Evidence map›Paper›PMID 25585701›Full record

ArticleEuropean journal of human genetics : EJHG2016

Reply to Sajantila and Budowle.

David E Barton, Mireille Claustres, Viktor Kozich, Els Dequeker, Brian Fowler, Jayne Y Hehir-Kwa, Konstantin Miller, Cor Oosterwijk, Borut Peterlin, Conny van Ravenswaaij-Arts and 3 more

Abstract readLetterComment
PubMed Full text at PMC Publisher
In one paragraph

Article in European journal of human genetics : EJHG, 2016. 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

13 authors.

David E BartonNational Centre for Medical Genetics, School of Medicine & Medical Sciences, University College Dublin, Our Lady's Children's Hospital, Dublin, Ireland.
Mireille ClaustresMolecular Genetics of Rare Disorders, University Hospital of Montpellier and INSERM U827, IURC (Institut Universitaire de Recherche Clinique), Montpellier, France.
Viktor KozichInstitute of Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague, Prague, Czech Republic.
Els DequekerBiomedical Quality Assurance Research Unit, Department of Human Genetics, University of Leuven, Leuven, Belgium.
Brian FowlerDepartment of Paediatrics, Universitats-Kinderspital Beider Basel (UKBB), Basel, Switzerland.
Jayne Y Hehir-KwaDepartment of Human Genetics, Radboud University Medical Centre, Nijmegen, The Netherlands.
Konstantin MillerInstitute of Human Genetics, Hannover Medical School, Hannover, Germany.
Cor OosterwijkVSOP-National Patient Alliance for Rare and Genetic Disorders, Soest, The Netherlands.
Borut PeterlinDivision of Obstetrics and Gynecology, Clinical Institute of Medical Genetics, University Medical Center, Ljubljana, Slovenia.
Conny van Ravenswaaij-ArtsDepartment of Genetics, University of Groningen, University Medical Centre Groningen, Groningen, The Netherlands.ORCID http://orcid.org/0000-0002-8744-1305
Uwe ZimmermannDivision 3 Health/Forensics, Deutsche Akkreditierungsstelle GmbH (DAkkS), Frankfurt am Main, Germany.
Orsetta ZuffardiDepartment of Medical Genetics, University of Pavia, Pavia, Italy.
Rosalind J HastingsCEQAS, John Radcliffe Hospital, Oxford University Hospitals NHS Trust, Oxford, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

DisclosureGenetic TestingHumans

Identifiers

PMID25585701
PMCPMC4755362

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.