Evidence map›Paper›PMID 28989339›Full record

ArticleFrontiers in immunology2017

Corrigendum: Clinical and Molecular Heterogeneity of RTEL1 Deficiency.

Carsten Speckmann, Sushree Sangita Sahoo, Marta Rizzi, Shinsuke Hirabayashi, Axel Karow, Nina Kathrin Serwas, Marc Hoemberg, Natalja Damatova, Detlev Schindler, Jean-Baptiste Vannier and 20 more

Abstract readPublished Erratum
PubMed Full text at PMC Publisher
In one paragraph

Article in Frontiers in immunology, 2017. 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
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

30 authors.

Carsten SpeckmannFaculty of Medicine, Department of Pediatrics and Adolescent Medicine, Division of Pediatric Hematology and Oncology, Medical Centre, University of Freiburg, Freiburg, Germany.
Sushree Sangita SahooFaculty of Medicine, Department of Pediatrics and Adolescent Medicine, Division of Pediatric Hematology and Oncology, Medical Centre, University of Freiburg, Freiburg, Germany.
Marta RizziCenter for Chronic Immunodeficiency, Medical Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Shinsuke HirabayashiFaculty of Medicine, Department of Pediatrics and Adolescent Medicine, Division of Pediatric Hematology and Oncology, Medical Centre, University of Freiburg, Freiburg, Germany.
Axel KarowDepartment of Pediatrics, University of Bern, Bern, Switzerland.
Nina Kathrin SerwasLudwig Boltzmann Institute for Rare and Undiagnosed Diseases, Vienna, Austria.
Marc HoembergDepartment of Pediatric Hematology and Oncology, Children's Hospital, University of Cologne, Cologne, Germany.
Natalja DamatovaDepartment of Medical Genetics, Biozentrum, University of Wuerzburg, Wuerzburg, Germany.
Detlev SchindlerDepartment of Medical Genetics, Biozentrum, University of Wuerzburg, Wuerzburg, Germany.
Jean-Baptiste VannierTelomere Replication and Stability Group, MRC London Institute of Medical Sciences (LMS), London, United Kingdom.
Simon J BoultonTelomere Replication and Stability Group, MRC London Institute of Medical Sciences (LMS), London, United Kingdom.
Ulrich PannickeInstitute for Transfusion Medicine, Institute for Clinical Transfusion Medicine and Immunogenetics Ulm, German Red Cross Blood Service Baden-Wuerttemberg - Hessen, University Ulm, Ulm, Germany.
Gudrun GöhringDepartment of Human Genetics, Hannover Medical School, Hannover, Germany.
Kathrin ThomayDepartment of Pediatric Hematology and Oncology, Justus Liebig-University, Giessen, Germany.
J J Verdu-AmorosDepartment of Pediatric Hematology and Oncology, Justus Liebig-University, Giessen, Germany.
Holger HauchDepartment of Pediatric Hematology and Oncology, Justus Liebig-University, Giessen, Germany.
Wilhelm WoessmannDepartment of Pediatric Hematology and Oncology, Justus Liebig-University, Giessen, Germany.
Gabriele EscherichClinic of Pediatric Hematology and Oncology, University Medical Center Hamburg Eppendorf, Hamburg, Germany.
Eckart LaackHemato-Oncology Clinic Hamburg, Hamburg, Germany.
Liliana RindleFaculty of Medicine, Department of Pediatrics and Adolescent Medicine, Division of Pediatric Hematology and Oncology, Medical Centre, University of Freiburg, Freiburg, Germany.
Maximilian SeidlCenter for Chronic Immunodeficiency, Medical Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Anne Rensing-EhlCenter for Chronic Immunodeficiency, Medical Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Ekkehart LauschFaculty of Medicine, Department of Pediatrics and Adolescent Medicine, Division of Pediatric Hematology and Oncology, Medical Centre, University of Freiburg, Freiburg, Germany.
Christine JandrasitsCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria.
Brigitte StrahmFaculty of Medicine, Department of Pediatrics and Adolescent Medicine, Division of Pediatric Hematology and Oncology, Medical Centre, University of Freiburg, Freiburg, Germany.
Klaus SchwarzInstitute for Transfusion Medicine, Institute for Clinical Transfusion Medicine and Immunogenetics Ulm, German Red Cross Blood Service Baden-Wuerttemberg - Hessen, University Ulm, Ulm, Germany.
Stephan R EhlFaculty of Medicine, Department of Pediatrics and Adolescent Medicine, Division of Pediatric Hematology and Oncology, Medical Centre, University of Freiburg, Freiburg, Germany.
Charlotte NiemeyerFaculty of Medicine, Department of Pediatrics and Adolescent Medicine, Division of Pediatric Hematology and Oncology, Medical Centre, University of Freiburg, Freiburg, Germany.
Kaan BoztugLudwig Boltzmann Institute for Rare and Undiagnosed Diseases, Vienna, Austria.
Marcin W WlodarskiFaculty of Medicine, Department of Pediatrics and Adolescent Medicine, Division of Pediatric Hematology and Oncology, Medical Centre, University of Freiburg, Freiburg, Germany.

Funding

Austrian Science Fund FWF Y 595
6 · The paper itself

Abstract

[This corrects the article on p. 449 in vol. 8, PMID: 28507545.].

Indexed as

bone marrow failuredyskeratosis congenitaimmunodeficiencylymphopeniaRTEL1

Identifiers

PMID28989339
PMCPMC5630696

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.