ArticleBrain communications2021
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In one paragraph
Article in Brain communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.
0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.4field-weighted citation impact, top 10% of its field
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.
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.
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Who cites it
22 citing papers in PubMed, 36 citations in OpenAlex.
- Article
- Infantile Cerebellar-Retinal Degeneration Associated With Novel ACO2 Variants: Clinical Features and Insights From a Drosophila Model.Clinical genetics · 2025Article
- Analysis and identification of mitochondria-related genes associated with age-related hearing loss.BMC genomics · 2025Article
- Imaging flow cytometry reveals divergent mitochondrial phenotypes in mitochondrial disease patients.iScience · 2025Article
- Mutation of CRYAB encoding a conserved mitochondrial chaperone and antiapoptotic protein causes hereditary optic atrophy.JCI insight · 2024Article
- 18-Years of single-centre DNA testing in over 7000 index cases with inherited retinal dystrophies and optic neuropathies.Scientific reports · 2024Article
- Vitamin B5 is a context-dependent dietary regulator of nociception.G3 (Bethesda, Md.) · 2024Article
- Unveiling the double-edged sword: SOD1 trimers possess tissue-selective toxicity and bind septin-7 in motor neuron-like cells.Structure (London, England : 1993) · 2024Article
- Mitochondrial Aconitase and Its Contribution to the Pathogenesis of Neurodegenerative Diseases.International journal of molecular sciences · 2024Review
- Mitochondria in Retinal Ganglion Cells: Unraveling the Metabolic Nexus and Oxidative Stress.International journal of molecular sciences · 2024Review
- Limited Added Diagnostic Value of Whole Genome Sequencing in Genetic Testing of Inherited Retinal Diseases in a Swiss Patient Cohort.International journal of molecular sciences · 2024Article
- Anaplerotic Therapy Using Triheptanoin in Two Brothers Suffering from Aconitase 2 Deficiency.Metabolites · 2024Article
- Hereditary Optic Neuropathies: A Systematic Review on the Interplay between Biomaterials and Induced Pluripotent Stem Cells.Bioengineering (Basel, Switzerland) · 2024Review
- Biochemical characterization on muscle tissue of a novel biallelicJIMD reports · 2024Article
- Transcriptome analyses reveal molecular mechanisms of novel compound heterozygousFrontiers in cellular neuroscience · 2024Article
- Child Neurology: Progressive Cerebellar Atrophy and Retinal Dystrophy: Clues to an UltrarareNeurology · 2023Article
- Variants in the WDR45 Gene Within the OPA-2 Locus Associate With Isolated X-Linked Optic Atrophy.Investigative ophthalmology & visual science · 2023Article
- The Italian reappraisal of the most frequent genetic defects in hereditary optic neuropathies and the global top 10.Brain : a journal of neurology · 2023Article
- Variants in Mitochondrial ATP Synthase Cause Variable Neurologic Phenotypes.Annals of neurology · 2022Article
- Mitochondrial Retinopathies.International journal of molecular sciences · 2021Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
38 authors at 11 institutions in 5 countries.
Majida CharifUniversité Angers, MitoLab Team, UMR CNRS 6015 - INSERM U1083, Institut MitoVasc, SFR ICAT, Angers, France.
Naïg GueguenUniversité Angers, MitoLab Team, UMR CNRS 6015 - INSERM U1083, Institut MitoVasc, SFR ICAT, Angers, France.
Marc FerréUniversité Angers, MitoLab Team, UMR CNRS 6015 - INSERM U1083, Institut MitoVasc, SFR ICAT, Angers, France.
Zouhair ElkarhatLaboratory of Genomics and Human Genetics, Institut Pasteur du Maroc, Casablanca, Morocco.ORCID https://orcid.org/0000-0002-6778-380X
Salim KhiatiUniversité Angers, MitoLab Team, UMR CNRS 6015 - INSERM U1083, Institut MitoVasc, SFR ICAT, Angers, France.
Morgane LeMaoUniversité Angers, MitoLab Team, UMR CNRS 6015 - INSERM U1083, Institut MitoVasc, SFR ICAT, Angers, France.
Arnaud ChevrollierUniversité Angers, MitoLab Team, UMR CNRS 6015 - INSERM U1083, Institut MitoVasc, SFR ICAT, Angers, France.
Valerie Desquiret-DumasUniversité Angers, MitoLab Team, UMR CNRS 6015 - INSERM U1083, Institut MitoVasc, SFR ICAT, Angers, France.
David GoudenègeUniversité Angers, MitoLab Team, UMR CNRS 6015 - INSERM U1083, Institut MitoVasc, SFR ICAT, Angers, France.
Céline BrisUniversité Angers, MitoLab Team, UMR CNRS 6015 - INSERM U1083, Institut MitoVasc, SFR ICAT, Angers, France.
