Moilanen JS - Search Results

1

Analysis of mitochondrial DNA sequences in patients with isolated or combined oxidative phosphorylation system deficiency.

Hinttala R, Smeets R, Moilanen JS, Ugalde C, Uusimaa J, Smeitink JA, Majamaa K. Hinttala R, et al. Among authors: moilanen js. J Med Genet. 2006 Nov;43(11):881-6. doi: 10.1136/jmg.2006.042168. Epub 2006 May 31. J Med Genet. 2006. PMID: 16738010 Free PMC article.

2

Epidemiology of A3243G, the mutation for mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes: prevalence of the mutation in an adult population.

Majamaa K, Moilanen JS, Uimonen S, Remes AM, Salmela PI, Kärppä M, Majamaa-Voltti KA, Rusanen H, Sorri M, Peuhkurinen KJ, Hassinen IE. Majamaa K, et al. Among authors: moilanen js. Am J Hum Genet. 1998 Aug;63(2):447-54. doi: 10.1086/301959. Am J Hum Genet. 1998. PMID: 9683591 Free PMC article.

3

Relative fitness of carriers of the mitochondrial DNA mutation 3243A > G.

Moilanen JS, Majamaa K. Moilanen JS, et al. Eur J Hum Genet. 2001 Jan;9(1):59-62. doi: 10.1038/sj.ejhg.5200550. Eur J Hum Genet. 2001. PMID: 11175302

4

Complex segregation analysis of Parkinson's disease in the Finnish population.

Moilanen JS, Autere JM, Myllylä VV, Majamaa K. Moilanen JS, et al. Hum Genet. 2001 Mar;108(3):184-9. doi: 10.1007/s004390100470. Hum Genet. 2001. PMID: 11354627

5

Hearing impairment in patients with 3243A-->G mtDNA mutation: phenotype and rate of progression.

Uimonen S, Moilanen JS, Sorri M, Hassinen IE, Majamaa K. Uimonen S, et al. Among authors: moilanen js. Hum Genet. 2001 Apr;108(4):284-9. doi: 10.1007/s004390100475. Hum Genet. 2001. PMID: 11379873

6

Phylogenetic network and physicochemical properties of nonsynonymous mutations in the protein-coding genes of human mitochondrial DNA.

Moilanen JS, Majamaa K. Moilanen JS, et al. Mol Biol Evol. 2003 Aug;20(8):1195-210. doi: 10.1093/molbev/msg121. Epub 2003 May 30. Mol Biol Evol. 2003. PMID: 12777521

7

Increased variation in mtDNA in patients with familial sensorineural hearing impairment.

Lehtonen MS, Moilanen JS, Majamaa K. Lehtonen MS, et al. Among authors: moilanen js. Hum Genet. 2003 Aug;113(3):220-7. doi: 10.1007/s00439-003-0966-9. Epub 2003 Jun 12. Hum Genet. 2003. PMID: 12802679

8

Epidemiology of the mitochondrial DNA 8344A>G mutation for the myoclonus epilepsy and ragged red fibres (MERRF) syndrome.

Remes AM, Kärppä M, Moilanen JS, Rusanen H, Hassinen IE, Majamaa K, Uimonen S, Sorri M, Salmela PI, Karvonen SL, Karvonen SL. Remes AM, et al. Among authors: moilanen js. J Neurol Neurosurg Psychiatry. 2003 Aug;74(8):1158-9. doi: 10.1136/jnnp.74.8.1158. J Neurol Neurosurg Psychiatry. 2003. PMID: 12876264 Free PMC article. No abstract available.

9

Lineage-specific selection in human mtDNA: lack of polymorphisms in a segment of MTND5 gene in haplogroup J.

Moilanen JS, Finnila S, Majamaa K. Moilanen JS, et al. Mol Biol Evol. 2003 Dec;20(12):2132-42. doi: 10.1093/molbev/msg230. Epub 2003 Aug 29. Mol Biol Evol. 2003. PMID: 12949126

10

Mitochondrial DNA polymorphisms as risk factors for Parkinson's disease and Parkinson's disease dementia.

Autere J, Moilanen JS, Finnilä S, Soininen H, Mannermaa A, Hartikainen P, Hallikainen M, Majamaa K. Autere J, et al. Among authors: moilanen js. Hum Genet. 2004 Jun;115(1):29-35. doi: 10.1007/s00439-004-1123-9. Epub 2004 Apr 24. Hum Genet. 2004. PMID: 15108120

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