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Peer Review reports

From: Exome sequencing reveals neurodevelopmental genes in simplex consanguineous Iranian families with syndromic autism

Original Submission
16 May 2023 Submitted Original manuscript
Resubmission - Version 2
Submitted Manuscript version 2
4 Jul 2023 Reviewed Reviewer Report
26 Jul 2023 Reviewed Reviewer Report
28 Jul 2023 Reviewed Reviewer Report
31 Jul 2023 Reviewed Reviewer Report
31 Aug 2023 Author responded Author comments - Hyung-Goo Kim
Resubmission - Version 3
31 Aug 2023 Submitted Manuscript version 3
4 Sep 2023 Author responded Author comments - Hyung-Goo Kim
Resubmission - Version 4
4 Sep 2023 Submitted Manuscript version 4
17 Sep 2023 Reviewed Reviewer Report
16 Nov 2023 Reviewed Reviewer Report
28 Nov 2023 Author responded Author comments - Hyung-Goo Kim
Resubmission - Version 5
28 Nov 2023 Submitted Manuscript version 5
13 Dec 2023 Author responded Author comments - Hyung-Goo Kim
Resubmission - Version 6
13 Dec 2023 Submitted Manuscript version 6
2 Jan 2024 Reviewed Reviewer Report
26 Jun 2024 Author responded Author comments - Hyung-Goo Kim
Resubmission - Version 7
26 Jun 2024 Submitted Manuscript version 7
Publishing
23 Jul 2024 Editorially accepted
5 Aug 2024 Article published 10.1186/s12920-024-01969-6

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