• PL 20 (Tukholmankatu 8)

    00014

    Finland

19992019
If you made any changes in Pure these will be visible here soon.

Publications 1999 2019

  • 50 Article
  • 3 Review Article
  • 2 Conference article
Filter
Article
2019

CACNG2 polymorphisms associate with chronic pain following mastectomy

Bortsov, A. V., Devor, M., Kaunisto, M. A., Kalso, E., Brufsky, A., Kehlet, H., Aasvang, E., Bittner, R., Diatchenko, L. & Belfer, I., Mar 2019, In : Pain. 160, 3, p. 561-568 8 p.

Research output: Contribution to journalArticleScientificpeer-review

Common Inflammation-Related Candidate Gene Variants and Acute Kidney Injury in 2647 Critically Ill Finnish Patients

Vilander, L. M., Vaara, S. T., Kaunisto, M. A., Pettilä, V., FINNAKI Study Grp, Laru-Sompa, R., Pulkkinen, A., Saarelainen, M., Reilama, M., Tolmunen, S., Rantalainen, U., Miettinen, M., Suvela, M., Pesola, K., Saastamoinen, P., Kauppinen, S., Kaukonen, K-M., Korhonen, A-M., Nisula, S., Vaara, S. & 81 othersSuojaranta-Ylinen, R., Mildh, L., Haapio, M., Nurminen, L., Sutinen, S., Pettilä, L., Laitinen, H., Syrja, H., Henttonen, K., Lappi, E., Boman, H., Varpula, T., Porkka, P., Sivula, M., Rahkonen, M., Tsurkka, A., Nieminen, T., Prittinen, N., Alaspaa, A., Salanto, V., Juntunen, H., Sanisalo, T., Parviainen, I., Uusaro, A., Ruokonen, E., Bendel, S., Rissanen, N., Lång, M., Rahikainen, S., Rissanen, S., Ahonen, M., Halonen, E., Vaskelainen, E., Poukkanen, M., Lintula, E., Suominen, S., Heikkinen, J., Lavander, T., Heinonen, K., Juopperi, A-M., Kaminski, T., Gäddnäs, F., Kuusela, T., Roiko, J., Karlsson, S., Reinikainen, M., Surakka, T., Jyrkönen, H., Eiserbeck, T., Kallinen, J., Lund, V., Tuominen, P., Perkola, P., Tuominen, R., Hietaranta, M., Johansson, S., Hovilehto, S., Kirsi, A., Tiainen, P., Myllärinen, T., Leino, P., Toropainen, A., Kuitunen, A., Leppänen, I., Levoranta, M., Hoppu, S., Sauranen, J., Tenhunen, J., Kukkurainen, A., Kortelainen, S., Varila, S., Inkinen, O., Koivuviita, N., Kotamäki, J., Laine, A., Ala-Kokko, T., Laurila, J. J., Sälkiö, S., Koivisto, S-P., Hautamäki, R. & Skinnar, M., 11 Mar 2019, In : Journal of clinical medicine. 8, 3, 13 p., 342.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
File

Genetic architecture of human plasma lipidome and its link to cardiovascular disease

FinnGen Project, 24 Sep 2019, In : Nature Communications. 10, 1, 14 p., 4329.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
File

Heme oxygenase-1 repeat polymorphism in septic acute kidney injury

FINNAKI Study Grp, Vilander, L. M., Vaara, S. T., Donner, K. M., Lakkisto, P., Kaunisto, M. A. & Pettilä, V., 23 May 2019, In : PLoS One. 14, 5, 13 p., 0217291.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
File
2018

Analgesic Plasma Concentrations of Oxycodone After Surgery for Breast CancerWhich Factors Matter?

Cajanus, K., Neuvonen, M., Koskela, O., Kaunisto, M. A., Neuvonen, P. J., Niemi, M. & Kalso, E., Apr 2018, In : Clinical Pharmacology and Therapeutics. 103, 4, p. 653-662 10 p.

