Towards an understanding of genetic predisposition to migraine

par Anttila, Verneri, Wessman, Maija, Kallela, Mikko, Palotie, Aarno
Publié 2011

Mapping ESTs by Fiber–FISH

par Horelli-Kuitunen, Nina, Aaltonen, Johanna, Yaspo, Marie-Laure, Eeva, Mervi, Wessman, Maija, Peltonen, Leena, Palotie, Aarno
Publié 1999

Assignment of a Novel Locus for Autosomal Recessive Congenital Ichthyosis to Chromosome 19p13.1-p13.2

par Virolainen, Elina, Wessman, Maija, Hovatta, Iiris, Niemi, Kirsti-Maria, Ignatius, Jaakko, Kere, Juha, Peltonen, Leena, Palotie, Aarno
Publié 2000

High-resolution population-specific recombination rates and their effect on phasing and genotype imputation

par Hassan, Shabbeer, Surakka, Ida, Taskinen, Marja-Riitta, Salomaa, Veikko, Palotie, Aarno, Wessman, Maija, Tukiainen, Taru, Pirinen, Matti, Palta, Priit, Ripatti, Samuli
Publié dans Eur J Hum Genet (2020)

Quantitative-Trait-Locus Analysis of Body-Mass Index and of Stature, by Combined Analysis of Genome Scans of Five Finnish Study Groups

par Perola, Markus, Öhman, Miina, Hiekkalinna, Tero, Leppävuori, Jenni, Pajukanta, Päivi, Wessman, Maija, Koskenvuo, Markku, Palotie, Aarno, Lange, Kenneth, Kaprio, Jaakko, Peltonen, Leena
Publié 2001

Elevated MBL Concentrations Are Not an Indication of Association Between the MBL2 Gene and Type 1 Diabetes or Diabetic Nephropathy

par Kaunisto, Mari A., Sjölind, Lisa, Sallinen, Riitta, Pettersson-Fernholm, Kim, Saraheimo, Markku, Fröjdö, Sara, Forsblom, Carol, Fagerudd, Johan, Hansen, Troels K., Flyvbjerg, Allan, Wessman, Maija, Groop, Per-Henrik
Publié 2009

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

par Wessman, Maija, Forsblom, Carol, Kaunisto, Mari A., Söderlund, Jenny, Ilonen, Jorma, Sallinen, Riitta, Hiekkalinna, Tero, Parkkonen, Maija, Maxwell, Alexander P., Tarnow, Lise, Parving, Hans-Henrik, Hadjadj, Samy, Marre, Michel, Peltonen, Leena, Groop, Per-Henrik
Publié 2011

Chromosome 19p13 Loci in Finnish Migraine With Aura Families

par Kaunisto, Mari A., Tikka, Päivi J., Kallela, Mikko, Leal, Suzanne M., Papp, Jeanette C., Korhonen, Arja, Hämäläinen, Eija, Harno, Hanna, Havanka, Hannele, Nissilä, Markku, Säkö, Erkki, Ilmavirta, Matti, Kaprio, Jaakko, Färkkilä, Markus, Ophoff, Roel A., Palotie, Aarno, Wessman, Maija
Publié dans Am J Med Genet B Neuropsychiatr Genet (2005)

Consistently Replicating Locus Linked to Migraine on 10q22-q23

par Anttila, Verneri, Nyholt, Dale R., Kallela, Mikko, Artto, Ville, Vepsäläinen, Salli, Jakkula, Eveliina, Wennerström, Annika, Tikka-Kleemola, Päivi, Kaunisto, Mari A., Hämäläinen, Eija, Widén, Elisabeth, Terwilliger, Joseph, Merikangas, Kathleen, Montgomery, Grant W., Martin, Nicholas G., Daly, Mark, Kaprio, Jaakko, Peltonen, Leena, Färkkilä, Markus, Wessman, Maija, Palotie, Aarno
Publié 2008

