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Items: 1 to 50 of 68

1.

Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families.

Gormley P, Kurki MI, Hiekkala ME, Veerapen K, Häppölä P, Mitchell AA, Lal D, Palta P, Surakka I, Kaunisto MA, Hämäläinen E, Vepsäläinen S, Havanka H, Harno H, Ilmavirta M, Nissilä M, Säkö E, Sumelahti ML, Liukkonen J, Sillanpää M, Metsähonkala L, Koskinen S, Lehtimäki T, Raitakari O, Männikkö M, Ran C, Belin AC, Jousilahti P, Anttila V, Salomaa V, Artto V, Färkkilä M; 23andMe Research Team; International Headache Genetics Consortium (IHGC), Runz H, Daly MJ, Neale BM, Ripatti S, Kallela M, Wessman M, Palotie A.

Neuron. 2018 Sep 5;99(5):1098. doi: 10.1016/j.neuron.2018.08.029. No abstract available.

PMID:
30189203
2.

Molecular genetic overlap between migraine and major depressive disorder.

Yang Y, Zhao H, Boomsma DI, Ligthart L, Belin AC, Smith GD, Esko T, Freilinger TM, Hansen TF, Ikram MA, Kallela M, Kubisch C, Paraskevi C, Strachan DP, Wessman M; International Headache Genetics Consortium, van den Maagdenberg AMJM, Terwindt GM, Nyholt DR.

Eur J Hum Genet. 2018 Aug;26(8):1202-1216. doi: 10.1038/s41431-018-0150-2. Epub 2018 Jul 11.

PMID:
29995844
3.

Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families.

Gormley P, Kurki MI, Hiekkala ME, Veerapen K, Häppölä P, Mitchell AA, Lal D, Palta P, Surakka I, Kaunisto MA, Hämäläinen E, Vepsäläinen S, Havanka H, Harno H, Ilmavirta M, Nissilä M, Säkö E, Sumelahti ML, Liukkonen J, Sillanpää M, Metsähonkala L, Koskinen S, Lehtimäki T, Raitakari O, Männikkö M, Ran C, Belin AC, Jousilahti P, Anttila V, Salomaa V, Artto V, Färkkilä M; 23andMe Research Team; International Headache Genetics Consortium (IHGC), Runz H, Daly MJ, Neale BM, Ripatti S, Kallela M, Wessman M, Palotie A.

Neuron. 2018 May 16;98(4):743-753.e4. doi: 10.1016/j.neuron.2018.04.014. Epub 2018 May 3. Erratum in: Neuron. 2018 Sep 5;99(5):1098.

PMID:
29731251
4.

The contribution of CACNA1A, ATP1A2 and SCN1A mutations in hemiplegic migraine: A clinical and genetic study in Finnish migraine families.

Hiekkala ME, Vuola P, Artto V, Häppölä P, Häppölä E, Vepsäläinen S, Cuenca-León E, Lal D, Gormley P, Hämäläinen E, Ilmavirta M, Nissilä M, Säkö E, Sumelahti ML, Harno H, Havanka H, Keski-Säntti P, Färkkilä M, Palotie A, Wessman M, Kaunisto MA, Kallela M.

Cephalalgia. 2018 Oct;38(12):1849-1863. doi: 10.1177/0333102418761041. Epub 2018 Feb 27.

PMID:
29486580
5.

Genetics of migraine.

Anttila V, Wessman M, Kallela M, Palotie A.

Handb Clin Neurol. 2018;148:493-503. doi: 10.1016/B978-0-444-64076-5.00031-4. Review.

PMID:
29478595
6.

Corrigendum: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine.

