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Page 1
Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1.
Anttila V, Stefansson H, Kallela M, Todt U, Terwindt GM, Calafato MS, Nyholt DR, Dimas AS, Freilinger T, Müller-Myhsok B, Artto V, Inouye M, Alakurtti K, Kaunisto MA, Hämäläinen E, de Vries B, Stam AH, Weller CM, Heinze A, Heinze-Kuhn K, Goebel I, Borck G, Göbel H, Steinberg S, Wolf C, Björnsson A, Gudmundsson G, Kirchmann M, Hauge A, Werge T, Schoenen J, Eriksson JG, Hagen K, Stovner L, Wichmann HE, Meitinger T, Alexander M, Moebus S, Schreiber S, Aulchenko YS, Breteler MM, Uitterlinden AG, Hofman A, van Duijn CM, Tikka-Kleemola P, Vepsäläinen S, Lucae S, Tozzi F, Muglia P, Barrett J, Kaprio J, Färkkilä M, Peltonen L, Stefansson K, Zwart JA, Ferrari MD, Olesen J, Daly M, Wessman M, van den Maagdenberg AM, Dichgans M, Kubisch C, Dermitzakis ET, Frants RR, Palotie A; International Headache Genetics Consortium. Anttila V, et al. Among authors: palotie a. Nat Genet. 2010 Oct;42(10):869-73. doi: 10.1038/ng.652. Epub 2010 Aug 29. Nat Genet. 2010. PMID: 20802479 Free PMC article.
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: palotie a. 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.
Kinetic alterations due to a missense mutation in the Na,K-ATPase alpha2 subunit cause familial hemiplegic migraine type 2.
Segall L, Scanzano R, Kaunisto MA, Wessman M, Palotie A, Gargus JJ, Blostein R. Segall L, et al. Among authors: palotie a. J Biol Chem. 2004 Oct 15;279(42):43692-6. doi: 10.1074/jbc.M407471200. Epub 2004 Aug 11. J Biol Chem. 2004. PMID: 15308625 Free article.
A., Harno, H., Vanmolkot, K. R., Gargus, J. J., Sun, G., Hamalainen, E., Liukkonen, E., Kallela, M., van den Maagdenberg, A. M., Frants, R. R., Farkkila, M., Palotie, A., and Wessman, M. (2004) Neurogenetics 5, 141-146). Introducing T345A into the cons …
A., Harno, H., Vanmolkot, K. R., Gargus, J. J., Sun, G., Hamalainen, E., Liukkonen, E., Kallela, M., van den Maagdenberg, A. M …
Chromosome 19p13 loci in Finnish migraine with aura families.
Kaunisto MA, Tikka PJ, Kallela M, Leal SM, Papp JC, Korhonen A, Hämäläinen E, Harno H, Havanka H, Nissilä M, Säkö E, Ilmavirta M, Kaprio J, Färkkilä M, Ophoff RA, Palotie A, Wessman M. Kaunisto MA, et al. Among authors: palotie a. Am J Med Genet B Neuropsychiatr Genet. 2005 Jan 5;132B(1):85-9. doi: 10.1002/ajmg.b.30082. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 15449251 Free PMC article.
The molecular genetics of migraine.
Wessman M, Kaunisto MA, Kallela M, Palotie A. Wessman M, et al. Among authors: palotie a. Ann Med. 2004;36(6):462-73. doi: 10.1080/07853890410018060. Ann Med. 2004. PMID: 15513297 Free article. Review.
Lessons from studying monogenic disease for common disease.
Peltonen L, Perola M, Naukkarinen J, Palotie A. Peltonen L, et al. Among authors: palotie a. Hum Mol Genet. 2006 Apr 15;15 Spec No 1:R67-74. doi: 10.1093/hmg/ddl060. Hum Mol Genet. 2006. PMID: 16651371 Review. No abstract available.
Comorbidity in Finnish migraine families.
Artto V, Wessman M, Nissilä M, Säkö E, Liukkonen J, Teirmaa H, Harno H, Havanka H, Ilmavirta M, Palotie A, Färkkilä M, Kallela M. Artto V, et al. Among authors: palotie a. J Headache Pain. 2006 Oct;7(5):324-30. doi: 10.1007/s10194-006-0319-x. Epub 2006 Oct 25. J Headache Pain. 2006. PMID: 17058048 Free PMC article.
The enhancement of homogenous mass extension reaction: comparison of two enzymes.
Tikka-Kleemola P, Hämäläinen E, Tuomainen K, Suvela M, Artma A, Kahre O, Wessman M, Palotie A, Silander K. Tikka-Kleemola P, et al. Among authors: palotie a. Mol Cell Probes. 2007 Jun;21(3):216-21. doi: 10.1016/j.mcp.2006.12.003. Epub 2007 Jan 12. Mol Cell Probes. 2007. PMID: 17331699
840 results