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Large-scale mapping of cortical alterations in 22q11.2 deletion syndrome: Convergence with idiopathic psychosis and effects of deletion size.
Sun D, Ching CRK, Lin A, Forsyth JK, Kushan L, Vajdi A, Jalbrzikowski M, Hansen L, Villalon-Reina JE, Qu X, Jonas RK, van Amelsvoort T, Bakker G, Kates WR, Antshel KM, Fremont W, Campbell LE, McCabe KL, Daly E, Gudbrandsen M, Murphy CM, Murphy D, Craig M, Vorstman J, Fiksinski A, Koops S, Ruparel K, Roalf DR, Gur RE, Schmitt JE, Simon TJ, Goodrich-Hunsaker NJ, Durdle CA, Bassett AS, Chow EWC, Butcher NJ, Vila-Rodriguez F, Doherty J, Cunningham A, van den Bree MBM, Linden DEJ, Moss H, Owen MJ, Murphy KC, McDonald-McGinn DM, Emanuel B, van Erp TGM, Turner JA, Thompson PM, Bearden CE. Sun D, et al. Among authors: linden dej. Mol Psychiatry. 2020 Aug;25(8):1822-1834. doi: 10.1038/s41380-018-0078-5. Epub 2018 Jun 13. Mol Psychiatry. 2020. PMID: 29895892 Free PMC article.
Dysbindin-1 genotype effects on emotional working memory.
Wolf C, Jackson MC, Kissling C, Thome J, Linden DE. Wolf C, et al. Mol Psychiatry. 2011 Feb;16(2):145-55. doi: 10.1038/mp.2009.129. Epub 2009 Dec 15. Mol Psychiatry. 2011. PMID: 20010894 Free PMC article.
Schizophrenia risk variants modulate white matter volume across the psychosis spectrum: evidence from two independent cohorts.
Oertel-Knöchel V, Lancaster TM, Knöchel C, Stäblein M, Storchak H, Reinke B, Jurcoane A, Kniep J, Prvulovic D, Mantripragada K, Tansey KE, O'Donovan MC, Owen MJ, Linden DE. Oertel-Knöchel V, et al. Neuroimage Clin. 2015 Mar 13;7:764-70. doi: 10.1016/j.nicl.2015.03.005. eCollection 2015. Neuroimage Clin. 2015. PMID: 25844328 Free PMC article.
CACNA1C risk variant is associated with increased amygdala volume.
Lancaster TM, Foley S, Tansey KE, Linden DE, Caseras X. Lancaster TM, et al. Eur Arch Psychiatry Clin Neurosci. 2016 Apr;266(3):269-75. doi: 10.1007/s00406-015-0609-x. Epub 2015 Jun 6. Eur Arch Psychiatry Clin Neurosci. 2016. PMID: 26048451
A national population-based e-cohort of people with psychosis (PsyCymru) linking prospectively ascertained phenotypically rich and genetic data to routinely collected records: overview, recruitment and linkage.
Lloyd K, McGregor J, John A, Craddock N, Walters JT, Linden D, Jones I, Bentall R, Lyons RA, Ford DV, Owen MJ. Lloyd K, et al. Schizophr Res. 2015 Aug;166(1-3):131-6. doi: 10.1016/j.schres.2015.05.036. Epub 2015 Jun 29. Schizophr Res. 2015. PMID: 26139629
Common alleles contribute to schizophrenia in CNV carriers.
Tansey KE, Rees E, Linden DE, Ripke S, Chambert KD, Moran JL, McCarroll SA, Holmans P, Kirov G, Walters J, Owen MJ, O'Donovan MC. Tansey KE, et al. Mol Psychiatry. 2016 Aug;21(8):1085-9. doi: 10.1038/mp.2015.143. Epub 2015 Sep 22. Mol Psychiatry. 2016. PMID: 26390827 Free PMC article.
353 results