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Lack of aggregation of ischemic stroke subtypes within affected sibling pairs.
Wiklund PG, Brown WM, Brott TG, Stegmayr B, Brown RD Jr, Nilsson-Ardnor S, Hardy JA, Kissela BM, Singleton A, Holmberg D, Rich SS, Meschia JF. Wiklund PG, et al. Among authors: nilsson ardnor s. Neurology. 2007 Feb 6;68(6):427-31. doi: 10.1212/01.wnl.0000252955.17126.6a. Neurology. 2007. PMID: 17283317
Genome-wide linkage scan of common stroke in families from northern Sweden.
Nilsson-Ardnor S, Janunger T, Wiklund PG, Lackovic K, Nilsson AK, Lindgren P, Escher SA, Stegmayr B, Asplund K, Holmberg D. Nilsson-Ardnor S, et al. Stroke. 2007 Jan;38(1):34-40. doi: 10.1161/01.STR.0000251643.37454.16. Epub 2006 Nov 22. Stroke. 2007. PMID: 17122438
The CTLA4 region as a general autoimmunity factor: an extended pedigree provides evidence for synergy with the HLA locus in the etiology of type 1 diabetes mellitus, Hashimoto's thyroiditis and Graves' disease.
Einarsdottir E, Söderström I, Löfgren-Burström A, Haraldsson S, Nilsson-Ardnor S, Penha-Goncalves C, Lind L, Holmgren G, Holmberg M, Asplund K, Holmberg D. Einarsdottir E, et al. Among authors: nilsson ardnor s. Eur J Hum Genet. 2003 Jan;11(1):81-4. doi: 10.1038/sj.ejhg.5200903. Eur J Hum Genet. 2003. PMID: 12529710
Spectrum of perforin gene mutations in familial hemophagocytic lymphohistiocytosis.
Göransdotter Ericson K, Fadeel B, Nilsson-Ardnor S, Söderhäll C, Samuelsson A, Janka G, Schneider M, Gürgey A, Yalman N, Révész T, Egeler R, Jahnukainen K, Storm-Mathiesen I, Haraldsson A, Poole J, de Saint Basile G, Nordenskjöld M, Henter J. Göransdotter Ericson K, et al. Among authors: nilsson ardnor s. Am J Hum Genet. 2001 Mar;68(3):590-7. doi: 10.1086/318796. Epub 2001 Feb 6. Am J Hum Genet. 2001. PMID: 11179007 Free PMC article.