Varilo T - Search Results

1

A balanced translocation truncates Neurotrimin in a family with intracranial and thoracic aortic aneurysm.

Luukkonen TM, Pöyhönen M, Palotie A, Ellonen P, Lagström S, Lee JH, Terwilliger JD, Salonen R, Varilo T. Luukkonen TM, et al. Among authors: varilo t. J Med Genet. 2012 Oct;49(10):621-9. doi: 10.1136/jmedgenet-2012-100977. J Med Genet. 2012. PMID: 23054244 Free PMC article.

2

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.

3

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.

4

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.

5

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.

6

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

7

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

8

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: varilo t. Hum Mol Genet. 2001 Jul 15;10(15):1611-7. doi: 10.1093/hmg/10.15.1611. Hum Mol Genet. 2001. PMID: 11468279

9

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. Among authors: varilo t. Hum Mol Genet. 2001 Dec 15;10(26):3037-48. doi: 10.1093/hmg/10.26.3037. Hum Mol Genet. 2001. PMID: 11751686

10

A genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27.

Auranen M, Vanhala R, Varilo T, Ayers K, Kempas E, Ylisaukko-Oja T, Sinsheimer JS, Peltonen L, Järvelä I. Auranen M, et al. Among authors: varilo t. Am J Hum Genet. 2002 Oct;71(4):777-90. doi: 10.1086/342720. Epub 2002 Aug 21. Am J Hum Genet. 2002. PMID: 12192642 Free PMC article.

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