Varilo T - Search Results

1

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.

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

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.

7

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.

8

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.

9

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

10

Linkage disequilibrium in isolated populations: Finland and a young sub-population of Kuusamo.

Varilo T, Laan M, Hovatta I, Wiebe V, Terwilliger JD, Peltonen L. Varilo T, et al. Eur J Hum Genet. 2000 Aug;8(8):604-12. doi: 10.1038/sj.ejhg.5200482. Eur J Hum Genet. 2000. PMID: 10951523

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