Works by Finnilä, Saara

Results: 11

Sequence Variation in the tRNA Genes of Human Mitochondrial DNA.

Published in:

Journal of Molecular Evolution, 2005, v. 60, n. 5, p. 587, doi. 10.1007/s00239-003-0202-1

By:

Vilmi, Tiina;
Moilanen, Jukka S.;
Finnilä, Saara;
Majamaa, Kari;
Cerff, Rüdiger

Publication type:

Article

Adult‐onset ataxia and polyneuropathy caused by mitochondrial 8993T→C mutation.

Published in:

Annals of Neurology, 2005, v. 58, n. 2, p. 337

By:

Maria T. Rantamäki;
Heidi K. Soini;
Saara M. Finnilä;
Kari Majamaa;
Bjarne Udd

Publication type:

Article

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

Published in:

Human Genetics, 2004, v. 115, n. 1, p. 29, doi. 10.1007/s00439-004-1123-9

By:

Autere, Jaana;
Moilanen, Jukka S.;
Finnilä, Saara;
Soininen, Hilkka;
Mannermaa, Arto;
Hartikainen, Päivi;
Hallikainen, Merja;
Majamaa, Kari

Publication type:

Article

A novel mitochondrial DNA mutation and a mutation in the Notch3 gene in a patient with myopathy and CADASIL.

Published in:

Journal of Molecular Medicine, 2001, v. 79, n. 11, p. 641, doi. 10.1007/s001090100268

By:

Finnilä, Saara;
Tuisku, Seppo;
Herva, Riitta;
Majamaa, Kari

Publication type:

Article

Mitochondrial DNA variant m.15218A > G in Finnish epilepsy patients who have maternal relatives with epilepsy, sensorineural hearing impairment or diabetes mellitus.

Published in:

BMC Medical Genetics, 2013, v. 14, n. 1, p. 1, doi. 10.1186/1471-2350-14-73

By:

Soini, Heidi K.;
Moilanen, Jukka S.;
Vilmi-Kerälä, Tiina;
Finnilä, Saara;
Majamaa, Kari

Publication type:

Article

POLG1 p.R722H mutation associated with multiple mtDNA deletions and a neurological phenotype.

Published in:

BMC Neurology, 2010, v. 10, p. 29, doi. 10.1186/1471-2377-10-29

By:

Komulainen, Tuomas;
Hinttala, Reetta;
Kärppä, Mikko;
Pajunen, Leila;
Finnilä, Saara;
Tuominen, Hannu;
Rantala, Heikki;
Hassinen, Ilmo;
Majamaa, Kari;
Uusimaa, Johanna

Publication type:

Article

Mitochondrial DNA sequence variation and mutation rate in patients with CADASIL.

Published in:

2006

By:

Annunen-Rasila, Johanna;
Finnilä, Saara;
Mykkänen, Kati;
Moilanen, Jukka;
Veijola, Johanna;
Pöyhönen, Minna;
Viitanen, Matti;
Kalimo, Hannu;
Majamaa, Kari

Publication type:

Correction Notice

Mitochondrial DNA sequence variation and mutation rate in patients with CADASIL.

Published in:

Neurogenetics, 2006, v. 7, n. 3, p. 185, doi. 10.1007/s10048-006-0049-x

By:

Annunen-Rasila, Johanna;
Finnilä, Saara;
Mykkänen, Kati;
Moilanen, Jukka S.;
Veijola, Johanna;
Pöyhönen, Minna;
Viitanen, Matti;
Kalimo, Hannu;
Majamaa, Kari

Publication type:

Article

Hydrolethalus syndrome is caused by a missense mutation in a novel gene HYLS1.

Published in:

Human Molecular Genetics, 2005, v. 14, n. 11, p. 1475, doi. 10.1093/hmg/ddi157

By:

Mee, Lisa;
Honkala, Heli;
Kopra, Outi;
Vesa, Jouni;
Finnilä, Saara;
Visapää, Ilona;
Sang, Tzu-Kang;
Jackson, George R.;
Salonen, Riitta;
Kestilä, Marjo;
Peltonen, Leena

Publication type:

Article

Fine mapping of a multiple sclerosis locus to 2.5 Mb on chromosome 17q22–q24.

Published in:

Human Molecular Genetics, 2002, v. 11, n. 19, p. 2257, doi. 10.1093/hmg/11.19.2257

By:

Saarela, Janna;
Schoenberg Fejzo, Marlena;
Chen, Daniel;
Finnilä, Saara;
Parkkonen, Maikki;
Kuokkanen, Satu;
Sobel, Eric;
Tienari, Pentti J.;
Sumelahti, Marja-Liisa;
Wikström, Juhani;
Elovaara, Irina;
Koivisto, Keijo;
Pirttilä, Tuula;
Reunanen, Mauri;
Palotie, Aarno;
Peltonen, Leena

Publication type:

Article

Evidence for mtDNA Admixture between the Finns and the Saami.

Published in:

Human Heredity, 2001, v. 52, n. 3, p. 160, doi. 10.1159/000053372

By:

Meinilä, Maria;
Finnilä, Saara;
Majamaa, Kari

Publication type:

Article