Peltonen L - Search Results

1

Genome-wide scan for schizophrenia in the Finnish population: evidence for a locus on chromosome 7q22.

Ekelund J, Lichtermann D, Hovatta I, Ellonen P, Suvisaari J, Terwilliger JD, Juvonen H, Varilo T, Arajärvi R, Kokko-Sahin ML, Lönnqvist J, Peltonen L. Ekelund J, et al. Among authors: peltonen l. Hum Mol Genet. 2000 Apr 12;9(7):1049-57. doi: 10.1093/hmg/9.7.1049. Hum Mol Genet. 2000. PMID: 10767329

2

Linkage analysis in two schizophrenic families originating from a restricted subpopulation of Finland.

Hovatta I, Seppälä J, Pekkarinen P, Tanskanen A, Lönnqvist J, Peltonen L. Hovatta I, et al. Among authors: peltonen l. Psychiatr Genet. 1994 Fall;4(3):143-52. doi: 10.1097/00041444-199400430-00004. Psychiatr Genet. 1994. PMID: 7719700

3

Random search for shared chromosomal regions in four affected individuals: the assignment of a new hereditary ataxia locus.

Nikali K, Suomalainen A, Terwilliger J, Koskinen T, Weissenbach J, Peltonen L. Nikali K, et al. Among authors: peltonen l. Am J Hum Genet. 1995 May;56(5):1088-95. Am J Hum Genet. 1995. PMID: 7726163 Free PMC article.

4

The age of human mutation: genealogical and linkage disequilibrium analysis of the CLN5 mutation in the Finnish population.

Varilo T, Savukoski M, Norio R, Santavuori P, Peltonen L, Järvelä I. Varilo T, et al. Among authors: peltonen l. Am J Hum Genet. 1996 Mar;58(3):506-12. Am J Hum Genet. 1996. PMID: 8644710 Free PMC article.

5

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: peltonen l. Am J Med Genet. 1997 Jul 25;74(4):353-60. Am J Med Genet. 1997. PMID: 9259368

6

Genomewide scan of multiple sclerosis in Finnish multiplex families.

Kuokkanen S, Gschwend M, Rioux JD, Daly MJ, Terwilliger JD, Tienari PJ, Wikström J, Palo J, Stein LD, Hudson TJ, Lander ES, Peltonen L. Kuokkanen S, et al. Among authors: peltonen l. Am J Hum Genet. 1997 Dec;61(6):1379-87. doi: 10.1086/301637. Am J Hum Genet. 1997. PMID: 9399895 Free PMC article.

7

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: peltonen l. Am J Hum Genet. 1998 Feb;62(2):362-72. doi: 10.1086/301722. Am J Hum Genet. 1998. PMID: 9463329 Free PMC article.

8

Linkage of familial combined hyperlipidaemia to chromosome 1q21-q23.

Pajukanta P, Nuotio I, Terwilliger JD, Porkka KV, Ylitalo K, Pihlajamäki J, Suomalainen AJ, Syvänen AC, Lehtimäki T, Viikari JS, Laakso M, Taskinen MR, Ehnholm C, Peltonen L. Pajukanta P, et al. Among authors: peltonen l. Nat Genet. 1998 Apr;18(4):369-73. doi: 10.1038/ng0498-369. Nat Genet. 1998. PMID: 9537421

9

Assignment of the locus for congenital lactase deficiency to 2q21, in the vicinity of but separate from the lactase-phlorizin hydrolase gene.

Järvelä I, Enattah NS, Kokkonen J, Varilo T, Savilahti E, Peltonen L. Järvelä I, et al. Among authors: peltonen l. Am J Hum Genet. 1998 Oct;63(4):1078-85. doi: 10.1086/302064. Am J Hum Genet. 1998. PMID: 9758622 Free PMC article.

10

Concordance for sex and the pseudoautosomal gene hypothesis revisited: no evidence of increased sex concordance in a nationwide Finnish sample of siblings with paternally derived schizophrenia.

Lichtermann D, Hovatta I, Terwilliger JD, Peltonen L, Lönnqvist J. Lichtermann D, et al. Among authors: peltonen l. Am J Psychiatry. 1998 Oct;155(10):1365-75. doi: 10.1176/ajp.155.10.1365. Am J Psychiatry. 1998. PMID: 9766768

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