Evidence map›Paper›PMID 29235362›Full record

ArticleAmyotrophic lateral sclerosis & frontotemporal degeneration2018

Reconsidering the causality of TIA1 mutations in ALS.

Rick A van der Spek, Wouter van Rheenen, Sara L Pulit, Kevin P Kenna, Nicola Ticozzi, Maarten Kooyman, Russell L Mclaughlin, Matthieu Moisse, Kristel R van Eijk, Joke J F A van Vugt and 27 more

Erratum issuedOpen access · bronzeAbstract readEditorial
In one paragraph

Article in Amyotrophic lateral sclerosis & frontotemporal degeneration, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

11 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Recent advances in the genetics of frontotemporal dementia.Current genetic medicine reports · 2019
    Article
  10. Review
  11. Myopathy WithFrontiers in neurology · 2018
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

37 authors at 20 institutions in 15 countries.

Rick A van der Speka Department of Neurology , Brain Center Rudolf Magnus University Medical Center Utrecht , Utrecht , The Netherlands.ORCID 0000-0001-9983-204X
Wouter van Rheenena Department of Neurology , Brain Center Rudolf Magnus University Medical Center Utrecht , Utrecht , The Netherlands.
Sara L Pulita Department of Neurology , Brain Center Rudolf Magnus University Medical Center Utrecht , Utrecht , The Netherlands.ORCID 0000-0002-2502-3669
Kevin P Kennab Department of Neurology , University of Massachusetts Medical School , Worcester , MA , USA.
Nicola Ticozzic Department of Neurology and Laboratory of Neuroscience , IRCCS Istituto Auxologico Italiano , Milan , Italy.
Maarten Kooymane SURFsara , Amsterdam , The Netherlands.
Russell L Mclaughlinf Population Genetics Laboratory , Smurfit Institute of Genetics, Trinity College Dublin , Dublin , Republic of Ireland.
Matthieu Moisseg Department of Neurosciences, Experimental Neurology and Leuven Research Institute for Neuroscience and Disease (LIND) , KU Leuven - University of Leuven , Leuven , Belgium.ORCID 0000-0001-8880-9311
Kristel R van Eijka Department of Neurology , Brain Center Rudolf Magnus University Medical Center Utrecht , Utrecht , The Netherlands.
Joke J F A van Vugta Department of Neurology , Brain Center Rudolf Magnus University Medical Center Utrecht , Utrecht , The Netherlands.
Alfredo Iacoangelij Department of Biostatistics and Health Informatics , Institute of Psychiatry, Psychology and Neuroscience, King's College London , London , UK.
Peter Andersenk Department of Pharmacology and Clinical Neuroscience , Umeå University , Umeå , Sweden.
A Nazli Basakl Suna and Inan Kırac Foundatıon Neurodegeneration Research Laboratory , Bogazici University , Istanbul , Turkey.
Ian Blairm Department of Biomedical Sciences, Faculty of Medicine and Health Sciences , Macquarie University , Sydney , New South Wales , Australia.
Mamede de Carvalhon Institute of Physiology, Institute of Molecular Medicine, Faculty of Medicine , University of Lisbon , Lisbon , Portugal.
Adriano Chiop 'Rita Levi Montalcini' Department of Neuroscience , ALS Centre, University of Torino , Turin , Italy.ORCID 0000-0001-9579-5341
Philippe Corciar Centre SLA , CHRU de Tours , Tours , France.
Phillipe Couratierr Centre SLA , CHRU de Tours , Tours , France.
Vivian E Droryt Department of Neurology Tel-Aviv Sourasky Medical Centre , Israel.
Jonathan D Glassu Department Neurology , Emory University School of Medicine , Atlanta , GA , USA.
Orla Hardimanf Population Genetics Laboratory , Smurfit Institute of Genetics, Trinity College Dublin , Dublin , Republic of Ireland.
Jesús S Morax ALS Unit , Hospital San Rafael , Madrid , Spain.
Karen E Morrisony Faculty of Medicine , University of Southampton , Southampton , UK.
Miguel Mitne-Netoz Human Genome Research Center , Bioscience Institute, University of São Paulo , SP , Brazil.
Wim Robberechtg Department of Neurosciences, Experimental Neurology and Leuven Research Institute for Neuroscience and Disease (LIND) , KU Leuven - University of Leuven , Leuven , Belgium.
Pamela J Shawaa Sheffield Institute for Translational Neuroscience (SITraN) , University of Sheffield , Sheffield , UK.ORCID 0000-0002-8925-2567
Monica P Panadésab Neurology Department , Hospital Universitari de Bellvitge , Barcelona , Spain.
Philip van Dammeg Department of Neurosciences, Experimental Neurology and Leuven Research Institute for Neuroscience and Disease (LIND) , KU Leuven - University of Leuven , Leuven , Belgium.
Vincenzo Silanic Department of Neurology and Laboratory of Neuroscience , IRCCS Istituto Auxologico Italiano , Milan , Italy.
Marc Gotkineac Department of Neurology , The Agnes Ginges Center for Human Neurogenetics, Hadassah-Hebrew University Medical Center , Israel.
Markus Weberad Neuromuscular Diseases Unit/ALS Clinic , Kantonsspital St. Gallen , St. Gallen , Switzerland.
Michael A van Esa Department of Neurology , Brain Center Rudolf Magnus University Medical Center Utrecht , Utrecht , The Netherlands.
John E Landersb Department of Neurology , University of Massachusetts Medical School , Worcester , MA , USA.
Ammar Al-Chalabiae Department of Basic and Clinical Neuroscience , Maurice Wohl Clinical Neuroscience Institute, King's College London , London , UK.ORCID 0000-0002-4924-7712
Leonard H van den Berga Department of Neurology , Brain Center Rudolf Magnus University Medical Center Utrecht , Utrecht , The Netherlands.
Jan H Veldinka Department of Neurology , Brain Center Rudolf Magnus University Medical Center Utrecht , Utrecht , The Netherlands.ORCID 0000-0001-5572-9657
PROJECT MINE ALS SEQUENCING CONSORTIUM
University Medical Center Utrecht · NLVIB-KU Leuven Center for Brain & Disease Research · BECentre Hospitalier Universitaire de Tours · FRKing's College London · GBTrinity College Dublin · IEUniversity of Massachusetts Chan Medical School · USUniversity of Milan · ITAzienda Ospedaliera Citta' della Salute e della Scienza di Torino · ITBellvitge University Hospital · ESBoğaziçi University · TREmory University · USHebrew University of Jerusalem · ILHospital Universitario San Rafael · ESKantonsspital St. Gallen · CHMacquarie University · AUSURFsara (Netherlands) · NLTel Aviv Sourasky Medical Center · ILUmeå University · SEUniversidade de São Paulo · BRUniversity of Lisbon · PT

Funding

Identification of genes causative for familial ALS gene using exome sequencingR01NS073873 · NINDS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI LANDERS, JOHN E · 2011 to 2019
$4.6M
Medical Research Council G0600974Medical Research Council MR/L501529/1Medical Research Council MR/R024804/1Motor Neurone Disease Association ALCHALABI-DOBSON/APR14/829-791Motor Neurone Disease Association MCLAUGHLIN/OCT15/957-799NINDS NIH HHS R01 NS073873
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Genetic Predisposition to DiseaseAmyotrophic Lateral SclerosisGenetic TestingHumansMutationT-Cell Intracellular Antigen-1T-Cell Intracellular Antigen-1TIA1 protein, human

Identifiers

PMID29235362
PMCPMC6516059
OpenAlexW2773963984

What OpenQuestion holds

Textmetadata
LicenceTDM
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.