Evidence map›Paper›PMID 35456477›Full record

ReviewGenes2022

Electrophysiological and Behavioral Evidence for Hyper- and Hyposensitivity in Rare Genetic Syndromes Associated with Autism.

Anastasia Neklyudova, Kirill Smirnov, Anna Rebreikina, Olga Martynova, Olga Sysoeva

Open access · goldAbstract readReview
In one paragraph

Review in Genes, 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
3.0field-weighted citation impact, top 9% 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, 17 citations in OpenAlex.

  1. Variability in sensory processing and evoked potentials in Rett syndrome.medRxiv : the preprint server for health sciences · 2026
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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

5 authors at 2 institutions in 1 country.

Anastasia NeklyudovaInstitute of Higher Nervous Activity and Neurophysiology, Russian Academy of Science, 117485 Moscow, Russia.
Kirill SmirnovInstitute of Higher Nervous Activity and Neurophysiology, Russian Academy of Science, 117485 Moscow, Russia.ORCID 0000-0002-0384-647X
Anna RebreikinaInstitute of Higher Nervous Activity and Neurophysiology, Russian Academy of Science, 117485 Moscow, Russia.ORCID 0000-0001-5714-2040
Olga MartynovaInstitute of Higher Nervous Activity and Neurophysiology, Russian Academy of Science, 117485 Moscow, Russia.ORCID 0000-0001-9047-2893
Olga SysoevaInstitute of Higher Nervous Activity and Neurophysiology, Russian Academy of Science, 117485 Moscow, Russia.
Institute of Higher Nervous Activity and Neurophysiology · RUSirius University of Science and Technology · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Our study reviewed abnormalities in spontaneous, as well as event-related, brain activity in syndromes with a known genetic underpinning that are associated with autistic symptomatology. Based on behavioral and neurophysiological evidence, we tentatively subdivided the syndromes on primarily hyper-sensitive (Fragile X, Angelman) and hypo-sensitive (Phelan-McDermid, Rett, Tuberous Sclerosis, Neurofibromatosis 1), pointing to the way of segregation of heterogeneous idiopathic ASD, that includes both hyper-sensitive and hypo-sensitive individuals. This segmentation links abnormalities in different genes, such as

Indexed as

Autistic DisorderBrainFragile X Messenger Ribonucleoprotein 1HumansSyndromeFMR1 protein, humanFragile X Messenger Ribonucleoprotein 1Angelman syndromeautism spectrum disorder (ASD)biomarkerselectroencephalogram (EEG)event-related potentials (ERP)Fragile X syndromeneurofibromatosis type 1Phelan–McDermid syndromeRett syndromesensory deficitstuberous sclerosis

Identifiers

PMID35456477
PMCPMC9027402
OpenAlexW4223535443

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.