Järvelä I - Search Results

1

Genome-wide scan of exfoliation syndrome.

Lemmelä S, Forsman E, Sistonen P, Eriksson A, Forsius H, Järvelä I. Lemmelä S, et al. Among authors: jarvela i. Invest Ophthalmol Vis Sci. 2007 Sep;48(9):4136-42. doi: 10.1167/iovs.06-1092. Invest Ophthalmol Vis Sci. 2007. PMID: 17724198

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

The role of TIGR and OPTN in Finnish glaucoma families: a clinical and molecular genetic study.

Forsman E, Lemmelä S, Varilo T, Kristo P, Forsius H, Sankila EM, Järvelä I. Forsman E, et al. Among authors: jarvela i. Mol Vis. 2003 May 30;9:217-22. Mol Vis. 2003. PMID: 12789137 Free article.

4

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

5

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

6

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.

7

Penetrance and phenotype of the Thr377Met Myocilin mutation in a large Finnish family with juvenile- and adult-onset primary open-angle glaucoma.

Puska P, Lemmelä S, Kristo P, Sankila EM, Järvelä I. Puska P, et al. Among authors: jarvela i. Ophthalmic Genet. 2005 Mar;26(1):17-23. doi: 10.1080/13816810590918208. Ophthalmic Genet. 2005. PMID: 15823921

8

Sequence analysis of the genes encoding for H+/K+-ATPase in autoimmune gastritis.

Oksanen AM, Lemmelä SM, Järvelä IE, Rautelin HI. Oksanen AM, et al. Among authors: jarvela ie. Ann Med. 2006;38(4):287-93. doi: 10.1080/07853890600673260. Ann Med. 2006. PMID: 16754260

9

Analysis of variants in the complement factor H, the elongation of very long chain fatty acids-like 4 and the hemicentin 1 genes of age-related macular degeneration in the Finnish population.

Seitsonen S, Lemmelä S, Holopainen J, Tommila P, Ranta P, Kotamies A, Moilanen J, Palosaari T, Kaarniranta K, Meri S, Immonen I, Järvelä I. Seitsonen S, et al. Among authors: jarvela i. Mol Vis. 2006 Jul 20;12:796-801. Mol Vis. 2006. PMID: 16885922 Free article.

10

Exfoliation syndrome: prevalence and inheritance in a subisolate of the Finnish population.

Forsman E, Cantor RM, Lu A, Eriksson A, Fellman J, Järvelä I, Forsius H. Forsman E, et al. Among authors: jarvela i. Acta Ophthalmol Scand. 2007 Aug;85(5):500-7. doi: 10.1111/j.1600-0420.2007.00978.x. Acta Ophthalmol Scand. 2007. PMID: 17655611 Free article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

223 results

Search Page