No evidence for shared etiology in two demyelinative disorders, MS and PLOSL

Por Sulonen, Anna-Maija, Kallio, Suvi P., Ellonen, Pekka, Suvela, Minna, Elovaara, Irina, Koivisto, Keijo, Pirttilä, Tuula, Reunanen, Mauri, Tienari, Pentti J., Palotie, Aarno, Peltonen, Leena, Saarela, Janna
Publicado em 2008

PRKCA and Multiple Sclerosis: Association in Two Independent Populations

Por Saarela, Janna, Kallio, Suvi P, Chen, Daniel, Montpetit, Alexandre, Jokiaho, Anne, Choi, Eva, Asselta, Rosanna, Bronnikov, Denis, Lincoln, Matthew R, Sadovnick, A. Dessa, Tienari, Pentti J, Koivisto, Keijo, Palotie, Aarno, Ebers, George C, Hudson, Thomas J, Peltonen, Leena
Publicado em 2006

Use of a genetic isolate to identify rare disease variants: C7 on 5p associated with MS

Por Kallio, Suvi P., Jakkula, Eveliina, Purcell, Shaun, Suvela, Minna, Koivisto, Keijo, Tienari, Pentti J., Elovaara, Irina, Pirttilä, Tuula, Reunanen, Mauri, Bronnikov, Denis, Viander, Markku, Meri, Seppo, Hillert, Jan, Lundmark, Frida, Harbo, Hanne F., Lorentzen, Åslaug R., De Jager, Philip L., Daly, Mark J., Hafler, David A., Palotie, Aarno, Peltonen, Leena, Saarela, Janna
Publicado em 2009

Genome-wide Association Study in a High-Risk Isolate for Multiple Sclerosis Reveals Associated Variants in STAT3 Gene

Por Jakkula, Eveliina, Leppä, Virpi, Sulonen, Anna-Maija, Varilo, Teppo, Kallio, Suvi, Kemppinen, Anu, Purcell, Shaun, Koivisto, Keijo, Tienari, Pentti, Sumelahti, Marja-Liisa, Elovaara, Irina, Pirttilä, Tuula, Reunanen, Mauri, Aromaa, Arpo, Oturai, Annette Bang, Søndergaard, Helle Bach, Harbo, Hanne F., Mero, Inger-Lise, Gabriel, Stacey B., Mirel, Daniel B., Hauser, Stephen L., Kappos, Ludwig, Polman, Chris, De Jager, Philip L., Hafler, David A., Daly, Mark J., Palotie, Aarno, Saarela, Janna, Peltonen, Leena
Publicado em 2010