ArticleGenome medicine2019
Correction to: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith-Magenis syndrome.
Abstract readPublished Erratum
In one paragraph
Article in Genome 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.
0numbers the graph read from it
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0citing 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
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
- Erratum for
Authors and funding
58 authors.
Francesco VetriniBaylor Genetics, Houston, TX, 77021, USA.
Shane McKeeNorthern Ireland Regional Genetics Service, Belfast City Hospital, Belfast, UK.
Jill A RosenfeldDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA.
Mohnish SuriNottingham Genetics Service, Nottingham City Hospital, Nottingham, UK.
Andrea M LewisDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA.
Kimberly Margaret NugentDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA.
Elizabeth RoederDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA.
Rebecca O LittlejohnDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA.
Sue HolderNorth West Thames Regional Genetics Service, 759 Northwick Park Hospital, London, UK.
Wenmiao ZhuBaylor Genetics, Houston, TX, 77021, USA.
Joseph T AlaimoDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA.
Brett GrahamDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA.
Jill M HarrisDell Children's Medical Group, Austin, TX, 78723, USA.
James B GibsonDell Children's Medical Group, Austin, TX, 78723, USA.
Matthew PastoreDivision of Genetic and Genomic Medicine, Nationwide Children's Hospital; and Department of Pediatrics, College of Medicine, Ohio State University, Columbus, OH, 43205, USA.
Kim L McBrideDivision of Genetic and Genomic Medicine, Nationwide Children's Hospital; and Department of Pediatrics, College of Medicine, Ohio State University, Columbus, OH, 43205, USA.
Makanko KomaraDepartment of Pediatrics, College of Medicine & Health Sciences, United Arab University, Al Ain, UAE.
Lihadh Al-GazaliDepartment of Pediatrics, College of Medicine & Health Sciences, United Arab University, Al Ain, UAE.
Aisha Al ShamsiDepartment of Pediatrics, Tawam Hospital, Al-Ain, UAE.
Elizabeth A FanningDepartment of Pediatrics, Section of Genetics, University of Oklahoma Health Sciences Center, Oklahoma City, OK, 73104, USA.
Klaas J WierengaDepartment of Pediatrics, Section of Genetics, University of Oklahoma Health Sciences Center, Oklahoma City, OK, 73104, USA.
Daryl A ScottDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA.
Ziva Ben-NeriahDepartment of Human Genetics and Metabolic Diseases, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.
Vardiella MeinerDepartment of Human Genetics and Metabolic Diseases, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.
Hanoch CassutoThe Hebrew University of Jerusalem, Jerusalem, Israel.
Orly ElpelegMonique and Jacques Roboh Department of Genetic Research, Hadassah-Hebrew University Medical Center, 91120, Jerusalem, Israel.
J Lloyd HolderDepartment of Pediatrics, Texas Children's Hospital, Houston, TX, 77030, USA.
Lindsay C BurrageDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA.
Laurie H SeaverDepartment of Pediatrics, University of Hawaii, Honolulu, HI, 96826, USA.
Lionel Van MaldergemCentre de Génétique Humaine, Université de Franche-Comté, Besançon, France.
Sonal MahidaDepartment of Neurology, Boston Children's Hospital, Boston, MA, 0211, USA.
Janet S SoulDepartment of Neurology, Boston Children's Hospital, Boston, MA, 0211, USA.
Margaret MarlattDepartment of Neurology, Boston Children's Hospital, Boston, MA, 0211, USA.
Ludmila MatyakhinaGene DX, Gaithersburg, MD, 20877, USA.
Julie VogtWest Midlands Regional Clinical Genetics Service and Birmingham Health Partners, Women's and Children's Hospitals NHS Foundation Trust, Birmingham, UK.
June-Anne GoldEast Anglia Regional Genetics Service, Addenbrooke's Hospital, Cambridge, UK.
Soo-Mi ParkEast Anglia Regional Genetics Service, Addenbrooke's Hospital, Cambridge, UK.
Vinod VargheseAll-Wales Medical Genetics Service, University Hospital of Wales, Cardiff, UK.
Anne K LampeSouth East of Scotland Clinical Genetic Service, Western General Hospital, Edinburgh, UK.
Ajith KumarNorth East Thames Regional Genetics Service, Great Ormond Street Hospital, London, UK.
Melissa LeesNorth East Thames Regional Genetics Service, Great Ormond Street Hospital, London, UK.
Muriel Holder-EspinasseSouth East Thames Regional Genetics Service, Guy's Hospital, London, UK.
Vivienne McConnellNorthern Ireland Regional Genetics Service, Belfast City Hospital, Belfast, UK.
Birgitta BernhardNorth West Thames Regional Genetics Service, 759 Northwick Park Hospital, London, UK.
Ed BlairOxford Regional Genetics Service, Oxford University Hospitals, Oxford, UK.
Victoria HarrisonWessex Clinical Genetics Service, Princess Anne Hospital, Southampton, UK.
DDD study
Donna M MuznyDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA.
Richard A GibbsDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA.
Sarah H ElseaBaylor Genetics, Houston, TX, 77021, USA.
Jennifer E PoseyDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA.
Weimin BiBaylor Genetics, Houston, TX, 77021, USA.
Seema LalaniBaylor Genetics, Houston, TX, 77021, USA.
Fan XiaBaylor Genetics, Houston, TX, 77021, USA.
Yaping YangBaylor Genetics, Houston, TX, 77021, USA.
Christine M EngBaylor Genetics, Houston, TX, 77021, USA.
James R LupskiBaylor Genetics, Houston, TX, 77021, USA.
Pengfei LiuBaylor Genetics, Houston, TX, 77021, USA. pengfeil@bcm.edu.
Funding
Individual genomic analyses to discover the molecular basis and mechanisms contributing to adult-onset diseaseK08HG008986 · NHGRI · BAYLOR COLLEGE OF MEDICINE · PI POSEY, JENNIFER ELLEN · 2017 to 2021
$831kMedical Research Council MC_PC_16018NHGRI NIH HHS K08 HG008986
Abstract
It was highlighted that the original article [1] contained a typographical error in the Results section. Subject 17 was incorrectly cited as Subject 1. This Correction article shows the revised statement. The original article has been updated.
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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.