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Genome-wide association analysis identifies susceptibility loci for migraine without aura.
Freilinger T, Anttila V, de Vries B, Malik R, Kallela M, Terwindt GM, Pozo-Rosich P, Winsvold B, Nyholt DR, van Oosterhout WP, Artto V, Todt U, Hämäläinen E, Fernández-Morales J, Louter MA, Kaunisto MA, Schoenen J, Raitakari O, Lehtimäki T, Vila-Pueyo M, Göbel H, Wichmann E, Sintas C, Uitterlinden AG, Hofman A, Rivadeneira F, Heinze A, Tronvik E, van Duijn CM, Kaprio J, Cormand B, Wessman M, Frants RR, Meitinger T, Müller-Myhsok B, Zwart JA, Färkkilä M, Macaya A, Ferrari MD, Kubisch C, Palotie A, Dichgans M, van den Maagdenberg AM; International Headache Genetics Consortium. Freilinger T, et al. Among authors: kallela m. Nat Genet. 2012 Jun 10;44(7):777-82. doi: 10.1038/ng.2307. Nat Genet. 2012. PMID: 22683712 Free PMC article.
Endothelin in migraine patients.
Kallela M, Färkkilä M, Saijonmaa O, Fyhrquist F. Kallela M, et al. Cephalalgia. 1998 Jul-Aug;18(6):329-32. doi: 10.1046/j.1468-2982.1998.1806329.x. Cephalalgia. 1998. PMID: 9731937
A susceptibility locus for migraine with aura, on chromosome 4q24.
Wessman M, Kallela M, Kaunisto MA, Marttila P, Sobel E, Hartiala J, Oswell G, Leal SM, Papp JC, Hämäläinen E, Broas P, Joslyn G, Hovatta I, Hiekkalinna T, Kaprio J, Ott J, Cantor RM, Zwart JA, Ilmavirta M, Havanka H, Färkkilä M, Peltonen L, Palotie A. Wessman M, et al. Among authors: kallela m. Am J Hum Genet. 2002 Mar;70(3):652-62. doi: 10.1086/339078. Epub 2002 Feb 8. Am J Hum Genet. 2002. PMID: 11836652 Free PMC article.
Novel splice site CACNA1A mutation causing episodic ataxia type 2.
Kaunisto MA, Harno H, Kallela M, Somer H, Sallinen R, Hämäläinen E, Miettinen PJ, Vesa J, Orpana A, Palotie A, Färkkilä M, Wessman M. Kaunisto MA, et al. Among authors: kallela m. Neurogenetics. 2004 Feb;5(1):69-73. doi: 10.1007/s10048-003-0161-0. Epub 2003 Oct 7. Neurogenetics. 2004. PMID: 14530926
120 results