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Peer Review reports

From: Identification of de novo mutations for ARID1B haploinsufficiency associated with Coffin–Siris syndrome 1 in three Chinese families via array-CGH and whole exome sequencing

Original Submission
2 Aug 2021 Submitted Original manuscript
16 Aug 2021 Author responded Author comments - Guanting Lu
Resubmission - Version 2
16 Aug 2021 Submitted Manuscript version 2
15 Sep 2021 Reviewed Reviewer Report
18 Sep 2021 Reviewed Reviewer Report - Tri Indah Winarni
18 Sep 2021 Reviewed Reviewer Report - Mawaddah Rochmah
18 Sep 2021 Reviewed Reviewer Report
23 Sep 2021 Reviewed Reviewer Report
28 Sep 2021 Reviewed Reviewer Report - TIAGO FERNANDO CHAVES
12 Oct 2021 Author responded Author comments - Guanting Lu
Resubmission - Version 3
12 Oct 2021 Submitted Manuscript version 3
12 Oct 2021 Reviewed Reviewer Report - Mawaddah Rochmah
15 Oct 2021 Reviewed Reviewer Report - Tri Indah Winarni
31 Oct 2021 Author responded Author comments - Guanting Lu
Resubmission - Version 4
31 Oct 2021 Submitted Manuscript version 4
2 Nov 2021 Author responded Author comments - Guanting Lu
Resubmission - Version 5
2 Nov 2021 Submitted Manuscript version 5
3 Nov 2021 Author responded Author comments - Guanting Lu
Resubmission - Version 6
3 Nov 2021 Submitted Manuscript version 6
4 Nov 2021 Author responded Author comments - Guanting Lu
Resubmission - Version 7
4 Nov 2021 Submitted Manuscript version 7
Publishing
5 Nov 2021 Editorially accepted
14 Nov 2021 Article published 10.1186/s12920-021-01119-2

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