Evidence map›Paper›PMID 25537359›Full record

ArticleEuropean journal of human genetics : EJHG2015

Reply to Pembrey et al: 'ZNF277 microdeletions, specific language impairment and the meiotic mismatch methylation (3M) hypothesis'.

Fabiola Ceroni, Nuala H Simpson, Clyde Francks, Gillian Baird, Gina Conti-Ramsden, Ann Clark, Patrick F Bolton, Elizabeth R Hennessy, Peter Donnelly, David R Bentley and 10 more

Abstract readComment
PubMed Full text at PMC Publisher
In one paragraph

Article in European journal of human genetics : EJHG, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors.

Fabiola CeroniWellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.
Nuala H SimpsonWellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.
Clyde Francks1] Max Planck Institute for Psycholinguistics, Nijmegen, The Netherlands [2] Donders Institute for Brain, Cognition & Behaviour, Nijmegen, The Netherlands.
Gillian BairdGuy's & St Thomas NHS Foundation Trust, Newcomen Children's Neurosciences Centre, St Thomas' Hospital, London, UK.
Gina Conti-RamsdenSchool of Psychological Sciences, The University of Manchester, Manchester, UK.
Ann ClarkSpeech and Hearing Sciences, Queen Margaret University, Edinburgh, UK.
Patrick F BoltonDepartments of Child & Adolescent Psychiatry & Social Genetic & Developmental Psychiatry Centre, Institute of Psychiatry, Kings College London, London, UK.
Elizabeth R HennessyUniversity Child Health and DMDE, University of Aberdeen, Aberdeen, UK.
Peter DonnellyWellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.
David R BentleyIllumina Cambridge Ltd, Chesterford Research Park, Little Chesterford, Essex, UK.
Hilary MartinWellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.
IMGSAC
SLI Consortium
WGS500 Consortium
Jeremy ParrInstitute of Neuroscience and Health and Society, Newcastle University, Newcastle upon Tyne, UK.
Alistair T Pagnamenta1] Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK [2] NIHR Biomedical Research Centre, Oxford and Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.
Elena MaestriniDipartimento di Farmacia e Biotecnologie, University of Bologna, Bologna, Italy.
Elena BacchelliDipartimento di Farmacia e Biotecnologie, University of Bologna, Bologna, Italy.
Simon E Fisher1] Max Planck Institute for Psycholinguistics, Nijmegen, The Netherlands [2] Donders Institute for Brain, Cognition & Behaviour, Nijmegen, The Netherlands.
Dianne F NewburyWellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.

Funding

Medical Research Council MR/J003719/1
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

ExonsSequence DeletionDNA-Binding ProteinsFemaleHumansLanguage Development DisordersMaleDNA-Binding Proteins

Identifiers

PMID25537359
PMCPMC4538219

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.