7 results on '"Sulonen, Anna-Maija"'
Search Results
2. No evidence for shared etiology in two demyelinative disorders, MS and PLOSL
- Author
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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, and Saarela, Janna
- Published
- 2009
- Full Text
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3. Genome-wide association study in a high-risk isolate for multiple sclerosis reveals associated variants in STAT3 gene
- Author
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Jakkula, Eveliina, Sulonen, Anna-Maija, Leppa, Virpi, Varilo, Teppo, Kallio, Suvi, Kemppinen, Anu, Purcell, Shaun, Tienari, Pentti, Koivisto, Keijo, Sumelahti, Marja-Liisa, Elovaara, Irina, Pirttila, Tuula, Reunanen, Mauri, Sondergaard, Helle Bach, Aromaa, Arpo, Oturai, Annette Bang, Harbo, Hanne F., Mero, Inger-Lise, Gabriel, Stacey B., Kappos, Ludwig, Polamn, Chris, De Jager, Philip L., Mirel, Daniel B., Hauser, Stephen L., Hafler, David A., Daly, Mark J., Palotie, Aarno, Saarela, Janna, and Peltonen, Leena
- Subjects
Multiple sclerosis -- Genetic aspects ,Multiple sclerosis -- Risk factors ,Genetic variation -- Research ,Biological sciences - Abstract
A genome-wide association study is undertaken in a high-risk isolate for multiple sclerosis (MS) in order to identify previously unreported high-impact variants associated with MS. Results reveal that SNP (rs744166) within the STAT3 gene is associated with MS.
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- 2010
4. Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
- Author
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Sawcer, Stephen, Hellenthal, Garrett, Pirinen, Matti, Spencer, Chris C. A., Patsopoulos, Nikolaos A., Moutsianas, Loukas, Dilthey, Alexander, Su, Zhan, Freeman, Colin, Hunt, Sarah E., Edkins, Sarah, Gray, Emma, Booth, David R., Potter, Simon C., Goris, An, Band, Gavin, Bang Oturai, Annette, Strange, Amy, Saarela, Janna, Bellenguez, Céline, Fontaine, Bertrand, Gillman, Matthew, Hemmer, Bernhard, Gwilliam, Rhian, Zipp, Frauke, Jayakumar, Alagurevathi, Martin, Roland, Leslie, Stephen, Hawkins, Stanley, Giannoulatou, Eleni, D’alfonso, Sandra, Blackburn, Hannah, Martinelli Boneschi, Filippo, Liddle, Jennifer, Harbo, Hanne F., Perez, Marc L., Spurkland, Anne, Waller, Matthew J., Mycko, Marcin P., Ricketts, Michelle, Comabella, Manuel, Hammond, Naomi, Kockum, Ingrid, McCann, Owen T., Ban, Maria, Whittaker, Pamela, Kemppinen, Anu, Weston, Paul, Hawkins, Clive, Widaa, Sara, Zajicek, John, Dronov, Serge, Robertson, Neil, Bumpstead, Suzannah J., Barcellos, Lisa F., Ravindrarajah, Rathi, Abraham, Roby, Alfredsson, Lars, Ardlie, Kristin, Aubin, Cristin, Baker, Amie, Baker, Katharine, Baranzini, Sergio E., Bergamaschi, Laura, Bergamaschi, Roberto, Bernstein, Allan, Berthele, Achim, Boggild, Mike, Bradfield, Jonathan P., Brassat, David, Broadley, Simon A., Buck, Dorothea, Butzkueven, Helmut, Capra, Ruggero, Carroll, William M., Cavalla, Paola, Celius, Elisabeth G., Cepok, Sabine, Chiavacci, Rosetta, Clerget-Darpoux, Françoise, Clysters, Katleen, Comi, Giancarlo, Cossburn, Mark, Cournu-Rebeix, Isabelle, Cox, Mathew B., Cozen, Wendy, Cree, Bruce A. C., Cross, Anne H., Cusi, Daniele, Daly, Mark J., Davis, Emma, de Bakker, Paul I. W., Debouverie, Marc, D’hooghe, Marie Beatrice, Dixon, Katherine, Dobosi, Rita, Dubois, Bénédicte, Ellinghaus, David, Elovaara, Irina, Esposito, Federica, Fontenille, Claire, Foote, Simon, Franke, Andre, Galimberti, Daniela, Ghezzi, Angelo, Glessner, Joseph, Gomez, Refujia, Gout, Olivier, Graham, Colin, Grant, Struan F. A., Rosa Guerini, Franca, Hakonarson, Hakon, Hall, Per, Hamsten, Anders, Hartung, Hans-Peter, Heard, Rob N., Heath, Simon, Hobart, Jeremy, Hoshi, Muna, Infante-Duarte, Carmen, Ingram, Gillian, Ingram, Wendy, Islam, Talat, Jagodic, Maja, Kabesch, Michael, Kermode, Allan G., Kilpatrick, Trevor J., Kim, Cecilia, Klopp, Norman, Koivisto, Keijo, Larsson, Malin, Lathrop, Mark, Lechner-Scott, Jeannette S., Leone, Maurizio A., Leppä, Virpi, Liljedahl, Ulrika, Lima Bomfim, Izaura, Lincoln, Robin R., Link, Jenny, Liu, Jianjun, Lorentzen, Åslaug R., Lupoli, Sara, Macciardi, Fabio, Mack, Thomas, Marriott, Mark, Martinelli, Vittorio, Mason, Deborah, McCauley, Jacob L., Mentch, Frank, Mero, Inger-Lise, Mihalova, Tania, Montalban, Xavier, Mottershead, John, Myhr, Kjell-Morten, Naldi, Paola, Ollier, William, Page, Alison, Palotie, Aarno, Pelletier, Jean, Piccio, Laura, Pickersgill, Trevor, Piehl, Fredrik, Pobywajlo, Susan, Quach, Hong L., Ramsay, Patricia P., Reunanen, Mauri, Reynolds, Richard, Rioux, John D., Rodegher, Mariaemma, Roesner, Sabine, Rubio, Justin P., Rückert, Ina-Maria, Salvetti, Marco, Salvi, Erika, Santaniello, Adam, Schaefer, Catherine A., Schreiber, Stefan, Schulze, Christian, Scott, Rodney