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Peer Review reports

From: A novel missense variant in ESRRB gene causing autosomal recessive non-syndromic hearing loss: in silico analysis of a case

Original Submission
8 Jul 2021 Submitted Original manuscript
3 Aug 2021 Reviewed Reviewer Report
8 Sep 2021 Reviewed Reviewer Report - Janakiramaiah Mekala
4 Oct 2021 Author responded Author comments - Sima Mansoori Derakhshan
6 Oct 2021 Author responded Author comments - Sima Mansoori Derakhshan
Resubmission - Version 2
4 Oct 2021 Submitted Manuscript version 2
8 Oct 2021 Author responded Author comments - Sima Mansoori Derakhshan
Resubmission - Version 3
8 Oct 2021 Submitted Manuscript version 3
21 Oct 2021 Reviewed Reviewer Report
5 Nov 2021 Reviewed Reviewer Report - Janakiramaiah Mekala
21 Nov 2021 Author responded Author comments - Sima Mansoori Derakhshan
Resubmission - Version 4
21 Nov 2021 Submitted Manuscript version 4
26 Nov 2021 Author responded Author comments - Sima Mansoori Derakhshan
Resubmission - Version 5
26 Nov 2021 Submitted Manuscript version 5
5 Dec 2021 Reviewed Reviewer Report
30 Dec 2021 Author responded Author comments - Sima Mansoori Derakhshan
Resubmission - Version 6
30 Dec 2021 Submitted Manuscript version 6
16 Jan 2022 Reviewed Reviewer Report
Resubmission - Version 7
Submitted Manuscript version 7
Publishing
24 Jan 2022 Editorially accepted
1 Feb 2022 Article published 10.1186/s12920-022-01165-4

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