Janna Saarela

Bilde av Janna Saarela
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Besøksadresse Gaustadalléen 21 Forskningsparken 0349 Oslo
Postadresse Postboks 1137 Blindern 0318 Oslo

Publikasjoner

  • Hakonen, Anna H; Lehtonen, Johanna; Kivirikko, Sirpa; Keski‐Filppula, Riikka; Moilanen, Jukka; Kivisaari, Reetta; Almusa, Henrikki; Jakkula, Eveliina; Saarela, Janna; Avela, Kristiina & Aittomäki, Kristiina (2020). Recessive MYH3 variants cause “Contractures, pterygia, and variable skeletal fusions syndrome 1B” mimicking Escobar variant multiple pterygium syndrome. American Journal of Medical Genetics. Part A.  ISSN 1552-4825.  182(11), s 2605- 2610 . doi: https://doi.org/10.1002/ajmg.a.61836 Vis sammendrag
  • Hannula-Jouppi, Katariina; Harjama, Liisa; Einarsdottir, Elisabet; Elomaa, Outi; Kettunen, Kaisa; Saarela, Janna; Soronen, Minna; Bouchard, Laura; Lappalainen, Katriina; Heikkilä, Hannele; Kivirikko, Sirpa; Seppänen, Mikko R J; Kere, Juha & Ranki, Annamari (2020). Nagashima-type palmoplantar keratosis in Finland caused by a SERPINB7 founder mutation. Journal of American Academy of Dermatology.  ISSN 0190-9622.  83(2), s 643- 645 . doi: https://doi.org/10.1016/j.jaad.2019.11.004 Fulltekst i vitenarkiv.
  • Harjama, Liisa; Kettunen, Kaisa; Elomaa, Outi; Einarsdottir, Elisabet; Heikkilä, Hannele; Kivirikko, Sirpa; Lappalainen, Katriina; Saarela, Janna; Alby, Caroline; Ranki, Annamari; Kere, Juha; Hadj-Rabia, Smaïl & Hannula-Jouppi, Katariina (2020). Phenotypic Variability with SLURP1 Mutations and Diffuse Palmoplantar Keratoderma. Acta Dermato-Venereologica.  ISSN 0001-5555.  100(4) . doi: https://doi.org/10.2340/00015555-3404 Fulltekst i vitenarkiv.
  • Hautala, Timo; Chen, Jie; Tervonen, Laura; Partanen, Terhi; Winqvist, Satu; Lehtonen, Johanna; Saarela, Janna; Kraatari, Minna; Kuismin, Outi; Vuorinen, Tytti; Glumoff, Virpi; Åström, Pirjo; Huuskonen, Usko; Lorenzo, Lazaro; Casanova, Jean-Laurent; Zhang, Shen-Ying & Seppänen, Mikko R.J. (2020). Herpes simplex virus 2 encephalitis in a patient heterozygous for a TLR3 mutation. Neurology: Genetics.  ISSN 2376-7839.  6(6) . doi: https://doi.org/10.1212/NXG.0000000000000532 Fulltekst i vitenarkiv.
  • Partanen, Terhi; Chen, Jie; Lehtonen, Johanna; Kuismin, Outi; Rusanen, Harri; Vapalahti, Olli; Vaheri, Antti; Anttila, Veli-Jukka; Bode, Michaela; Hautala, Nina; Vuorinen, Tytti; Glumoff, Virpi; Kraatari, Minna; Åström, Pirjo; Saarela, Janna; Kauma, Heikki; Lorenzo, Lazaro; Casanova, Jean-Laurent; Zhang, Shen-Ying; Seppänen, Mikko & Hautala, Timo (2020). Heterozygous TLR3 Mutation in Patients with Hantavirus Encephalitis. Journal of Clinical Immunology.  ISSN 0271-9142.  40(8) . doi: https://doi.org/10.1007/s10875-020-00834-2 Fulltekst i vitenarkiv. Vis sammendrag
  • Tuovinen, Elina A.; Grönholm, Juha; Ohman, Tiina; Pöysti, Sakari; Toivonen, Raine; Kreutzman, Anna; Heiskanen, Kaarina; Trotta, Luca; Toiviainen-Salo, Sanna; Routes, John M.; Verbsky, James; Mustjoki, Satu; Saarela, Janna; Kere, Juha; Varjosalo, Markku; Hänninen, Arno & Seppänen, Mikko (2020). Novel Hemizygous IL2RG p.(Pro58Ser) Mutation Impairs IL-2 Receptor Complex Expression on Lymphocytes Causing X-Linked Combined Immunodeficiency. Journal of Clinical Immunology.  ISSN 0271-9142.  40(3), s 503- 514 . doi: 10.1007/s10875-020-00745-2 Fulltekst i vitenarkiv.
  • Madireddy, Lohith; Patsopoulos, Nikolaos A.; Cotsapas, Chris; Bos, Steffan Daniel; Beecham, Ashley; McCauley, Jacob; Kim, Kicheol; Jia, Xiaoming; Santaniello, Adam; Caillier, Stacy J.; Andlauer, Till F.M.; Barcellos, Lisa F.; Berge, Tone; Bernardinelli, Luisa; Martinelli-Boneschi, Filippo; Booth, David R.; Briggs, Farren; Celius, Elisabeth Gulowsen; Comabella, Manuel; Comi, Giancarlo; Cree, Bruce A.C.; D'Alfonso, Sandra; Dedham, Katrina; Duquette, Pierre; Efthimios, Dardiotis; Esposito, Federica; Fontaine, Bertrand; Gasperi, Christiane; Goris, An; Dubois, Bénédicte; Gourraud, Pierre-Antoine; Hadjigeorgiou, Georgios; Haines, Jonathan; Hawkins, Clive; Hemmer, Bernhard; Hintzen, Rogier; Horakova, Dana; Isobe, Noriko; Kalra, Seema; Kira, Jun-ichi; Khalil, Michael; Kockum, Ingrid; Lill, Christina M.; Lincoln, Matthew R; Luessi, Felix; Martin, Roland; Oturai, Annette; Palotie, Aarno; Pericak-Vance, Margaret A.; Henry, Roland; Saarela, Janna; Ivinson, Adrian; Olsson, Tomas; Taylor, Bruce V.; Stewart, Graeme J.; Harbo, Hanne Flinstad; Compston, Alastair; Hauser, Stephen L.; Hafler, David A.; Zipp, Frauke; De Jager, Philip; Sawcer, Stephen; Oksenberg, Jorge R. & Baranzini, Sergio E. (2019). A systems biology approach uncovers cell-specific gene regulatory effects of genetic associations in multiple sclerosis. Nature Communications.  ISSN 2041-1723.  10:2236, s 1- 12 . doi: 10.1038/s41467-019-09773-y Fulltekst i vitenarkiv.