Gormley P, Anttila V, Winsvold BS, Palta P, Esko T, Pers TH, Farh KH, Cuenca-Leon E, Muona M, Furlotte NA, Kurth T, Ingason A, McMahon G, Ligthart L, Terwindt GM, Kallela M, Freilinger TM, Ran C, Gordon SG, Stam AH, Steinberg S, Borck G, Koiranen M, Quaye L, Adams HH, Lehtimäki T, Sarin AP, Wedenoja J, Hinds DA, Buring JE, Schürks M, Ridker PM, Hrafnsdottir MG, Stefansson H, Ring SM, Hottenga JJ, Penninx BW, Färkkilä M, Artto V, Kaunisto M, Vepsäläinen S, Malik R, Heath AC, Madden PA, Martin NG, Montgomery GW, Kurki MI, Kals M, Mägi R, Pärn K, Hämäläinen E, Huang H, Byrnes AE, Franke L, Huang J, Stergiakouli E, Lee PH, Sandor C, Webber C, Cader Z, Muller-Myhsok B, Schreiber S, Meitinger T, Eriksson JG, Salomaa V, Heikkilä K, Loehrer E, Uitterlinden AG, Hofman A, van Duijn CM, Cherkas L, Pedersen LM, Stubhaug A, Nielsen CS, Männikkö M, Mihailov E, Milani L, Göbel H, Esserlind AL, Christensen AF, Hansen TF, Werge T; International Headache Genetics Consortium, Kaprio J, Aromaa AJ, Raitakari O, Ikram MA, Spector T, Järvelin MR, Metspalu A, Kubisch C, Strachan DP, Ferrari MD, Belin AC, Dichgans M, Wessman M, van den Maagdenberg AM, Zwart JA, Boomsma DI, Smith GD, Stefansson K, Eriksson N, Daly MJ, Neale BM, Olesen J, Chasman DI, Nyholt DR, Palotie A.

Nat Genet. 2016 Sep 28;48(10):1296. doi: 10.1038/ng1016-1296c. No abstract available.

PMID:
27681292
7.

Migraine genetics: from genome-wide association studies to translational insights.

Gormley P, Winsvold BS, Nyholt DR, Kallela M, Chasman DI, Palotie A.

Genome Med. 2016 Aug 19;8(1):86. doi: 10.1186/s13073-016-0346-4. No abstract available.

8.

Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine.

Gormley P, Anttila V, Winsvold BS, Palta P, Esko T, Pers TH, Farh KH, Cuenca-Leon E, Muona M, Furlotte NA, Kurth T, Ingason A, McMahon G, Ligthart L, Terwindt GM, Kallela M, Freilinger TM, Ran C, Gordon SG, Stam AH, Steinberg S, Borck G, Koiranen M, Quaye L, Adams HH, Lehtimäki T, Sarin AP, Wedenoja J, Hinds DA, Buring JE, Schürks M, Ridker PM, Hrafnsdottir MG, Stefansson H, Ring SM, Hottenga JJ, Penninx BW, Färkkilä M, Artto V, Kaunisto M, Vepsäläinen S, Malik R, Heath AC, Madden PA, Martin NG, Montgomery GW, Kurki MI, Kals M, Mägi R, Pärn K, Hämäläinen E, Huang H, Byrnes AE, Franke L, Huang J, Stergiakouli E, Lee PH, Sandor C, Webber C, Cader Z, Muller-Myhsok B, Schreiber S, Meitinger T, Eriksson JG, Salomaa V, Heikkilä K, Loehrer E, Uitterlinden AG, Hofman A, van Duijn CM, Cherkas L, Pedersen LM, Stubhaug A, Nielsen CS, Männikkö M, Mihailov E, Milani L, Göbel H, Esserlind AL, Christensen AF, Hansen TF, Werge T; International Headache Genetics Consortium, Kaprio J, Aromaa AJ, Raitakari O, Ikram MA, Spector T, Järvelin MR, Metspalu A, Kubisch C, Strachan DP, Ferrari MD, Belin AC, Dichgans M, Wessman M, van den Maagdenberg AM, Zwart JA, Boomsma DI, Smith GD, Stefansson K, Eriksson N, Daly MJ, Neale BM, Olesen J, Chasman DI, Nyholt DR, Palotie A.

Nat Genet. 2016 Aug;48(8):856-66. doi: 10.1038/ng.3598. Epub 2016 Jun 20. Erratum in: Nat Genet. 2016 Sep 28;48(10 ):1296.

9.

Genetic analysis for a shared biological basis between migraine and coronary artery disease.

Winsvold BS, Nelson CP, Malik R, Gormley P, Anttila V, Vander Heiden J, Elliott KS, Jacobsen LM, Palta P, Amin N, de Vries B, Hämäläinen E, Freilinger T, Ikram MA, Kessler T, Koiranen M, Ligthart L, McMahon G, Pedersen LM, Willenborg C, Won HH, Olesen J, Artto V, Assimes TL, Blankenberg S, Boomsma DI, Cherkas L, Davey Smith G, Epstein SE, Erdmann J, Ferrari MD, Göbel H, Hall AS, Jarvelin MR, Kallela M, Kaprio J, Kathiresan S, Lehtimäki T, McPherson R, März W, Nyholt DR, O'Donnell CJ, Quaye L, Rader DJ, Raitakari O, Roberts R, Schunkert H, Schürks M, Stewart AF, Terwindt GM, Thorsteinsdottir U, van den Maagdenberg AM, van Duijn C, Wessman M, Kurth T, Kubisch C, Dichgans M, Chasman DI, Cotsapas C, Zwart JA, Samani NJ, Palotie A; CARDIoGRAM Consortium and the International Headache Genetics Consortium.