Selma KaneUniversité Angers, MitoLab Team, UMR CNRS 6015 - INSERM U1083, Institut MitoVasc, SFR ICAT, Angers, France.
Jennifer AlbanUniversité Angers, MitoLab Team, UMR CNRS 6015 - INSERM U1083, Institut MitoVasc, SFR ICAT, Angers, France.
Stéphanie ChupinDépartement de Biochimie et Génétique, CHU d'Angers, Angers, France.
Céline WetterwaldDépartement de Biochimie et Génétique, CHU d'Angers, Angers, France.
Leonardo CaporaliUnit of Neurology, Department of Biomedical and NeuroMotor Sciences (DIBINEM), University of Bologna, Bologna, Italy.ORCID https://orcid.org/0000-0002-0666-4380
Francesca TagliaviniUnit of Neurology, Department of Biomedical and NeuroMotor Sciences (DIBINEM), University of Bologna, Bologna, Italy.
Chiara LaMorgiaUnit of Neurology, Department of Biomedical and NeuroMotor Sciences (DIBINEM), University of Bologna, Bologna, Italy.
Michele CarbonelliUnit of Neurology, Department of Biomedical and NeuroMotor Sciences (DIBINEM), University of Bologna, Bologna, Italy.
Neringa JurkuteMoorfields Eye Hospital, London, UK.ORCID https://orcid.org/0000-0002-3092-7451
Abdelhamid BarakatLaboratory of Genomics and Human Genetics, Institut Pasteur du Maroc, Casablanca, Morocco.
Philippe GohierUniversité Angers, MitoLab Team, UMR CNRS 6015 - INSERM U1083, Institut MitoVasc, SFR ICAT, Angers, France.
Christophe VernyUniversité Angers, MitoLab Team, UMR CNRS 6015 - INSERM U1083, Institut MitoVasc, SFR ICAT, Angers, France.
Magalie BarthDepartment of Pediatrics, Competence Center of Inherited Metabolic Disorders, Angers Hospital, Angers, France.
Vincent ProcaccioUniversité Angers, MitoLab Team, UMR CNRS 6015 - INSERM U1083, Institut MitoVasc, SFR ICAT, Angers, France.
Dominique BonneauUniversité Angers, MitoLab Team, UMR CNRS 6015 - INSERM U1083, Institut MitoVasc, SFR ICAT, Angers, France.
Xavier ZanlonghiEye Clinic, Sourdille Jules Verne, Nantes, France.
Isabelle MeunierNational Center for Rare Diseases, Genetics of Sensory Diseases, University Hospital, Montpellier, France.
Nicole WeisschuhInstitute for Ophthalmic Research, Centre for Ophthalmology, University of Tübingen, Tübingen, Germany.
Simone Schimpf-LinzenboldPraxis für Humangenetik, Tübingen, Germany.
Felix TonagelCentre for Ophthalmology, University of Tübingen, Tübingen, Germany.
Ulrich KellnerRare Retinal Disease Center, AugenZentrum Siegburg, MVZ ADTC Siegburg GmbH, Siegburg, Germany.ORCID https://orcid.org/0000-0001-5221-4631
Patrick Yu-Wai-ManMoorfields Eye Hospital, London, UK.
Valerio CarelliUnit of Neurology, Department of Biomedical and NeuroMotor Sciences (DIBINEM), University of Bologna, Bologna, Italy.
Bernd WissingerInstitute for Ophthalmic Research, Centre for Ophthalmology, University of Tübingen, Tübingen, Germany.
Patrizia Amati-BonneauUniversité Angers, MitoLab Team, UMR CNRS 6015 - INSERM U1083, Institut MitoVasc, SFR ICAT, Angers, France.
Pascal ReynierUniversité Angers, MitoLab Team, UMR CNRS 6015 - INSERM U1083, Institut MitoVasc, SFR ICAT, Angers, France.ORCID https://orcid.org/0000-0003-0802-4608
European ION Group
Guy LenaersUniversité Angers, MitoLab Team, UMR CNRS 6015 - INSERM U1083, Institut MitoVasc, SFR ICAT, Angers, France.
Centre National de la Recherche Scientifique · FRUniversity of Bologna · ITCentre Hospitalier Universitaire d'Angers · FRInstitute of Neurological Sciences · ITInstitut Pasteur du Maroc · MAMoorfields Eye Hospital NHS Foundation Trust · GBSTZ eyetrial · DECentre Hospitalier Universitaire de Montpellier · FRClinique Jules Verne · FRPraxis für Humangenetik Tübingen · DEUniversity of Tübingen · DE
Funding
Medical Research Council G0701386Medical Research Council G1002570
Abstract
Biallelic mutations in
Indexed as
ACO2aconitase 2Krebs cyclemitochondriaoptic neuropathy
Identifiers
What OpenQuestion holds
Textmetadata
LicenceCC BY
Read underepoch 390
Registered trials
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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.