  • Patsopoulos, Nikolaos A.; Baranzini, Sergio E.; Santaniello, Adam; Shoostari, Parisa; Cotsapas, Chris; Wong, Garrett; Beecham, Ashley H.; James, Tojo; Replogle, Joseph; Vlachos, Ioannis S.; McCabe, Cristin; Pers, Tune H.; Brandes, Aaron; White, Charles; Keenan, Brendan; Cimpean, Maria; Winn, Phoebe; Panteliadis, Ioannis-Pavlos; Robbins, Allison; Andlauer, Till F.M.; Zarzycki, Onigiusz; Dubois, Benedicte; Goris, An; Søndergaard, Helle Bach; Sellebjerg, Finn; Sørensen, Per Sølberg; Ullum, Henrik; Thørner, Lise Wegner; Saarela, Janna; Cournu-Rebeix, Isabelle; Damotte, Vincent; Fontaine, Bertrand; Guillot-Noel, Lena; Lathrop, Mark; Vukusic, Sandra; Berthele, Achim; Pongratz, Viola; Buck, Dorothea; Gasperi, Christiane; Graetz, Christiane; Grummel, Verena; Hemmer, Bernhard; Hoshi, Muni; Knier, Benjamin; Korn, Thomas S.; Lill, Christina M.; Luessi, Felix; Muhlau, Mark; Zipp, Frauke; Dardiotis, Efthimios; Agliardi, Cristina; Amoroso, Antonio; Barizzone, Nadia; Benedetti, Maria D.; Bernardinelli, Luisa; Cavalla, Paola; Clarelli, Ferdinando; Comi, Giancarlo; Cusi, Daniele; Esposito, Federica; Ferré, Laura; Galimberti, Daniela; Guaschino, Clara; Leone, Maurizio A.; Martinelli, Vittorio; Moiola, Lucia; Salvetti, Marco; Sorosina, Melissa; Vecchio, Domizia; Zauli, Andrea; Santoro, Silvia; Mancini, Nicasio; Zuccalà, Miriam; Mescheriakova, Julia; van Duijn, Cornelia M.; Bos-Haugen, Steffan Daniël; Celius, Elisabeth Gulowsen; Spurkland, Anne; Comabella, Manuel; Montalban, Xavier; Alfredsson, Lars; Bomfim, Izaura L.; Gomez-Cabrero, David; Hillert, Jan; Jagodić, Maja; Lindén, Magdalena; Piehl, Fredrik; Jelcic, Ilijas; Martin, Roland; Sospedra, Mirela; Baker, Amie; Ban, Maria; Hawkins, Clive; Hysi, Pirro; Kalra, Seema; Karpe, Fredrik; Khadake, Jyoti; Lachance, Genevieve; Molyneux, Paul; Neville, Matthew; Thorpe, John; Bradshaw, Elizabeth; Caillier, Stacy J.; Calabresi, Peter; Cree, Bruce A.C.; Cross, Anne; Davis, Mary; de Bakker, Paul W.I.; Delgado, Silvia; Dembele, Marieme; Edwards, Keith; Fitzgerald, Kate; Frohlich, Irene Y.; Gourraud, Pierre-Antoine; Haines, Jonathan L.; Hákonarson, Hákon H.; Kimbrough, Dorlan; Isobe, Noriko; Konidari, Ioanna; Lathi, Ellen; Lee, Michelle H.; Li, Taibo; An, David; Zimmer, Andrew; Madireddy, Lohith; Manrique, Clara P.; Mitrovic, Mitja; Olah, Marta; Patrick, Ellis; Pericak-Vance, Margaret A.; Piccio, Laura; Schaefer, Cathy; Weiner, Howard; Lage, Kasper; Compston, Alastair; Hafler, David; Harbo, Hanne Flinstad; Hauser, Stephen L.; Stewart, Graeme; D'Alfonso, Sandra; Hadjigeorgiou, Georgios; Taylor, Bruce; Barcellos, Lisa F.; Booth, David; Hintzen, Rogier; Kockum, Ingrid; Martinelli-Boneschi, Filippo; McCauley, Jacob L.; Oksenberg, Jorge R.; Oturai, Annette; Sawcer, Stephen; Ivinson, Adrian J.; Olsson, Tomas & de Jager, Philip L. (2019). Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility. Science.  ISSN 0036-8075.  365:eaav7188(6460), s 1- 12 . doi: 10.1126/science.aav7188 Vis sammendrag
  • Mitrovic, Mitja; Patsopoulos, Nikolaos A.; Beecham, Ashley H.; Dankowski, Theresa; Goris, An; Dubois, Benedicte; D’hooghe, Marie B.; Lemmens, Robin; Van Damme, Philip; Bach Søndergaard, Helle; Sellebjerg, Finn; Soelberg Sorensen, Per; Ullum, Henrik; Thørner, Lise Wegner; Werge, Thomas; Saarela, Janna; Cournu-Rebeix, Isabelle; Damotte, Vincent; Fontaine, Bertrand; Guillot-Noel, Lena; Lathrop, Mark; Vukusik, Sandra; Gourraud, Pierre-Antoine; Andlauer, Till F.M.; Pongratz, Viola; Buck, Dorothea; Gasperi, Christiane; Antonios, Bayas; Heesen, Christoph; Kümpfel, Tania; Linker, Ralf; Paul, Friedemann; Stangel, Martin; Tackenberg, Björn; Bergh, Florian Then; Warnke, Clemens; Wiendl, Heinz; Wildemann, Brigitte; Zettl, Uwe; Ziemann, Ulf; Tumani, Hayrettin; Gold, Ralf; Grummel, Verena; Hemmer, Bernhard; Knier, Benjamin; Lill, Christina M.; Myhr, Kjell-Morten; Celius, Elisabeth Gulowsen; Lie, Benedicte Alexandra; Spurkland, Anne; Harbo, Hanne Flinstad & Cotsapas, Chris (2018). Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk. Cell.  ISSN 0092-8674.  175(6), s 1679- 1687 . doi: 10.1016/j.cell.2018.09.049 Fulltekst i vitenarkiv.
