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Peer Review reports

From: Whole-genome sequencing, as a powerful diagnostic tool in hearing loss, reveals novel variants in PTPRQ missed by whole-exome sequencing

Original Submission
11 Nov 2024 Submitted Original manuscript
Resubmission - Version 2
Submitted Manuscript version 2
Resubmission - Version 3
Submitted Manuscript version 3
3 Dec 2024 Author responded Author comments - Asuman Koparir
Resubmission - Version 4
3 Dec 2024 Submitted Manuscript version 4
3 Jan 2025 Reviewed Reviewer Report
11 Feb 2025 Reviewed Reviewer Report
19 Feb 2025 Author responded Author comments - Asuman Koparir
Resubmission - Version 5
19 Feb 2025 Submitted Manuscript version 5
25 Feb 2025 Reviewed Reviewer Report
5 Mar 2025 Reviewed Reviewer Report
7 Mar 2025 Author responded Author comments - Asuman Koparir
Resubmission - Version 6
7 Mar 2025 Submitted Manuscript version 6
Publishing
10 Mar 2025 Editorially accepted
31 Mar 2025 Article published 10.1186/s12920-025-02122-7

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