Evidence map›Paper›PMID 37115209›Full record

ArticleActa neuropathologica2023

Correction to: Ganglioglioma with adverse clinical outcome and atypical histopathological features were defined by alterations in PTPN11/KRAS/NF1 and other RAS-/MAP-Kinase pathway genes.

Lucas Hoffmann, Roland Coras, Katja Kobow, Javier A López-Rivera, Dennis Lal, Costin Leu, Imad Najm, Peter Nürnberg, Jochen Herms, Patrick N Harter and 11 more

Open access · hybridAbstract readPublished Erratum
In one paragraph

Article in Acta neuropathologica, 2023. 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
0.3field-weighted citation impact, top 37% of its field
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, 2 citations in OpenAlex.

  1. Article
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

21 authors at 8 institutions in 3 countries.

Lucas HoffmannDepartment of Neuropathology, Partner of the European Reference Network (ERN) EpiCARE, Universitätsklinikum Erlangen, FAU Erlangen-Nürnberg, Erlangen, 91054, Germany.ORCID http://orcid.org/0000-0002-3801-1595
Roland CorasDepartment of Neuropathology, Partner of the European Reference Network (ERN) EpiCARE, Universitätsklinikum Erlangen, FAU Erlangen-Nürnberg, Erlangen, 91054, Germany.ORCID http://orcid.org/0000-0002-8352-2773
Katja KobowDepartment of Neuropathology, Partner of the European Reference Network (ERN) EpiCARE, Universitätsklinikum Erlangen, FAU Erlangen-Nürnberg, Erlangen, 91054, Germany.ORCID http://orcid.org/0000-0002-0074-2480
Javier A López-RiveraDepartment of Molecular Medicine, Cleveland Clinic Lerner College of Medicine, Case Western Reserve University, Cleveland, USA.ORCID http://orcid.org/0000-0002-3563-9977
Dennis LalGenomic Medicine Institute, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, 44195, USA.ORCID http://orcid.org/0000-0002-5173-9636
Costin LeuGenomic Medicine Institute, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, 44195, USA.ORCID http://orcid.org/0000-0003-0598-3301
Imad NajmCharles Shor Epilepsy Center, Neurological Institute, Cleveland Clinic, Cleveland, USA.ORCID http://orcid.org/0000-0001-5192-2089
Peter NürnbergCologne Center for Genomics (CCG), Medical Faculty of the University of Cologne, University Hospital of Cologne, 50931, Cologne, Germany.ORCID http://orcid.org/0000-0002-7228-428X
Jochen HermsCenter for Neuropathology and Prion Research, LMU Munich, Munich, Germany.ORCID http://orcid.org/0000-0002-6201-1042
Patrick N HarterCenter for Neuropathology and Prion Research, LMU Munich, Munich, Germany.ORCID http://orcid.org/0000-0001-5530-6910
Christian G BienDepartment of Epileptology (Krankenhaus Mara), Medical School, Bielefeld University, Bielefeld, 33617, Germany.ORCID http://orcid.org/0000-0003-2225-8654
Thilo KalbhennDepartment of Epileptology (Krankenhaus Mara), Medical School, Bielefeld University, Bielefeld, 33617, Germany.ORCID http://orcid.org/0000-0001-6249-629X
Markus MüllerDepartment of Epileptology (Krankenhaus Mara), Medical School, Bielefeld University, Bielefeld, 33617, Germany.
Tom PieperCenter for Pediatric Neurology, Neurorehabilitation, and Epileptology, Schoen-Clinic, Vogtareuth, 83569, Rosenheim, Germany.ORCID http://orcid.org/0000-0001-7623-5058
Till HartliebCenter for Pediatric Neurology, Neurorehabilitation, and Epileptology, Schoen-Clinic, Vogtareuth, 83569, Rosenheim, Germany.ORCID http://orcid.org/0000-0002-0854-5537
Manfred KudernatschCenter for Pediatric Neurology, Neurorehabilitation, and Epileptology, Schoen-Clinic, Vogtareuth, 83569, Rosenheim, Germany.ORCID http://orcid.org/0000-0003-0876-0146
Hajo HamerEpilepsy Center, EpiCARE Partner, Universitätsklinikum Erlangen, FAU Erlangen-Nürnberg, Erlangen, 91054, Germany.ORCID http://orcid.org/0000-0003-1709-8617
Sebastian BrandnerDepartment of Neurosurgery, EpiCARE Partner, Universitätsklinikum Erlangen, FAU Erlangen-Nürnberg, Erlangen, Germany.ORCID http://orcid.org/0000-0002-8635-7195
Karl RösslerDepartment of Neurosurgery, EpiCARE Partner, Universitätsklinikum Erlangen, FAU Erlangen-Nürnberg, Erlangen, Germany.ORCID http://orcid.org/0000-0002-9249-8082
Ingmar BlümckeDepartment of Neuropathology, Partner of the European Reference Network (ERN) EpiCARE, Universitätsklinikum Erlangen, FAU Erlangen-Nürnberg, Erlangen, 91054, Germany.ORCID http://orcid.org/0000-0001-8676-0788
Samir JabariDepartment of Neuropathology, Partner of the European Reference Network (ERN) EpiCARE, Universitätsklinikum Erlangen, FAU Erlangen-Nürnberg, Erlangen, 91054, Germany. Samir.jabari@uk-erlangen.de.ORCID http://orcid.org/0000-0002-3037-7170
Universitätsklinikum Erlangen · DEBielefeld University · DESchön Klinik Vogtareuth · DEBroad Institute · USCleveland Clinic · USLudwig-Maximilians-Universität München · DEUniversity of Cologne · DEVienna General Hospital · AT

Funding

Clinical genetics of drug-resistant epilepsy with focal cortical dysplasiaR01NS117544 · NINDS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI DENNIS LAL, Costin Leu · 2021 to 2026
$3.4M
NINDS NIH HHS R01 NS117544
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID37115209
PMCPMC10175382
OpenAlexW4367315199

What OpenQuestion holds

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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.