  • Saarela, Jan & Skirbekk, Vegard Fykse (2018). Forced migration in childhood and subsequent fertility: The Karelian displaced population in Finland. Population, Space and Place.  ISSN 1544-8444. . doi: 10.1002/psp.2223
  • Kontro, Mika; Kumar, Anil; Majumder, Muntasir Mamun; Eldfors, Samuli; Parsons, Alun; Pemovska, Tea; Saarela, Janna; Yadav, Bhagwan; Malani, Disha; Fløisand, Yngvar; Höglund, Martin; Remes, Kari Juhani; Gjertsen, Bjørn Tore; Kallioniemi, Olli; Wennerberg, Krister; Heckman, Caroline Akemi & Porkka, Kimmo (2017). HOX gene expression predicts response to BCL-2 inhibition in acute myeloid leukemia. Leukemia.  ISSN 0887-6924.  31(2), s 301- 309 . doi: 10.1038/leu.2016.222
  • Moutsianas, Loukas; Jostins, Luke; Beecham, Ashley H.; Dilthey, Alexander T.; Xifara, Dionysia K.; Ban, Maria; Shah, Tejas S.; Patsopoulos, Nikolaos A.; Alfredsson, Lars; Anderson, Carl A.; Attfield, Katherine E.; Baranzini, Sergio E.; Barrett, Jeffrey; Binder, Thomas M.C.; Booth, David; Buck, Dorothea; Celius, Elisabeth Gulowsen; Cotsapas, Chris; D'Alfonso, Sandra; Dendrou, Calliope A.; Donnelly, Peter; Dubois, Bénédicte; Fontaine, Bertrand; Fugger, Lars; Goris, An; Gourraud, Pierr-Antoine; Graetz, Christiane; Hemmer, Bernhard; Hillert, Jan; Kockum, Ingrid; Leslie, Stephen; Lill, Christina M.; Martinelli-Boneschi, Filippo; Oksenberg, Jorge R.; Olsson, Tomas; Oturai, Annette; Saarela, Janna; Søndergaard, Helle Bach; Spurkland, Anne; Taylor, Bruce; Winkelmann, Juliane; Zipp, Frauke; Haines, Jonathan L.; Pericak-Vance, Margaret A.; Spencer, Chris C.A.; Stewart, Graeme; Hafler, David A; Ivinson, Adrian J.; Harbo, Hanne Flinstad; Hauser, Stephen L.; De Jager, Philip L.; Compston, Alastair; McCauley, Jacob L.; Sawcer, Stephen & McVean, Gil (2015). Class II HLA interactions modulate genetic risk for multiple sclerosis. Nature Genetics.  ISSN 1061-4036.  47(10), s 1107- 1113 . doi: 10.1038/ng.3395
  • Damotte, V; Guillot-Noel, Lena; Patsopoulos, Nikolaos A.; Madireddy, L; Behi, M El; Ban, Maria; Baranzini, Sergio; Barcellos, Lisa; Beecham, Gary; Beecham, Ashley; Bernardinelli, L; Booth, David; Bos, Steffan Daniel; Buck, Dorothea; Bush, William; Comabella, Manuel; Compston, Alastair; Cotsapas, Chris; Cournu-rebeixisabelle, Isabelle; Cree, Bruce; d'Alfonso, Sandra; Daly, Mark; Damotte, Vincent; Davis, Mary; Bakker, Paul de; De Jager, Philip L; Dubois, Benedicte; Esposito, Federica; Fontaine, Bertrand; Goris, An; Gourraud, Pierre-Antoine; Green, Todd; Celius, Elisabeth Gulowsen; Hadjixenofontos, Athena; Hafler, David; Haines, Jonathan; Harbo, Hanne Flinstad; Hauser, Stephen; Hawkins, Clive; Hemmer, Bernhard; Hillert, Jan; Hintzen, Rogier; Horáková, Dana; Ivinson, Adrian J; Kemppinen, Anu; Kira, Jun-ichi; Kockum, Ingrid; Lincoln, Robin; Martin, Roland; Boneschi, Filippo martinelli; McCauley, Jacob L.; Mero, Inger-Lise; Oksenberg, Jorge; Olsson, Tomas; Oturai, Annette; Palotie, Aarno; Pericak-Vance, Margaret; Rioux, John; Saarela, Janna; Sawcer, Stephen; Schnetz-boutaud, Nathalie; Sellebjerg, Finn; Soendergaard, Helle; Sorensen, Per Soelberg; Spurkland, Anne; Stankovich, Jim; Stewart, Graeme; Taylor, Bruce; Ticca, Anna; West, Sandra; Zipp, Frauke; Blackwell, Jenefer m; Bramon, Elvira; Brown, Matthew A; Casas, Juan Pablo; Corvin, Aiden; Jankowski, Janusz; Markus, Hugh s; Mathew, Christopher G.; Palmer, Colin NA; Plomin, Robert; Rautanen, Anna; Trembath, Richard c; Viswanathan, Ananth c; Wood, Nicholas W.; Spencer, Chris ca; Band, Gavin; Bellenguez, Celine; Freeman, Colin; Hellenthal, Garrett; Giannoulatou, Eleni; Pirinen, Matti; Pearson, Richard; Strange, Amy; Su, Zhan; Vukcevic, Damjan; Donnelly, Peter; Langford, Cordelia; Hunt, Sarah E; Edkins, Sarah; Gwilliam, Rhian; Blackburn, Hannah; Bumpstead, Suzannah J.; Dronov, Serge; Gillman, Matthew; Gray, Emma; Hammond, Naomi; Jayakumar, Alagurevathi; Mccann, Owen t; Liddle, Jennifer; Potter, Simon C; Ravindrarajah, Rathi; Ricketts, Michelle; Waller, Matthew J; Weston, Paul; Widaa, Sara; Whittaker, Pamela; Barroso, Ines; Deloukas, Panos; Dilthey, Alexander; Leslie, Stephen; Moutsianas, Loukas; Perez, Marc l; Mcvean, Gil; Mccarthy, Mark i; Baranzini, SE; Cournu-Rebeix, I & Fontaine, B. (2014). A gene pathway analysis highlights the role of cellular adhesion molecules in multiple sclerosis susceptibility. Genes and Immunity.  ISSN 1466-4879.  15, s 126- 132 . doi: 10.1038/gene.2013.70