A Susceptibility Locus for Migraine with Aura, on Chromosome 4q24

par Wessman, Maija, Kallela, Mikko, Kaunisto, Mari A., Marttila, Pia, Sobel, Eric, Hartiala, Jaana, Oswell, Greg, Leal, Suzanne M., Papp, Jeanette C., Hämäläinen, Eija, Broas, Petra, Joslyn, Geoffrey, Hovatta, Iiris, Hiekkalinna, Tero, Kaprio, Jaakko, Ott, Jürg, Cantor, Rita M., Zwart, John-Anker, Ilmavirta, Matti, Havanka, Hannele, Färkkilä, Markus, Peltonen, Leena, Palotie, Aarno
Publié 2002

Molecular genetic overlap between migraine and major depressive disorder

par Yang, Yuanhao, Zhao, Huiying, Boomsma, Dorret I, Ligthart, Lannie, Belin, Andrea C., Smith, George Davey, Esko, Tonu, Freilinger, Tobias M., Hansen, Thomas Folkmann, Ikram, M. Arfan, Kallela, Mikko, Kubisch, Christian, Paraskevi, Christofidou, Strachan, David P., Wessman, Maija, van den Maagdenberg, Arn M. J. M., Terwindt, Gisela M., Nyholt, Dale R.
Publié dans Eur J Hum Genet (2018)

Confirmation of the Type 2 Myotonic Dystrophy (CCTG)(n) Expansion Mutation in Patients with Proximal Myotonic Myopathy/Proximal Myotonic Dystrophy of Different European Origins: A...

par Bachinski, Linda L., Udd, Bjarne, Meola, Giovanni, Sansone, Valeria, Bassez, Guillaume, Eymard, Bruno, Thornton, Charles A., Moxley, Richard T., Harper, Peter S., Rogers, Mark T., Jurkat-Rott, Karin, Lehmann-Horn, Frank, Wieser, Thomas, Gamez, Josep, Navarro, Carmen, Bottani, Armand, Kohler, Andre, Shriver, Mark D., Sallinen, Riitta, Wessman, Maija, Zhang, Shanxiang, Wright, Fred A., Krahe, Ralf
Publié 2003

WNT1 Mutations in Early-onset Osteoporosis and Osteogenesis Imperfecta

par Laine, Christine M., Joeng, Kyu Sang, Campeau, Philippe M., Kiviranta, Riku, Tarkkonen, Kati, Grover, Monica, Lu, James T., Pekkinen, Minna, Wessman, Maija, Heino, Terhi J., Nieminen-Pihala, Vappu, Aronen, Mira, Laine, Tero, Kröger, Heikki, Cole, William G., Lehesjoki, Anna-Elina, Nevarez, Lisette, Krakow, Deborah, Curry, Cynthia J.R., Cohn, Daniel H., Gibbs, Richard A., Lee, Brendan H., Mäkitie, Outi
Publié 2013

Common variant burden contributes to the familial aggregation of migraine in 1,589 families

par Gormley, Padhraig, Kurki, Mitja I., Hiekkala, Marjo Eveliina, Veerapen, Kumar, Häppölä, Paavo, Mitchell, Adele A., Lal, Dennis, Palta, Priit, Surakka, Ida, Kaunisto, Mari Anneli, Hämäläinen, Eija, Vepsäläinen, Salli, Havanka, Hannele, Harno, Hanna, Ilmavirta, Matti, Nissilä, Markku, Säkö, Erkki, Sumelahti, Marja-Liisa, Liukkonen, Jarmo, Sillanpää, Matti, Metsähonkala, Liisa, Koskinen, Seppo, Lehtimäki, Terho, Raitakari, Olli, Männikkö, Minna, Ran, Caroline, Belin, Andrea Carmine, Jousilahti, Pekka, Anttila, Verneri, Salomaa, Veikko, Artto, Ville, Färkkilä, Markus, Runz, Heiko, Daly, Mark J., Neale, Benjamin M., Ripatti, Samuli, Kallela, Mikko, Wessman, Maija, Palotie, Aarno
Publié dans Neuron (2018)

