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Peer Review reports

From: Screening of BRCA1/2 genes mutations and copy number variations in patients with high risk for hereditary breast and ovarian cancer syndrome (HBOC)

Original Submission
2 Mar 2020 Submitted Original manuscript
10 Mar 2020 Author responded Author comments - Fatima Zahra El Ansari
Resubmission - Version 2
10 Mar 2020 Submitted Manuscript version 2
15 Mar 2020 Author responded Author comments - Fatima Zahra El Ansari
Resubmission - Version 3
15 Mar 2020 Submitted Manuscript version 3
5 Apr 2020 Reviewed Reviewer Report - Uri David Akavia
15 Apr 2020 Reviewed Reviewer Report - Wareed Ahmed
16 Apr 2020 Reviewed Reviewer Report - Chiara Agnoletto
27 Apr 2020 Reviewed Reviewer Report - Yoshimitsu Akiyama
5 May 2020 Reviewed Reviewer Report
10 May 2020 Reviewed Reviewer Report - Ajay Abraham
11 May 2020 Reviewed Reviewer Report - Venkateshwari Ananthapur
6 Jun 2020 Author responded Author comments - Fatima Zahra El Ansari
Resubmission - Version 4
6 Jun 2020 Submitted Manuscript version 4
11 Jun 2020 Reviewed Reviewer Report
12 Jun 2020 Reviewed Reviewer Report
20 Jun 2020 Reviewed Reviewer Report
22 Jun 2020 Reviewed Reviewer Report
27 Jun 2020 Reviewed Reviewer Report - Ajay Abraham
20 Jul 2020 Author responded Author comments - Fatima Zahra El Ansari
Resubmission - Version 5
20 Jul 2020 Submitted Manuscript version 5
25 Jul 2020 Reviewed Reviewer Report
30 Jul 2020 Author responded Author comments - Fatima Zahra El Ansari
Resubmission - Version 6
30 Jul 2020 Submitted Manuscript version 6
31 Jul 2020 Author responded Author comments - Fatima Zahra El Ansari
Resubmission - Version 7
31 Jul 2020 Submitted Manuscript version 7
Publishing
3 Aug 2020 Editorially accepted
10 Aug 2020 Article published 10.1186/s12885-020-07250-0

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