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Children with Early-Onset Psychosis Have Increased Burden of Rare GRIN2A Variants.
Hojlo MA, Ghebrelul M, Genetti CA, Smith R, Rockowitz S, Deaso E, Beggs AH, Agrawal PB, Glahn DC, Gonzalez-Heydrich J, Brownstein CA. Hojlo MA, et al. Among authors: glahn dc. Genes (Basel). 2023 Mar 23;14(4):779. doi: 10.3390/genes14040779. Genes (Basel). 2023. PMID: 37107537 Free PMC article.
Copy-number variants differ in frequency across genetic ancestry groups.
Schultz LM, Knighton A, Huguet G, Saci Z, Jean-Louis M, Mollon J, Knowles EEM, Glahn DC, Jacquemont S, Almasy L. Schultz LM, et al. Among authors: glahn dc. HGG Adv. 2024 Oct 10;5(4):100340. doi: 10.1016/j.xhgg.2024.100340. Epub 2024 Aug 12. HGG Adv. 2024. PMID: 39138864 Free PMC article.
Impact of Copy Number Variants and Polygenic Risk Scores on Psychopathology in the UK Biobank.
Mollon J, Schultz LM, Huguet G, Knowles EEM, Mathias SR, Rodrigue A, Alexander-Bloch A, Saci Z, Jean-Louis M, Kumar K, Douard E, Almasy L, Jacquemont S, Glahn DC. Mollon J, et al. Among authors: glahn dc. Biol Psychiatry. 2023 Oct 1;94(7):591-600. doi: 10.1016/j.biopsych.2023.01.028. Epub 2023 Feb 9. Biol Psychiatry. 2023. PMID: 36764568 Free PMC article.
Subcortical Brain Alterations in Carriers of Genomic Copy Number Variants.
Kumar K, Modenato C, Moreau C, Ching CRK, Harvey A, Martin-Brevet S, Huguet G, Jean-Louis M, Douard E, Martin CO, Younis N, Tamer P, Maillard AM, Rodriguez-Herreros B, Pain A; 16p11.2 European Consortium, Simons Searchlight Consortium; Kushan L, Isaev D, Alpert K, Ragothaman A, Turner JA, Wang L, Ho TC, Schmaal L, Silva AI, van den Bree MBM, Linden DEJ, Owen MJ, Hall J, Lippé S, Dumas G, Draganski B, Gutman BA, Sønderby IE, Andreassen OA, Schultz LM, Almasy L, Glahn DC, Bearden CE, Thompson PM, Jacquemont S. Kumar K, et al. Among authors: glahn dc. Am J Psychiatry. 2023 Sep 1;180(9):685-698. doi: 10.1176/appi.ajp.20220304. Epub 2023 Jul 12. Am J Psychiatry. 2023. PMID: 37434504 Free PMC article.
375 results