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

par Nyholt, Dale R., LaForge, K. Steven, Kallela, Mikko, Alakurtti, Kirsi, Anttila, Verneri, Färkkilä, Markus, Hämaläinen, Eija, Kaprio, Jaakko, Kaunisto, Mari A., Heath, Andrew C., Montgomery, Grant W., Göbel, Hartmut, Todt, Unda, Ferrari, Michel D., Launer, Lenore J., Frants, Rune R., Terwindt, Gisela M., de Vries, Boukje, Verschuren, W.M. Monique, Brand, Jan, Freilinger, Tobias, Pfaffenrath, Volker, Straube, Andreas, Ballinger, Dennis G., Zhan, Yiping, Daly, Mark J., Cox, David R., Dichgans, Martin, van den Maagdenberg, Arn M.J.M., Kubisch, Christian, Martin, Nicholas G., Wessman, Maija, Peltonen, Leena, Palotie, Aarno
Publié 2008

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

par Zhao, Huiying, Eising, Else, de Vries, Boukje, Vijfhuizen, Lisanne S, Anttila, Verneri, Winsvold, Bendik S, Kurth, Tobias, Stefansson, Hreinn, Kallela, Mikko, Malik, Rainer, Stam, Anine H, Ikram, M Arfan, Ligthart, Lannie, Freilinger, Tobias, Alexander, Michael, Muller-Myhsok, Bertram, Schreiber, Stefan, Meitinger, Thomas, Aromaa, Arpo, Eriksson, Johan G, Boomsma, Dorret I, van Duijn, Cornelia M, Zwart, John-Anker, Quaye, Lydia, Kubisch, Christian, Dichgans, Martin, Wessman, Maija, Stefansson, Kari, Chasman, Daniel I, Palotie, Aarno, Martin, Nicholas G, Montgomery, Grant W, Ferrari, Michel D, Terwindt, Gisela M, van den Maagdenberg, Arn M J M, Nyholt, Dale R
Publié dans Cephalalgia (2015)

Migraine without aura: genome-wide association analysis identifies several novel susceptibility

par de Vries, Boukje, Freilinger, Tobias, Anttila, Verneri, Malik, Rainer, Kallela, Mikko, Terwindt, Gisela M, Pozo-Rosich, Patricia, Winsvold, Bendik, Nyholt, Dale R, van Oosterhout, Willebrordus PJ, Artto, Ville, Todt, Unda, Hämäläinen, Eija, Fernández-Morales, Jèssica, Louter, Mark A, Kaunisto, Mari A, Schoenen, Jean, Raitakari, Olli, Lehtimäki, Terho, Vila-Pueyo, Marta, Göbel, Hartmut, Wichmann, Erich, Sintas, Cèlia, Uitterlinden, Andre G, Hofman, Albert, Rivadeneira, Fernando, Heinze, Axel, Tronvik, Erling, van Duijn, Cornelia M, Kaprio, Jaakko, Cormand, Bru, Wessman, Maija, Frants, Rune R, Meitinger, Thomas, Müller-Myhsok, Bertram, Zwart, John-Anker, Färkkilä, Markus, Macaya, Alfons, Ferrari, Michel D, Kubisch, Christian, Palotie, Aarno, Dichgans, Martin, van den Maagdenberg, Arn MJM
Publié 2013