Research output: Contribution to journalArticleScientificpeer-review

Analysis of shared heritability in common disorders of the brain

Brainstorm Consortium, Anttila, V., Bulik-Sullivan, B., Finucane, H. K., Walters, R. K., Bras, J., Duncan, L., Escott-Price, V., Falcone, G. J., Gormley, P., Malik, R., Patsopoulos, N. A., Ripke, S., Wei, Z., Yu, D., Lee, P. H., Turley, P., Grenier-Boley, B., Chouraki, V., Kamatani, Y. & 33 othersBerr, C., Letenneur, L., Hannequin, D., Amouyel, P., Boland, A., Deleuze, J-F., Duron, E., Vardarajan, B. N., Reitz, C., Goate, A. M., Huentelman, M. J., Kamboh, M. I., Larson, E. B., Rogaeva, E., St George-Hyslop, P., Hakonarson, H., Kukull, W. A., Palta, P., Wedenoja, J., Artto, V., Kaunisto, M., Vepsäläinen, S., Kurki, M. I., Hämäläinen, E., Kaprio, J., Metspalu, A., Keski-Rahkonen, A., Raevuori, A., Ripatti, S., Lönnqvist, J., Daly, M., Palotie, A. & Neale, B. M., 22 Jun 2018, In : Science. 360, 6395, p. 1313-+ 13 p., 8757.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
File

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

23 Me Res Team, IHGC, Gormley, P., Kurki, M. I., Hiekkala, M. E., Häppölä, P., Palta, P., Surakka, I., Kaunisto, M. A., Hämäläinen, E., Vepsäläinen, S., Havanka, H., Harno, H., Ilmavirta, M., Nissilä, M., Säkö, E., Sumelahti, M-L., Liukkonen, J., Sillanpaa, M., Metsähonkala, L. & 15 othersKoskinen, S., Lehtimaki, T., Raitakari, O., Männikko, M., Jousilahti, P., Anttila, V., Salomaa, V., Artto, V., Färkkilä, M., Daly, M. J., Neale, B. M., Ripatti, S., Kallela, M., Wessman, M. & Palotie, A., 16 May 2018, In : Neuron. 98, 4, p. 743–753 11 p.

Research output: Contribution to journalArticleScientificpeer-review

Development of an AmpliSeq (TM) Panel for Next-Generation Sequencing of a Set of Genetic Predictors of Persisting Pain

Kringel, D., Kaunisto, M. A., Lippmann, C., Kalso, E. & Lötsch, J., 19 Sep 2018, In : Frontiers in Pharmacology. 9, 22 p., 1008.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
File

Genetic variation in P2RX7 and pain tolerance

Kambur, O., Kaunisto, M. A., Winsvold, B. S., Wilsgaard, T., Stubhaug, A., Zwart, J. A., Kalso, E. & Nielsen, C. S., Jun 2018, In : Pain. 159, 6, p. 1064-1073 10 p.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
File

Genomitiedon arkaluonteisuus on tiukassa elävä myytti

Palotie, A., Kaunisto, M., Kääriäinen, H., Perola, M., Pitkänen, K., Ripatti, S., Soini, S. & Widén, E., 2018, In : Suomen lääkärilehti. 73, 15, p. 916-917 2 p.

Research output: Contribution to journalArticleProfessional

Open Access
File

Molecular genetic overlap between migraine and major depressive disorder

Int Headache Genetics Consortium, Yang, Y., Zhao, H., Boomsma, D. I., Kallela, M., Wessman, M., Anttila, V., Palta, P., Muona, M., Sarin, A-P., Wedenoja, J., Färkkilä, M., Artto, V., Kaunisto, M., Vepsäläinen, S., Hämäläinen, E., Eriksson, J. G., Heikkilä, K., Kaprio, J., Wessman, M. & 4 othersPalotie, A., Kurki, M. I., Pärn, K. & Neale, B. M., Aug 2018, In : European Journal of Human Genetics. 26, 8, p. 1202-1216 15 p.

Research output: Contribution to journalArticleScientificpeer-review

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

Hiekkala, M. E., Vuola, P., Artto, V., Häppölä, P., Häppölä, E., Vepsäläinen, S., Cuenca-Leon, E., Lal, D., Gormley, P., Hämäläinen, E., Ilmavirta, M., Nissilä, M., Säkö, E., Sumelahti, M-L., Harno, H., Havanka, H., Keski-Säntti, P., Färkkilä, M., Palotie, A., Wessman, M. & 2 othersKaunisto, M. A. & Kallela, M., Oct 2018, In : Cephalalgia. 38, 12, p. 1849-1863 15 p.

