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Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.
Marshall CR, Howrigan DP, Merico D, Thiruvahindrapuram B, Wu W, Greer DS, Antaki D, Shetty A, Holmans PA, Pinto D, Gujral M, Brandler WM, Malhotra D, Wang Z, Fajarado KVF, Maile MS, Ripke S, Agartz I, Albus M, Alexander M, Amin F, Atkins J, Bacanu SA, Belliveau RA Jr, Bergen SE, Bertalan M, Bevilacqua E, Bigdeli TB, Black DW, Bruggeman R, Buccola NG, Buckner RL, Bulik-Sullivan B, Byerley W, Cahn W, Cai G, Cairns MJ, Campion D, Cantor RM, Carr VJ, Carrera N, Catts SV, Chambert KD, Cheng W, Cloninger CR, Cohen D, Cormican P, Craddock N, Crespo-Facorro B, Crowley JJ, Curtis D, Davidson M, Davis KL, Degenhardt F, Del Favero J, DeLisi LE, Dikeos D, Dinan T, Djurovic S, Donohoe G, Drapeau E, Duan J, Dudbridge F, Eichhammer P, Eriksson J, Escott-Price V, Essioux L, Fanous AH, Farh KH, Farrell MS, Frank J, Franke L, Freedman R, Freimer NB, Friedman JI, Forstner AJ, Fromer M, Genovese G, Georgieva L, Gershon ES, Giegling I, Giusti-Rodríguez P, Godard S, Goldstein JI, Gratten J, de Haan L, Hamshere ML, Hansen M, Hansen T, Haroutunian V, Hartmann AM, Henskens FA, Herms S, Hirschhorn JN, Hoffmann P, Hofman A, Huang H, Ikeda M, Joa I, Kähler AK, Kahn RS, Kalaydjieva L, Karjalainen J, Kavanagh … See abstract for full author list ➔ Marshall CR, et al. Among authors: lonnqvist j. Nat Genet. 2017 Jan;49(1):27-35. doi: 10.1038/ng.3725. Epub 2016 Nov 21. Nat Genet. 2017. PMID: 27869829 Free PMC article.
Schizophrenia in the genetic isolate of Finland.
Hovatta I, Terwilliger JD, Lichtermann D, Mäkikyrö T, Suvisaari J, Peltonen L, Lönnqvist J. Hovatta I, et al. Among authors: lonnqvist j. Am J Med Genet. 1997 Jul 25;74(4):353-60. Am J Med Genet. 1997. PMID: 9259368
Assignment of the locus for PLO-SL, a frontal-lobe dementia with bone cysts, to 19q13.
Pekkarinen P, Hovatta I, Hakola P, Järvi O, Kestilä M, Lenkkeri U, Adolfsson R, Holmgren G, Nylander PO, Tranebjaerg L, Terwilliger JD, Lönnqvist J, Peltonen L. Pekkarinen P, et al. Among authors: lonnqvist j. Am J Hum Genet. 1998 Feb;62(2):362-72. doi: 10.1086/301722. Am J Hum Genet. 1998. PMID: 9463329 Free PMC article.
Tyrosine hydroxylase polymorphism and phenotypic heterogeneity in bipolar affective disorder: a multicenter association study.
Souery D, Lipp O, Rivelli SK, Massat I, Serretti A, Cavallini C, Ackenheil M, Adolfsson R, Aschauer H, Blackwood D, Dam H, Dikeos D, Fuchshuber S, Heiden M, Jakovljevic M, Kaneva R, Kessing L, Lerer B, Lönnqvist J, Mellerup T, Milanova V, Muir W, Nylander PO, Oruc L, Mendlewicz J, et al. Souery D, et al. Among authors: lonnqvist j. Am J Med Genet. 1999 Oct 15;88(5):527-32. doi: 10.1002/(sici)1096-8628(19991015)88:5<527::aid-ajmg17>3.0.co;2-4. Am J Med Genet. 1999. PMID: 10490711
Decreasing seasonal variation of births in schizophrenia.
Suvisaari JM, Haukka JK, Tanskanen AJ, Lönnqvist JK. Suvisaari JM, et al. Among authors: lonnqvist jk. Psychol Med. 2000 Mar;30(2):315-24. doi: 10.1017/s0033291700001756. Psychol Med. 2000. PMID: 10824652
593 results