Skip to main content

Peer Review reports

From: Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies in a consanguineous Iranian family is associated with a homozygous start loss variant in the PRUNE1 gene

Original Submission
7 Aug 2021 Submitted Original manuscript
16 Sep 2021 Reviewed Reviewer Report - Serdar Ceylaner
24 Oct 2021 Reviewed Reviewer Report - Tadashi Kaname
9 Nov 2021 Reviewed Reviewer Report - Yaping Yang
26 Nov 2021 Author responded Author comments - Masoud Garshasbi
8 Dec 2021 Author responded Author comments - Masoud Garshasbi
Resubmission - Version 2
26 Nov 2021 Submitted Manuscript version 2
23 Dec 2021 Reviewed Reviewer Report - Serdar Ceylaner
3 Jan 2022 Reviewed Reviewer Report - Tadashi Kaname
24 Jan 2022 Author responded Author comments - Masoud Garshasbi
Resubmission - Version 3
24 Jan 2022 Submitted Manuscript version 3
17 Feb 2022 Author responded Author comments - Masoud Garshasbi
Resubmission - Version 4
17 Feb 2022 Submitted Manuscript version 4
22 Mar 2022 Author responded Author comments - Masoud Garshasbi
Resubmission - Version 5
22 Mar 2022 Submitted Manuscript version 5
24 Mar 2022 Author responded Author comments - Masoud Garshasbi
Resubmission - Version 6
24 Mar 2022 Submitted Manuscript version 6
Publishing
30 Mar 2022 Editorially accepted
4 Apr 2022 Article published 10.1186/s12920-022-01228-6

You can find further information about peer review here.

Back to article page