Järvelä I - Search Results

1

Association and Promoter Analysis of AVPR1A in Finnish Autism Families.

Kantojärvi K, Oikkonen J, Kotala I, Kallela J, Vanhala R, Onkamo P, Järvelä I. Kantojärvi K, et al. Among authors: jarvela i. Autism Res. 2015 Oct;8(5):634-9. doi: 10.1002/aur.1473. Epub 2015 Feb 23. Autism Res. 2015. PMID: 25707602

2

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

3

MECP2 gene analysis in classical Rett syndrome and in patients with Rett-like features.

Auranen M, Vanhala R, Vosman M, Levander M, Varilo T, Hietala M, Riikonen R, Peltonen L, Järvelä I. Auranen M, et al. Among authors: jarvela i. Neurology. 2001 Mar 13;56(5):611-7. doi: 10.1212/wnl.56.5.611. Neurology. 2001. PMID: 11245712

4

[First gene connected to autism spectrum disorders has been found].

Auranen M, Vanhala R, Järvelä I. Auranen M, et al. Among authors: jarvela i. Duodecim. 2000;116(20):2185-7. Duodecim. 2000. PMID: 12017623 Finnish. No abstract available.

5

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.

6

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

7

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. Among authors: jarvela i. Hum Genet. 2004 Jan;114(2):211-3. doi: 10.1007/s00439-003-1048-8. Epub 2003 Nov 4. Hum Genet. 2004. PMID: 14598163

8

The genetic variant of lactase persistence C (-13910) T as a risk factor for type I and II diabetes in the Finnish population.

Enattah NS, Forsblom C, Rasinperä H, Tuomi T, Groop PH, Järvelä I; FinnDiane Study Group. Enattah NS, et al. Among authors: jarvela i. Eur J Clin Nutr. 2004 Sep;58(9):1319-22. doi: 10.1038/sj.ejcn.1601971. Eur J Clin Nutr. 2004. PMID: 15054412

9

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

10

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. Among authors: jarvela i. 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

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