Evidence map›Paper›PMID 32451403›Full record

ArticleGenetics in medicine : official journal of the American College of Medical Genetics2020

Correction: The genomic and clinical landscape of fetal akinesia.

Matthias Pergande, Susanne Motameny, Özkan Özdemir, Mona Kreutzer, Haicui Wang, Hülya-Sevcan Daimagüler, Kerstin Becker, Mert Karakaya, Harald Ehrhardt, Nursel Elcioglu and 21 more

Abstract readPublished Erratum
PubMed Publisher
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 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

31 authors.

Matthias PergandeUniversity of Cologne, Center for Molecular Medicine Cologne (CMMC), Cologne, Germany.
Susanne MotamenyUniversity of Cologne, Cologne Center for Genomics CCG, Cologne, Germany.
Özkan ÖzdemirUniversity of Cologne, Center for Molecular Medicine Cologne (CMMC), Cologne, Germany.
Mona KreutzerUniversity of Cologne, Center for Molecular Medicine Cologne (CMMC), Cologne, Germany.
Haicui WangUniversity of Cologne, Center for Molecular Medicine Cologne (CMMC), Cologne, Germany.
Hülya-Sevcan DaimagülerUniversity of Cologne, Center for Molecular Medicine Cologne (CMMC), Cologne, Germany.
Kerstin BeckerUniversity of Cologne, Center for Molecular Medicine Cologne (CMMC), Cologne, Germany.
Mert KarakayaUniversity of Cologne, Center for Molecular Medicine Cologne (CMMC), Cologne, Germany.
Harald EhrhardtDepartment of General Pediatrics and Neonatology, Justus-Liebig-University, Gießen, Germany.
Nursel ElciogluDepartment of Pediatric Genetics, Marmara University Medical School, Istanbul, Turkey.
Slavica OstojicDepartment of Neurology, Mother and Child Health Care Institute of Serbia "Dr. Vukan Cupic", Belgrade, Serbia.
Cho-Ming ChaoDepartment of General Pediatrics and Neonatology, Justus-Liebig-University, Gießen, Germany.
Amit KawaliaUniversity of Cologne, Cologne Center for Genomics CCG, Cologne, Germany.
Özgür DumanDepartment of Pediatric Neurology, Akdeniz University Hospital, Antalya, Turkey.
Anne KoyUniversity of Cologne, University Hospital Cologne and Faculty of Medicine, Department of Pediatrics, Cologne, Germany.
Andreas HahnDepartment of Pediatric Neurology, Social Pediatrics and Epileptology, Justus-Liebig-University, Gießen, Germany.
Jens ReimannDepartment of Neurology, Rheinische Friedrich-Wilhelms-University, Bonn, Germany.
Katharina SchonerInstitute of Pathology, Philipps University of Marburg, Marburg, Germany.
Anne SchänzerInstitute of Neuropathology, Justus-Liebig-University, Gießen, Germany.
Jens H WesthoffHeidelberg University, University Children's Hospital Heidelberg, Department of Pediatrics, Heidelberg, Germany.
Eva Maria Christina SchwaiboldInstitute of Human Genetics, Heidelberg University, Institute of Human Genetics, Heidelberg, Germany.
Mireille CosseeUniversity of Montpellier, University Hospital of Montpellier, Molecular Diagnostic Laboratory, Montpellier, France.
Marion Imbert-BouteilleUniversity of Montpellier, University Hospital of Montpellier, Medical Genetics Department, Montpellier, France.
Harald von PeinJohannes-Gutenberg University Mainz, University Medical Center Mainz, Institute of Neuropathology, Mainz, Germany.
Göknur HalilogluHacettepe University, Children's Hospital, Department of Pediatric Neurology, Ankara, Turkey.
Haluk TopalogluHacettepe University, Children's Hospital, Department of Pediatric Neurology, Ankara, Turkey.
Janine AltmüllerUniversity of Cologne, Center for Molecular Medicine Cologne (CMMC), Cologne, Germany.
Peter NürnbergUniversity of Cologne, Center for Molecular Medicine Cologne (CMMC), Cologne, Germany.
Holger ThieleUniversity of Cologne, Cologne Center for Genomics CCG, Cologne, Germany.
Raoul HellerUniversity of Cologne, University Hospital Cologne, Institute of Human Genetics, Cologne, Germany.
Sebahattin CirakUniversity of Cologne, Center for Molecular Medicine Cologne (CMMC), Cologne, Germany. sebahattin.cirak@uk-koeln.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

Identifiers

PMID32451403

What 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.