Varilo T - Search Results

1

Linkage and linkage disequilibrium scan for autism loci in an extended pedigree from Finland.

Kilpinen H, Ylisaukko-oja T, Rehnström K, Gaál E, Turunen JA, Kempas E, von Wendt L, Varilo T, Peltonen L. Kilpinen H, et al. Among authors: varilo t. Hum Mol Genet. 2009 Aug 1;18(15):2912-21. doi: 10.1093/hmg/ddp229. Epub 2009 May 19. Hum Mol Genet. 2009. PMID: 19454485 Free PMC article.

2

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. Am J Hum Genet. 1996 Mar;58(3):506-12. Am J Hum Genet. 1996. PMID: 8644710 Free PMC article.

3

Tracing an ancestral mutation: genealogical and haplotype analysis of the infantile onset spinocerebellar ataxia locus.

Varilo T, Nikali K, Suomalainen A, Lönnqvist T, Peltonen L. Varilo T, et al. Genome Res. 1996 Sep;6(9):870-5. doi: 10.1101/gr.6.9.870. Genome Res. 1996. PMID: 8889554 Free article.

4

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: varilo t. Am J Hum Genet. 1998 Oct;63(4):1078-85. doi: 10.1086/302064. Am J Hum Genet. 1998. PMID: 9758622 Free PMC article.

5

Assignment of the locus for a new lethal neonatal metabolic syndrome to 2q33-37.

Visapää I, Fellman V, Varilo T, Palotie A, Raivio KO, Peltonen L. Visapää I, et al. Among authors: varilo t. Am J Hum Genet. 1998 Nov;63(5):1396-403. doi: 10.1086/302123. Am J Hum Genet. 1998. PMID: 9792866 Free PMC article.

6

Fine-scale mapping of a novel dementia gene, PLOSL, by linkage disequilibrium.

Pekkarinen P, Kestilä M, Paloneva J, Terwillign J, Varilo T, Järvi O, Hakola P, Peltonen L. Pekkarinen P, et al. Among authors: varilo t. Genomics. 1998 Dec 1;54(2):307-15. doi: 10.1006/geno.1998.5591. Genomics. 1998. PMID: 9828133 Free article.

7

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.

8

Assignment of the locus for hydrolethalus syndrome to a highly restricted region on 11q23-25.

Visapää I, Salonen R, Varilo T, Paavola P, Peltonen L. Visapää I, et al. Among authors: varilo t. Am J Hum Genet. 1999 Oct;65(4):1086-95. doi: 10.1086/302603. Am J Hum Genet. 1999. PMID: 10486328 Free PMC article.

9

A genomewide screen for schizophrenia genes in an isolated Finnish subpopulation, suggesting multiple susceptibility loci.

Hovatta I, Varilo T, Suvisaari J, Terwilliger JD, Ollikainen V, Arajärvi R, Juvonen H, Kokko-Sahin ML, Väisänen L, Mannila H, Lönnqvist J, Peltonen L. Hovatta I, et al. Among authors: varilo t. Am J Hum Genet. 1999 Oct;65(4):1114-24. doi: 10.1086/302567. Am J Hum Genet. 1999. PMID: 10486331 Free PMC article.

10

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: varilo t. Hum Mol Genet. 2000 Apr 12;9(7):1049-57. doi: 10.1093/hmg/9.7.1049. Hum Mol Genet. 2000. PMID: 10767329

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