Neurol Genet. 2015 Jul 2;1(1):e10. doi: 10.1212/NXG.0000000000000010. eCollection 2015 Jun.

10.

Headache as symptom of intracranial hemorrhage.

Mäkitie L, Korja M, Kangasniemi M, Kallela M, Forss N, Niemelä M, Lindsberg PJ.

Duodecim. 2016;132(21):1993-9.

PMID:
29190051
11.

Gene-based pleiotropy across migraine with aura and migraine without aura patient groups.

Zhao H, Eising E, de Vries B, Vijfhuizen LS; International Headache Genetics Consortium, Anttila V, Winsvold BS, Kurth T, Stefansson H, Kallela M, Malik R, Stam AH, Ikram MA, Ligthart L, Freilinger T, Alexander M, Müller-Myhsok B, Schreiber S, Meitinger T, Aromas A, Eriksson JG, Boomsma DI, van Duijn CM, Zwart JA, Quaye L, Kubisch C, Dichgans M, Wessman M, Stefansson K, Chasman DI, Palotie A, Martin NG, Montgomery GW, Ferrari MD, Terwindt GM, van den Maagdenberg AM, Nyholt DR.

Cephalalgia. 2016 Jun;36(7):648-57. doi: 10.1177/0333102415591497. Epub 2015 Dec 8.

12.

Premonitory symptoms in migraine: A cross-sectional study in 2714 persons.

Laurell K, Artto V, Bendtsen L, Hagen K, Häggström J, Linde M, Söderström L, Tronvik E, Wessman M, Zwart JA, Kallela M.

Cephalalgia. 2016 Sep;36(10):951-9. doi: 10.1177/0333102415620251. Epub 2015 Dec 6.

PMID:
26643378
13.

Shared genetic basis for migraine and ischemic stroke: A genome-wide analysis of common variants.

Malik R, Freilinger T, Winsvold BS, Anttila V, Vander Heiden J, Traylor M, de Vries B, Holliday EG, Terwindt GM, Sturm J, Bis JC, Hopewell JC, Ferrari MD, Rannikmae K, Wessman M, Kallela M, Kubisch C, Fornage M, Meschia JF, Lehtimäki T, Sudlow C, Clarke R, Chasman DI, Mitchell BD, Maguire J, Kaprio J, Farrall M, Raitakari OT, Kurth T, Ikram MA, Reiner AP, Longstreth WT Jr, Rothwell PM, Strachan DP, Sharma P, Seshadri S, Quaye L, Cherkas L, Schürks M, Rosand J, Ligthart L, Boncoraglio GB, Davey Smith G, van Duijn CM, Stefansson K, Worrall BB, Nyholt DR, Markus HS, van den Maagdenberg AM, Cotsapas C, Zwart JA, Palotie A; International Headache Genetics Consortium, Dichgans M; METASTROKE Collaboration of the International Stroke Genetics Consortium.

Neurology. 2015 May 26;84(21):2132-45. doi: 10.1212/WNL.0000000000001606. Epub 2015 May 1.

14.

Systematic re-evaluation of genes from candidate gene association studies in migraine using a large genome-wide association data set.

de Vries B, Anttila V, Freilinger T, Wessman M, Kaunisto MA, Kallela M, Artto V, Vijfhuizen LS, Göbel H, Dichgans M, Kubisch C, Ferrari MD, Palotie A, Terwindt GM, van den Maagdenberg AM; International Headache Genetics Consortium.

Cephalalgia. 2016 Jun;36(7):604-14. doi: 10.1177/0333102414566820. Epub 2015 Jan 29.

PMID:
25633374
15.

Concordance of genetic risk across migraine subgroups: Impact on current and future genetic association studies.

