Järvelä I - Search Results

1

Search for autism loci by combined analysis of Autism Genetic Resource Exchange and Finnish families.

Ylisaukko-oja T, Alarcón M, Cantor RM, Auranen M, Vanhala R, Kempas E, von Wendt L, Järvelä I, Geschwind DH, Peltonen L. Ylisaukko-oja T, et al. Among authors: jarvela i. Ann Neurol. 2006 Jan;59(1):145-55. doi: 10.1002/ana.20722. Ann Neurol. 2006. PMID: 16288458

2

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: jarvela i. 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.

3

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. Among authors: jarvela i. Mol Vis. 2004 Apr 2;10:260-4. Mol Vis. 2004. PMID: 15073581 Free article.

4

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. Among authors: jarvela i. Eur J Hum Genet. 2005 Jan;13(1):127-30. doi: 10.1038/sj.ejhg.5201272. Eur J Hum Genet. 2005. PMID: 15470369

5

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. Among authors: jarvela i. Eur J Hum Genet. 2005 Dec;13(12):1285-92. doi: 10.1038/sj.ejhg.5201474. Eur J Hum Genet. 2005. PMID: 16077734

6

Allelic variants in HTR3C show association with autism.

Rehnström K, Ylisaukko-oja T, Nummela I, Ellonen P, Kempas E, Vanhala R, von Wendt L, Järvelä I, Peltonen L. Rehnström K, et al. Among authors: jarvela i. Am J Med Genet B Neuropsychiatr Genet. 2009 Jul 5;150B(5):741-6. doi: 10.1002/ajmg.b.30882. Am J Med Genet B Neuropsychiatr Genet. 2009. PMID: 19035560 Free PMC article.

7

Analysis of autism susceptibility gene loci on chromosomes 1p, 4p, 6q, 7q, 13q, 15q, 16p, 17q, 19q and 22q in Finnish multiplex families.

Auranen M, Nieminen T, Majuri S, Vanhala R, Peltonen L, Järvelä I. Auranen M, et al. Among authors: jarvela i. Mol Psychiatry. 2000 May;5(3):320-2. doi: 10.1038/sj.mp.4000708. Mol Psychiatry. 2000. PMID: 10889536

8

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. Among authors: jarvela i. Mol Psychiatry. 2003 Oct;8(10):879-84. doi: 10.1038/sj.mp.4001299. Mol Psychiatry. 2003. PMID: 14515138

9

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. Among authors: jarvela i. Mol Psychiatry. 2004 Feb;9(2):161-8. doi: 10.1038/sj.mp.4001385. Mol Psychiatry. 2004. PMID: 14966474

10

Analysis of 9p24 and 11p12-13 regions in autism spectrum disorders: rs1340513 in the JMJD2C gene is associated with ASDs in Finnish sample.

Kantojärvi K, Onkamo P, Vanhala R, Alen R, Hedman M, Sajantila A, Nieminen-von Wendt T, Järvelä I. Kantojärvi K, et al. Among authors: jarvela i. Psychiatr Genet. 2010 Jun;20(3):102-8. doi: 10.1097/YPG.0b013e32833a2080. Psychiatr Genet. 2010. PMID: 20410850

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