ArticleNPJ genomic medicine2019
Erratum: Author Correction: A framework to identify contributing genes in patients with Phelan-McDermid syndrome.
Abstract readPublished Erratum
In one paragraph
Article in NPJ genomic medicine, 2019. 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.
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0 citing papers in PubMed.
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Corrections and comments
- Erratum for
Authors and funding
62 authors.
Anne-Claude Tabet *1Genetics Department, Robert Debré Hospital, APHP, Paris, France.ORCID 0000-0003-2910-7744
Thomas Rolland *2Human Genetics and Cognitive Functions, Institut Pasteur, Paris, France.
Marie Ducloy2Human Genetics and Cognitive Functions, Institut Pasteur, Paris, France.
Jonathan Lévy1Genetics Department, Robert Debré Hospital, APHP, Paris, France.
Julien Buratti2Human Genetics and Cognitive Functions, Institut Pasteur, Paris, France.
Alexandre Mathieu2Human Genetics and Cognitive Functions, Institut Pasteur, Paris, France.
Damien Haye1Genetics Department, Robert Debré Hospital, APHP, Paris, France.
Laurence Perrin1Genetics Department, Robert Debré Hospital, APHP, Paris, France.
Céline Dupont1Genetics Department, Robert Debré Hospital, APHP, Paris, France.ORCID 0000-0001-8329-0346
Sandrine Passemard1Genetics Department, Robert Debré Hospital, APHP, Paris, France.
Yline Capri1Genetics Department, Robert Debré Hospital, APHP, Paris, France.
Alain Verloes1Genetics Department, Robert Debré Hospital, APHP, Paris, France.
Séverine Drunat1Genetics Department, Robert Debré Hospital, APHP, Paris, France.
Boris Keren5Cytogenetics Unit, Pitié Salpetrière Hospital, APHP, Paris, France.
Cyril Mignot6Neurogenetics Unit, Pitié Salpetrière Hospital, APHP, Paris, France.
Isabelle Marey7Clinical Genetics Unit, Pitié Salpetrière Hospital, APHP, Paris, France.
Aurélia Jacquette7Clinical Genetics Unit, Pitié Salpetrière Hospital, APHP, Paris, France.
Sandra Whalen7Clinical Genetics Unit, Pitié Salpetrière Hospital, APHP, Paris, France.
Eva Pipiras8Cytogenetics Unit, Jean Verdier Hospital, APHP, Bondy, France.
Brigitte Benzacken8Cytogenetics Unit, Jean Verdier Hospital, APHP, Bondy, France.
Sandra Chantot-Bastaraud9Cytogenetics Unit, Trousseau Hospital, APHP, Paris, France.
Alexandra Afenjar10Clinical Genetics Unit, Trousseau Hospital, APHP, Paris, France.
Delphine Héron10Clinical Genetics Unit, Trousseau Hospital, APHP, Paris, France.
Cédric Le Caignec11Clinical Genetics Unit, Nantes Hospital, Nantes, France.
Claire Beneteau11Clinical Genetics Unit, Nantes Hospital, Nantes, France.
Olivier Pichon11Clinical Genetics Unit, Nantes Hospital, Nantes, France.
Bertrand Isidor11Clinical Genetics Unit, Nantes Hospital, Nantes, France.
Albert David11Clinical Genetics Unit, Nantes Hospital, Nantes, France.
Laila El Khattabi12Cytogenetics Unit, Cochin Hospital, APHP, Paris, France.
Stephan Kemeny13Genetics Unit, CHU Estaing, Clermont-Ferrand, France.
Laetitia Gouas13Genetics Unit, CHU Estaing, Clermont-Ferrand, France.
Philippe Vago13Genetics Unit, CHU Estaing, Clermont-Ferrand, France.
Anne-Laure Mosca-BoidronCytogenetics Unit, Dijon Hospital, Dijon, France.
Laurence FaivreClinical Genetics Unit, Dijon Hospital, Dijon, France.
Chantal Missirian16Genetics Unit, La Timone Hospital, Marseille, France.
Nicole Philip16Genetics Unit, La Timone Hospital, Marseille, France.
Damien SanlavilleCytogenetics Unit, Lyon Civil Hospital, Lyon, France.
Patrick EderyClinical Genetics Unit, Lyon Civil Hospital, Lyon, France.
Véronique Satre19Cytogenetics Unit, Grenoble Hospital, Grenoble, France.
Charles Coutton19Cytogenetics Unit, Grenoble Hospital, Grenoble, France.
Françoise Devillard19Cytogenetics Unit, Grenoble Hospital, Grenoble, France.
Klaus Dieterich20Clinical Genetics Unit, Grenoble Hospital, Grenoble, France.
Marie-Laure Vuillaume21Genetics Unit, Bordeaux Hospital, Bordeaux, France.
Caroline Rooryck21Genetics Unit, Bordeaux Hospital, Bordeaux, France.
Didier Lacombe21Genetics Unit, Bordeaux Hospital, Bordeaux, France.
Lucile Pinson22Genetics Unit, Montpellier Hospital, Montpellier, France.
Vincent Gatinois22Genetics Unit, Montpellier Hospital, Montpellier, France.
Jacques Puechberty22Genetics Unit, Montpellier Hospital, Montpellier, France.
Jean ChiesaGenetics Unit, CHRU Nimes, Nimes, France.
James LespinasseCytogenetics Unit, Chambéry-Hôtel-Dieu Hospital, Chambéry, France.
Christèle Dubourg25Genetics Unit, CHU Rennes, Rennes, France.
Chloé Quelin25Genetics Unit, CHU Rennes, Rennes, France.
Mélanie Fradin25Genetics Unit, CHU Rennes, Rennes, France.
Hubert JournelGenetics Unit, Chubert Hospital, Vannes, France.
Annick Toutain27Genetics Unit, Bretonneau Hospital, Tours, France.
Dominique Martin28Genetics Unit, CH Le Mans, Le Mans, France.
Abdelamdjid Benmansour1Genetics Department, Robert Debré Hospital, APHP, Paris, France.
Claire S Leblond2Human Genetics and Cognitive Functions, Institut Pasteur, Paris, France.
Roberto Toro2Human Genetics and Cognitive Functions, Institut Pasteur, Paris, France.
Frédérique Amsellem29Department of Child and Adolescent Psychiatry, Robert Debré Hospital, APHP, Paris, France.
Richard Delorme2Human Genetics and Cognitive Functions, Institut Pasteur, Paris, France.
Thomas Bourgeron2Human Genetics and Cognitive Functions, Institut Pasteur, Paris, France.
Funding
No grant is acknowledged in the PubMed record.
Abstract
[This corrects the article DOI: 10.1038/s41525-017-0035-2.].
Indexed as
Clinical geneticsNeurodevelopmental disorders
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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.