Association of genetic markers with CSF oligoclonal bands in multiple sclerosis patients von Leone, Maurizio A, Barizzone, Nadia, Esposito, Federica, Lucenti, Ausiliatrice, Harbo, Hanne F, Goris, An, Kockum, Ingrid, Oturai, Annette Bang, Celius, Elisabeth Gulowsen, Mero, Inger L, Dubois, Bénédicte, Olsson, Tomas, Søndergaard, Helle Bach, Cusi, Daniele, Lupoli, Sara, Andreassen, Bettina Kulle, Myhr, Kjell-Morten, Guerini, Franca R, Comi, Giancarlo, Martinelli-Boneschi, Filippo, D'Alfonso, Sandra

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Association of Genetic Markers with CSF Oligoclonal Bands in Multiple Sclerosis Patients. e64408 von Leone, Maurizio A, Barizzone, Nadia, Esposito, Federica, Lucenti, Ausiliatrice, Harbo, Hanne F, Goris, An, Kockum, Ingrid, Oturai, Annette Bang, Celius, Elisabeth Gulowsen, Mero, Inger L

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Gain-of-function and loss-of-function GABRB3 variants lead to distinct clinical phenotypes in patients with developmental and epileptic encephalopathies von Absalom, Nathan L., Liao, Vivian W. Y., Johannesen, Katrine M. H., Gardella, Elena, Jacobs, Julia, Lesca, Gaetan, Gokce-Samar, Zeynep, Arzimanoglou, Alexis, Zeidler, Shimriet, Striano, Pasquale, Meyer, Pierre, Benkel-Herrenbrueck, Ira, Mero, Inger-Lise, Rummel, Jutta, Chebib, Mary, Møller, Rikke S., Ahring, Philip K.

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Assessment of gene-disease associations and recommendations for genetic testing for somatic variants in vascular anomalies by VASCERN-VASCA von Revencu, Nicole, Eijkelenboom, Astrid, Bracquemart, Claire, Alhopuro, Pia, Armstrong, Judith, Baselga, Eulalia, Cesario, Claudia, Dentici, Maria Lisa, Eyries, Melanie, Frisk, Sofia, Karstensen, Helena Gásdal, Gene-Olaciregui, Nagore, Kivirikko, Sirpa, Lavarino, Cinzia, Mero, Inger-Lise, Michiels, Rodolphe, Pisaneschi, Elisa, Schönewolf-Greulich, Bitten, Wieland, Ilse, Zenker, Martin, Vikkula, Miikka

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No evidence of association between mutant alleles of the CYP27B1 gene and multiple sclerosis von Ban, Maria, Caillier, Stacy, Mero, Inger-Lise, Myhr, Kjell-Morten, Celius, Elisabeth G., Aarseth, Jan, Torkildsen, Øivind, Harbo, Hanne F., Oksenberg, Jorge, Hauser, Stephen L., Sawcer, Stephen, Compston, Alastair

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

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Oligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles von Mero, Inger-Lise, Gustavsen, Marte W, Sæther, Hanne S, Flåm, Siri T, Berg-Hansen, Pål, Søndergaard, Helle B, Jensen, Poul Erik H, Berge, Tone, Bjølgerud, Anja, Muggerud, Aslaug, Aarseth, Jan H, Myhr, Kjell-Morten, Celius, Elisabeth G, Sellebjerg, Finn, Hillert, Jan, Alfredsson, Lars, Olsson, Tomas, Oturai, Annette Bang, Kockum, Ingrid, Lie, Benedicte A, Andreassen, Bettina Kulle, Harbo, Hanne F

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Oligoclonal bands and age at onset correlate with genetic risk score in multiple sclerosis von Harbo, Hanne F, Isobe, Noriko, Berg-Hansen, Pål, Bos, Steffan D, Caillier, Stacy J, Gustavsen, Marte W, Mero, Inger-Lise, Celius, Elisabeth Gulowsen, Hauser, Stephen L, Oksenberg, Jorge R, Gourraud, Pierre-Antoine

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A rare variant of the TYK2 gene is confirmed to be associated with multiple sclerosis von MERO, Inger-Lise, LORENTZEN, Aslaug R, KOCKUM, Ingrid, MASTERMAN, Thomas, OTURAI, Annette Bang, SONDERGAARD, Helle Bach, SELLEBJERG, Finn, SAARELA, Janna, KEMPPINEN, Anu, ELOVAARA, Irina, SPURKLAND, Anne, DUDBRIDGE, Frank, BAN, Maria, LIE, Benedicte A, HARBO, Hanne F, SMESTAD, Cathrine, CELIUS, Elisabeth G, AARSETH, Jan H, MYHR, Kjell-Morten, LINK, Jenny, HILLERT, Jan, OLSSON, Tomas

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Oligoclonal band phenotypes in MS differ in their HLA class II association, while specific KIR ligands at HLA class I show association to MS in general von Gustavsen, Marte W, Viken, Marte K, Celius, Elisabeth G, Berge, Tone, Mero, Inger-Lise, Berg-Hansen, Pål, Aarseth, Jan H, Myhr, Kjell-Morten, Søndergaard, Helle B, Sellebjerg, Finn, Oturai, Annette B, Hillert, Jan, Alfredsson, Lars, Olsson, Tomas, Kockum, Ingrid, Lie, Benedicte A, Harbo, Hanne F

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Alterations in KLRB1 gene expression and a Scandinavian multiple sclerosis association study of the KLRB1 SNP rs4763655 von SØNDERGAARD, Helle Bach, SELLEBJERG, Finn, ROMME CHRISTENSEN, Jeppe, BÖRNSEN, Lars, SOELBERG SORENSEN, Per, BANG OTURAI, Annette, HILLERT, Jan, OLSSON, Tomas, KOCKUM, Ingrid, LINDEN, Magdalena, MERO, Inger-Lise, MYHR, Kjell-Morten, CELIUS, Elisabeth G, HARBO, Hanne F

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The genetic association of variants in CD6, TNFRSF1A and IRF8 to multiple sclerosis: a multicenter case-control study von International, Multiple Sclerosis Genetics Consortium

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No evidence of association between mutant alleles of the CYP27B1 gene and MS von Ban, Maria, Caillier, Stacy, Mero, Inger-Lise, Myhr, Kjell-Morten, Celius, Elisabeth G., Aarseth, Jan, Torkildsen, Øivind, Harbo, Hanne F., Oksenberg, Jorge, Hauser, Stephen L., Sawcer, Stephen, Compston, Alastair

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