Publisher Correction

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

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 & 23 andre 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

*Kontaktforfatter for dette arbejde

Publikation: Bidrag til tidsskriftKommentar/debatForskningpeer review

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Resumé

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
Artikelnummer2162
TidsskriftNature Communications
Vol/bind9
Udgave nummer1
ISSN2041-1723
DOI
StatusUdgivet - 30. maj 2018

Fingeraftryk

Research Ethics Committees
Clinical Medicine
Medical problems
Computational Biology
Type 2 Diabetes Mellitus
Single Nucleotide Polymorphism
Epidemiology
clinical medicine
Joints
document markup languages
epidemiology
HTML
chromosomes
Spain
Chromosomes
biology
Research
Medicine

Citer dette

Bonàs-Guarch, S., Guindo-Martínez, M., Miguel-Escalada, I., Grarup, N., Sebastian, D., Rodriguez-Fos, E., ... Torrents, D. (2018). Publisher Correction: Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes. Nature Communications, 9(1), [2162]. https://doi.org/10.1038/s41467-018-04170-3
Bonàs-Guarch, Sílvia ; Guindo-Martínez, Marta ; Miguel-Escalada, Irene ; Grarup, Niels ; Sebastian, David ; Rodriguez-Fos, Elias ; Sánchez, Friman ; Planas-Fèlix, Mercè ; Cortes-Sánchez, Paula ; González, Santi ; Timshel, Pascal ; Pers, Tune H. ; Morgan, Claire C. ; Moran, Ignasi ; Atla, Goutham ; González, Juan R. ; Puiggros, Montserrat ; Martí, Jonathan ; Andersson, Ehm A. ; Díaz, Carlos ; Badia, Rosa M. ; Udler, Miriam ; Leong, Aaron ; Kaur, Varindepal ; Flannick, Jason ; Jørgensen, Torben ; Linneberg, Allan ; Jørgensen, Marit E. ; Witte, Daniel R. ; Christensen, Cramer ; Brandslund, Ivan ; Appel, Emil V. ; Scott, Robert A. ; Luan, Jian'An ; Langenberg, Claudia ; Wareham, Nicholas J. ; Pedersen, Oluf ; Zorzano, Antonio ; Florez, Jose C. ; Hansen, Torben ; Ferrer, Jorge ; Mercader, Josep Maria ; Torrents, David. / Publisher Correction : Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes. I: Nature Communications. 2018 ; Bind 9, Nr. 1.
@article{89f1f37a75be46389f939c204694cbc6,
title = "Publisher Correction: Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes",
abstract = "In the originally published version of this Article, the affiliation details for Santi Gonz{\'a}lez, Jian'an Luan and Claudia Langenberg were inadvertently omitted. Santi Gonz{\'a}lez 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.",
author = "S{\'i}lvia Bon{\`a}s-Guarch and Marta Guindo-Mart{\'i}nez and Irene Miguel-Escalada and Niels Grarup and David Sebastian and Elias Rodriguez-Fos and Friman S{\'a}nchez and Merc{\`e} Planas-F{\`e}lix and Paula Cortes-S{\'a}nchez and Santi Gonz{\'a}lez and Pascal Timshel and Pers, {Tune H.} and Morgan, {Claire C.} and Ignasi Moran and Goutham Atla and Gonz{\'a}lez, {Juan R.} and Montserrat Puiggros and Jonathan Mart{\'i} and Andersson, {Ehm A.} and Carlos D{\'i}az and Badia, {Rosa M.} and Miriam Udler and Aaron Leong and Varindepal Kaur and Jason Flannick and Torben J{\o}rgensen and Allan Linneberg and J{\o}rgensen, {Marit E.} and Witte, {Daniel R.} and Cramer Christensen and Ivan Brandslund and Appel, {Emil V.} and Scott, {Robert A.} and Jian'An Luan and Claudia Langenberg and Wareham, {Nicholas J.} and Oluf Pedersen and Antonio Zorzano and Florez, {Jose C.} and Torben Hansen and Jorge Ferrer and Mercader, {Josep Maria} and David Torrents",
year = "2018",
month = "5",
day = "30",
doi = "10.1038/s41467-018-04170-3",
language = "English",
volume = "9",
journal = "Nature Communications",
issn = "2041-1723",
publisher = "Nature Publishing Group",
number = "1",

