ArticleNature communications2020
Author Correction: Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders.
Abstract readPublished Erratum
In one paragraph
Article in Nature communications, 2020. 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
–field-weighted citation impact
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
7 citing papers in PubMed.
- Correlated protein-RNA associations and a requirement for HNRNPU in the long-range recruitment of Polycomb Repressive Complexes by the lncRNAs Airn and Kcnq1ot1.PLoS genetics · 2026Article
- Microglia Mitochondrial Metabolism in Neurological Diseases.Molecular neurobiology · 2026Review
- Genome Sequencing Identifies 13 Novel Candidate Risk Genes for Autism Spectrum Disorder in a Qatari Cohort.International journal of molecular sciences · 2024Article
- A cryptic microdeletion del(12)(p11.21p11.23) within an unbalanced translocation t(7;12)(q21.13;q23.1) implicates new candidate loci for intellectual disability and Kallmann syndrome.Scientific reports · 2023Article
- Reanalysis of exome sequencing data reveals a treatable neurometabolic origin in two previously undiagnosed siblings with neurodevelopmental disorder.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2023Article
- A microdeletion del(12)(p11.21p11.23) with a cryptic unbalanced translocation t(7;12)(q21.13;q23.1) implicates new candidate loci for intellectual disability and Kallmann syndrome.Research square · 2023Article
- A rigorousFrontiers in molecular neuroscience · 2022Article
Corrections and comments
- Erratum for
Authors and funding
72 authors.
Tianyun WangDepartment of Genome Sciences, University of Washington, Seattle, WA, USA.ORCID http://orcid.org/0000-0002-5179-087X
Kendra HoekzemaDepartment of Genome Sciences, University of Washington, Seattle, WA, USA.
Davide VecchioRare Disease and Medical Genetics, Academic Department of Pediatrics, Bambino Gesù Children's Hospital, Rome, Italy.ORCID http://orcid.org/0000-0003-2907-3206
Huidan WuCenter for Medical Genetics & Hunan Provincial Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China.
Arvis SulovariDepartment of Genome Sciences, University of Washington, Seattle, WA, USA.ORCID http://orcid.org/0000-0003-4354-9020
Bradley P CoeDepartment of Genome Sciences, University of Washington, Seattle, WA, USA.
Madelyn A GillentineDepartment of Genome Sciences, University of Washington, Seattle, WA, USA.ORCID http://orcid.org/0000-0002-8989-2214
Amy B WilfertDepartment of Genome Sciences, University of Washington, Seattle, WA, USA.
Luis A Perez-JuradoPaediatric and Reproductive Genetics unit, Women's and Children's Hospital, Adelaide, SA, Australia.
Malin KvarnungDepartment of Molecular Medicine and Surgery, Center for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden.
Yoeri SleypCentre for Human Genetics, KU Leuven and Leuven Autism Research (LAuRes), Leuven, Belgium.
Rachel K EarlDepartment of Psychiatry and Behavioral Sciences, University of Washington, Seattle, WA, USA.
Jill A RosenfeldDepartment of Molecular & Human Genetics, Baylor College of Medicine, Houston, TX, USA.ORCID http://orcid.org/0000-0001-5664-7987
Madeleine R GeishekerDepartment of Genome Sciences, University of Washington, Seattle, WA, USA.ORCID http://orcid.org/0000-0002-4166-3236
Lin HanCenter for Medical Genetics & Hunan Provincial Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China.
Bing DuCenter for Medical Genetics & Hunan Provincial Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China.
Chris BarnettPaediatric and Reproductive Genetics unit, Women's and Children's Hospital, Adelaide, SA, Australia.
Elizabeth ThompsonPaediatric and Reproductive Genetics unit, Women's and Children's Hospital, Adelaide, SA, Australia.
Marie ShawAdelaide Medical School and the Robinson Research Institute, the University of Adelaide, Adelaide, SA, Australia.
Renee CarrollAdelaide Medical School and the Robinson Research Institute, the University of Adelaide, Adelaide, SA, Australia.
Kathryn FriendGenetics and Molecular Pathology, SA Pathology, Adelaide, SA, Australia.
Rachael CatfordGenetics and Molecular Pathology, SA Pathology, Adelaide, SA, Australia.
Elizabeth E PalmerGenetics of Learning Disability Service, Hunter New England Health Service, Waratah, NSW, Australia.
Xiaobing ZouChildren Development Behavior Center, The Third Affiliated Hospital, Sun Yat-Sen University, Guangzhou, Guangdong, China.
Jianjun OuMental Health Institute of the Second Xiangya Hospital, Central South University, Changsha, China.
Honghui LiKey Laboratory of Developmental Disorders in Children, Liuzhou Maternity and Child Healthcare Hospital, Liuzhou, China.
Hui GuoCenter for Medical Genetics & Hunan Provincial Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China.ORCID http://orcid.org/0000-0002-1570-2545
Jennifer GerdtsDepartment of Psychiatry and Behavioral Sciences, University of Washington, Seattle, WA, USA.
Emanuela AvolaOasi Research Institute-IRCCS, Troina, Italy.
Giuseppe CalabreseOasi Research Institute-IRCCS, Troina, Italy.
Maurizio EliaOasi Research Institute-IRCCS, Troina, Italy.
Donatella GrecoOasi Research Institute-IRCCS, Troina, Italy.
Anna LindstrandDepartment of Molecular Medicine and Surgery, Center for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden.ORCID http://orcid.org/0000-0003-0806-5602
Ann NordgrenDepartment of Molecular Medicine and Surgery, Center for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden.ORCID http://orcid.org/0000-0003-3285-4281
Britt-Marie AnderlidDepartment of Molecular Medicine and Surgery, Center for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden.