Nyholt DR; International Headache Genetics Consortium, Anttila V, Winsvold BS, Kurth T, Stefansson H, Kallela M, Malik R, Vries Bd, Terwindt GM, Ikram MA, Stam AH, Ligthart L, Freilinger T, Alexander M, Muller-Myhsok B, Schreiber S, Meitinger T, Aromaa A, Eriksson JG, Kaprio J, Boomsma DI, Duijn Cv, Raitakari O, Järvelin MR, Zwart JA, Quaye L, Strachan DP, Kubisch C, Ferrari MD, van den Maagdenberg AM, Dichgans M, Wessman M, Smith GD, Stefansson K, Chasman DI, Palotie A.

Cephalalgia. 2015 May;35(6):489-99. doi: 10.1177/0333102414547784. Epub 2014 Sep 1.

PMID:
25179292
16.

[Vertigo from the practitioner's standpoint].

Kallela M, Kentala E.

Duodecim. 2014;130(4):400-12. Review. Finnish.

PMID:
24673009
17.

[Unconsciousness].

Kallela M, Häppölä O, Eriksson H.

Duodecim. 2014;130(4):368-82. Review. Finnish.

PMID:
24673006
18.

The relationship between headache and religious attendance (the Nord-Trøndelag health study-HUNT).

Tronvik E, Sørensen T, Linde M, Bendtsen L, Artto V, Laurell K, Kallela M, Zwart JA, Hagen K.

J Headache Pain. 2014 Jan 3;15:1. doi: 10.1186/1129-2377-15-1.

19.

Genome-wide meta-analysis identifies new susceptibility loci for migraine.

Anttila V, Winsvold BS, Gormley P, Kurth T, Bettella F, McMahon G, Kallela M, Malik R, de Vries B, Terwindt G, Medland SE, Todt U, McArdle WL, Quaye L, Koiranen M, Ikram MA, Lehtimäki T, Stam AH, Ligthart L, Wedenoja J, Dunham I, Neale BM, Palta P, Hamalainen E, Schürks M, Rose LM, Buring JE, Ridker PM, Steinberg S, Stefansson H, Jakobsson F, Lawlor DA, Evans DM, Ring SM, Färkkilä M, Artto V, Kaunisto MA, Freilinger T, Schoenen J, Frants RR, Pelzer N, Weller CM, Zielman R, Heath AC, Madden PAF, Montgomery GW, Martin NG, Borck G, Göbel H, Heinze A, Heinze-Kuhn K, Williams FMK, Hartikainen AL, Pouta A, van den Ende J, Uitterlinden AG, Hofman A, Amin N, Hottenga JJ, Vink JM, Heikkilä K, Alexander M, Muller-Myhsok B, Schreiber S, Meitinger T, Wichmann HE, Aromaa A, Eriksson JG, Traynor B, Trabzuni D; North American Brain Expression Consortium; UK Brain Expression Consortium, Rossin E, Lage K, Jacobs SBR, Gibbs JR, Birney E, Kaprio J, Penninx BW, Boomsma DI, van Duijn C, Raitakari O, Jarvelin MR, Zwart JA, Cherkas L, Strachan DP, Kubisch C, Ferrari MD, van den Maagdenberg AMJM, Dichgans M, Wessman M, Smith GD, Stefansson K, Daly MJ, Nyholt DR, Chasman D, Palotie A.

Nat Genet. 2013 Aug;45(8):912-917. doi: 10.1038/ng.2676. Epub 2013 Jun 23.

20.

Probing the brain of comorbidity.

Palotie A, Kallela M, Anttila V.

Sci Transl Med. 2013 May 1;5(183):183fs15, 1-3. doi: 10.1126/scitranslmed.3006229. No abstract available.

PMID:
23636091
21.

[Treatment of prolonged migraine attack (status migrenosus)].

Artto V, Kallela M.

Duodecim. 2012;128(15):1577-82. Review. Finnish.

PMID:
22970609
22.

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.

Nat Genet. 2012 Jun 10;44(7):777-82. doi: 10.1038/ng.2307.

23.

[How do I distinguish migraine aura from TIA attack?].

Kallela M, Lindsberg PJ.

Duodecim. 2012;128(9):971-7. Finnish.

PMID:
22667050
24.

Shared loci for migraine and epilepsy on chromosomes 14q12-q23 and 12q24.2-q24.3.

Polvi A, Siren A, Kallela M, Rantala H, Artto V, Sobel EM, Palotie A, Lehesjoki AE, Wessman M.

Neurology. 2012 Jan 17;78(3):202-9. doi: 10.1212/WNL.0b013e31823fcd87. Epub 2012 Jan 4.

