Ylisaukko-Oja T - Search Results

1

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. 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.

2

Evidence for allelic association on chromosome 3q25-27 in families with autism spectrum disorders originating from a subisolate of Finland.

Auranen M, Varilo T, Alen R, Vanhala R, Ayers K, Kempas E, Ylisaukko-Oja T, Peltonen L, Järvelä I. Auranen M, et al. Mol Psychiatry. 2003 Oct;8(10):879-84. doi: 10.1038/sj.mp.4001299. Mol Psychiatry. 2003. PMID: 14515138

3

Identification of two AGTR2 mutations in male patients with non-syndromic mental retardation.

Ylisaukko-oja T, Rehnström K, Vanhala R, Tengström C, Lähdetie J, Järvelä I. Ylisaukko-oja T, et al. Hum Genet. 2004 Jan;114(2):211-3. doi: 10.1007/s00439-003-1048-8. Epub 2003 Nov 4. Hum Genet. 2004. PMID: 14598163

4

Genome-wide scan for loci of Asperger syndrome.

Ylisaukko-oja T, Nieminen-von Wendt T, Kempas E, Sarenius S, Varilo T, von Wendt L, Peltonen L, Järvelä I. Ylisaukko-oja T, et al. Mol Psychiatry. 2004 Feb;9(2):161-8. doi: 10.1038/sj.mp.4001385. Mol Psychiatry. 2004. PMID: 14966474

5

Exclusion of 14 candidate loci for primary open angle glaucoma in Finnish families.

Lemmelä S, Ylisaukko-oja T, Forsman E, Järvelä I. Lemmelä S, et al. Mol Vis. 2004 Apr 2;10:260-4. Mol Vis. 2004. PMID: 15073581 Free article.

6

Family-based association study of DYX1C1 variants in autism.

Ylisaukko-Oja T, Peyrard-Janvid M, Lindgren CM, Rehnström K, Vanhala R, Peltonen L, Järvelä I, Kere J. Ylisaukko-Oja T, et al. Eur J Hum Genet. 2005 Jan;13(1):127-30. doi: 10.1038/sj.ejhg.5201272. Eur J Hum Genet. 2005. PMID: 15470369

7

MECP2 mutation analysis in patients with mental retardation.

Ylisaukko-Oja T, Rehnström K, Vanhala R, Kempas E, von Koskull H, Tengström C, Mustonen A, Ounap K, Lähdetie J, Järvelä I. Ylisaukko-Oja T, et al. Am J Med Genet A. 2005 Jan 15;132A(2):121-4. doi: 10.1002/ajmg.a.30416. Am J Med Genet A. 2005. PMID: 15578581

8

Subjective face recognition difficulties, aberrant sensibility, sleeping disturbances and aberrant eating habits in families with Asperger syndrome.

Nieminen-von Wendt T, Paavonen JE, Ylisaukko-Oja T, Sarenius S, Källman T, Järvelä I, von Wendt L. Nieminen-von Wendt T, et al. BMC Psychiatry. 2005 Apr 12;5:20. doi: 10.1186/1471-244X-5-20. BMC Psychiatry. 2005. PMID: 15826308 Free PMC article.

9

Analysis of four neuroligin genes as candidates for autism.

Ylisaukko-oja T, Rehnström K, Auranen M, Vanhala R, Alen R, Kempas E, Ellonen P, Turunen JA, Makkonen I, Riikonen R, Nieminen-von Wendt T, von Wendt L, Peltonen L, Järvelä I. Ylisaukko-oja T, et al. Eur J Hum Genet. 2005 Dec;13(12):1285-92. doi: 10.1038/sj.ejhg.5201474. Eur J Hum Genet. 2005. PMID: 16077734

10

A heterogeneity-based genome search meta-analysis for autism-spectrum disorders.

Trikalinos TA, Karvouni A, Zintzaras E, Ylisaukko-oja T, Peltonen L, Järvelä I, Ioannidis JP. Trikalinos TA, et al. Mol Psychiatry. 2006 Jan;11(1):29-36. doi: 10.1038/sj.mp.4001750. Mol Psychiatry. 2006. PMID: 16189507

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