  • Goris, An; Van Setten, Jessica; Diekstra, Frank; Ripke, Stephan; Patsopoulos, Nikolaos A.; Sawcer, Stephen; Ban, Maria; Baranzini, Sergio; Barcellos, Lisa; Beecham, Gary; Beecham, Ashley; Bernardinelli, L; Booth, David; Bos, Steffan Daniel; Buck, Dorothea; Bush, William; Comabella, Manuel; Compston, Alastair; Cotsapas, Chris; Cournu-Rebeix, Isabelle; Cree, Bruce; d'Alfonso, Sandra; Daly, Mark; Damotte, Vincent; Davis, Mary; Bakker, Paul de; De Jager, Philip L; Dubois, Benedicte; Esposito, Federica; Fontaine, Bertrand; Gourraud, Pierre-Antoine; Green, Todd; Celius, Elisabeth Gulowsen; Hadjixenofontos, Athena; Hafler, David; Haines, Jonathan; Harbo, Hanne Flinstad; Hauser, Stephen; Hawkins, Clive; Hemmer, Bernhard; Hillert, Jan; Hintzen, Rogier; Horáková, Dana; Ivinson, Adrian J; Kemppinen, Anu; Kira, Jun-ichi; Kockum, Ingrid; Lincoln, Robin; Martin, Roland; Boneschi, Filippo martinelli; McCauley, Jacob L.; Mero, Inger-Lise; Oksenberg, Jorge; Olsson, Tomas; Oturai, Annette; Palotie, Aarno; Pericak-Vance, Margaret; Rioux, John; Saarela, Janna; Schnetz-boutaud, Nathalie; Sellebjerg, Finn; Soendergaard, Helle; Sorensen, Per Soelberg; Spurkland, Anne; Stankovich, Jim; Stewart, Graeme; Taylor, Bruce; Ticca, Anna; West, Sandra; Zipp, Frauke; van Es, Michael; Bahlo, M; Booth, DR; Broadley, SA; Brown, MA; Foote, SJ; Griffiths, LR; Kilpatrick, TJ; Lechner-Scott, J; Moscato, P; Perreau, VM; Rubio, JP; Scott, RJ; Stankovich, J; Taylor, BV; Wiley, J; Clarke, G; Cox, MB; Csurhes, PA; Danoy, P; Drysdale, K; Field, J; Greer, JM; Guru, P; Hadler, J; Mcmorran, BJ; Jensen, CJ; Johnson, JL; McCallum, R.; Merriman, M.; Merriman, T.; Pryce, K; Stewart, GJ; Tajouri, L; Wilkins, EJ; Browning, BL; Browning, SR; Perera, D; Broadley, S.; Butzkueven, H.; Carroll, WM; Chapman, C.; Kermode, AG; Marriott, M; Mason, D; Heard, RN; Pender, MP; Slee, M.; Tubridy, N; Willoughby, E; Andersen, Peter M.; Melki, Judith; Meininger, Vincent; Hardiman, Orla; Landers, John E; Brown, Robert H; Shatunov, Aleksey; Leigh, Nigel; Al-Chalabi, Ammar; Shaw, Christopher E; Traynor, Bryan J.; Chio, Adriano; Restagno, Gabriella; Mora, Gabriele; Ophoff, Roel A.; Oksenberg, Jorge R.; Van Damme, Philip; Robberecht, Wim; van den Berg, Leonard H.; Veldink, Jan H & de Bakker, Paul I.W. (2014). No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis. Human Molecular Genetics.  ISSN 0964-6906.  23(7), s 1916- 1922 . doi: 10.1093/hmg/ddt574
  • Sundqvist, Emilie; Buck, Dorothea; Warnke, Clemens; Albrecht, Eva; Gieger, Christian; Khademi, Mohsen; Lima Bomfim, Izaura; Fogdell-Hahn, Anna; Link, Jenny; Alfredsson, Lars; Søndergaard, Helle Bach; Hillert, Jan; Barcellos, Lisa; Booth, David; McCauley, Jacob L.; Comabella, Manuel; Compston, Alastair; d'Alfonso, Sandra; de Jager, Philip; Fontaine, Bertrand; Goris, An; Hafler, David; Haines, Jonathan; Harbo, Hanne Flinstad; Hauser, Stephen L; Hawkins, Clive; Ivinson, Adrian; Martin, Roland; Boneschi, Fillippo Martinelli; Oksenberg, Jorge; Patsopoulos, Nikolaos; Pericak-Vance, Margaret; Saarela, Janna; Sawcer, Stephen; Spurkland, Anne; Stewart, Graeme; Zipp, Frauke; Oturai, Annette B.; Hemmer, Bernhard; Kockum, Ingrid & Olsson, Tomas (2014). JC Polyomavirus Infection Is Strongly Controlled by Human Leucocyte Antigen Class II Variants. PLoS Pathogens.  ISSN 1553-7366.  10(4) . doi: 10.1371/journal.ppat.1004084
  • Baranzini, SE; Celius, E.G.; Elovaara, I; Harbo, HF; Hillert, J; Myhr, Kjell-Morten; Sørensen, PS; Spurkland, A; Sawcer, S; Hauser, SL; Oksenberg, JR; Khankhanian, Pouya; Patsopoulos, Nikolaos A.; Li, Michael; Stankovich, Jim; Cotsapas, Chris; Søndergaard, Helle Bach; Ban, Maria; Barizzone, Nadia; Bergamaschi, Laura; Booth, David; Buck, Dorothea; Cavalla, Paola; Celius, Elisabeth G.; Comabella, Manuel; Comi, Giancarlo; Compston, Alastair; Cournu-Rebeix, Isabelle; D’alfonso, Sandra; Damotte, Vincent; Din, Lennox; Dubois, Benedicte; Elovaara, Irina; Esposito, Federica; Fontaine, Bertrand; Franke, Andre; Goris, An; Gourraud, Pierre-Antoine; Graetz, Christiane; Guerini, Franca R.; Guillot-Noel, Lena; Hafler, David A; Hakonarson, Hakon; Hall, Per; Hamsten, Anders; Harbo, Hanne Flinstad; Bernhard, Hemmer; Hillert, Jan; Kemppinen, Anu; Ingrid, Kockum; Koivisto, Keijo; Larsson, Malin; Lathrop, Mark; Leone, Maurizio; Lill, Christina M.; Macciardi, Fabio; Martin, Roland; Martinelli, Vittorio; Martinelli-Boneschi, Filippo; McCauley, Jacob L.; Naldi, Paoloa; Olsson, Tomas; Oturai, Annette; Pericak-Vance, Margaret A.; Perla, Franco; Reunanen, Mauri; Saarela, Janna; Saker-Delye, Safa; Salvetti, Marco; Sellebjerg, Finn; Sørensen, Per Soelberg; Spurkland, Anne; Stewart, Graeme; Taylor, Bruce; Tienari, Pentti; Winkelmann, Juliane; Wellcome Trust Case Control, Consortium 2; Zipp, Frauke; Ivinson, Adrian J; Haines, Jonathan L.; Sawcer, Stephen; DeJager, Philip; Hauser, Stephen L & Oksenberg, Jorge R. (2013). Network-based multiple sclerosis pathway analysis with GWAS data from 15,000 cases and 30,000 controls. American Journal of Human Genetics.  ISSN 0002-9297.  s 854- 865 . doi: 10.1016/j.ajhg.2013.04.019
