ArticleGenetics in medicine : official journal of the American College of Medical Genetics2020
Correction: The CHD4-related syndrome: a comprehensive investigation of the clinical spectrum, genotype-phenotype correlations, and molecular basis.
Abstract readPublished Erratum
In one paragraph
Article in Genetics in medicine : official journal of the American College of Medical Genetics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
0numbers the graph read from it
0cells of the map it votes in
3citing 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
3 citing papers in PubMed.
- Genomic transcription factor binding site selection is edited by the chromatin remodeling factor CHD4.Nucleic acids research · 2024Article
- The role of auxiliary domains in modulating CHD4 activity suggests mechanistic commonality between enzyme families.Nature communications · 2022Article
- A rigorousFrontiers in molecular neuroscience · 2022Article
Corrections and comments
- Erratum for
Authors and funding
49 authors.
Karin WeissThe Genetics Institute, Rambam Health Care Campus, Haifa, Israel. k_weiss@rambam.health.gov.il.
Hayley P LazarEpigenetics and Stem Cell Biology Laboratory, National Institute of Environmental Health Sciences, Research Triangle Park, NC, USA.
Alina KurolapThe Genetics Institute, Rambam Health Care Campus, Haifa, Israel.
Ariel F MartinezMedical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.
Tamar PapernaThe Genetics Institute, Rambam Health Care Campus, Haifa, Israel.
Lior CohenGenetics Institute, Schneider Children's Medical Center, Petah Tikva, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Marie F SmelandDepartment of Medical Genetics, University Hospital of North Norway, Tromsø, Norway.
Sandra WhalenUF de génétique clinique, Centre de Référence Maladies Rares des Anomalies du développement et syndromes malformatifs, APHP, Hôpital Trousseau, Paris, France.
Solveig HeideAP-HP, Département de Génétique, Centre de Référence Maladies Rares "Anomalies du développement et syndromes malformatifs" Hôpital de la Pitié Salpêtrière, Paris, France.
Boris KerenAP-HP, Département de Génétique, Centre de Référence Maladies Rares "Anomalies du développement et syndromes malformatifs" Hôpital de la Pitié Salpêtrière, Paris, France.
Pauline TerhalDepartment of Genetics, Utrecht University Medical Center, Utrecht, the Netherlands.
Melita IrvingDepartment of Clinical Genetics, Guy's Hospital, London, UK.
Motoki TakakuEpigenetics and Stem Cell Biology Laboratory, National Institute of Environmental Health Sciences, Research Triangle Park, NC, USA.
John D RobertsEpigenetics and Stem Cell Biology Laboratory, National Institute of Environmental Health Sciences, Research Triangle Park, NC, USA.
Robert M PetrovichEpigenetics and Stem Cell Biology Laboratory, National Institute of Environmental Health Sciences, Research Triangle Park, NC, USA.
Samantha A Schrier VerganoDivision of Medical Genetics and Metabolism, Children's Hospital of The King's Daughters, Norfolk, VA, USA.
Amy KenneyDivision of Medical Genetics and Metabolism, Children's Hospital of The King's Daughters, Norfolk, VA, USA.
Hanne HoveCentre for Rare Diseases, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.
Elizabeth DeCheneDivision of Genomic Diagnostics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Shane C QuinonezDepartment of Pediatrics, Division of Genetics, Metabolism and Genomic Medicine, University of Michigan, Ann Arbor, MI, USA.
Estelle ColinDepartment of Biochemistry and Genetics, University Hospital Angers, Angers, France.
Alban ZieglerDepartment of Biochemistry and Genetics, University Hospital Angers, Angers, France.
Melissa RumpleBanner Child Neurology, Glendale, AZ, USA.
Mahim JainMedical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.
Danielle MonteilDepartment of Pediatrics, Naval Medical Center Portsmouth, Portsmouth, VA, USA.
Elizabeth R RoederDepartments of Pediatrics and Molecular and Human Genetics, Baylor College of Medicine, San Antonio, TX, USA.
Kimberly NugentDepartments of Pediatrics and Molecular and Human Genetics, Baylor College of Medicine, San Antonio, TX, USA.
Arie van HaeringenDepartment of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.
Michael GambelloDepartment of Human Genetics, School of Medicine, Emory University, Atlanta, GA, USA.
Avni SantaniDivision of Genomic Diagnostics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Līvija MedneDivision of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Bryan KrockDivision of Genomic Diagnostics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Cara M SkrabanDivision of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Elaine H ZackaiDivision of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Holly A DubbsDivision of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Thomas SmolDepartment of Clinical Genetics, Lille University Hospital, CHU Lille, Lille, France.
Jamal GhoumidDepartment of Clinical Genetics, Lille University Hospital, CHU Lille, Lille, France.
Michael J ParkerSheffield Children's Hospital NHS Foundation Trust, Western Bank, Sheffield, UK.
Michael WrightNorthern Genetics Service, Newcastle Upon Tyne Hospitals NHS Foundation Trust, Institute of Human Genetics, International Centre for Life, Newcastle upon Tyne, UK.
Peter TurnpennyUniversity of Exeter Medical School, Clinical Genetics Royal Devon & Exeter Hospital, Exeter, UK.
Jill Clayton-SmithInstitute of Evolution, Systems and Genomics, Faculty of Medical and Human Sciences, University of Manchester, Manchester Academic Health Science Centre, Manchester, UK.
Kay MetcalfeInstitute of Evolution, Systems and Genomics, Faculty of Medical and Human Sciences, University of Manchester, Manchester Academic Health Science Centre, Manchester, UK.
Hitoshi KurumizakaLaboratory of Structural Biology, Graduate School of Advanced Science & Engineering, Waseda University, Tokyo, Japan.
Bruce D GelbMindich Child Health and Development Institute and Department of Pediatrics, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Hagit Baris FeldmanThe Genetics Institute, Rambam Health Care Campus, Haifa, Israel.
Philippe M CampeauDepartment of Pediatrics, University of Montreal and CHU Sainte-Justine, Montreal, QC, Canada.
Maximilian MuenkeMedical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.
Paul A Wade *Epigenetics and Stem Cell Biology Laboratory, National Institute of Environmental Health Sciences, Research Triangle Park, NC, USA.
Katherine Lachlan *Wessex Clinical Genetics Service, University Hospital Southampton NHS Trust. Department of Human Genetics and Genomic Medicine, Southampton University, Southampton, UK.
Funding
No grant is acknowledged in the PubMed record.
Abstract
An amendment to this paper has been published and can be accessed via a link at the top of the paper.
Identifiers
PMID
31844176What OpenQuestion holds
Textmetadata
Read underepoch 390
Registered trials
None linked
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.