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BMC Neurology

Open Access
Open Peer Review

This article has Open Peer Review reports available.

How does Open Peer Review work?

The utility of exome sequencing for genetic diagnosis in a familial microcephaly epilepsy syndrome

  • Laura M McDonell1,
  • Jodi Warman Chardon2,
  • Jeremy Schwartzentruber3,
  • Denise Foster4,
  • Chandree L Beaulieu1,
  • FORGE Canada Consortium1,
  • Jacek Majewski5,
  • Dennis E Bulman1, 6 and
  • Kym M Boycott1, 2, 6Email author
Contributed equally
BMC Neurology201414:22

https://doi.org/10.1186/1471-2377-14-22

Received: 11 November 2013

Accepted: 22 January 2014

Published: 31 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
11 Nov 2013 Submitted Original manuscript
6 Dec 2013 Reviewed Reviewer Report - Wasim Ahmad
10 Dec 2013 Reviewed Reviewer Report - Bobby Koeleman
8 Jan 2014 Author responded Author comments - Kym Boycott
Resubmission - Version 2
8 Jan 2014 Submitted Manuscript version 2
17 Jan 2014 Author responded Author comments - Kym Boycott
Resubmission - Version 3
17 Jan 2014 Submitted Manuscript version 3
Publishing
22 Jan 2014 Editorially accepted
31 Jan 2014 Article published 10.1186/1471-2377-14-22

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)
Children’s Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Canada
(2)
Department of Genetics, Children’s Hospital of Eastern Ontario, Ottawa, Canada
(3)
McGill University and Genome Quebec Innovation Centre, Montréal, Canada
(4)
Algoma Public Health, Sault Ste Marie, Canada
(5)
Department of Human Genetics, McGill University, Montréal, Canada
(6)
Department of Pediatrics, University of Ottawa, Ottawa, Canada

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