Research output: Contribution to journalArticleScientificpeer-review

2017

Genetic variants in SERPINA4 and SERPINA5, but not BCL2 and SIK3 are associated with acute kidney injury in critically ill patients with septic shock

Vilander, L., Kaunisto, M. A., Vaara, S., Pettila, V. & FINNAKI Study Grp, 8 Mar 2017, In : Critical Care. 21, 11 p., 47.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
File

PRKCDBP (CAVIN3) and CRY2 associate with major depressive disorder

Kovanen, L., Donner, K., Kaunisto, M. & Partonen, T., Jan 2017, In : Journal of Affective Disorders. 207, p. 136-140 5 p.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
File

Terveydenhoitaja vastaavana tutkimushoitajana SUPER-tutkimuksessa - mielenkiintoista työtä tärkeän asian ympärillä

Kaunisto, M. & Ristiluoma, N., 2017, In : Terveydenhoitaja. 50, 3-4, p. 40-41 2 p.

Research output: Contribution to journalArticleProfessional

Two missense mutations in KCNQ1 cause pituitary hormone deficiency and maternally inherited gingival fibromatosis

Tommiska, J., Känsäkoski, J., Skibsbye, L., Vaaralahti, K., Liu, X., Lodge, E. J., Tang, C., Yuan, L., Fagerholm, R., Kanters, J. K., Lahermo, P., Kaunisto, M., Keski-Filppula, R., Vuoristo, S., Pulli, K., Ebeling, T., Valanne, L., Sankila, E-M., Kivirikko, S., Lääperi, M. & 15 othersCasoni, F., Giacobini, P., Phan-Hug, F., Buki, T., Tena-Sempere, M., Pitteloud, N., Veijola, R., Lipsanen-Nyman, M., Kaunisto, K., Mollard, P., Andoniadou, C. L., Hirsch, J. A., Varjosalo, M., Jespersen, T. & Raivio, T., 3 Nov 2017, In : Nature Communications. 8, 11 p., 1289.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
File
2016

CRY1 and CRY2 genetic variants in seasonality: A longitudinal and cross-sectional study

Kovanen, L., Donner, K., Kaunisto, M. & Partonen, T., 30 Aug 2016, In : Psychiatry Research. 242, p. 101-110 10 p.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
File

Effect of endocannabinoid degradation on pain: role of FAAH polymorphisms in experimental and postoperative pain in women treated for breast cancer

Cajanus, K., Holmström, E., Wessman, M. A., Holmström, E. J., Wessman, M., Anttila, V., Kaunisto, M. A. & Kalso, E., 2016, In : Pain. 157, 2, p. 361-9 9 p.

Research output: Contribution to journalArticleScientificpeer-review

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

Gormley, P., Anttila, V., Winsvold, B. S., Palta, P., Esko, T., Pers, T. H., Farh, K-H., Cuenca-Leon, E., Muona, M., Furlotte, N. A., Kurth, T., Ingason, A., McMahon, G., Ligthart, L., Terwindt, G. M., Kallela, M., Freilinger, T. M., Ran, C., Gordon, S. G., Stam, A. H. & 32 othersSteinberg, S., Borck, G., Koiranen, M., Quaye, L., Adams, H. H. H., Lehtimaki, T., Sarin, A-P., Wedenoja, J., Hinds, D. A., Buring, J. E., Schurks, M., Ridker, P. M., Hrafnsdottir, M. G., Stefansson, H., Ring, S. M., Hottenga, J-J., Penninx, B. W. J. H., Färkkilä, M., Artto, V., Kaunisto, M., Vepsalainen, S., Malik, R., Heath, A. C., Pärn, K., Hämäläinen, E., Eriksson, J. G., Heikkila, K., Kaprio, J., Wessman, M., Daly, M. J., Palotie, A. & Int Headache Genetics Consortium, Aug 2016, In : Nature Genetics. 48, 8, p. 856-+ 14 p.

Research output: Contribution to journalArticleScientificpeer-review

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, M. A., Kallela, K. M., Artto, V., Vijfhuizen, L. S., Goebel, H., Dichgans, M., Kubisch, C., Ferrari, M. D., Palotie, A., Terwindt, G. M., van den Maagdenberg, A. M. J. M. & Int Headache Genetics Consortium, Jun 2016, In : Cephalalgia. 36, 7, p. 604-614 11 p.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
File
2015

A Novel Splice Mutation in PLS3 Causes X-linked Early Onset Low-Turnover Osteoporosis

Laine, C. M., Wessman, M., Toiviainen-Salo, S., Kaunisto, M. A., Mayranpaa, M. K., Laine, T., Pekkinen, M., Kroger, H., Valimaki, V-V., Valimaki, M. J., Lehesjoki, A-E. & Makitie, O., Mar 2015, In : Journal of Bone and Mineral Research. 30, 3, p. 437-445 9 p.

