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Peer Review reports

From: Whole exome sequencing in adult-onset hearing loss reveals a high load of predicted pathogenic variants in known deafness-associated genes and identifies new candidate genes

Original Submission
31 Jan 2018 Submitted Original manuscript
3 May 2018 Reviewed Reviewer Report - Ambroise Wonkam
17 May 2018 Reviewed Reviewer Report - Giulia Soldà
11 Jul 2018 Author responded Author comments - Morag Lewis
Resubmission - Version 2
11 Jul 2018 Submitted Manuscript version 2
26 Jul 2018 Reviewed Reviewer Report - Ambroise Wonkam
6 Aug 2018 Reviewed Reviewer Report - Giulia Soldà
15 Aug 2018 Author responded Author comments - Morag Lewis
Resubmission - Version 3
15 Aug 2018 Submitted Manuscript version 3
Publishing
21 Aug 2018 Editorially accepted
4 Sep 2018 Article published 10.1186/s12920-018-0395-1

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BMC Medical Genomics

ISSN: 1755-8794

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