  • Beecham, Ashley H.; Patsopoulos, NA; Xifara, DK; Davis, MF; Kemppinen, A; Cotsapas, C; Shah, TS; Spencer, C; Booth, D; Goris, A; Oturai, A; Saarela, J; Fontaine, B; Hemmer, B; Martin, C; Zipp, F; D'Alfonso, S; Martinelli-Boneschi, F; Taylor, B; Harbo, Hanne Flinstad; Kockum, I; Hillert, J; Olsson, T; Ban, M; Oksenberg, JR; Hintzen, R; Barcellos, LF; Agliardi, C; Alfredsson, L; Alizadeh, M; Anderson, C; Andrews, R; Sondergaard, HB; Baker, A; Band, G; Baranzini, SE; Barizzone, N; Barrett, J; Bellenguez, C; Bergamaschi, L; Bernardinelli, L; Berthele, A; Biberacher, V; Binder, TMC; Blackburn, H; Bomfim, IL; Brambilla, P; Broadley, S; Brochet, B; Brundin, L; Buck, D; Butzkueven, H; Caillier, SJ; Camu, W; Carpentier, W; Cavalla, P; Celius, Elisabeth Gulowsen; Coman, I; Comi, G; Corrado, L; Cosemans, L; Cournu-Rebeix, I; Cree, BAC; Cusi, D; Damotte, V; Defer, G; Delgado, SR; Deloukas, P; di Sapio, A; Dilthey, AT; Donnelly, P; Dubois, B; Duddy, M; Edkins, S; Elovaara, I; Esposito, F; Evangelou, N; Fiddes, B; Field, J; Franke, A; Freeman, C; Frohlich, IY; Galimberti, D; Gieger, C; Gourraud, PA; Graetz, C; Graham, A; Grummel, V; Guaschino, C; Hadjixenofontos, A; Hakonarson, H; Halfpenny, C; Hall, G; Hall, P; Hamsten, A; Harley, J; Harrower, T; Hawkins, C; Hellenthal, G; Hillier, C; Hobart, J; Hoshi, M; Hunt, SE; Jagodic, M; Jelcic, I; Jochim, A; Kendall, B; Kermode, A; Kilpatrick, T; Koivisto, K; Konidari, I; Korn, T; Kronsbein, H; Langford, C; Larsson, M; Lathrop, M; Lebrun-Frenay, C; Lechner-Scott, J; Lee, MH; Leone, MA; Leppa, V; Liberatore, G; Lie, Benedicte Alexandra; Lill, CM; Linden, M; Link, J; Luessi, F; Lycke, J; Macciardi, F; Mannisto, S; Manrique, CP; Martin, R; Martinelli, V; Mason, D; Mazibrada, G; McCabe, C; Mero, Inger-Lise; Mescheriakova, J; Moutsianas, L; Myhr, Kjell-Morten; Nagels, G; Nicholas, R; Nilsson, P; Piehl, F; Pirinen, M; Price, SE; Quach, H; Reunanen, M; Robberecht, W; Robertson, NP; Rodegher, M; Rog, D; Salvetti, M; Schnetz-Boutaud, NC; Sellebjerg, F; Selter, RC; Schaefer, C; Shaunak, S; Shen, L; Shields, S; Siffrin, V; Slee, M; Sorensen, PS; Sorosina, M; Sospedra, M; Spurkland, Anne; Strange, A; Sundqvist, E; Thijs, V; Thorpe, J; Ticca, A; Tienari, P; van Duijn, C; Visser, EM; Vucic, S; Westerlind, H; Wiley, JS; Wilkins, A; Wilson, JF; Winkelmann, J; Zajicek, J; Zindler, E; Haines, JL; Pericak-Vance, MA; Ivinson, AJ; Stewart, G; Hafler, D; Hauser, SL; Compston, A; McVean, G; De Jager, P; Sawcer, SJ & McCauley, JL (2013). Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis. Nature Genetics.  ISSN 1061-4036.  45(11), s 1353- 1360 . doi: 10.1038/ng.2770
  • Liu, Jimmy Z.; Hov, Johannes Espolin Roksund; Folseraas, Trine; Ellinghaus, E; Rushbrook, SM; Doncheva, NT; Andreassen, Ole Andreas; Weersma, RK; Weismuller, TJ; Eksteen, B; Invernizzi, P; Hirschfield, GM; Gotthardt, DN; Pares, A; Ellinghaus, D; Shah, T; Juran, BD; Milkiewicz, P; Rust, C; Schramm, C; Muller, T; Srivastava, B; Dalekos, G; Nothen, MM; Herms, S; Winkelmann, J; Mitrovic, M; Braun, F; Ponsioen, CY; Croucher, PJP; Sterneck, M; Teufel, A; Mason, AL; Saarela, J; Leppa, V; Dorfman, R; Alvaro, D; Floreani, A; Onengut-Gumuscu, S; Rich, SS; Thompson, WK; Schork, AJ; Næss, Sigrid; Thomsen, I; Mayr, G; Konig, IR; Hveem, Kristian; Cleynen, I; Gutierrez-Achury, J; Ricano-Ponce, I; van Heel, D; Bjornsson, E; Sandford, RN; Durie, PR; Melum, Espen; Vatn, Morten H; Silverberg, MS; Duerr, RH; Padyukov, L; Brand, S; Sans, M; Annese, V; Achkar, JP; Boberg, Kirsten Muri; Marschall, HU; Chazouilleres, O; Bowlus, CL; Wijmenga, C; Schrumpf, Erik; Vermeire, S; Albrecht, M; Rioux, JD; Alexander, G; Bergquist, A; Cho, J; Schreiber, S; Manns, MP; Farkkila, M; Dale, AM; Chapman, RW; Lazaridis, KN; Franke, A; Anderson, Carl A. & Karlsen, Tom Hemming (2013). Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis. Nature Genetics.  ISSN 1061-4036.  45(6), s 670- 675 . doi: 10.1038/ng.2616