Research output: Contribution to journalArticleScientificpeer-review

CRY1, CRY2 and PRKCDBP genetic variants in metabolic syndrome

Kovanen, L., Donner, K., Kaunisto, M. & Partonen, T., Mar 2015, In : Hypertension Research. 38, 3, p. 186-192 7 p.

Research output: Contribution to journalArticleScientificpeer-review

Genome wide association study identifies variants in NBEA associated with migraine in bipolar disorder

Jacobsen, K. K., Nievergelt, C. M., Zayats, T., Greenwood, T. A., Anttila, V., Akiskal, H. S., Haavik, J., Fasmer, O. B., Kelsoe, J. R., Johansson, S., Oedegaard, K. J., BiGs Consortium IHG Consortium, Liu, C., Wedenoja, J. O., Kaunisto, M. A., Heikkilä, K. V., Kaprio, J. A., Wessman, M., Kallela, M., Färkkilä, M. & 4 othersArtto, V., Eriksson, J., Palotie, A. V. & Daly, M., 1 Feb 2015, In : Journal of Affective Disorders. 172, p. 453-461 9 p.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
File
2014

High Risk Population Isolate Reveals Low Frequency Variants Predisposing to Intracranial Aneurysms

Kurki, M. I., Gaal, E. I., Kettunen, J., Lappalainen, T., Menelaou, A., Anttila, V., van't Hof, F. N. G., von und zu Fraunberg, M., Helisalmi, S., Hiltunen, M., Lehto, H., Laakso, A., Kivisaari, R., Koivisto, T., Ronkainen, A., Rinne, J., Kiemeney, L. A. L., Vermeulen, S. H., Kaunisto, M. A., Eriksson, J. G. & 15 othersAromaa, A., Perola, M., Lehtimaki, T., Raitakari, O. T., Salomaa, V., Gunel, M., Dermitzakis, E. T., Ruigrok, Y. M., Rinkel, G. J. E., Niemela, M., Hernesniemi, J., Ripatti, S., de Bakker, P. I. W., Palotie, A. & Jaaskelainen, J. E., Jan 2014, In : PLoS Genetics. 10, 1, 12 p., 1004134.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
File

How much oxycodone is needed for adequate analgesia after breast cancer surgery: effect of the OPRM1 118A>G polymorphism

Cajanus, K., Kaunisto, M., Tallgren, M., Jokela, R. & Kalso, E., Dec 2014, In : Journal of Pain. 15, 12, p. 1248-1256 9 p.

Research output: Contribution to journalArticleScientificpeer-review

Massive Withdrawal Symptoms and Affective Vulnerability Are Associated with Variants of the CHRNA4 Gene in a Subgroup of Smokers

Lazary, J., Dome, P., Csala, I., Kovacs, G., Faludi, G., Kaunisto, M. & Dome, B., 30 Jan 2014, In : PLoS One. 9, 1, 6 p., 87141.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
File
2013

CRY2 Genetic Variants Associate with Dysthymia

Kovanen, L., Kaunisto, M., Donner, K., Saarikoski, S. T. & Partonen, T., 8 Aug 2013, In : PLoS One. 8, 8, p. Article Number: e71450 9 p.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
File

Effect of Catechol-o-methyltransferase-gene (COMT) Variants on Experimental and Acute Postoperative Pain in 1,000 Women undergoing Surgery for Breast Cancer

Kambur, O., Kaunisto, M., Tikkanen, E., Leal, S., Ripatti, S. O. & Kalso, E., Dec 2013, In : Anesthesiology. 119, 6, p. 1422-1433 12 p.

Research output: Contribution to journalArticleScientificpeer-review

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

Anttila, V., Winsvold, B. S., Gormley, P., Kurth, T., Bettella, F., McMahon, G., Kallela, K. M. J., Malik, R., de Vries, B., Terwindt, G., Medland, S. E., Todt, U., McArdle, W. L., Quaye, L., Koiranen, M., Ikram, M. A., Lehtimaki, T., Stam, A. H., Ligthart, L., Wedenoja, J. & 33 othersDunham, I., Neale, B. M., Palta, P., Hämäläinen, E., Schuerks, M., Rose, L. M., Buring, J. E., Ridker, P. M., Steinberg, S., Stefansson, H., Jakobsson, F., Lawlor, D. A., Evans, D. M., Ring, S. M., Färkkilä, M., Artto, V., Kaunisto, M. A., Freilinger, T., Schoenen, J., Frants, R. R., Pelzer, N., Weller, C. M., Zielman, R., Heath, A. C., Madden, P. A. F., Heikkila, K., Eriksson, J. G., Kaprio, J., Wessman, M., Palotie, A., North Amer Brain Expression, UK Brain Expression Consortium & Int Headache Genetics Consortium, Aug 2013, In : Nature Genetics. 45, 8, p. 912-U255 8 p.

