Evidence map›Paper›PMID 30568165›Full record

ArticleNature communications2018

Author Correction: Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits.

Arthur Gilly, Daniel Suveges, Karoline Kuchenbaecker, Martin Pollard, Lorraine Southam, Konstantinos Hatzikotoulas, Aliki-Eleni Farmaki, Thea Bjornland, Ryan Waples, Emil V R Appel and 14 more

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

Article in Nature communications, 2018. 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. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

24 authors.

Arthur GillyDepartment of Human Genetics, Wellcome Sanger Institute, Hinxton, CB10 1SA, United Kingdom.
Daniel SuvegesDepartment of Human Genetics, Wellcome Sanger Institute, Hinxton, CB10 1SA, United Kingdom.
Karoline KuchenbaeckerDepartment of Human Genetics, Wellcome Sanger Institute, Hinxton, CB10 1SA, United Kingdom.
Martin PollardDepartment of Human Genetics, Wellcome Sanger Institute, Hinxton, CB10 1SA, United Kingdom.ORCID http://orcid.org/0000-0001-8738-0920
Lorraine SouthamDepartment of Human Genetics, Wellcome Sanger Institute, Hinxton, CB10 1SA, United Kingdom.ORCID http://orcid.org/0000-0002-7546-9650
Konstantinos HatzikotoulasDepartment of Human Genetics, Wellcome Sanger Institute, Hinxton, CB10 1SA, United Kingdom.ORCID http://orcid.org/0000-0002-4699-3672
Aliki-Eleni FarmakiDepartment of Health Sciences, College of Life Sciences, University of Leicester, Leicester, LE1 6TP, United Kingdom.
Thea BjornlandDepartment of Mathematical Sciences, Norwegian Institute of Science and Technology, Trondheim 7491, Norway.
Ryan WaplesDepartment of Biology, The Bioinformatics Centre, University of Copenhagen, 2200, Copenhagen, Denmark.
Emil V R AppelSection for Metabolic Genetics, Novo Nordisk Foundation Center for Basic Metabolic Research, University of Copenhagen, Copenhagen 2200, Denmark.ORCID http://orcid.org/0000-0001-7704-6611
Elisabetta CasaloneHuman Genetics Foundation, University of Torino, Torino IT-10126, Italy.
Giorgio MelloniDepartment of Biomedical Informatics, Harvard Medical School, Boston 02115, MA, USA.ORCID http://orcid.org/0000-0001-6371-1334
Britt KilianDepartment of Human Genetics, Wellcome Sanger Institute, Hinxton, CB10 1SA, United Kingdom.
Nigel W RaynerDepartment of Human Genetics, Wellcome Sanger Institute, Hinxton, CB10 1SA, United Kingdom.
Ioanna NtallaWilliam Harvey Research Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, EC1M 6BQ, United Kingdom.
Kousik KunduDepartment of Human Genetics, Wellcome Sanger Institute, Hinxton, CB10 1SA, United Kingdom.ORCID http://orcid.org/0000-0002-1019-8351
Klaudia WalterDepartment of Human Genetics, Wellcome Sanger Institute, Hinxton, CB10 1SA, United Kingdom.ORCID http://orcid.org/0000-0003-4448-0301
John DaneshDepartment of Human Genetics, Wellcome Sanger Institute, Hinxton, CB10 1SA, United Kingdom.
Adam ButterworthThe National Institute for Health Research Blood and Transplant Unit (NIHR BTRU) in Donor Health and Genomics at the University of Cambridge, Strangeways Research Laboratory, Wort's Causeway, University of Cambridge, Cambridge, CB1 8RN, United Kingdom.ORCID http://orcid.org/0000-0002-6915-9015
Inês BarrosoDepartment of Human Genetics, Wellcome Sanger Institute, Hinxton, CB10 1SA, United Kingdom.ORCID http://orcid.org/0000-0001-5800-4520
Emmanouil TsafantakisAnogia Medical Centre, 740 51, Anogia, Greece.
George DedoussisDepartment of Nutrition and Dietetics, School of Health Science and Education, Harokopio University of Athens, Athens 176-71, Greece.
Ida MoltkeDepartment of Biology, The Bioinformatics Centre, University of Copenhagen, 2200, Copenhagen, Denmark.ORCID http://orcid.org/0000-0001-7052-8554
Eleftheria ZegginiDepartment of Human Genetics, Wellcome Sanger Institute, Hinxton, CB10 1SA, United Kingdom. Eleftheria@sanger.ac.uk.

Funding

Medical Research Council G0800270
6 · The paper itself

Abstract

The original version of this Article contained an error in Fig. 2. In panel a, the two legend items "rare" and "common" were inadvertently swapped. This has been corrected in both the PDF and HTML versions of the Article.

Identifiers

PMID30568165
PMCPMC6300593

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.