  • Rosella, Mechelli; Renato, Umeton; Policano, Claudia; Annibali, Viviana; Giulia, Coarelli; Ricigliano, Vito A. G.; Vittori, Danila; Fornasiero, Arianna; Buscarinu, Maria Chiara; Sawcer, Stephen; Hellenthal, Garrett; Pirinen, Matti; Spencer, Chris C A; Patsopoulos, Nikolaos; Mousianas, Loukas; Dithey, Alexander; Su, Zhan; Freeman, Colin; Hunt, Sarah E; Edkins, Sarah; Gray, Emma; Booth, David R; Potter, Simon C; Goris, An; Band, Gavin; Oturai, Annette Bang; Strange, Amy; Saarela, Janna; Bellenguez, Celine; Fontaine, Bertrand; Gillman, Matthew; Hemmer, Bernhard; Gwilliam, Rhian; Zipp, Frauke; Jayakumar, Akagurevathi; Martin, Roland; Leslie, Stephen; Hawkins, Stanley; Giannolatou, Eleni; D`alfonso, Sandra; Blackburn, Hannah; Boneschi, Fillippo Martinelli; Liddle, Jennifer; Harbo, Hanne Flinstad; Perez, Marc L; Spurkland, Anne; Waller, Matthew J; Mycko, Marcin P; Ricketts, Michelle; Comabella, Manuel; Celius, Elisabeth Gulowsen; Lorentzen, Åslaug Rudjord; Mero, Inger-Lise; Myhr, Kjell-Morten & SMESTAD, CATHRINE (2013). A ‘‘candidate-interactome’’ aggregate analysis of genome-wide association data in multiple sclerosis. PLOS ONE.  ISSN 1932-6203.  8(5) . doi: 10.1371/journal.pone.0063300
  • Sawcer, S; Hellenthal, G; Pirinen, M; Spencer, CCA; Patsopoulos, NA; Moutsianas, L; Dilthey, A; Su, Z; Freeman, C; Hunt, SE; Edkins, S; Gray, E; Booth, DR; Potter, SC; Goris, A; Band, G; Oturai, AB; Strange, A; Saarela, J; Bellenguez, C; Fontaine, B; Gillman, M; Hemmer, B; Gwilliam, R; Zipp, F; Jayakumar, A; Martin, R; Leslie, S; Hawkins, S; Giannoulatou, E; D'alfonso, S; Blackburn, H; Boneschi, FM; Liddle, J; Harbo, Hanne Flinstad; Perez, ML; Spurkland, Anne; Waller, MJ; Mycko, MP; Ricketts, M; Comabella, M; Hammond, N; Kockum, I; McCann, OT; Ban, M; Whittaker, P; Kemppinen, A; Weston, P; Hawkins, C; Widaa, S; Zajicek, J; Dronov, S; Robertson, N; Bumpstead, SJ; Barcellos, LF; Ravindrarajah, R; Abraham, R; Alfredsson, L; Ardlie, K; Aubin, C; Baker, A; Baker, K; Baranzini, SE; Bergamaschi, L; Bergamaschi, R; Bernstein, A; Berthele, A; Boggild, M; Bradfield, JP; Brassat, D; Broadley, SA; Buck, D; Butzkueven, H; Capra, R; Carroll, WM; Cavalla, P; Celius, Elisabeth Gulowsen; Cepok, S; Chiavacci, R; Clerget-Darpoux, F; Clysters, K; Comi, G; Cossburn, M; Cournu-Rebeix, I; Cox, MB; Cozen, W; Cree, BAC; Cross, AH; Cusi, D; Daly, MJ; Davis, E; de Bakker, PIW; Debouverie, M; D'hooghe, MB; Dixon, K; Dobosi, R; Dubois, B; Ellinghaus, D; Elovaara, I; Esposito, F; Fontenille, C; Foote, S; Franke, A; Galimberti, D; Ghezzi, A; Glessner, J; Gomez, R; Gout, O; Graham, C; Grant, SFA; Guerini, FR; Hakonarson, H; Hall, P; Hamsten, A; Hartung, HP; Heard, RN; Heath, S; Hobart, J; Hoshi, M; Infante-Duarte, C; Ingram, G; Ingram, W; Islam, T; Jagodic, M; Kabesch, M; Kermode, AG; Kilpatrick, TJ; Kim, C; Klopp, N; Koivisto, K; Larsson, M; Lathrop, M; Lechner-Scott, JS; Leone, MA; Leppa, V; Liljedahl, U; Bomfim, IL; Lincoln, RR; Link, J; Liu, JJ; Lorentzen, Åslaug Rudjord; Lupoli, S; Macciardi, F; Mack, T; Marriott, M; Martinelli, V; Mason, D; McCauley, JL; Mentch, F; Mero, Inger-Lise; Mihalova, T; Montalban, X; Mottershead, J; Myhr, Kjell-Morten; Naldi, P; Ollier, W; Page, A; Palotie, A; Pelletier, J; Piccio, L; Pickersgill, T; Piehl, F; Pobywajlo, S; Quach, HL; Ramsay, PP; Reunanen, M; Reynolds, R; Rioux, J; Rodegher, M; Roesner, S; Rubio, JP; Ruckert, IM; Salvetti, M; Salvi, E; Santaniello, A; Schaefer, CA; Schreiber, S; Schulze, C; Scott, RJ; Sellebjerg, F; Selmaj, KW; Sexton, D; Shen, L; Simms-Acuna, B; Skidmore, S; Sleiman, PMA; SMESTAD, CATHRINE; Sorensen, PS; Sondergaard, HB; Stankovich, J; Strange, RC; Sulonen, AM; Sundqvist, E; Syvanen, AC; Taddeo, F; Taylor, B; Blackwell, JM; Tienari, P; Bramon, E; Tourbah, A; Brown, MA; Tronczynska, E; Casas, JP; Tubridy, N; Corvin, A; Vickery, J; Jankowski, J; Villoslada, P; Markus, HS; Wang, K; Mathew, CG; Wason, J; Palmer, CNA; Wichmann, HE; Plomin, R; Willoughby, E; Rautanen, A; Winkelmann, J; Wittig, M; Trembath, RC; Yaouanq, J; Viswanathan, AC; Zhang, HT; Wood, NW; Zuvich, R; Deloukas, P; Langford, C; Duncanson, A; Oksenberg, JR; Pericak-Vance, MA; Haines, JL; Olsson, T; Hillert, J; Ivinson, AJ; De Jager, PL; Peltonen, L; Stewart, GJ; Hafler, DA; Hauser, SL; McVean, G; Donnelly, Peter & Compston, Alastair (2011). Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. Nature.  ISSN 0028-0836.  476(7359), s 214- 219 . doi: 10.1038/nature10251
