Evidence map›Paper›PMID 35782384›Full record

ArticleFrontiers in molecular neuroscience2022

Amjad Khan, Lucia Pia Bruno, Fadhel Alomar, Muhammad Umair, Anna Maria Pinto, Abid Ali Khan, Alamzeb Khan, Saima, Alessandra Fabbiani, Kristina Zguro and 9 more

Open access · goldAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Frontiers in molecular neuroscience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
4.0field-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

11 citing papers in PubMed, 26 citations in OpenAlex.

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  10. Commentary:Frontiers in molecular neuroscience · 2022
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  11. Commentary:Frontiers in molecular neuroscience · 2022
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 5 institutions in 5 countries.

Amjad KhanFaculty of Science, Department of Biological Sciences (Zoology), University of Lakki Marwat, Lakki Marwat, Pakistan.
Lucia Pia BrunoMedical Genetics, University of Siena, Siena, Italy.
Fadhel AlomarDepartment of Pharmacology and Toxicology, College of Clinical Pharmacy, Imam Abdulrahman, Bin Faisal University, Dammam, Saudi Arabia.
Muhammad UmairMedical Genomics Research Department, King Abdullah International Medical Research Center (KAIMRC), King Saud bin Abdulaziz University for Health Sciences, Ministry of National Guard Health Affairs, Riyadh, Saudi Arabia.
Anna Maria PintoGenetica Medica, Azienda Ospedaliera Universitaria Senese, Siena, Italy.
Abid Ali KhanFaculty of Science, Department of Chemical Sciences, University of Lakki Marwat, Lakki Marwat, Pakistan.
Alamzeb KhanDepartment of Pediatrics, Yale School of Medicine, Yal University, New Heaven, CT, United States.
SaimaDepartment of Biotechnology, Abdul Wali Khan University Mardan, Mardan, Pakistan.
Alessandra FabbianiMedical Genetics, University of Siena, Siena, Italy.
Kristina ZguroMed Biotech Hub and Competence Center, Department of Medical Biotechnologies, University of Siena, Siena, Italy.
Simone FuriniMed Biotech Hub and Competence Center, Department of Medical Biotechnologies, University of Siena, Siena, Italy.
Maria Antonietta MencarelliGenetica Medica, Azienda Ospedaliera Universitaria Senese, Siena, Italy.
Alessandra RenieriMedical Genetics, University of Siena, Siena, Italy.
Sara RescinitiMedical Genetics, University of Siena, Siena, Italy.
Karla A Peña-GuerraComputational Bioscience Research Center (CBRC), Biological and Environmental Science and Engineering (BESE), King Abdullah University of Science and Technology (KAUST), Thuwal, Saudi Arabia.
Francisco J Guzmán-VegaComputational Bioscience Research Center (CBRC), Biological and Environmental Science and Engineering (BESE), King Abdullah University of Science and Technology (KAUST), Thuwal, Saudi Arabia.
Stefan T AroldComputational Bioscience Research Center (CBRC), Biological and Environmental Science and Engineering (BESE), King Abdullah University of Science and Technology (KAUST), Thuwal, Saudi Arabia.
Francesca ArianiMedical Genetics, University of Siena, Siena, Italy.
Shahid Niaz KhanDepartment of Zoology, Kohat University of Science and Technology, Kohat, Pakistan.
University of Siena · ITAzienda Ospedaliera Universitaria Senese · ITKing Saud bin Abdulaziz University for Health Sciences · SAKohat University of Science and Technology · PKCentre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Whole exome sequencing has provided significant opportunities to discover novel candidate genes for intellectual disability and autism spectrum disorders. Variants in the spectrin genes

Indexed as

heterozygous mutationintellectual disability (ID)protein modeling 3SPTBN5whole exome sequencing (WES)

Identifiers

PMID35782384
PMCPMC9248767
OpenAlexW4283008574

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.