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Peer Review reports

From: Whole-exome sequencing identifies a de novo PDE3A variant causing autosomal dominant hypertension with brachydactyly type E syndrome: a case report

Original Submission
25 Aug 2019 Submitted Original manuscript
14 Oct 2019 Author responded Author comments - Xianqing Li
Resubmission - Version 2
14 Oct 2019 Submitted Manuscript version 2
16 Dec 2019 Reviewed Reviewer Report - Lisong Shi
3 Jan 2020 Reviewed Reviewer Report
19 Jan 2020 Reviewed Reviewer Report - Kamwing Jair
21 Mar 2020 Author responded Author comments - Xianqing Li
Resubmission - Version 3
21 Mar 2020 Submitted Manuscript version 3
6 May 2020 Reviewed Reviewer Report
14 May 2020 Reviewed Reviewer Report - Kamwing Jair
26 May 2020 Author responded Author comments - Xianqing Li
Resubmission - Version 4
26 May 2020 Submitted Manuscript version 4
13 Jun 2020 Author responded Author comments - Xianqing Li
Resubmission - Version 5
13 Jun 2020 Submitted Manuscript version 5
18 Jun 2020 Author responded Author comments - Xianqing Li
Resubmission - Version 6
18 Jun 2020 Submitted Manuscript version 6
19 Jun 2020 Author responded Author comments - Xianqing Li
Resubmission - Version 7
19 Jun 2020 Submitted Manuscript version 7
23 Jun 2020 Author responded Author comments - Xianqing Li
Resubmission - Version 8
23 Jun 2020 Submitted Manuscript version 8
Publishing
25 Jun 2020 Editorially accepted
6 Jul 2020 Article published 10.1186/s12881-020-01077-z

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