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Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.
Nature. 2011 Aug 10;476(7359):214-9. doi: 10.1038/nature10251.
Nature. 2011.
PMID: 21833088
Free PMC article.
Genome-wide association study in a high-risk isolate for multiple sclerosis reveals associated variants in STAT3 gene.
Jakkula E, Leppä V, Sulonen AM, Varilo T, Kallio S, Kemppinen A, Purcell S, Koivisto K, Tienari P, Sumelahti ML, Elovaara I, Pirttilä T, Reunanen M, Aromaa A, Oturai AB, Søndergaard HB, Harbo HF, Mero IL, Gabriel SB, Mirel DB, Hauser SL, Kappos L, Polman C, De Jager PL, Hafler DA, Daly MJ, Palotie A, Saarela J, Peltonen L.
Jakkula E, et al. Among authors: sulonen am.
Am J Hum Genet. 2010 Feb 12;86(2):285-91. doi: 10.1016/j.ajhg.2010.01.017.
Am J Hum Genet. 2010.
PMID: 20159113
Free PMC article.
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A "candidate-interactome" aggregate analysis of genome-wide association data in multiple sclerosis.
Mechelli R, Umeton R, Policano C, Annibali V, Coarelli G, Ricigliano VA, Vittori D, Fornasiero A, Buscarinu MC; International Multiple Sclerosis Genetics Consortium; Wellcome Trust Case Control Consortium,2; Romano S, Salvetti M, Ristori G.
Mechelli R, et al.
PLoS One. 2013 May 16;8(5):e63300. doi: 10.1371/journal.pone.0063300. Print 2013.
PLoS One. 2013.
PMID: 23696811
Free PMC article.
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mtDNA nt13708A variant increases the risk of multiple sclerosis.
Yu X, Koczan D, Sulonen AM, Akkad DA, Kroner A, Comabella M, Costa G, Corongiu D, Goertsches R, Camina-Tato M, Thiesen HJ, Nyland HI, Mørk SJ, Montalban X, Rieckmann P, Marrosu MG, Myhr KM, Epplen JT, Saarela J, Ibrahim SM.
Yu X, et al. Among authors: sulonen am.
PLoS One. 2008 Feb 13;3(2):e1530. doi: 10.1371/journal.pone.0001530.
PLoS One. 2008.
PMID: 18270557
Free PMC article.
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No evidence for shared etiology in two demyelinative disorders, MS and PLOSL.
Sulonen AM, Kallio SP, Ellonen P, Suvela M, Elovaara I, Koivisto K, Pirttilä T, Reunanen M, Tienari PJ, Palotie A, Peltonen L, Saarela J.
Sulonen AM, et al.
J Neuroimmunol. 2009 Jan 3;206(1-2):86-90. doi: 10.1016/j.jneuroim.2008.10.005. Epub 2008 Nov 18.
J Neuroimmunol. 2009.
PMID: 19019460
Free PMC article.
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Comparison of solution-based exome capture methods for next generation sequencing.
Sulonen AM, Ellonen P, Almusa H, Lepistö M, Eldfors S, Hannula S, Miettinen T, Tyynismaa H, Salo P, Heckman C, Joensuu H, Raivio T, Suomalainen A, Saarela J.
Sulonen AM, et al.
Genome Biol. 2011 Sep 28;12(9):R94. doi: 10.1186/gb-2011-12-9-r94.
Genome Biol. 2011.
PMID: 21955854
Free PMC article.
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Haplotype information of large neuromuscular disease genes provided by linked-read sequencing has a potential to increase diagnostic yield.
Lehtonen J, Sulonen AM, Almusa H, Lehtokari VL, Johari M, Palva A, Hakonen AH, Wartiovaara K, Lehesjoki AE, Udd B, Wallgren-Pettersson C, Pelin K, Savarese M, Saarela J.
Lehtonen J, et al. Among authors: sulonen am.
Sci Rep. 2024 Feb 21;14(1):4306. doi: 10.1038/s41598-024-54866-4.
Sci Rep. 2024.
PMID: 38383731
Free PMC article.
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