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Genome-wide significant association with seven novel multiple sclerosis risk loci.
Lill CM, Luessi F, Alcina A, Sokolova EA, Ugidos N, de la Hera B, Guillot-Noël L, Malhotra S, Reinthaler E, Schjeide BM, Mescheriakova JY, Mashychev A, Wohlers I, Akkad DA, Aktas O, Alloza I, Antigüedad A, Arroyo R, Astobiza I, Blaschke P, Boyko AN, Buttmann M, Chan A, Dörner T, Epplen JT, Favorova OO, Fedetz M, Fernández O, García-Martínez A, Gerdes LA, Graetz C, Hartung HP, Hoffjan S, Izquierdo G, Korobko DS, Kroner A, Kubisch C, Kümpfel T, Leyva L, Lohse P, Malkova NA, Montalban X, Popova EV, Rieckmann P, Rozhdestvenskii AS, Schmied C, Smagina IV, Tsareva EY, Winkelmann A, Zettl UK, Binder H, Cournu-Rebeix I, Hintzen R, Zimprich A, Comabella M, Fontaine B, Urcelay E, Vandenbroeck K, Filipenko M, Matesanz F, Zipp F, Bertram L. Lill CM, et al. Among authors: hoffjan s. J Med Genet. 2015 Dec;52(12):848-55. doi: 10.1136/jmedgenet-2015-103442. Epub 2015 Oct 16. J Med Genet. 2015. PMID: 26475045
A 21-year-old woman with progressive asymptomatic skin laxity in flexural regions.
Gambichler T, Hoffjan S, Nagel M, Terschlüsen M, Mansour R, Würfel L, Hoffmann K, Susok L, Dickel H, Doerler M. Gambichler T, et al. Among authors: hoffjan s. Clin Exp Dermatol. 2023 Sep 19;48(10):1198-1201. doi: 10.1093/ced/llad170. Clin Exp Dermatol. 2023. PMID: 37171041 No abstract available.
Polymorphisms in NACHT-LRR (NLR) genes in atopic dermatitis.
Macaluso F, Nothnagel M, Parwez Q, Petrasch-Parwez E, Bechara FG, Epplen JT, Hoffjan S. Macaluso F, et al. Among authors: hoffjan s. Exp Dermatol. 2007 Aug;16(8):692-8. doi: 10.1111/j.1600-0625.2007.00589.x. Exp Dermatol. 2007. PMID: 17620097
100 results