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Peer Review reports

From: Genome sequencing reveals novel causative structural and single nucleotide variants in Pakistani families with congenital hypogonadotropic hypogonadism

Original Submission
23 Oct 2023 Submitted Original manuscript
24 Jan 2024 Author responded Author comments - Nelly Pitteloud
25 Jan 2024 Author responded Author comments - Nelly Pitteloud
Resubmission - Version 2
24 Jan 2024 Submitted Manuscript version 2
25 Jan 2024 Author responded Author comments - Nelly Pitteloud
Resubmission - Version 3
25 Jan 2024 Submitted Manuscript version 3
11 Mar 2024 Reviewed Reviewer Report
14 Mar 2024 Reviewed Reviewer Report
24 Mar 2024 Reviewed Reviewer Report
24 Apr 2024 Author responded Author comments - Nelly Pitteloud
Resubmission - Version 4
24 Apr 2024 Submitted Manuscript version 4
25 Apr 2024 Author responded Author comments - Nelly Pitteloud
Resubmission - Version 5
25 Apr 2024 Submitted Manuscript version 5
26 Apr 2024 Reviewed Reviewer Report
3 May 2024 Reviewed Reviewer Report
2 Jul 2024 Author responded Author comments - Nelly Pitteloud
Resubmission - Version 6
2 Jul 2024 Submitted Manuscript version 6
Publishing
5 Jul 2024 Editorially accepted
14 Aug 2024 Article published 10.1186/s12864-024-10598-3

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