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

par Freilinger, Tobias, Anttila, Verneri, de Vries, Boukje, Malik, Rainer, Kallela, Mikko, Terwindt, Gisela M, Pozo-Rosich, Patricia, Winsvold, Bendik, Nyholt, Dale R, van Oosterhout, Willebrordus P J, Artto, Ville, Todt, Unda, Hämäläinen, Eija, Fernández-Morales, Jèssica, Louter, Mark A, Kaunisto, Mari A, Schoenen, Jean, Raitakari, Olli, Lehtimäki, Terho, Vila-Pueyo, Marta, Göbel, Hartmut, Wichmann, Erich, Sintas, Cèlia, Uitterlinden, Andre G, Hofman, Albert, Rivadeneira, Fernando, Heinze, Axel, Tronvik, Erling, van Duijn, Cornelia M., Kaprio, Jaakko, Cormand, Bru, Wessman, Maija, Frants, Rune R, Meitinger, Thomas, Müller-Myhsok, Bertram, Zwart, John-Anker, Färkkilä, Markus, Macaya, Alfons, Ferrari, Michel D, Kubisch, Christian, Palotie, Aarno, Dichgans, Martin, van den Maagdenberg, Arn M J M
Publié 2012

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

par Malik, Rainer, Freilinger, Tobias, Winsvold, Bendik S., Anttila, Verneri, Vander Heiden, Jason, Traylor, Matthew, de Vries, Boukje, Holliday, Elizabeth G., Terwindt, Gisela M., Sturm, Jonathan, Bis, Joshua C., Hopewell, Jemma C., Ferrari, Michel D., Rannikmae, Kristiina, Wessman, Maija, Kallela, Mikko, Kubisch, Christian, Fornage, Myriam, Meschia, James F., Lehtimäki, Terho, Sudlow, Cathie, Clarke, Robert, Chasman, Daniel I., Mitchell, Braxton D., Maguire, Jane, Kaprio, Jaakko, Farrall, Martin, Raitakari, Olli T., Kurth, Tobias, Ikram, M. Arfan, Reiner, Alex P., Longstreth, W.T., Rothwell, Peter M., Strachan, David P., Sharma, Pankaj, Seshadri, Sudha, Quaye, Lydia, Cherkas, Lynn, Schürks, Markus, Rosand, Jonathan, Ligthart, Lannie, Boncoraglio, Giorgio B., Davey Smith, George, van Duijn, Cornelia M., Stefansson, Kari, Worrall, Bradford B., Nyholt, Dale R., Markus, Hugh S., van den Maagdenberg, Arn M.J.M., Cotsapas, Chris, Zwart, John A., Palotie, Aarno, Dichgans, Martin
Publié dans Neurology (2015)

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

par Anttila, Verneri, Stefansson, Hreinn, Kallela, Mikko, Todt, Unda, Terwindt, Gisela M, Calafato, M Stella, Nyholt, Dale R, Dimas, Antigone S, Freilinger, Tobias, Müller-Myhsok, Bertram, Artto, Ville, Inouye, Michael, Alakurtti, Kirsi, Kaunisto, Mari A, Hämäläinen, Eija, de Vries, Boukje, Stam, Anine H, Weller, Claudia M, Heinze, Axel, Heinze-Kuhn, Katja, Goebel, Ingrid, Borck, Guntram, Göbel, Hartmut, Steinberg, Stacy, Wolf, Christiane, Björnsson, Asgeir, Gudmundsson, Gretar, Kirchmann, Malene, Hauge, Anne, Werge, Thomas, Schoenen, Jean, Eriksson, Johan G, Hagen, Knut, Stovner, Lars, Wichmann, H-Erich, Meitinger, Thomas, Alexander, Michael, Moebus, Susanne, Schreiber, Stefan, Aulchenko, Yurii S, Breteler, Monique M B, Uitterlinden, Andre G, Hofman, Albert, van Duijn, Cornelia M, Tikka-Kleemola, Päivi, Vepsäläinen, Salli, Lucae, Susanne, Tozzi, Federica, Muglia, Pierandrea, Barrett, Jeffrey, Kaprio, Jaakko, Färkkilä, Markus, Peltonen, Leena, Stefansson, Kari, Zwart, John-Anker, Ferrari, Michel D, Olesen, Jes, Daly, Mark, Wessman, Maija, van den Maagdenberg, Arn M J M, Dichgans, Martin, Kubisch, Christian, Dermitzakis, Emmanouil T, Frants, Rune R, Palotie, Aarno
Publié 2010