J., Sellebjerg, Finn, Selmaj, Krzysztof W., Sexton, David, Shen, Ling, Simms-Acuna, Brigid, Skidmore, Sheila, Sleiman, Patrick M. A., Smestad, Cathrine, Sørensen, Per Soelberg, Søndergaard, Helle Bach, Stankovich, Jim, Strange, Richard C., Sulonen, Anna-Maija, Sundqvist, Emilie, Syvänen, Ann-Christine, Taddeo, Francesca, Taylor, Bruce, Blackwell, Jenefer M., Tienari, Pentti, Bramon, Elvira, Tourbah, Ayman, Brown, Matthew A., Tronczynska, Ewa, Casas, Juan P., Tubridy, Niall, Corvin, Aiden, Vickery, Jane, Jankowski, Janusz, Villoslada, Pablo, Markus, Hugh S., Wang, Kai, Mathew, Christopher G., Wason, James, Palmer, Colin N. A., Wichmann, H-Erich, Plomin, Robert, Willoughby, Ernest, Rautanen, Anna, Winkelmann, Juliane, Wittig, Michael, Trembath, Richard C., Yaouanq, Jacqueline, Viswanathan, Ananth C., Zhang, Haitao, Wood, Nicholas W., Zuvich, Rebecca, Deloukas, Panos, Langford, Cordelia, Duncanson, Audrey, Oksenberg, Jorge R., Pericak-Vance, Margaret A., Haines, Jonathan L., Olsson, Tomas, Hillert, Jan, Ivinson, Adrian J., De Jager, Philip L., Peltonen, Leena, Stewart, Graeme J., Hafler, David A., Hauser, Stephen L., McVean, Gil, Donnelly, Peter, and Compston, Alastair
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- 2011
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5. Comparison of solution-based exome capture methods for next generation sequencing
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Sulonen, Anna-Maija, primary, Ellonen, Pekka, additional, Almusa, Henrikki, additional, Lepistö, Maija, additional, Eldfors, Samuli, additional, Hannula, Sari, additional, Miettinen, Timo, additional, Tyynismaa, Henna, additional, Salo, Perttu, additional, Heckman, Caroline, additional, Joensuu, Heikki, additional, Raivio, Taneli, additional, Suomalainen, Anu, additional, and Saarela, Janna, additional
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- 2011
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6. mtDNA nt13708A Variant Increases the Risk of Multiple Sclerosis
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Yu, Xinhua, primary, Koczan, Dirk, additional, Sulonen, Anna-Maija, additional, Akkad, Denis A., additional, Kroner, Antje, additional, Comabella, Manuel, additional, Costa, Gianna, additional, Corongiu, Daniela, additional, Goertsches, Robert, additional, Camina-Tato, Montserrat, additional, Thiesen, Hans-Juergen, additional, Nyland, Harald I., additional, Mørk, Sverre J., additional, Montalban, Xavier, additional, Rieckmann, Peter, additional, Marrosu, Maria G., additional, Myhr, Kjell-Morten, additional, Epplen, Joerg T., additional, Saarela, Janna, additional, and Ibrahim, Saleh M., additional
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- 2008
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7. mtDNA nt13708A Variant Increases the Risk of Multiple Sclerosis.
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Xinhua Yu, Koczan, Dirk, Sulonen, Anna-Maija, Akkad, Denis A., Kroner, Antje, Comabella, Manuel, Costa, Gianna, Corongiu, Daniela, Goertsches, Robert, Camina-Tato, Montserrat, Thiesen, Hans-Juergen, Nyland, Harald I., Mørk, Sverre J., Montalban, Xavier, Rieckmann, Peter, Marrosu, Maria G., Myhr, Kjell-Morten, Epplen, Joerg T., Saarela, Janna, and Ibrahim, Saleh M.
- Subjects
MITOCHONDRIAL DNA ,GENETIC polymorphisms ,MULTIPLE sclerosis ,NUCLEOTIDES ,DISEASE progression ,DISEASE susceptibility ,NUCLEOTIDE sequence ,MEDICAL research - Abstract
Background: Mitochondrial DNA (mtDNA) polymorphism is a possible factor contributing to the maternal parent-of-origin effect in multiple sclerosis (MS) susceptibility. Methods and Findings: In order to investigate the role of mtDNA variations in MS, we investigated six European MS case-control cohorts comprising >5,000 individuals. Three well matched cohorts were genotyped with seven common, potentially functional mtDNA single nucleotide polymorphisms (SNPs). A SNP, nt13708 G/A, was significantly associated with MS susceptibility in all three cohorts. The nt13708A allele was associated with an increased risk of MS (OR = 1.71, 95% CI 1.28-2.26, P = 0.0002). Subsequent sequencing of the mtDNA of 50 individuals revealed that the nt13708 itself, rather than SNPs linked to it, was responsible for the association. However, the association of nt13708 G/A with MS was not significant in MS cohorts which were not well case-control matched, indicating that the significance of association was affected by the population structure of controls. Conclusions: Taken together, our finding identified the nt13708A variant as a susceptibility allele to MS, which could contribute to defining the role of the mitochondrial genome in MS pathogenesis. [ABSTRACT FROM AUTHOR]
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- 2008
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