Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Anna-Maija Kristiina Sulonen"'
Autor:
Teppo Varilo, Chris H. Polman, Maria-Liisa Sumelahti, Stacey Gabriel, Anna-Maija Kristiina Sulonen, Arpo Aromaa, David A. Hafler, Pentti J. Tienari, Inger-Lise Mero, Eveliina Jakkula, Stephen L. Hauser, Aarno Palotie, Daniel B. Mirel, Mauri Reunanen, Leena Peltonen, Ludwig Kappos, Shaun Purcell, Annette Bang Oturai, Anu Kemppinen, Helle Bach Søndergaard, Irina Elovaara, Hanne F. Harbo, Philip L. De Jager, Tuula Pirttilä, Keijo Koivisto, Virpi Leppa, Janna Saarela, Mark J. Daly, Suvi P. Kallio
Publikováno v:
American journal of human genetics, 86(2), 285-291. Cell Press
Jakkula, E, Leppa, V, Sulonen, A M, Varilo, T, Kallio, S, Kemppinen, A, Purcell, S, Koivisto, K, Tienari, P, Sumelahti, M L, Elovaara, I, Pirttila, T, Reunanen, M, Aromaa, A, Oturai, A B, Sondergaard, H B, Harbo, H F, Mero, I L, Gabriel, S B, Mirel, D B, Hauser, S L, Kappos, L, Polman, C H, de Jager, P L, Hafler, D A, Daly, M J, Palotie, A, Saarela, J & Peltonen, L 2010, ' Genome-wide Association Study in a High-Risk Isolate for Multiple Sclerosis Reveals Associated Variants in STAT3 Gene ', American journal of human genetics, vol. 86, no. 2, pp. 285-291 . https://doi.org/10.1016/j.ajhg.2010.01.017
Jakkula, E, Leppa, V, Sulonen, A M, Varilo, T, Kallio, S, Kemppinen, A, Purcell, S, Koivisto, K, Tienari, P, Sumelahti, M L, Elovaara, I, Pirttila, T, Reunanen, M, Aromaa, A, Oturai, A B, Sondergaard, H B, Harbo, H F, Mero, I L, Gabriel, S B, Mirel, D B, Hauser, S L, Kappos, L, Polman, C H, de Jager, P L, Hafler, D A, Daly, M J, Palotie, A, Saarela, J & Peltonen, L 2010, ' Genome-wide Association Study in a High-Risk Isolate for Multiple Sclerosis Reveals Associated Variants in STAT3 Gene ', American journal of human genetics, vol. 86, no. 2, pp. 285-291 . https://doi.org/10.1016/j.ajhg.2010.01.017
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d1ddbb7bb17173c8b5e8e0d4ba16514
https://doi.org/10.1016/j.ajhg.2010.01.017
https://doi.org/10.1016/j.ajhg.2010.01.017
Autor:
Keijo Koivisto, Irina Elovaara, Anna-Maija Kristiina Sulonen, Pentti J. Tienari, Aarno Palotie, Leena Peltonen, Janna Saarela, Mauri Reunanen, Tuula Pirttilä, Minna Suvela, Pekka Ellonen, Suvi P. Kallio
Loss-of-function mutations of DAP12 and TREM2 cause a recessively inherited disease PLOSL, manifesting in brain white matter. The genes of the DAP12-TREM2 signaling receptor are located on 19q13.12 and 6p21.1, to which linkage has been observed also
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::169c276050971b5828635c5892c5be2e
https://europepmc.org/articles/PMC2682253/
https://europepmc.org/articles/PMC2682253/
Autor:
Harald Nyland, Hans-Juergen Thiesen, Xinhua Yu, Peter Rieckmann, Montserrat Camina-Tato, Saleh M. Ibrahim, Manuel Comabella, Denis A. Akkad, Janna Saarela, Daniela Corongiu, Anna-Maija Kristiina Sulonen, Dirk Koczan, Sverre Mørk, Joerg T. Epplen, Robert Goertsches, Kjell-Morten Myhr, Xavier Montalban, Maria Giovanna Marrosu, Gianna Costa, Antje Kroner
Publikováno v:
PLoS ONE, Vol 3, Iss 2, p e1530 (2008)
PLoS ONE
PLoS ONE
BackgroundMitochondrial DNA (mtDNA) polymorphism is a possible factor contributing to the maternal parent-of-origin effect in multiple sclerosis (MS) susceptibility.Methods and findingsIn order to investigate the role of mtDNA variations in MS, we in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15969d24816f85b8609309d373d5f13b
https://hdl.handle.net/1956/2704
https://hdl.handle.net/1956/2704
Autor:
Caroline A. Heckman, Perttu Salo, Maija Lepistö, Taneli Raivio, Anna-Maija Kristiina Sulonen, Samuli Eldfors, Anu Suomalainen, Timo Miettinen, Janna Saarela, Henna Tyynismaa, Henrikki Almusa, Heikki Joensuu, Pekka Ellonen, Sari Hannula
Publikováno v:
Genome Biology
Background Techniques enabling targeted re-sequencing of the protein coding sequences of the human genome on next generation sequencing instruments are of great interest. We conducted a systematic comparison of the solution-based exome capture kits p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22de4c9f82c0fffc90aa4a1e2101670d
https://doi.org/10.1186/gb-2011-12-9-r94
https://doi.org/10.1186/gb-2011-12-9-r94