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802 results

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A high-density association screen of 155 ion transport genes for involvement with common migraine.
Nyholt DR, LaForge KS, Kallela M, Alakurtti K, Anttila V, Färkkilä M, Hämaläinen E, Kaprio J, Kaunisto MA, Heath AC, Montgomery GW, Göbel H, Todt U, Ferrari MD, Launer LJ, Frants RR, Terwindt GM, de Vries B, Verschuren WM, Brand J, Freilinger T, Pfaffenrath V, Straube A, Ballinger DG, Zhan Y, Daly MJ, Cox DR, Dichgans M, van den Maagdenberg AM, Kubisch C, Martin NG, Wessman M, Peltonen L, Palotie A. Nyholt DR, et al. Among authors: palotie a. Hum Mol Genet. 2008 Nov 1;17(21):3318-31. doi: 10.1093/hmg/ddn227. Epub 2008 Aug 2. Hum Mol Genet. 2008. PMID: 18676988 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.
Fine mapping of a multiple sclerosis locus to 2.5 Mb on chromosome 17q22-q24.
Saarela J, Schoenberg Fejzo M, Chen D, Finnilä S, Parkkonen M, Kuokkanen S, Sobel E, Tienari PJ, Sumelahti ML, Wikström J, Elovaara I, Koivisto K, Pirttilä T, Reunanen M, Palotie A, Peltonen L. Saarela J, et al. Among authors: palotie a. Hum Mol Genet. 2002 Sep 15;11(19):2257-67. doi: 10.1093/hmg/11.19.2257. Hum Mol Genet. 2002. PMID: 12217954
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 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.
802 results