Research output: Contribution to journalArticleScientificpeer-review

Ischemic Stroke Is Associated with the ABO Locus: The EuroCLOT Study

Williams, F. M. K., Carter, A. M., Hysi, P. G., Surdulescu, G., Hodgkiss, D., Soranzo, N., Traylor, M., Bevan, S., Dichgans, M., Rothwell, P. M. W., Sudlow, C., Farrall, M., Silander, K., Kaunisto, M., Wagner, P., Saarela, O., Kuulasmaa, K., Virtamo, J., Salomaa, V., Amouyel, P. & 33 othersArveiler, D., Ferrieres, J., Wiklund, P-G., Ikram, M. A., Hofman, A., Boncoraglio, G. B., Parati, E. A., Helgadottir, A., Gretarsdottir, S., Thorsteinsdottir, U., Thorleifsson, G., Stefansson, K., Seshadri, S., DeStefano, A., Gschwendtner, A., Psaty, B., Longstreth, W., Mitchell, B. D., Cheng, Y-C., Clarke, R., Ferrario, M., Bis, J. C., Levi, C., Attia, J., Holliday, E. G., Scott, R. J., Fornage, M., Sharma, P., Furie, K. L., Palotie, A., EuroCLOT Investigators, Wellcome Trust Case Control Consor & Int Stroke Genetics Consortium, Jan 2013, In : Annals of Neurology. 73, 1, p. 16-31 16 p.

Research output: Contribution to journalArticleScientificpeer-review

Pain in 1,000 women treated for breast cancer: a prospective study of pain sensitivity and postoperative pain

Kaunisto, M., Jokela, R., Tallgren, M., Kambur, O., Tikkanen, E., Tasmuth, T., Reetta, S., Palotie, A., Estlander, A-M., Leidenius, M. H., Ripatti, S. O. & Kalso, E., Dec 2013, In : Anesthesiology. 119, 6, p. 1410-1421 12 p.

Research output: Contribution to journalArticleScientificpeer-review

2012

Genome-wide association analysis identifies susceptibility loci for migraine without aura

Freilinger, T., Anttila, V., de Vries, B., Malik, R., Kallela, K. M. J., Terwindt, G. M., Pozo-Rosich, P., Winsvold, B., Nyholt, D. R., van Oosterhout, W. P. J., Artto, V., Todt, U., Hämäläinen, E., Fernandez-Morales, J., Louter, M. A., Kaunisto, M. A., Schoenen, J., Raitakari, O., Lehtimaki, T., Vila-Pueyo, M. & 24 othersGoebel, H., Wichmann, E., Sintas, C., Uitterlinden, A. G., Hofman, A., Rivadeneira, F., Heinze, A., Tronvik, E., van Duijn, C. M., Kaprio, J., Cormand, B., Wessman, M., Frants, R. R., Meitinger, T., Mueller-Myhsok, B., Zwart, J-A., Färkkilä, M., Macaya, A., Ferrari, M. D., Kubisch, C., Palotie, A., Dichgans, M., van den Maagdenberg, A. M. J. M. & Int Headache Genetics Consortium, 2012, In : Nature Genetics. 44, 7, p. 777-U205 8 p.

Research output: Contribution to journalArticleScientificpeer-review

2011

Novel Susceptibility Locus at 22q11 for Diabetic Nephropathy in Type 1 Diabetes

Wessman, M., Forsblom, C., Kaunisto, M. A., Soderlund, J., Ilonen, J., Sallinen, R., Hiekkalinna, T., Parkkonen, M., Maxwell, A. P., Tarnow, L., Parving, H-H., Hadjadj, S., Marre, M., Peltonen, L. & Groop, P-H., 2011, In : PLoS One. 6, 9, p. Article Number: e24053 9 p.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
File
2010

Association of the SLC22A1, SLC22A2, and SLC22A3 genes encoding organic cation transporters with diabetic nephropathy and hypertension

Sallinen, R., Kaunisto, M. A., Forsblom, C., Thomas, M., Fagerudd, J., Pettersson-Fernholm, K., Groop, P-H., Wessman, M. & Finnish Diabetic Nephropathy Study, 2010, In : Annals of Medicine. 42, p. 296-304 9 p.

