Whole-exome sequencing in moyamoya patients of Northern-European origin identifies gene variants involved in Nitric Oxide metabolism: A pilot study by Markus K.H. Wiedmann, Ingunn V. Steinsvåg, Tovy Dinh, Magnus D. Vigeland, Pål G. Larsson, Hanne Hjorthaug, Ying Sheng, Inger-Lise Mero, Kaja K. Selmer

Get full text

Novel Loss of Function Variants in <i>CENPF</i> Including a Large Intragenic Deletion in Patients with Strømme Syndrome by Doriana Misceo, Lokuliyanage Dona Samudita Senaratne, Inger-Lise Mero, Arvind Y. M. Sundaram, Pål Marius Bjørnstad, Krzysztof Szczałuba, Piotr Gasperowicz, Benjamin Kamien, Bård Nedregaard, Asbjørn Holmgren, Petter Strømme, Eirik Frengen

Get full text

Associations between APOE genotypes and disease susceptibility, joint damage and lipid levels in patients with rheumatoid arthritis. by Marthe T Maehlen, Sella A Provan, Diederik P C de Rooy, Annette H M van der Helm-van Mil, Annemarie Krabben, Tore Saxne, Elisabet Lindqvist, Anne Grete Semb, Till Uhlig, Désirée van der Heijde, Inger Lise Mero, Inge C Olsen, Tore K Kvien, Benedicte A Lie

Get full text

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

Get full text