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Page 1
Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders.
Singh T, Kurki MI, Curtis D, Purcell SM, Crooks L, McRae J, Suvisaari J, Chheda H, Blackwood D, Breen G, Pietiläinen O, Gerety SS, Ayub M, Blyth M, Cole T, Collier D, Coomber EL, Craddock N, Daly MJ, Danesh J, DiForti M, Foster A, Freimer NB, Geschwind D, Johnstone M, Joss S, Kirov G, Körkkö J, Kuismin O, Holmans P, Hultman CM, Iyegbe C, Lönnqvist J, Männikkö M, McCarroll SA, McGuffin P, McIntosh AM, McQuillin A, Moilanen JS, Moore C, Murray RM, Newbury-Ecob R, Ouwehand W, Paunio T, Prigmore E, Rees E, Roberts D, Sambrook J, Sklar P, St Clair D, Veijola J, Walters JT, Williams H; Swedish Schizophrenia Study; INTERVAL Study; DDD Study; UK10 K Consortium; Sullivan PF, Hurles ME, O'Donovan MC, Palotie A, Owen MJ, Barrett JC. Singh T, et al. Among authors: paunio t. Nat Neurosci. 2016 Apr;19(4):571-7. doi: 10.1038/nn.4267. Epub 2016 Mar 14. Nat Neurosci. 2016. PMID: 26974950 Free PMC article.
Chromosome 1 loci in Finnish schizophrenia families.
Ekelund J, Hovatta I, Parker A, Paunio T, Varilo T, Martin R, Suhonen J, Ellonen P, Chan G, Sinsheimer JS, Sobel E, Juvonen H, Arajärvi R, Partonen T, Suvisaari J, Lönnqvist J, Meyer J, Peltonen L. Ekelund J, et al. Among authors: paunio t. Hum Mol Genet. 2001 Jul 15;10(15):1611-7. doi: 10.1093/hmg/10.15.1611. Hum Mol Genet. 2001. PMID: 11468279
Bipolar disorder susceptibility region on Xq24-q27.1 in Finnish families.
Ekholm JM, Pekkarinen P, Pajukanta P, Kieseppä T, Partonen T, Paunio T, Varilo T, Perola M, Lönnqvist J, Peltonen L. Ekholm JM, et al. Among authors: paunio t. Mol Psychiatry. 2002;7(5):453-9. doi: 10.1038/sj.mp.4001104. Mol Psychiatry. 2002. PMID: 12082562
Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia.
Lewis CM, Levinson DF, Wise LH, DeLisi LE, Straub RE, Hovatta I, Williams NM, Schwab SG, Pulver AE, Faraone SV, Brzustowicz LM, Kaufmann CA, Garver DL, Gurling HM, Lindholm E, Coon H, Moises HW, Byerley W, Shaw SH, Mesen A, Sherrington R, O'Neill FA, Walsh D, Kendler KS, Ekelund J, Paunio T, Lönnqvist J, Peltonen L, O'Donovan MC, Owen MJ, Wildenauer DB, Maier W, Nestadt G, Blouin JL, Antonarakis SE, Mowry BJ, Silverman JM, Crowe RR, Cloninger CR, Tsuang MT, Malaspina D, Harkavy-Friedman JM, Svrakic DM, Bassett AS, Holcomb J, Kalsi G, McQuillin A, Brynjolfson J, Sigmundsson T, Petursson H, Jazin E, Zoëga T, Helgason T. Lewis CM, et al. Among authors: paunio t. Am J Hum Genet. 2003 Jul;73(1):34-48. doi: 10.1086/376549. Epub 2003 Jun 11. Am J Hum Genet. 2003. PMID: 12802786 Free PMC article.
Evidence of susceptibility loci on 4q32 and 16p12 for bipolar disorder.
Ekholm JM, Kieseppä T, Hiekkalinna T, Partonen T, Paunio T, Perola M, Ekelund J, Lönnqvist J, Pekkarinen-Ijäs P, Peltonen L. Ekholm JM, et al. Among authors: paunio t. Hum Mol Genet. 2003 Aug 1;12(15):1907-15. doi: 10.1093/hmg/ddg199. Hum Mol Genet. 2003. PMID: 12874110
271 results