Research output: Contribution to journalArticleScientificpeer-review

A visual migraine aura locus maps to 9q21-q22

Tikka-Kleemola, P. J., Artto, V., Vepsalainen, S., Sobel, E. M., Raty, S., Kaunisto, M., Anttila, V., Hämäläinen, E., Sumelahti, M. -L., Ilmavirta, M., Färkkilä, M., Kallela, K. M. J., Palotie, A. & Wessman, M., 2010, In : Neurology. 74, 15, p. 1171-1177 7 p.

Research output: Contribution to journalArticleScientificpeer-review

Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1

Anttila, V., Stefansson, H., Kallela, M., Todt, U., Terwindt, G. M., Calafato, M. S., Nyholt, D. R., Dimas, A. S., Freilinger, T., Mueller-Myhsok, B., Artto, V., Inouye, M., Alakurtti, K., Kaunisto, M. A., Hämäläinen, E., de Vries, B., Stam, A. H., Weller, C. M., Heinze, A., Heinze-Kuhn, K. & 31 othersGoebel, I., Borck, G., Goebel, H., Steinberg, S., Wolf, C., Bjoernsson, A., Gudmundsson, G., Kirchmann, M., Hauge, A., Werge, T., Schoenen, J., Eriksson, J. G., Hagen, K., Stovner, L., Wichmann, E., Meitinger, T., Alexander, M., Moebus, S., Schreiber, S., Aulchenko, Y. S., Breteler, M. M. B., Uitterlinden, A. G., Hofman, A., van Duijn, C. M., Tikka-Kleemola, P., Kaprio, J., Färkkilä, M., Palotie, L., Wessman, M., Palotie, A. & Int Headache Genetics Consortium, 2010, In : Nature Genetics. 42, 10, p. 869-873 5 p.

Research output: Contribution to journalArticleScientificpeer-review

HEME OXYGENASE 1 POLYMORPHISMS AND PLASMA CONCENTRATIONS IN CRITICALLY ILL PATIENTS

Saukkonen, K., Lakkisto, P., Kaunisto, M. A., Varpula, M., Voipio-Pulkki, L-M., Varpula, T., Pettila, V. & Pulkki, K., 2010, In : Shock (Philadelphia). 34, 6, p. 558-564 7 p.

Research output: Contribution to journalArticleScientificpeer-review

2009

Elevated MBL concentrations are not an indication of association between the MBL2 gene and type 1 diabetes or diabetic nephropathy

Kaunisto, M. A., Sjölind, L., Sallinen, R. J., Pettersson-Fernholm, K., Saraheimo, M., Fröjdö, S., Forsblom, C., Fagerudd, J., Hansen, T. K., Flyvbjerg, A., Wessman, M., Groop, P-H. & FinnDiane Study Group, 2009, In : Diabetes. 58, 7, p. 1710-1714 5 p.

Research output: Contribution to journalArticleScientificpeer-review

Findings from bipolar disorder genome-wide association studies replicate in a Finnish bipolar family-cohort

Ollila, H. M., Soronen, P., Silander, K., Palo, O. M., Kieseppä, T., Kaunisto, M. A., Lönnqvist, J., Peltonen, L., Partonen, T. & Paunio, T., 2009, In : Molecular Psychiatry. 14, 4, p. 351-353 3 p.

Research output: Contribution to journalArticleScientificpeer-review

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

Tikka-Kleemola, P., Kaunisto, M. A., Hämäläinen, E., Todt, U., Goebel, H., Kaprio, J., Kubisch, C., Farkkila, M., Palotie, A., Wessman, M. & Kallela, M., 2009, In : Cephalalgia. 29, p. 1224-1231 8 p.

