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

Genetic risk for multiple sclerosis (MS) is thought to involve both common and rare risk alleles. Recent GWAS and subsequent meta-analysis have established the critical role of the HLA locus and identified new common variants associated to MS. These variants have small odds ratios (ORs) and explain...

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Main Authors: 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
格式: Artigo
語言:Inglês
出版: Elsevier 2010
主題:
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在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC2820168/
https://ncbi.nlm.nih.gov/pubmed/20159113
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajhg.2010.01.017
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