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Page 1
Prevalence and psychiatric comorbidity of attention-deficit/hyperactivity disorder in an adolescent Finnish population.
Smalley SL, McGough JJ, Moilanen IK, Loo SK, Taanila A, Ebeling H, Hurtig T, Kaakinen M, Humphrey LA, McCracken JT, Varilo T, Yang MH, Nelson SF, Peltonen L, Järvelin MR. Smalley SL, et al. Among authors: varilo t. J Am Acad Child Adolesc Psychiatry. 2007 Dec;46(12):1575-83. doi: 10.1097/chi.0b013e3181573137. J Am Acad Child Adolesc Psychiatry. 2007. PMID: 18030079
ADHD candidate gene study in a population-based birth cohort: association with DBH and DRD2.
Nyman ES, Ogdie MN, Loukola A, Varilo T, Taanila A, Hurtig T, Moilanen IK, Loo SK, McGough JJ, Järvelin MR, Smalley SL, Nelson SF, Peltonen L. Nyman ES, et al. Among authors: varilo t. J Am Acad Child Adolesc Psychiatry. 2007 Dec;46(12):1614-21. doi: 10.1097/chi.0b013e3181579682. J Am Acad Child Adolesc Psychiatry. 2007. PMID: 18030083
Genome-wide association analysis of metabolic traits in a birth cohort from a founder population.
Sabatti C, Service SK, Hartikainen AL, Pouta A, Ripatti S, Brodsky J, Jones CG, Zaitlen NA, Varilo T, Kaakinen M, Sovio U, Ruokonen A, Laitinen J, Jakkula E, Coin L, Hoggart C, Collins A, Turunen H, Gabriel S, Elliot P, McCarthy MI, Daly MJ, Järvelin MR, Freimer NB, Peltonen L. Sabatti C, et al. Among authors: varilo t. Nat Genet. 2009 Jan;41(1):35-46. doi: 10.1038/ng.271. Epub 2008 Dec 7. Nat Genet. 2009. PMID: 19060910 Free PMC article.
Molecular genetics of the Finnish disease heritage.
Peltonen L, Jalanko A, Varilo T. Peltonen L, et al. Among authors: varilo t. Hum Mol Genet. 1999;8(10):1913-23. doi: 10.1093/hmg/8.10.1913. Hum Mol Genet. 1999. PMID: 10469845 Review.
Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studies.
Service S, DeYoung J, Karayiorgou M, Roos JL, Pretorious H, Bedoya G, Ospina J, Ruiz-Linares A, Macedo A, Palha JA, Heutink P, Aulchenko Y, Oostra B, van Duijn C, Jarvelin MR, Varilo T, Peddle L, Rahman P, Piras G, Monne M, Murray S, Galver L, Peltonen L, Sabatti C, Collins A, Freimer N. Service S, et al. Among authors: varilo t. Nat Genet. 2006 May;38(5):556-60. doi: 10.1038/ng1770. Epub 2006 Apr 2. Nat Genet. 2006. PMID: 16582909
Deletion of TOP3β, a component of FMRP-containing mRNPs, contributes to neurodevelopmental disorders.
Stoll G, Pietiläinen OPH, Linder B, Suvisaari J, Brosi C, Hennah W, Leppä V, Torniainen M, Ripatti S, Ala-Mello S, Plöttner O, Rehnström K, Tuulio-Henriksson A, Varilo T, Tallila J, Kristiansson K, Isohanni M, Kaprio J, Eriksson JG, Raitakari OT, Lehtimäki T, Jarvelin MR, Salomaa V, Hurles M, Stefansson H, Peltonen L, Sullivan PF, Paunio T, Lönnqvist J, Daly MJ, Fischer U, Freimer NB, Palotie A. Stoll G, et al. Among authors: varilo t. Nat Neurosci. 2013 Sep;16(9):1228-1237. doi: 10.1038/nn.3484. Epub 2013 Aug 4. Nat Neurosci. 2013. PMID: 23912948 Free PMC article.
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: varilo t. Mol Psychiatry. 2002;7(5):453-9. doi: 10.1038/sj.mp.4001104. Mol Psychiatry. 2002. PMID: 12082562
65 results