  • Esposito, Floriana; Patsopoulos, NA; Cepok, Sabine; Kockum, I; Leppa, V; Booth, DR; Heard, RN; Stewart, GJ; Cox, M; Scott, RJ; Lechner-Scott, J; Goris, A; Dobosi, R; Dubois, B; Rioux, JD; Oturai, AB; Søndergaard, HB; Sellebjerg, F; Sørensen, PS; Reunanen, M; Koivisto, K; Cournu-Rebeix, I; Fontaine, B; Winkelmann, J; Gieger, C; Infante-Duarte, C; Zipp, F; Bergamaschi, L; Leone, M; Bergamaschi, R; Cavalla, P; Lorentzen, ÅR; Mero, Inger-Lise; Celius, Elisabeth Gulowsen; Harbo, Hanne Flinstad; Spurkland, Anne; Comabella, M; Brynedal, B; Alfredsson, L; Bernardinelli, L; Robertson, NB; Hawkins, CP; Barcellos, LF; Beecham, G; Bush, W; Cree, BAC; Daly, MJ; Ivinson, AJ; Aublin, C; Compston, A; D´Alfonso, S; Haines, JL; Hauser, SL; Hemmer, B; Hillert, J; McMcauley, JL; Oksenberg, Jorge; Olsson, T; Palotie, A; Peltonen, L; Pericak-Vance, MA; Saarela, J; Sawcer, SJ; Stranger, B; Boneschi, FM; Comi, G; Hafler, DA; de Bakker, PIW & De Jaeger, PL (2010). IL12A, MPHOSPH9/CDK2AP1 and RGS1 are novel multiple sclerosis susceptibility loci. Genes and Immunity.  ISSN 1466-4879.  11(5), s 397- 405 . doi: 10.1038/gene.2010.28
  • Jakkula, Eveliina; Leppa, Virpi; Sulonen, Anna-Maija; Varilo, Teppo; Kallio, Suvi; Kemppinen, Anu; Purcell, Shaun; Koivisto, Keijo; Tienari, Pentti; Sumelahti, Marja-Liisa; Elovaara, Irina; Pirttila, Tuula; Reunanen, Mauri; Aromaa, Arpo; Oturai, Annette Bang; Søndergaard, Helle Bach; Harbo, Hanne Flinstad; 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 (2010). Genome-wide Association Study in a High-Risk Isolate for Multiple Sclerosis Reveals Associated Variants in STAT3 Gene. American Journal of Human Genetics.  ISSN 0002-9297.  86(2), s 285- 291 . doi: 10.1016/j.ajhg.2010.01.017
  • Mero, Inger-Lise; Lorentzen, Åslaug Rudjord; SMESTAD, CATHRINE; Ban, Maria; Celius, Elisabeth Gulowsen; Aarseth, Jan; Myhr, Kjell-Morten; Link, Jenny; Olsson, Tomas; Hillert, Jan; Kockum, Ingrid; Masterman, T; Oturai, AB; Sondergaard, HB; Sellebjerg, F; Saarela, J; Kemppinen, A; Elovaara, I; Spurkland, Anne; Dudbridge, F; Lie, Benedicte Alexandra & Harbo, Hanne Flinstad (2010). A rare variant of the TYK2 gene is confirmed to be associated with multiple sclerosis. European Journal of Human Genetics.  ISSN 1018-4813.  18(4), s 502- 504 . doi: 10.1038/ejhg.2009.195
  • Jagodic, Maja; Colacios, Celine; Nohra, Rita; Dejean, Anne S.; Beyeen, Amennai Daniel; Khademi, Mohsen; Casemayou, Audrey; Lamouroux, Lucille; Duthoit, Christine; Papapietro, Olivier; Sjöholm, Louise; Bernard, Isabelle; Lagrange, Dominique; Dahlman, Ingrid; Lundmark, Frida; Oturai, Annette Bang; Soendergaard, Helle B; Kemppinen, Anu; Saarela, Janna; Tienari, Pentti J.; Harbo, Hanne Flinstad; Spurkland, Anne; Ramagopalan, Sreeram V.; Sadovnick, Dessa A.; Ebers, George C.; Seddighzadeh, Maria; Klareskog, Lars; Alfredsson, Lars; Padyukov, Leonid; Hillert, Jan; Clanet, Michel; Edan, Gilles; Fontaine, Bertrand; Fournie, Gilbert J.; Kockum, Ingrid; Saoudi, Abdelhadi & Olsson, Tomas (2009). A Role for VAV1 in Experimental Autoimmune Encephalomyelitis and Multiple Sclerosis. Science Translational Medicine.  ISSN 1946-6234.  1(10) . doi: 10.1126/scitranslmed.3000278
  • Kallio, SP; Jakkula, E; Purcell, S; Suvela, M; Koivisto, K; Tienari, PJ; Elovaara, I; Pirttila, T; Reunanen, M; bronnikov, D; Viander, M; Meri, S; Hillert, Jan; Lundmark, F; Harbo, Hanne Flinstad; Lorentzen, Åslaug Rudjord; De Jager, PL; Daly, MJ; Hafler, David A; Palotie, Aarno; Peltonen, L & Saarela, Janna (2009). Use of a genetic isolate to identify rare disease variants: C7 on 5p associated with MS. Human Molecular Genetics.  ISSN 0964-6906.  18(9), s 1670- 1683 . doi: 10.1093/hmg/ddp073
  • Kemppinen, Anu; Suvela, M; Tienari, PJ; Elovaara, I; Koivisto, K; Pirttila, T; Reunanen, M; Rautakorpi, I; Hillert, Jan; Lundmark, F; Oturai, A; Ryder, Lars P.; Harbo, Hanne Flinstad; Celius, Elisabeth G; Palotie, Aarno; Daly, Mark; Peltonen, L & Saarela, Janna (2009). MYO9B polymorphisms in multiple sclerosis. European Journal of Human Genetics.  ISSN 1018-4813.  17(6), s 840- 843 . doi: 10.1038/ejhg.2008.251
  • Lorentzen, Åslaug R; Smestad, Cathrine; Lie, Benedicte A; Lie, BA; Oturai, AB; Oturai, Annette; Åkesson, Eva; Akesson, E; Saarela, Janna; Myhr, Kjell-Morten; Vartdal, Frode; Celius, Elisabeth G; Sorensen, PS; Sørensen, Per S; Hillert, Jan; Spurkland, Anne; Harbo, Hanne F & Harbo, HF (2008). The SH2D2A gene and susceptibility to multiple sclerosis. Journal of Neuroimmunology.  ISSN 0165-5728.  197, s 152- 158 . doi: 10.1016/j.jneuroim.2008.04.037
