Peer review reports
From: A paradigmatic autistic phenotype associated with loss of PCDH11Y and NLGN4Y genes
Original Submission | ||
---|---|---|
2 Dec 2019 | Submitted | Original manuscript |
7 Mar 2020 | Reviewed | Reviewer Report |
2 Nov 2020 | Author responded | Author comments - Rosaria Nardello |
Resubmission - Version 2 | ||
2 Nov 2020 | Submitted | Manuscript version 2 |
13 Jan 2021 | Reviewed | Reviewer Report |
20 Jan 2021 | Author responded | Author comments - Rosaria Nardello |
Resubmission - Version 3 | ||
20 Jan 2021 | Submitted | Manuscript version 3 |
26 Feb 2021 | Author responded | Author comments - Rosaria Nardello |
Resubmission - Version 4 | ||
26 Feb 2021 | Submitted | Manuscript version 4 |
3 Mar 2021 | Author responded | Author comments - Rosaria Nardello |
Resubmission - Version 5 | ||
3 Mar 2021 | Submitted | Manuscript version 5 |
5 Mar 2021 | Author responded | Author comments - Rosaria Nardello |
Resubmission - Version 6 | ||
5 Mar 2021 | Submitted | Manuscript version 6 |
Publishing | ||
8 Mar 2021 | Editorially accepted | |
8 Apr 2021 | Article published | 10.1186/s12920-021-00934-x |