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Peer Review reports

From: Whole exome sequencing reveals a stop-gain mutation of PKD2 in an autosomal dominant polycystic kidney disease family complicated with aortic dissection

Original Submission
19 Mar 2017 Submitted Original manuscript
8 Jun 2017 Reviewed Reviewer Report - Yumay Chen
7 Jul 2017 Reviewed Reviewer Report - Federico Piscione
18 Jul 2017 Reviewed Reviewer Report - Andrew Paterson
25 Aug 2017 Author responded Author comments - Wenwen Zhang
Resubmission - Version 2
25 Aug 2017 Submitted Manuscript version 2
28 Aug 2017 Reviewed Reviewer Report - Andrew Paterson
12 Sep 2017 Reviewed Reviewer Report - Yumay Chen
2 Dec 2017 Author responded Author comments - Wenwen Zhang
Resubmission - Version 3
2 Dec 2017 Submitted Manuscript version 3
14 Dec 2017 Reviewed Reviewer Report - Yumay Chen
16 Jan 2018 Reviewed Reviewer Report - Andrew Paterson
23 Jan 2018 Author responded Author comments - Wenwen Zhang
Resubmission - Version 4
23 Jan 2018 Submitted Manuscript version 4
Publishing
24 Jan 2018 Editorially accepted
30 Jan 2018 Article published 10.1186/s12881-018-0536-6

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BMC Medical Genetics

ISSN: 1471-2350

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