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 |
You can find further information about peer review here.