Evidence map›Paper›PMID 35628442›Full record

ArticleInternational journal of molecular sciences2022

A Novel Loss-of-Function

Alyssa J J Paganoni, Federica Amoruso, Javier Porta Pelayo, Beatriz Calleja-Pérez, Valeria Vezzoli, Paolo Duminuco, Alessia Caramello, Roberto Oleari, Alberto Fernández-Jaén, Anna Cariboni

Open access · goldAbstract readCase Reports
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.8field-weighted citation impact, top 34% 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

7 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Identification of plasma SEMA3E as the diagnostic biomarker for human epilepsy based on integrated bioinformatics analysis.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2025
    Article
  5. Article
  6. Bilateral Testicular Regression Syndrome and Optic Nerve Atrophy: Clinical Aspects of a Child with a <italic>SEMA3E</italic> Loss-of-Function Variant.Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation · 2025
    Article
  7. 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

10 authors at 5 institutions in 3 countries.

Alyssa J J PaganoniDepartment of Pharmacological and Biomolecular Sciences, Università degli Studi di Milano, 20133 Milan, Italy.ORCID 0000-0001-9393-9356
Federica AmorusoDepartment of Pharmacological and Biomolecular Sciences, Università degli Studi di Milano, 20133 Milan, Italy.ORCID 0000-0002-6832-6053
Javier Porta PelayoGenologica Medica, 29015 Malaga, Spain.
Beatriz Calleja-PérezPediatric Primary Care, C. S. Doctor Cirajas, 28017 Madrid, Spain.
Valeria VezzoliDepartment of Endocrine and Metabolic Diseases and Laboratory of Endocrine and Metabolic Research, IRCCS Istituto Auxologico Italiano, 20145 Milan, Italy.
Paolo DuminucoDepartment of Endocrine and Metabolic Diseases and Laboratory of Endocrine and Metabolic Research, IRCCS Istituto Auxologico Italiano, 20145 Milan, Italy.
Alessia CaramelloUK Dementia Research Institute, Imperial College London, London SW7 2AZ, UK.
Roberto OleariDepartment of Pharmacological and Biomolecular Sciences, Università degli Studi di Milano, 20133 Milan, Italy.ORCID 0000-0002-5692-3328
Alberto Fernández-JaénNeuropediatric Department, Hospital Universitario Quirónsalud, School of Medicine, Universidad Europea de Madrid, 28670 Madrid, Spain.ORCID 0000-0003-3306-9832
Anna CariboniDepartment of Pharmacological and Biomolecular Sciences, Università degli Studi di Milano, 20133 Milan, Italy.ORCID 0000-0001-8630-8361
University of Milan · ITIRCCS Istituto Auxologico Italiano · ITHospital Universitario Quirónsalud Madrid · ESMadrid Health Service · ESUK Dementia Research Institute · GB

Funding

CHARGE Syndrome Foundation 2021 CHARGE Syndrome Foundation Research GrantMinistero della Salute GR-2016-02362389
6 · The paper itself

Abstract

Intellectual disability (ID) is a neurological disorder arising from early neurodevelopmental defects. The underlying genetic and molecular mechanisms are complex, but are thought to involve, among others, alterations in genes implicated in axon guidance and/or neural circuit formation as demonstrated by studies on mouse models. Here, by combining exome sequencing with in silico analyses, we identified a patient affected by severe ID and cognitive regression, carrying a novel loss-of-function variant in the semaphorin 3E (

Indexed as

Intellectual DisabilitySemaphorinsAnimalsCognitionHumansMiceMutationSignal TransductionSEMA3E protein, humanSema3e protein, mouseSemaphorinscognitive regressionintellectual disabilityneurodevelopmental disordersemaphorin 3E

Identifiers

PMID35628442
PMCPMC9143429
OpenAlexW4280622618

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.