ArticleEuropean journal of human genetics : EJHG2026
Correction: Comprehensive analysis of CNOT3-related neurodevelopmental disorders: phenotypic and genotypic characterization.
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In one paragraph
Article in European journal of human genetics : EJHG, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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0citing papers in PubMed
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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.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
- Erratum for
Authors and funding
77 authors.
Camille EngelUniversité de Franche-Comté, Centre de Génétique Humaine, CHU Besançon, Besançon, France. cengel@chu-besancon.fr.ORCID http://orcid.org/0000-0003-1531-7628
Michaela RendekUniversité de Franche-Comté, Centre de Génétique Humaine, CHU Besançon, Besançon, France.
Jessica AssoumaniUniversité de Franche-Comté, Centre de Génétique Humaine, CHU Besançon, Besançon, France.
Emanuela ArgilliDepartment of Neurology, University of California, San Francisco, San Francisco, CA, USA.
Francesca ArianiMedical Genetics, University of Siena, Siena, Italy.
Anne-Laude Avice-DenizetUniversité de Franche-Comté, Centre de Génétique Humaine, CHU Besançon, Besançon, France.
Emilia K BijlsmaDepartment of Clinical Genetics, Leiden University Medical Centre, Leiden, The Netherlands.
Pierre BlancLaboratoire Seqoia, Paris, France.ORCID http://orcid.org/0009-0003-8965-7171
Lucia Pia BrunoMedical Genetics, University of Siena, Siena, Italy.
Bert CallewaertReference centre for Mendelian connective tissue disorders-UZ Gent, Ghent University Hospital-UZ Gent, Gent, Belgium.ORCID http://orcid.org/0000-0002-9743-4205
Valeria CapraGenomics and Clinical Genetics, IRCCS Istituto Giannina Gaslini, Genoa, Italy.ORCID http://orcid.org/0000-0002-3097-0388
Michele CarulloFondazione Policlinico Universitario Agostino Gemelli IRCCS, Roma, Italy.ORCID http://orcid.org/0009-0008-0915-3923
Bertrand ChesneauService de Génétique Médicale, Hôpital Purpan, CHU de Toulouse, Toulouse, France.ORCID http://orcid.org/0000-0001-9729-7346
Sandra CoppensCenter for Medical Genetics, Hôpital Erasme, Hôpital Universitaire de Bruxelles, Université Libre de Bruxelles, Brussels, Belgium.
Cynthia CurryGenetic Medicine, University of California, San Francisco/Fresno, Fresno, CA, USA.
Breanne DaleGenetics and Metabolics Clinic, McMaster Children's Hospital, Hamilton, ON, Canada.ORCID http://orcid.org/0000-0001-5034-7457
Eric DahlenUniversité de Franche-Comté, CHU Besançon, Oncobiologie Génétique Bioinformatique, FHU-TRANSLAD et Institut GIMI, Besançon, France.
Andrée Delahaye-DuriezUF médecine génomique et génétique clinique, Hôpital Jean Verdier, Hôpitaux Universitaires de Paris Seine Saint Denis, AP-HP, Bondy, France.ORCID http://orcid.org/0000-0003-4324-7372
Anne-Sophie Denommé-PichonUniversité de Bourgogne, INSERM UMR1231 GAD "Génétique des Anomalies du Développement", Dijon, France.ORCID http://orcid.org/0000-0002-8986-8222
Bénédicte DemeerService de Génétique Clinique et Oncogénétique, CHU Amiens-Picardie, Amiens, France.
Lenka DvořákováDepartment of Biology and Medical Genetics, Charles University-2nd Faculty of Medicine and University Hospital Motol, Prague, Czech Republic.
Jan FischerInstitute for Clinical Genetics, University Hospital Carl Gustav Carus at TUD Dresden University of Technology, Dresden, Germany.ORCID http://orcid.org/0009-0002-7334-0842
David GenevièveUniversité Montpellier, Centre de référence anomalies du développement et syndromes malformatifs, Génétique Clinique, CHU Montpellier, Montpellier, France.ORCID http://orcid.org/0000-0001-6928-6287
Thea GiacominiDepartment of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genoa, Italy.
