Paunio T - Search Results

1

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: paunio 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.

2

Applications of PCR in the diseases of genetic isolates.

Peltonen L, Ikonen E, Paunio T. Peltonen L, et al. Among authors: paunio t. Ann Med. 1992 Jun;24(3):191-4. doi: 10.3109/07853899209147820. Ann Med. 1992. PMID: 1627315 No abstract available.

3

Haplotype analysis in gelsolin-related amyloidosis reveals independent origin of identical mutation (G654A) of gelsolin in Finland and Japan.

Paunio T, Sunada Y, Kiuru S, Makishita H, Ikeda S, Weissenbach J, Palo J, Peltonen L. Paunio T, et al. Hum Mutat. 1995;6(1):60-5. doi: 10.1002/humu.1380060112. Hum Mutat. 1995. PMID: 7550233

4

Toward understanding the pathogenic mechanisms in gelsolin-related amyloidosis: in vitro expression reveals an abnormal gelsolin fragment.

Paunio T, Kangas H, Kalkkinen N, Haltia M, Palo J, Peltonen L. Paunio T, et al. Hum Mol Genet. 1994 Dec;3(12):2223-9. doi: 10.1093/hmg/3.12.2223. Hum Mol Genet. 1994. PMID: 7881424

5

In vitro expression analysis shows that the secretory form of gelsolin is the sole source of amyloid in gelsolin-related amyloidosis.

Kangas H, Paunio T, Kalkkinen N, Jalanko A, Peltonen L. Kangas H, et al. Among authors: paunio t. Hum Mol Genet. 1996 Sep;5(9):1237-43. doi: 10.1093/hmg/5.9.1237. Hum Mol Genet. 1996. PMID: 8872462

6

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

7

Genome-wide scan in a nationwide study sample of schizophrenia families in Finland reveals susceptibility loci on chromosomes 2q and 5q.

Paunio T, Ekelund J, Varilo T, Parker A, Hovatta I, Turunen JA, Rinard K, Foti A, Terwilliger JD, Juvonen H, Suvisaari J, Arajärvi R, Suokas J, Partonen T, Lönnqvist J, Meyer J, Peltonen L. Paunio T, et al. Hum Mol Genet. 2001 Dec 15;10(26):3037-48. doi: 10.1093/hmg/10.26.3037. Hum Mol Genet. 2001. PMID: 11751686

8

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

9

Heritability and number of quantitative trait loci of neurocognitive functions in families with schizophrenia.

Tuulio-Henriksson A, Haukka J, Partonen T, Varilo T, Paunio T, Ekelund J, Cannon TD, Meyer JM, Lönnqvist J. Tuulio-Henriksson A, et al. Among authors: paunio t. Am J Med Genet. 2002 Jul 8;114(5):483-90. doi: 10.1002/ajmg.10480. Am J Med Genet. 2002. PMID: 12116181

10

RHD maternal-fetal genotype incompatibility increases schizophrenia susceptibility.

Palmer CG, Turunen JA, Sinsheimer JS, Minassian S, Paunio T, Lönnqvist J, Peltonen L, Woodward JA. Palmer CG, et al. Among authors: paunio t. Am J Hum Genet. 2002 Dec;71(6):1312-9. doi: 10.1086/344659. Epub 2002 Nov 18. Am J Hum Genet. 2002. PMID: 12439825 Free PMC article.

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