Geert VandeweyerDepartment of Medical Genetics, University of Antwerp, Antwerp, Belgium.
Anke Van DijckDepartment of Medical Genetics, University of Antwerp, Antwerp, Belgium.ORCID http://orcid.org/0000-0002-6713-2943
Nathalie Van der AaDepartment of Medical Genetics, University of Antwerp, Antwerp, Belgium.
Brooke McKennaDepartment of Psychology, Emory University, Atlanta, GA, USA.
Miroslava HancarovaDepartment of Biology and Medical Genetics, Charles University 2nd Faculty of Medicine and University Hospital Motol, Prague, Czech Republic.
Sarka BendovaDepartment of Biology and Medical Genetics, Charles University 2nd Faculty of Medicine and University Hospital Motol, Prague, Czech Republic.
Marketa HavlovicovaDepartment of Biology and Medical Genetics, Charles University 2nd Faculty of Medicine and University Hospital Motol, Prague, Czech Republic.
Giovanni MalerbaDepartment of Neurosciences, Biomedicine and Movement Sciences, University of Verona, Verona, Italy.
Bernardo Dalla BernardinaChild Neuropsychiatry Unit, AOUI, Verona, Italy.
Pierandrea MugliaUCB Pharma, Bruxelles, Belgium.
Arie van HaeringenDepartment of Clinical Genetics, Leiden University Medical Center (LUMC), Leiden, Netherlands.
Mariette J V HofferDepartment of Clinical Genetics, Leiden University Medical Center (LUMC), Leiden, Netherlands.ORCID http://orcid.org/0000-0002-1812-7670
Barbara FrankeDepartment of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, Netherlands.ORCID http://orcid.org/0000-0003-4375-6572
Gerarda CappuccioDepartment of Translational Medicine, Federico II University, Naples, Italy.
Martin DelatyckiMurdoch Children's Research Institute, Melbourne, Australia.
Paul J LockhartMurdoch Children's Research Institute, Melbourne, Australia.ORCID http://orcid.org/0000-0003-2531-8413
Melanie A ManningDivision of Medical Genetics, Department of Pediatrics, Stanford University, Stanford, CA, USA.
Pengfei LiuDepartment of Molecular & Human Genetics, Baylor College of Medicine, Houston, TX, USA.ORCID http://orcid.org/0000-0002-4177-709X
Ingrid E SchefferMurdoch Children's Research Institute, Melbourne, Australia.
Nicola Brunetti-PierriDepartment of Translational Medicine, Federico II University, Naples, Italy.ORCID http://orcid.org/0000-0002-6895-8819
Nanda RommelseDepartment of Psychiatry, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, Netherlands.
David G AmaralDepartment of Psychiatry and Behavioral Sciences and the MIND Institute, University of California, Davis, Sacramento, CA, USA.
Gijs W E SantenDepartment of Clinical Genetics, Leiden University Medical Center (LUMC), Leiden, Netherlands.
Elisabetta TrabettiDepartment of Neurosciences, Biomedicine and Movement Sciences, University of Verona, Verona, Italy.
Zdeněk SedláčekDepartment of Biology and Medical Genetics, Charles University 2nd Faculty of Medicine and University Hospital Motol, Prague, Czech Republic.
Jacob J MichaelsonDepartment of Psychiatry, University of Iowa Carver College of Medicine, Iowa City, IA, USA.ORCID http://orcid.org/0000-0001-9713-0992
Karen PierceDepartment of Neurosciences, UC San Diego Autism Center, School of Medicine, University of California San Diego, La Jolla, CA, USA.
Eric CourchesneDepartment of Neurosciences, UC San Diego Autism Center, School of Medicine, University of California San Diego, La Jolla, CA, USA.ORCID http://orcid.org/0000-0002-3772-5799
R Frank KooyDepartment of Medical Genetics, University of Antwerp, Antwerp, Belgium.ORCID http://orcid.org/0000-0003-2024-0485
SPARK Consortium
Magnus NordenskjöldDepartment of Molecular Medicine and Surgery, Center for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden.
Corrado RomanoOasi Research Institute-IRCCS, Troina, Italy.ORCID http://orcid.org/0000-0003-1049-0683
Hilde PeetersCentre for Human Genetics, KU Leuven and Leuven Autism Research (LAuRes), Leuven, Belgium.
Raphael A BernierDepartment of Psychiatry and Behavioral Sciences, University of Washington, Seattle, WA, USA.
Jozef GeczSouth Australian Health and Medical Research Institute, Adelaide, SA, Australia.ORCID http://orcid.org/0000-0002-7884-6861
Kun XiaCenter for Medical Genetics & Hunan Provincial Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China.ORCID http://orcid.org/0000-0001-8090-6002
Evan E EichlerDepartment of Genome Sciences, University of Washington, Seattle, WA, USA. eee@gs.washington.edu.ORCID http://orcid.org/0000-0002-8246-4014
Funding
Mechanisms of Brain Dysmorphology in MN1 C-Terminal Truncation Syndrome, a Novel Intellectual Developmental Disability Disorder P50HD103524 · NICHD · UNIVERSITY OF WASHINGTON · PI DANIEL DOHERTY · 2020 to 2026
$9.9MNICHD NIH HHS P50 HD103524
Abstract
An amendment to this paper has been published and can be accessed via a link at the top of the paper.
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Read underepoch 390
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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.