Mette M HandrupCenter for Rare Diseases, Pediatric and Adolescent Medicine, Aarhus University Hospital, Aarhus, Denmark.
Delphine HeronDépartement de génétique médicale, Hôpital Pitié-Salpêtrière, AP-HP.Sorbonne Université, Paris, France.
Irina HüningInstitute of Human Genetics, University Hospital Schleswig-Holstein, Lübeck, Germany.
Michelle IacominoMedical Genetics Unit, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Bertrand IsidorService de génétique médicale, Unité de génétique clinique, CHU Hôtel Dieu, 1 place Alexis Ricordeau, Nantes, France.
Boris KerenDépartement de génétique médicale, Hôpital Pitié-Salpêtrière, AP-HP.Sorbonne Université, Paris, France.
Stanislav KmochResearch Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, 1st Faculty of Medicine, Charles University in Prague, Prague, Czech Republic.ORCID http://orcid.org/0000-0002-6239-707X
David A KoolenDepartment of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.ORCID http://orcid.org/0000-0002-2152-4626
Andrea KüblerInstitute for Clinical Genetics, University Hospital Carl Gustav Carus at TUD Dresden University of Technology, Dresden, Germany.
Jana LaštůvkováDepartment of Medical Genetics, Masaryk Hospital in Ústí nad Labem, Regional Health Corporation, Ústí nad Labem, Czech Republic.
Carolyn LeDepartment of Neurology, University of California, San Francisco, San Francisco, CA, USA.ORCID http://orcid.org/0009-0001-1532-7685
Jonathan LevyGenetics Department, AP-HP, Robert-Debré University Hospital, Paris, France.ORCID http://orcid.org/0000-0002-8822-816X
Caterina Lo RizzoGenetica Medica, Azienda Ospedaliera Universitaria Senese, Siena, Italy.
Silvia MaitzService of Medical Genetics, Oncologic Institute of Southern Switzerland, EOC, Switzerland, Switzerland.
Sandrine MarlinCentre de référence « Surdités Génétiques », Service de Médecine génomique des Maladies rares, Hôpital Necker, Assistance Publique-Hôpitaux de Paris, Paris, France.ORCID http://orcid.org/0000-0002-4115-9806
Cyril MignotDépartement de génétique médicale, Hôpital Pitié-Salpêtrière, AP-HP.Sorbonne Université, Paris, France.
Ghayda MirzaaDepartment of Pediatrics, University of Washington, Seattle, WA, USA.ORCID http://orcid.org/0000-0003-2648-7657
Inga NagelInstitute of Human Genetics, University Hospital Schleswig-Holstein, Kiel, Germany.
Sebastian NeuensDepartment of Genetics, Hôpital Universitaire des Enfants Reine Fabiola, Hôpital Universitaire de Bruxelles, Université Libre de Bruxelles, Brussels, Belgium.ORCID http://orcid.org/0000-0003-2979-3764
Lenka NoskováResearch Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, 1st Faculty of Medicine, Charles University in Prague, Prague, Czech Republic.
Emily PaoCenter for Integrative Brain Research, Seattle Children's Research Institute, Seattle, WA, USA.
Anna PeckováDepartment of Medical Genetics, Masaryk Hospital in Ústí nad Labem, Regional Health Corporation, Ústí nad Labem, Czech Republic.
Julie PlaisancieService de Génétique Médicale, Hôpital Purpan, CHU de Toulouse, Toulouse, France.ORCID http://orcid.org/0000-0001-7551-248X
Joseph PorrmannInstitute for Clinical Genetics, University Hospital Carl Gustav Carus at TUD Dresden University of Technology, Dresden, Germany.