25.

Genome-wide association study reveals three susceptibility loci for common migraine in the general population.

Chasman DI, Schürks M, Anttila V, de Vries B, Schminke U, Launer LJ, Terwindt GM, van den Maagdenberg AM, Fendrich K, Völzke H, Ernst F, Griffiths LR, Buring JE, Kallela M, Freilinger T, Kubisch C, Ridker PM, Palotie A, Ferrari MD, Hoffmann W, Zee RY, Kurth T.

Nat Genet. 2011 Jun 12;43(7):695-8. doi: 10.1038/ng.856.

26.

Towards an understanding of genetic predisposition to migraine.

Anttila V, Wessman M, Kallela M, Palotie A.

Genome Med. 2011 Mar 21;3(3):17. doi: 10.1186/gm231.

27.

Migrainous infarction: a Nordic multicenter study.

Laurell K, Artto V, Bendtsen L, Hagen K, Kallela M, Meyer EL, Putaala J, Tronvik E, Zwart JA, Linde M.

Eur J Neurol. 2011 Oct;18(10):1220-6. doi: 10.1111/j.1468-1331.2011.03364.x. Epub 2011 Mar 18.

PMID:
21414105
28.

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.

Nat Genet. 2010 Oct;42(10):869-73. doi: 10.1038/ng.652. Epub 2010 Aug 29.

29.

Migraine with aura is a risk factor for cervical artery dissection: a case-control study.

Artto V, Metso TM, Metso AJ, Putaala J, Haapaniemi E, Wessman M, Färkkilä M, Kallela M, Tatlisumak T.

Cerebrovasc Dis. 2010;30(1):36-40. doi: 10.1159/000313608. Epub 2010 Apr 29.

PMID:
20431287
30.

A visual migraine aura locus maps to 9q21-q22.

Tikka-Kleemola P, Artto V, Vepsäläinen S, Sobel EM, Räty S, Kaunisto MA, Anttila V, Hämäläinen E, Sumelahti ML, Ilmavirta M, Färkkilä M, Kallela M, Palotie A, Wessman M.

Neurology. 2010 Apr 13;74(15):1171-7. doi: 10.1212/WNL.0b013e3181d8ffcb.

31.

Short-term frovatriptan for the prevention of difficult-to-treat menstrual migraine attacks.

Brandes JL, Poole Ac, Kallela M, Schreiber CP, MacGregor EA, Silberstein SD, Tobin J, Shaw R.

Cephalalgia. 2009 Nov;29(11):1133-48. doi: 10.1111/j.1468-2982.2009.01840.x.

PMID:
19811503
32.

Genetic association study of endothelin-1 and its receptors EDNRA and EDNRB in migraine with aura.

Tikka-Kleemola P, Kaunisto MA, Hämäläinen E, Todt U, Göbel H, Kaprio J, Kubisch C, Färkkilä M, Palotie A, Wessman M, Kallela M.

Cephalalgia. 2009 Nov;29(11):1224-31. doi: 10.1111/j.1468-2982.2009.01855.x. Epub 2009 Apr 9.

33.

Lateralization in cluster headache: a Nordic multicenter study.

Meyer EL, Laurell K, Artto V, Bendtsen L, Linde M, Kallela M, Tronvik E, Zwart JA, Jensen RM, Hagen K.

J Headache Pain. 2009 Aug;10(4):259-63. doi: 10.1007/s10194-009-0129-z. Epub 2009 Jun 3.

34.

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.

Hum Mol Genet. 2008 Nov 1;17(21):3318-31. doi: 10.1093/hmg/ddn227. Epub 2008 Aug 2.

35.

Valsalva maneuver as migraine inducer: a case report of a woman with patent foramen ovale and an ischemic stroke.

Artto V, Anttila V, Rantanen K, Kallela M, Färkkilä M.

Headache. 2009 Jan;49(1):146-7. doi: 10.1111/j.1526-4610.2008.01143.x. Epub 2008 Jun 11.

PMID:
18549412
36.

Consistently replicating locus linked to migraine on 10q22-q23.

Anttila V, Nyholt DR, Kallela M, Artto V, Vepsäläinen S, Jakkula E, Wennerström A, Tikka-Kleemola P, Kaunisto MA, Hämäläinen E, Widén E, Terwilliger J, Merikangas K, Montgomery GW, Martin NG, Daly M, Kaprio J, Peltonen L, Färkkilä M, Wessman M, Palotie A.