  • Yu, Xinhua; Koczan, Dirk; Sulonen, Anna-Maija; Akkad, Dennis A.; Kroner, Antje; Comabella, Manuel; Costa, Gianna; Corongiu, Daniela; Goertsches, Robert; Camina-Tato, Montserrat; Thiesen, Hans-Juergen; Nyland, Harald Inge; Mørk, Sverre; Montalban, Xavier; Rieckmann, Peter; Marrosu, Maria G.; Myhr, Kjell-Morten; Epplen, Joerg T.; Saarela, Janna & Ibrahim, Saleh M. (2008). mtDNA nt13708A Variant Increases the Risk of Multiple Sclerosis. PLOS ONE.  ISSN 1932-6203.  3(2), s 1- 7 . doi: 10.1371/journal.pone.0001530
  • Lundmark, F; Duvefelt, K; Iacobaeus, E; Kockum, I; Wallstrom, E; Khademi, M; Oturai, A; Ryder, LP; Saarela, J; Harbo, Hanne Flinstad; Celius, EG; Salter, H; Olsson, T & Hillert, J (2007). Variation in interleukin 7 receptor a chain (IL7R) influences risk of multiple sclerosis. Nature Genetics.  ISSN 1061-4036.  39, s 1108- 1113 . doi: 10.1038/ng2106
  • Lundmark, F; Harbo, Hanne Flinstad; Celius, Elisabeth Gulowsen; Saarela, J; Datta, Pameli; Oturai, Anette; Lindgren, CM; Masterman, T.; Salter, H & Hillert, Jan (2006). Association analysis of the LAG3 and CD4 genes in multiple sclerosis in two independent populations. Journal of Neuroimmunology.  ISSN 0165-5728.  180, s 193- 198
  • Booth, DR; Heard, RN; Stewart, GJ; Cox, M; Scott, RJ; Lechner-Scott, J; Goris, A; Dobosi, R; Dubois, B; Saarela, J; Leppa, V; Peltonen, L; Pirttila, T; Cournu-Rebeix, I; Fontaine, B; Bergamaschi, L; D'Alfonso, S; Leone, M; Lorentzen, A.R.; Harbo, Hanne Flinstad; Celius, Elisabeth Gulowsen; Spurkland, Anne; Link, J; Kockum, I; Olsson, T; Hillert, J; Ban, M; Baker, A; Kemppinen, A; Sawcer, S; Compston, A; Robertson, NP; De Jager, PL; Hafler, DA; Barcellos, LF; Ivinson, AJ; McCauley, JL; Pericak-Vance, MA; Oksenberg, JR; Hauser, SL; Sexton, D & Haines, J (2010). Lack of support for association between the KIF1B rs10492972[C] variant and multiple sclerosis. Nature Genetics.  ISSN 1061-4036.  42(6), s 469- 470
  • Mero, Inger-Lise; Lorentzen, AR; Ban, Maria; SMESTAD, CATHRINE; Celius, Elisabeth Gulowsen; Aarseth, JH; Myhr, Kjell Morten; Link, Jenny; Hillert, Jan; Olsson, Tomas; Kockum, Ingrid; Masterman, T.; Oturai, Anette; Søndergaard, Henrik; Sellebjerg, Finn; Saarela, J; Kemppinen, A; Spurkland, Anne; Lie, Benedicte Alexandra & Harbo, Hanne Flinstad (2009). The TYK2 gene is associated with susceptibility to multiple sclerosis. Multiple Sclerosis.  ISSN 1352-4585.  15(9), s S186- S186
  • Sawcer, Stephen; Booth, David; Heard, Robert; Stewart, Graeme; An, Goris; Dobosi, Rita; Dubois, Benedicte; Oturai, Annette; Soendergaard, Helle B; Sellebjerg, Finn; Saarela, Janna; Leppa, Virpi; Palotie, Aarno; Peltonen, Leena; Fontaine, Bertrand; Cournu-Rebeix, Isabelle; Clerget-Darpoux, Francoise; Weber, Frank; Holsboer, Florian; Muller-Myhsok, Bertram; Rieckmann, Peter; Kroner, Antje; Graham, Colin; Vandenbroeck, Koen; Hawkins, Stanley; D'Alfonso, Sandra; Bergamaschi, Laura; Naldi, Paola; Guerini, Franca R; Salvetti, Marco; Galimberti, Daniela; Hintzen, Rogier; Lorentzen, Åslaug Rudjord; Harbo, Hanne Flinstad; Celius, Elisabeth Gulowsen; Spurkland, Anne; Cucca, Francesco; Marrosu, Maria Giovanna; Comabella, Manuel; Montalban, Xavier; Villoslada, Pablo; Olsson, Tomas; Kockum, Ingrid; Hillert, Jan; Ban, Maria; Walton, Amie; Compston, Alastair; Hawkins, Clive; Mihalova, Tania; Robertson, Neil; Ingram, Gillian; De Jager, Philip L; Hafler, David A; Rioux, John; Daly, Mark; Barcellos, Lisa; Ivinson, Adrian; Periack-Vance, Margaret; Oksenberg, Jorge; Hauser, Stephen L; McCauley, Jacob; Sexton, David & Haines, Jonathan (2008). Refining genetic associations in multiple sclerosis. Lancet Neurology.  ISSN 1474-4422.  7(7), s 567- 569 . doi: 10.1016/S1474-4422(08)70122-4
  • Lorentzen, AR; SMESTAD, CATHRINE; Ekstrøm, Per Olaf; Oturai, Annette Bang; Åkesson, Eva; Saarela, Janna; Myhr, Kjell-Morten; Lie, Benedicte Alexandra; Celius, Elisabeth Gulowsen; Sorensen, PS; Hillert, Jan; Spurkland, Anne & Harbo, Hanne Flinstad (2006). The role of SH2D2A gene polymorphisms in multiple sclerosis. Multiple Sclerosis.  ISSN 1352-4585.  12(Suppl 1), s S72- S72
  • Lorentzen, Åslaug Rudjord; Smestad, C.; Ekström, Peter; Ekstrom, PO; Oturai, AB; Oturai, AB; Akesson, E; Åkesson, Elisabeth; Saarela, J. & Myhr, Kjell-Morten (2006). The role of SH2D2A gene polymorphisms in development of multiple sclerosis. Tissue Antigens.  ISSN 0001-2815.  67(6 - P-179), s 528- 529
Publisert 8. jan. 2019 14:30 - Sist endret 8. jan. 2019 14:30

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