Evidence map›Paper›PMID 28546572›Full record

ArticleNature genetics2017

Corrigendum: Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia.

Esther Meyer, Keren J Carss, Julia Rankin, John M E Nichols, Detelina Grozeva, Agnel P Joseph, Niccolo E Mencacci, Apostolos Papandreou, Joanne Ng, Serena Barral and 63 more

Abstract readPublished Erratum
PubMed Publisher
In one paragraph

Article in Nature genetics, 2017. 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
–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

2 citing papers in PubMed.

  1. Article
  2. The role of KMT2 gene in human tumors.Histology and histopathology · 2022
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

73 authors.

Esther Meyer
Keren J Carss
Julia Rankin
John M E Nichols
Detelina Grozeva
Agnel P Joseph
Niccolo E Mencacci
Apostolos Papandreou
Joanne Ng
Serena Barral
Adeline Ngoh
Hilla Ben-Pazi
Michel A Willemsen
David Arkadir
Angela Barnicoat
Hagai Bergman
Sanjay Bhate
Amber Boys
Niklas Darin
Nicola Foulds
Nicholas Gutowski
Alison Hills
Henry Houlden
Jane A Hurst
Zvi Israel
Margaret Kaminska
Patricia Limousin
Daniel Lumsden
Shane McKee
Shibalik Misra
Shekeeb S Mohammed
Vasiliki Nakou
Joost Nicolai
Magnus Nilsson
Hardev Pall
Kathryn J Peall
Gregory B Peters
Prab Prabhakar
Miriam S Reuter
Patrick Rump
Reeval Segel
Margje Sinnema
Martin Smith
Peter Turnpenny
Susan M White
Dagmar Wieczorek
Sarah Wiethoff
Brian T Wilson
Gidon Winter
Christopher Wragg
Simon Pope
Simon J H Heales
Deborah Morrogh
UK10K Consortium
Deciphering Developmental Disorders Study
NIHR BioResource Rare Diseases Consortium
Alan Pittman
Lucinda J Carr
Belen Perez-Dueñas
Jean-Pierre Lin
Andre Reis
William A Gahl
Camilo Toro
Kailash P Bhatia
Nicholas W Wood
Erik-Jan Kamsteeg
Wui K Chong
Paul Gissen
Maya Topf
Russell C Dale
Jonathan R Chubb
F Lucy Raymond
Manju A Kurian

Funding

NHGRI/DIR Clinical Support ServicesZIDHG200352 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI SOLOMON, BENJAMIN · 2009 to 2025
$182.8M
Human Biochemical GeneticsZIAHG000215 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI GAHL, WILLIAM · 2009 to 2025
$72.6M
Medical Research Council MR/K02342X/1Parkinson's UK G-1107
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID28546572

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.