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Publisher Correction: Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

DOI

  1. An atlas of O-linked glycosylation on peptide hormones reveals diverse biological roles

    Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

  2. A phenome-wide association and Mendelian Randomisation study of polygenic risk for depression in UK Biobank

    Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

  3. Author Correction: Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples

    Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

  4. SUCLA2 mutations cause global protein succinylation contributing to the pathomechanism of a hereditary mitochondrial disease

    Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

  5. PCM1 is necessary for focal ciliary integrity and is a candidate for severe schizophrenia

    Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

  • Sílvia Bonàs-Guarch
  • Marta Guindo-Martínez
  • Irene Miguel-Escalada
  • Niels Grarup
  • David Sebastian
  • Elias Rodriguez-Fos
  • Friman Sánchez
  • Mercè Planas-Fèlix
  • Paula Cortes-Sánchez
  • Santi González
  • Pascal Timshel
  • Tune H Pers
  • Claire C Morgan
  • Ignasi Moran
  • Goutham Atla
  • Juan R González
  • Montserrat Puiggros
  • Jonathan Martí
  • Ehm A Andersson
  • Carlos Díaz
  • Rosa M Badia
  • Miriam Udler
  • Aaron Leong
  • Varindepal Kaur
  • Jason Flannick
  • Torben Jørgensen
  • Allan Linneberg
  • Marit E Jørgensen
  • Daniel R Witte
  • Cramer Christensen
  • Ivan Brandslund
  • Emil V Appel
  • Robert A Scott
  • Jian'an Luan
  • Claudia Langenberg
  • Nicholas J Wareham
  • Oluf Pedersen
  • Antonio Zorzano
  • Jose C Florez
  • Torben Hansen
  • Jorge Ferrer
  • Josep Maria Mercader
  • David Torrents
Vis graf over relationer

In the originally published version of this Article, the affiliation details for Santi González, Jian'an Luan and Claudia Langenberg were inadvertently omitted. Santi González should have been affiliated with 'Barcelona Supercomputing Center (BSC), Joint BSC-CRG-IRB Research Program in Computational Biology, 08034 Barcelona, Spain', and Jian'an Luan and Claudia Langenberg should have been affiliated with 'MRC Epidemiology Unit, University of Cambridge School of Clinical Medicine, Cambridge Biomedical Campus, Cambridge CB2 0QQ, UK'. Furthermore, the abstract contained an error in the SNP ID for the rare variant in chromosome Xq23, which was incorrectly given as rs146662057 and should have been rs146662075. These errors have now been corrected in both the PDF and HTML versions of the Article.

OriginalsprogEngelsk
TidsskriftNature Communications
Vol/bind9
Udgave nummer1
Sider (fra-til)2162
ISSN2041-1723
DOI
StatusUdgivet - 30 maj 2018

ID: 54442826