Flavia PriviteraDepartment of Neurobiology and Molecular Medicine, IRCCS Fondazione Stella Maris, Pisa, Italy.ORCID http://orcid.org/0000-0002-0316-4903
André ReisInstitute of Human Genetics, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.ORCID http://orcid.org/0000-0002-6301-6363
Alessandra RenieriMedical Genetics, University of Siena, Siena, Italy.
Marlène RioNecker Hospital, APHP, Reference Center for Intellectual Disability, Genetics Department, Institut Imagine, University of Paris, Paris, France.ORCID http://orcid.org/0000-0003-2049-5058
Alyssa RippertDivision of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Lukáš RybaDepartment of Biology and Medical Genetics, Charles University-2nd Faculty of Medicine and University Hospital Motol, Prague, Czech Republic.
Marcello ScalaDepartment of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genoa, Italy.ORCID http://orcid.org/0000-0003-2194-7239
Jolanda H SchievingRadboud University Medical Center, Department of Neurology, Nijmegen, The Netherlands.
Elliott H SherrDepartment of Neurology, University of California, San Francisco, San Francisco, CA, USA.
Andrew ShuenDepartment of Pediatrics, Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, Toronto, ON, Canada.ORCID http://orcid.org/0000-0001-6094-4394
Richard SidlowDepartment of Medical Genetics and Metabolism, Valley Children's Hospital, Madera, CA, USA.
Thomas SmolInstitut de Génétique Médicale, CHU Lille, Avenue Oscar Lambret, Lille, France.ORCID http://orcid.org/0000-0002-0119-5896
Julie SobletDepartment of Genetics, Hôpital Universitaire des Enfants Reine Fabiola, Hôpital Universitaire de Bruxelles, Université Libre de Bruxelles, Brussels, Belgium.
Pasquale StrianoDepartment of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genoa, Italy.ORCID http://orcid.org/0000-0002-6065-1476
Mohnish SuriNottingham Clinical Genetics Service, Nottingham University Hospitals NHS Trust, City Hospital Campus, Nottingham, UK.
Hannes SyrynCenter for Medical Genetics, Ghent University Hospital, Ghent, Belgium.
Frédéric Tran Mau-ThemUniversité de Bourgogne, INSERM UMR1231 GAD "Génétique des Anomalies du Développement", Dijon, France.
Andre M TravessaDepartment of Medical Genetics, Hospital de Santa Maria, Centro Hospitalar Universitário Lisboa Norte, Lisbon, Portugal.
Julien Van GilsDepartment of Medical Genetics, University Hospital of Bordeaux and INSERM U1211, University of Bordeaux, Bordeaux, France.ORCID http://orcid.org/0000-0003-1497-9363
Georgia VasileiouInstitute of Human Genetics, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.
Jolijn J A VerseputDepartment of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
Catheline VilainDepartment of Genetics, Hôpital Universitaire des Enfants Reine Fabiola, Hôpital Universitaire de Bruxelles, Université Libre de Bruxelles, Brussels, Belgium.
Catherine Vincent-DelormeCHU Lille, Clinique de Génétique, Lille, France.
Emílie VyhnálkováDepartment of Biology and Medical Genetics, Charles University-2nd Faculty of Medicine and University Hospital Motol, Prague, Czech Republic.
Emma L WakelingNorth East Thames Regional Genetic Service, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
Pia ZacherEpilepsy Center Kleinwachau, Radeberg, Germany.ORCID http://orcid.org/0000-0002-0211-5763
Federico ZaraDepartment of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genoa, Italy.ORCID http://orcid.org/0000-0001-9744-5222
Paul KuentzUniversité de Bourgogne, INSERM UMR1231 GAD "Génétique des Anomalies du Développement", Dijon, France.ORCID http://orcid.org/0000-0003-2814-6303
Juliette PiardUniversité de Franche-Comté, Centre de Génétique Humaine, CHU Besançon, Besançon, France. jpiard@chu-besancon.fr.ORCID http://orcid.org/0000-0001-5244-5325
Funding
No grant is acknowledged in the PubMed record.
Abstract
PubMed holds no abstract for this paper.
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PMID
41927804What OpenQuestion holds
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