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A single nucleotide polymorphism in the coding region of PGC-1α is a male-specific modifier of Huntington disease age-at-onset in a large European cohort

  • Patrick Weydt1Email author,
  • Selma M Soyal2,
  • G Bernhard Landwehrmeyer1,
  • Wolfgang Patsch3 and
  • For the European Huntington Disease Network
BMC Neurology201414:1

DOI: 10.1186/1471-2377-14-1

Received: 8 September 2013

Accepted: 10 December 2013

Published: 2 January 2014

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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
8 Sep 2013 Submitted Original manuscript
17 Sep 2013 Author responded Author comments - Patrick Weydt
Resubmission - Version 2
17 Sep 2013 Submitted Manuscript version 2
16 Oct 2013 Reviewed Reviewer Report - Huu Phuc Nguyen
6 Nov 2013 Reviewed Reviewer Report - Larissa Arning
28 Nov 2013 Author responded Author comments - Patrick Weydt
Resubmission - Version 3
28 Nov 2013 Submitted Manuscript version 3
Publishing
10 Dec 2013 Editorially accepted
2 Jan 2014 Article published 10.1186/1471-2377-14-1

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. Pre-publication versions of the article and author comments to reviewers are available by contacting info@biomedcentral.com. 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)
Neurology, Ulm University
(2)
Laboratory Medicine, Paracelsus Medical University
(3)
Pharmacology, Paracelsus Medical University

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