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Using rare genetic mutations to revisit structural brain asymmetry.
Kopal J, Kumar K, Shafighi K, Saltoun K, Modenato C, Moreau CA, Huguet G, Jean-Louis M, Martin CO, Saci Z, Younis N, Douard E, Jizi K, Beauchamp-Chatel A, Kushan L, Silva AI, van den Bree MBM, Linden DEJ, Owen MJ, Hall J, Lippé S, Draganski B, Sønderby IE, Andreassen OA, Glahn DC, Thompson PM, Bearden CE, Zatorre R, Jacquemont S, Bzdok D. Kopal J, et al. Among authors: hall j. bioRxiv [Preprint]. 2023 Apr 18:2023.04.17.537199. doi: 10.1101/2023.04.17.537199. bioRxiv. 2023. Update in: Nat Commun. 2024 Mar 26;15(1):2639. doi: 10.1038/s41467-024-46784-w PMID: 37131672 Free PMC article. Updated. Preprint.
Psychiatric disorders in children with 16p11.2 deletion and duplication.
Niarchou M, Chawner SJRA, Doherty JL, Maillard AM, Jacquemont S, Chung WK, Green-Snyder L, Bernier RA, Goin-Kochel RP, Hanson E, Linden DEJ, Linden SC, Raymond FL, Skuse D, Hall J, Owen MJ, Bree MBMVD. Niarchou M, et al. Among authors: hall j. Transl Psychiatry. 2019 Jan 16;9(1):8. doi: 10.1038/s41398-018-0339-8. Transl Psychiatry. 2019. PMID: 30664628 Free PMC article.
Correction: Psychiatric disorders in children with 16p11.2 deletion and duplication.
Niarchou M, Chawner SJRA, Doherty JL, Maillard AM, Jacquemont S, Chung WK, Green-Snyder L, Bernier RA, Goin-Kochel RP, Hanson E, Linden DEJ, Linden SC, Raymond FL, Skuse D, Hall J, Owen MJ, van den Bree MBM. Niarchou M, et al. Among authors: hall j. Transl Psychiatry. 2019 Mar 5;9(1):107. doi: 10.1038/s41398-019-0441-6. Transl Psychiatry. 2019. PMID: 30837452 Free PMC article.
9,145 results