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Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification.
Hsu SC, Sears RL, Lemos RR, Quintáns B, Huang A, Spiteri E, Nevarez L, Mamah C, Zatz M, Pierce KD, Fullerton JM, Adair JC, Berner JE, Bower M, Brodaty H, Carmona O, Dobricić V, Fogel BL, García-Estevez D, Goldman J, Goudreau JL, Hopfer S, Janković M, Jaumà S, Jen JC, Kirdlarp S, Klepper J, Kostić V, Lang AE, Linglart A, Maisenbacher MK, Manyam BV, Mazzoni P, Miedzybrodzka Z, Mitarnun W, Mitchell PB, Mueller J, Novaković I, Paucar M, Paulson H, Simpson SA, Svenningsson P, Tuite P, Vitek J, Wetchaphanphesat S, Williams C, Yang M, Schofield PR, de Oliveira JR, Sobrido MJ, Geschwind DH, Coppola G. Hsu SC, et al. Among authors: fullerton jm. Neurogenetics. 2013 Feb;14(1):11-22. doi: 10.1007/s10048-012-0349-2. Epub 2013 Jan 20. Neurogenetics. 2013. PMID: 23334463 Free PMC article.
Predictive and diagnostic genetic testing in psychiatry.
Mitchell PB, Meiser B, Wilde A, Fullerton J, Donald J, Wilhelm K, Schofield PR. Mitchell PB, et al. Psychiatr Clin North Am. 2010 Mar;33(1):225-43. doi: 10.1016/j.psc.2009.10.001. Psychiatr Clin North Am. 2010. PMID: 20159347 Review.
Predictive and diagnostic genetic testing in psychiatry.
Mitchell PB, Meiser B, Wilde A, Fullerton J, Donald J, Wilhelm K, Schofield PR. Mitchell PB, et al. Clin Lab Med. 2010 Dec;30(4):829-46. doi: 10.1016/j.cll.2010.07.001. Clin Lab Med. 2010. PMID: 20832655 Review.
Investigation of circadian disruption in bipolar disorder.
Fullerton J, Heath A, Mitchell P, Schofield P. Fullerton J, et al. Acta Neuropsychiatr. 2006 Dec;18(6):251. doi: 10.1017/S0924270800030283. Acta Neuropsychiatr. 2006. PMID: 27397185 No abstract available.
148 results