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Open Peer Review

This article has Open Peer Review reports available.

How does Open Peer Review work?

Reassessing the role of mitochondrial DNA mutations in autism spectrum disorder

  • Vanesa Álvarez-Iglesias1,
  • Ana Mosquera-Miguel1,
  • Ivón Cuscó2, 3,
  • Ángel Carracedo1, 3, 4,
  • Luis Alberto Pérez-Jurado2, 3, 5, 6 and
  • Antonio Salas1Email author
Contributed equally
BMC Medical Genetics201112:50

DOI: 10.1186/1471-2350-12-50

Received: 13 November 2010

Accepted: 6 April 2011

Published: 6 April 2011

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Open Peer Review reports

Pre-publication versions of this article and author comments to reviewers are available by contacting info@biomedcentral.com.

Original Submission
13 Nov 2010 Submitted Original manuscript
Resubmission - Version 2
Submitted Manuscript version 2
13 Nov 2010 Author responded Author comments - Antonio Salas
Resubmission - Version 3
13 Nov 2010 Submitted Manuscript version 3
7 Dec 2010 Reviewed Reviewer Report - Richard Holt
10 Dec 2010 Reviewed Reviewer Report - Yong-Gang Yao
19 Dec 2010 Reviewed Reviewer Report - Antonio Persico
24 Dec 2010 Reviewed Reviewer Report - Sean Ennis
19 Jan 2011 Author responded Author comments - Antonio Salas
Resubmission - Version 4
19 Jan 2011 Submitted Manuscript version 4
21 Jan 2011 Reviewed Reviewer Report - Richard Holt
23 Jan 2011 Reviewed Reviewer Report - Yong-Gang Yao
7 Feb 2011 Reviewed Reviewer Report - Sean Ennis
Resubmission - Version 5
Submitted Manuscript version 5
Publishing
6 Apr 2011 Editorially accepted
6 Apr 2011 Article published 10.1186/1471-2350-12-50

How does Open Peer Review work?

Open peer review is a system where authors know who the reviewers are, and the reviewers know who the authors are. If the manuscript is accepted, the named reviewer reports are published alongside the article.. All previous versions of the manuscript and all author responses to the reviewers are also available.

You can find further information about the peer review system here.

Authors’ Affiliations

(1)
Unidade de Xenética, Instituto de Medicina Legal and Departamento de Anatomía Patolóxica e Ciencias Forenses, Facultade de Medicina, Universidade de Santiago de Compostela
(2)
Unidad de Genética, Universitat Pompeu Fabra
(3)
CIBER de enfermedades raras (CIBERER)
(4)
Fundación Pública Galega de Medicina Xenómica, SERGAS, Santiago de Compostela
(5)
Programa de Medicina Molecular y Genética, Hospital Universitari Vall d'Hebron
(6)
Dept. of Genome Sciences, University of Washington

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