Evidence map›Paper›PMID 31506600›Full record

ArticleEuropean journal of human genetics : EJHG2020

Correction: Phenotypic spectrum associated with a CRADD founder variant underlying frontotemporal predominant pachygyria in the Finnish population.

Daniel L Polla, Elisa Rahikkala, Michaela K Bode, Tuomo Määttä, Teppo Varilo, Thyrza Loman, Anju K Philips, Mitja Kurki, Aarno Palotie, Jarmo Körkkö and 9 more

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

Article in European journal of human genetics : EJHG, 2020. 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

19 authors.

Daniel L Polla *Department of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.ORCID http://orcid.org/0000-0002-5552-3488
Elisa Rahikkala *Department of Clinical Genetics, PEDEGO Research Unit and Medical Research Center Oulu, Oulu University Hospital and University of Oulu, Oulu, Finland.
Michaela K Bode *Department of Diagnostic Radiology, Oulu University Hospital and Medical Research Center Oulu, Oulu, Finland.
Tuomo MäättäDisability Services, Joint Authority for Kainuu, Kainuu, Finland.
Teppo VariloDepartment of Medical Genetics, University of Helsinki, Helsinki, Finland.
Thyrza LomanDepartment of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.
Anju K PhilipsDepartment of Medical Genetics, University of Helsinki, Helsinki, Finland.
Mitja KurkiPsychiatric & Neurodevelopmental Genetics Unit, Massachusetts General Hospital, Boston, MA, USA.
Aarno PalotiePsychiatric & Neurodevelopmental Genetics Unit, Massachusetts General Hospital, Boston, MA, USA.
Jarmo KörkköNorthern Ostrobothnia Hospital District, Center for Intellectual Disability Care, 90220, Oulu, Finland.
Päivi VieiraClinic for Children and Adolescents, PEDEGO Research Unit and Medical Research Center Oulu, Oulu University Hospital and University of Oulu, Oulu, Finland.
Kristiina AvelaDepartment of Clinical Genetics, Helsinki University Hospital, Helsinki, Finland.
Valérie JacqueminMedical Genetics, IRIBHM, Université Libre de Bruxelles, Brussels, Belgium.
Isabelle PirsonMedical Genetics, IRIBHM, Université Libre de Bruxelles, Brussels, Belgium.
Marc AbramowiczMedical Genetics, IRIBHM, Université Libre de Bruxelles, Brussels, Belgium.
Arjan P M de BrouwerDepartment of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.
Outi KuisminDepartment of Clinical Genetics, PEDEGO Research Unit and Medical Research Center Oulu, Oulu University Hospital and University of Oulu, Oulu, Finland.
Hans van Bokhoven *Department of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.
Irma Järvelä *Department of Medical Genetics, University of Helsinki, Helsinki, Finland. irma.jarvela@helsinki.fi.

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

PMID31506600
PMCPMC7080772

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.