Am J Hum Genet. 2008 May;82(5):1051-63. doi: 10.1016/j.ajhg.2008.03.003.

37.

Treatment of hemiplegic migraine with triptans.

Artto V, Nissilä M, Wessman M, Palotie A, Färkkilä M, Kallela M.

Eur J Neurol. 2007 Sep;14(9):1053-6.

PMID:
17718700
38.

Sweet taste preferences are partly genetically determined: identification of a trait locus on chromosome 16.

Keskitalo K, Knaapila A, Kallela M, Palotie A, Wessman M, Sammalisto S, Peltonen L, Tuorila H, Perola M.

Am J Clin Nutr. 2007 Jul;86(1):55-63.

PMID:
17616763
39.

No association of migraine to the GABA-A receptor complex on chromosome 15.

Oswell G, Kaunisto MA, Kallela M, Hämäläinen E, Anttila V, Kaprio J, Färkkilä M, Wessman M, Palotie A.

Am J Med Genet B Neuropsychiatr Genet. 2008 Jan 5;147B(1):33-6.

PMID:
17580321
40.

Food neophobia shows heritable variation in humans.

Knaapila A, Tuorila H, Silventoinen K, Keskitalo K, Kallela M, Wessman M, Peltonen L, Cherkas LF, Spector TD, Perola M.

Physiol Behav. 2007 Aug 15;91(5):573-8. Epub 2007 Mar 30.

PMID:
17459432
41.

Genetic component of identification, intensity and pleasantness of odours: a Finnish family study.

Knaapila A, Keskitalo K, Kallela M, Wessman M, Sammalisto S, Hiekkalinna T, Palotie A, Peltonen L, Tuorila H, Perola M.

Eur J Hum Genet. 2007 May;15(5):596-602. Epub 2007 Mar 7.

42.

Idiopaattinen intrakraniaalinen hypertensio, "pseudotumor cerebri".

Setälä K, Kallela M, Valanne L, Hernesniemi J, Dashti R, Pelaez J, Färkkilä M.

Duodecim. 2007;123(1):55-63. Finnish. No abstract available.

PMID:
17328294
43.

Testing of variants of the MTHFR and ESR1 genes in 1798 Finnish individuals fails to confirm the association with migraine with aura.

Kaunisto MA, Kallela M, Hämäläinen E, Kilpikari R, Havanka H, Harno H, Nissilä M, Säkö E, Ilmavirta M, Liukkonen J, Teirmaa H, Törnwall O, Jussila M, Terwilliger J, Färkkilä M, Kaprio J, Palotie A, Wessman M.

Cephalalgia. 2006 Dec;26(12):1462-72.

PMID:
17116097
44.

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.

J Headache Pain. 2006 Oct;7(5):324-30. Epub 2006 Oct 25.

45.

Door to thrombolysis: ER reorganization and reduced delays to acute stroke treatment.

Lindsberg PJ, Häppölä O, Kallela M, Valanne L, Kuisma M, Kaste M.

Neurology. 2006 Jul 25;67(2):334-6.

PMID:
16864834
46.

Trait components provide tools to dissect the genetic susceptibility of migraine.

Anttila V, Kallela M, Oswell G, Kaunisto MA, Nyholt DR, Hamalainen E, Havanka H, Ilmavirta M, Terwilliger J, Sobel E, Peltonen L, Kaprio J, Farkkila M, Wessman M, Palotie A.

Am J Hum Genet. 2006 Jul;79(1):85-99. Epub 2006 May 10.

47.

Eletriptan review.

Färkkilä M, Kallela M.

Expert Opin Pharmacother. 2005 Apr;6(4):625-30. Review.

PMID:
15934888
48.

[What is new in the pathophysiology and genetics of migraine?].

Kallela M.

Duodecim. 2005;121(6):665-73. Review. Finnish. No abstract available.

PMID:
15907094
49.

Decreased cerebellar total creatine in episodic ataxia type 2: a 1H MRS study.

Harno H, Heikkinen S, Kaunisto MA, Kallela M, Häkkinen AM, Wessman M, Färkkilä M, Lundbom N.

Neurology. 2005 Feb 8;64(3):542-4.

PMID:
15699392
50.

The molecular genetics of migraine.

Wessman M, Kaunisto MA, Kallela M, Palotie A.

Ann Med. 2004;36(6):462-73. Review.

PMID:
15513297

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