Research output: Contribution to journalArticleScientificpeer-review

2008

A high-density association screen of 155 ion transport genes for involvement with common migraine

Nyholt, D. R., LaForge, K. S., Kallela, M., Alakurtti, K., Anttila, V., Färkkilä, M., Hämäläinen, E., Kaprio, J., Kaunisto, M. A., Heath, A. C., Montgomery, G. W., Göbel, H., Todt, U., Ferrari, M. D., Launer, L. J., Frants, R. R., Terwindt, G. M., de Vries, B., Verschuren, W. M. M., Brand, J. & 14 othersFreilinger, T., Pfaffenrath, V., Straube, A., Ballinger, D. G., Zhan, Y., Daly, M. J., Cox, D. R., Dichgans, M., van den Maagdenberg, A. M. J. M., Kubisch, C., Martin, N. G., Wessman, M., Peltonen, L. & Palotie, A., 2008, In : Human Molecular Genetics. 17, 21, p. 3318-3331 14 p.

Research output: Contribution to journalArticleScientificpeer-review

Association analysis of podocyte slit diaphragm genes as candidates for diabetic nephropathy

Ihalmo, P., Wessman, M., Kaunisto, M. A., Kilpikari, R., Parkkonen, M., Forsblom, C. M., Holthöfer, H., Groop, P-H., Kaunisto, M. A., Forsblom, C. & FinnDiane Study Group, 2008, In : Diabetologia. 51, 1, p. 86-90 5 p.

Research output: Contribution to journalArticleScientificpeer-review

Consistently replicating locus linked to migraine on 10q22-q23

Anttila, V., Nyholt, D. R., Kallela, M., Artto, V., Vepsäläinen, S., Jakkula, E., Wennerström, A., Tikka-Kleemola, P., Kaunisto, M. A., Hämäläinen, E., Widen, E., Terwilliger, J., Merikangas, K., Montgomery, G. W., Martin, N. G., Daly, M., Kaprio, J., Peltonen, L., Färkkilä, M., Wessman, M. & 1 othersPalotie, A., 2008, In : American Journal of Human Genetics. 82, 5, p. 1051-1063 13 p.

Research output: Contribution to journalArticleScientificpeer-review

2007

Migraine: a complex genetic disorder

Wessman, M., Terwindt, G. M., Kaunisto, M. A., Palotie, A. & Ophoff, R. A., 2007, In : Lancet Neurology. 6, p. 521-532 12 p.

Research output: Contribution to journalArticleScientificpeer-review

2006

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

Kaunisto, M. A., 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., 2006, In : Cephalalgia. 26, 12, p. 1462-1472 11 p.

Research output: Contribution to journalArticleScientificpeer-review

Trait components provide tools to dissect the genetic susceptibility of migraine

Anttila, V., Kallela, M., Oswell, G., Kaunisto, M., Nyholt, D. R., Hämäläinen, E., Havanka, H., Ilmavirta, M., Terwilliger, J., Sobel, E., Peltonen, L., Kaprio, J., Färkkilä, M., Wessman, M. & Palotie, A., 2006, In : American Journal of Human Genetics. 79, 1, p. 85-99 15 p.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
File
2004

A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2

Kaunisto, MA., Harno, H., Vanmolkot, KRJ., Gargus, JJ., Sun, G., Hämäläinen, E., Liukkonen, E., Kallela, M., van den Maagdenberg, AMJM., Frants, RR., Färkkilä, M., Palotie, A. & Wessman, M., Jun 2004, In : Neurogenetics. 5, 2, p. 141-146 6 p.

Research output: Contribution to journalArticleScientificpeer-review

Novel splice site CACNA1A mutation causing episodic ataxia type 2

Kaunisto, M. A., Harno, H., Kallela, M., Somer, H., Sallinen, R., Hämäläinen, E., Miettinen, P. J., Vesa, J., Orpana, A., Palotie, A., Färkkilä, M. & Wessman, M., 2004, In : Neurogenetics. 5, p. 69-73 5 p.

Research output: Contribution to journalArticleScientificpeer-review

2002

A susceptibility locus for migraine with aura, on chromosome 4q24

Wessman, M., Kallela, M., Kaunisto, M. A., Marttila, P., Sobel, E., Hartiala, J., Oswell, G., Leal, S. M., Papp, J. C., Hämäläinen, E., Broas, P., Joslyn, G., Hovatta, I., Hiekkalinna, T., Kaprio, J., Ott, J., Cantor, R. M., Zwart, J. A., Ilmavirta, M., Havanka, H. & 3 othersFärkkilä, M., Peltonen, L. & Palotie, A., 2002, In : American Journal of Human Genetics. 70, p. 652-662 11 p.

Research output: Contribution to journalArticleScientificpeer-review