A Reshetov, Tatiana V Andreeva, Gilberto De Lima Garcias, Maria Da Graça Martino Roth, Andreas Papassotiropoulos, Evgeny I Rogaev

Open access · goldAbstract read
In one paragraph

Article in Cells, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
4.7field-weighted citation impact, top 5% 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

5 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Lurcher Mouse as a Model of Cerebellar Syndromes.Cerebellum (London, England) · 2025
    Review
  3. Article
  4. Mycoplasma DnaK increases DNA copy number variants in vivo.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  5. 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

9 authors at 5 institutions in 4 countries.

Anastasia P GrigorenkoCenter for Genetics and Life Science, Sirius University of Science and Technology, 354340 Sochi, Russia.
Maria S ProtasovaLaboratory of Evolutionary Genomics, Department of Genomics and Human Genetics, Vavilov Institute of General Genetics, Russian Academy of Sciences, 119333 Moscow, Russia.ORCID 0000-0002-2422-1540
Alexandra A LisenkovaLaboratory of Evolutionary Genomics, Department of Genomics and Human Genetics, Vavilov Institute of General Genetics, Russian Academy of Sciences, 119333 Moscow, Russia.
Denis A ReshetovLaboratory of Evolutionary Genomics, Department of Genomics and Human Genetics, Vavilov Institute of General Genetics, Russian Academy of Sciences, 119333 Moscow, Russia.
Tatiana V AndreevaCenter for Genetics and Life Science, Sirius University of Science and Technology, 354340 Sochi, Russia.
Gilberto De Lima GarciasCatholic University of Pelotas, Pelotas 96015-560, RS, Brazil.
Maria Da Graça Martino RothCatholic University of Pelotas, Pelotas 96015-560, RS, Brazil.
Andreas PapassotiropoulosTransfaculty Research Platform, University of Basel, CH-4055 Basel, Switzerland.ORCID 0000-0002-2210-9651
Evgeny I RogaevCenter for Genetics and Life Science, Sirius University of Science and Technology, 354340 Sochi, Russia.
Vavilov Institute of General Genetics · RUUniversidade Católica de Pelotas · BRUniversity of Massachusetts Chan Medical School · USLomonosov Moscow State University · RUUniversity of Basel · CH

Funding

Russian Science Foundation 19-75-30039
6 · The paper itself

Abstract

Bipedalism, speech, and intellect are the most prominent traits that emerged in the evolution of

Indexed as

Intellectual DisabilityNeurodevelopmental DisordersReceptors, GlutamateSpeech DisordersAdultExonsHumansSyndromeglutamate receptor delta 2Receptors, Glutamatecerebellum hypoplasiacongenital cerebellar ataxiadisequilibrium syndromeintellectual disabilitymental retardationquadrupedal locomotionspeech

Identifiers

PMID35159210
PMCPMC8834146
OpenAlexW4210283828

What OpenQuestion 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 OpenQuestion graph.