}

Bonàs-Guarch, S, Guindo-Martínez, M, Miguel-Escalada, I, Grarup, N, Sebastian, D, Rodriguez-Fos, E, Sánchez, F, Planas-Fèlix, M, Cortes-Sánchez, P, González, S, Timshel, P, Pers, TH, Morgan, CC, Moran, I, Atla, G, González, JR, Puiggros, M, Martí, J, Andersson, EA, Díaz, C, Badia, RM, Udler, M, Leong, A, Kaur, V, Flannick, J, Jørgensen, T, Linneberg, A, Jørgensen, ME, Witte, DR, Christensen, C, Brandslund, I, Appel, EV, Scott, RA, Luan, JA, Langenberg, C, Wareham, NJ, Pedersen, O, Zorzano, A, Florez, JC, Hansen, T, Ferrer, J, Mercader, JM & Torrents, D 2018, 'Publisher Correction: Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes', Nature Communications, bind 9, nr. 1, 2162. https://doi.org/10.1038/s41467-018-04170-3

Publisher Correction : Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes. / Bonàs-Guarch, Sílvia; Guindo-Martínez, Marta; Miguel-Escalada, Irene; Grarup, Niels; Sebastian, David; Rodriguez-Fos, Elias; Sánchez, Friman; Planas-Fèlix, Mercè; Cortes-Sánchez, Paula; González, Santi; Timshel, Pascal; Pers, Tune H.; Morgan, Claire C.; Moran, Ignasi; Atla, Goutham; González, Juan R.; Puiggros, Montserrat; Martí, Jonathan; Andersson, Ehm A.; Díaz, Carlos; Badia, Rosa M.; Udler, Miriam; Leong, Aaron; Kaur, Varindepal; Flannick, Jason; Jørgensen, Torben; Linneberg, Allan; Jørgensen, Marit E.; Witte, Daniel R.; Christensen, Cramer; Brandslund, Ivan; Appel, Emil V.; Scott, Robert A.; Luan, Jian'An; Langenberg, Claudia; Wareham, Nicholas J.; Pedersen, Oluf; Zorzano, Antonio; Florez, Jose C.; Hansen, Torben; Ferrer, Jorge; Mercader, Josep Maria; Torrents, David.

I: Nature Communications, Bind 9, Nr. 1, 2162, 30.05.2018.

Publikation: Bidrag til tidsskriftKommentar/debatForskningpeer review

TY - JOUR

T1 - Publisher Correction

T2 - Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes

AU - Bonàs-Guarch, Sílvia

AU - Guindo-Martínez, Marta

AU - Miguel-Escalada, Irene

AU - Grarup, Niels

AU - Sebastian, David

AU - Rodriguez-Fos, Elias

AU - Sánchez, Friman

AU - Planas-Fèlix, Mercè

AU - Cortes-Sánchez, Paula

AU - González, Santi

AU - Timshel, Pascal

AU - Pers, Tune H.

AU - Morgan, Claire C.

AU - Moran, Ignasi

AU - Atla, Goutham

AU - González, Juan R.

AU - Puiggros, Montserrat

AU - Martí, Jonathan

AU - Andersson, Ehm A.

AU - Díaz, Carlos

AU - Badia, Rosa M.

AU - Udler, Miriam

AU - Leong, Aaron

AU - Kaur, Varindepal

AU - Flannick, Jason

AU - Jørgensen, Torben

AU - Linneberg, Allan

AU - Jørgensen, Marit E.

AU - Witte, Daniel R.

AU - Christensen, Cramer

AU - Brandslund, Ivan

AU - Appel, Emil V.

AU - Scott, Robert A.

AU - Luan, Jian'An

AU - Langenberg, Claudia

AU - Wareham, Nicholas J.

AU - Pedersen, Oluf

AU - Zorzano, Antonio

AU - Florez, Jose C.

AU - Hansen, Torben

AU - Ferrer, Jorge

AU - Mercader, Josep Maria

AU - Torrents, David

PY - 2018/5/30

Y1 - 2018/5/30

N2 - 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.

AB - 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.

U2 - 10.1038/s41467-018-04170-3

DO - 10.1038/s41467-018-04170-3

M3 - Comment/debate

VL - 9

JO - Nature Communications

JF - Nature Communications

SN - 2041-1723

IS - 1

M1 - 2162

ER -

Bonàs-Guarch S, Guindo-Martínez M, Miguel-Escalada I, Grarup N, Sebastian D, Rodriguez-Fos E et al. Publisher Correction: Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes. Nature Communications. 2018 maj 30;9(1). 2162. https://doi.org/10.1038/s41467-018-04170-3