Anzahl der Publikationen: 6
Zeitschriftenartikel
Siewert, Katherine M ORCID: https://orcid.org/0000-0002-3658-5245; Klarin, Derek; Damrauer, Scott M; Chang, Kyong-Mi; Tsao, Philip S; Assimes, Themistocles L; Davey Smith, George; Voight, Benjamin F; Gormley, Padhraig; Anttila, Verneri; Winsvold, Bendik S; Palta, Priit; Esko, Tonu; Pers, Tune H.; Farh, Kai-How; Cuenca-Leon, Ester; Muona, Mikko; Furlotte, Nicholas A; Kurth, Tobias; Ingason, Andres; McMahon, George; Ligthart, Lannie; Terwindt, Gisela M; Kallela, Mikko; Freilinger, Tobias M; Ran, Caroline; Gordon, Scott G; Stam, Anine H; Steinberg, Stacy; Borck, Guntram; Koiranen, Markku; Quaye, Lydia; Adams, Hieab HH; Lehtimäki, Terho; Sarin, Antti-Pekka; Wedenoja, Juho; Hinds, David A; Buring, Julie E; Schürks, Markus; Ridker, Paul M; Hrafnsdottir, Maria Gudlaug; Stefansson, Hreinn; Ring, Susan M; Hottenga, Jouke-Jan; Penninx, Brenda WJH; Färkkilä, Markus; Artto, Ville; Kaunisto, Mari; Vepsäläinen, Salli; Malik, Rainer; Heath, Andrew C; Madden, Pamela A F; Martin, Nicholas G; Montgomery, Grant W; Kurki, Mitja; Kals, Mart; Mägi, Reedik; Pärn, Kalle; Hämäläinen, Eija; Huang, Hailiang; Byrnes, Andrea E; Franke, Lude; Huang, Jie; Stergiakouli, Evie; Lee, Phil H; Sandor, Cynthia; Webber, Caleb; Cader, Zameel; Muller-Myhsok, Bertram; Schreiber, Stefan; Meitinger, Thomas; Eriksson, Johan G; Salomaa, Veikko; Heikkilä, Kauko; Loehrer, Elizabeth; Uitterlinden, Andre G; Hofman, Albert; van Duijn, Cornelia M; Cherkas, Lynn; Pedersen, Linda M.; Stubhaug, Audun; Nielsen, Christopher S; Männikkö, Minna; Mihailov, Evelin; Milani, Lili; Göbel, Hartmut; Esserlind, Ann-Louise; Christensen, Anne Francke; Hansen, Thomas Folkmann; Werge, Thomas; Børte, Sigrid; Cormand, Bru; Eising, Else; Griffiths, Lyn; Hamalainen, Eija; Hiekkala, Marjo; Kajanne, Risto; Launer, Lenore; Lehtimaki, Terho; Lessel, Davor; Macaya, Alfons; Mangino, Massimo; Pedersen, Nancy; Posthuma, Danielle; Pozo-Rosich, Patricia; Pressman, Alice; Sintas, Celia; Vila-Pueyo, Marta; Zhao, Huiying; Kaprio, Jaakko; Aromaa, Arpo J; Raitakari, Olli; Ikram, M Arfan; Spector, Tim; Järvelin, Marjo-Riitta; Metspalu, Andres; Kubisch, Christian; Strachan, David P; Ferrari, Michel D; Belin, Andrea C; Dichgans, Martin; Wessman, Maija; van den Maagdenberg, Arn MJM; Zwart, John-Anker; Boomsma, Dorret I; Smith, George Davey; Stefansson, Kari; Eriksson, Nicholas; Daly, Mark J; Neale, Benjamin M; Olesen, Jes; Chasman, Daniel I; Nyholt, Dale R und Palotie, Aarno
(2020):
Cross-trait analyses with migraine reveal widespread pleiotropy and suggest a vascular component to migraine headache.
In: International Journal of Epidemiology, Bd. 49, Nr. 3: S. 1022-1031
[PDF, 823kB]
Cruz, Pedro M. Rodriguez; Cossins, Judith; Estephan, Eduardo de Paula; Munell, Francina; Selby, Kathryn; Hirano, Michio; Maroofin, Reza; Mehrjardi, Mohammad Yahya Vahidi; Chow, Gabriel; Carr, Aisling; Manzur, Adnan; Robb, Stephanie; Munot, Pinki; Liu, Wei Wei; Banka, Siddharth; Fraser, Harry; De Goede, Christian; Zanoteli, Edmar; Reed, Umbertina Conti; Sage, Abigail; Gratacos, Margarida; Macaya, Alfons; Dusl, Marina; Senderek, Jan; Topf, Ana; Hofer, Monika; Knight, Ravi; Ramdas, Sithara; Jayawant, Sandeep; Lochmüller, Hans; Palace, Jacqueline und Beeson, David
(2019):
The clinical spectrum of the congenital myasthenic syndrome resulting from COL13A1 mutations.
In: Brain, Bd. 142: S. 1547-1560
Dusl, Marina; Moreno, Teresa; Muneii, Francina; Macaya, Alfons; Gratacos, Margarida; Abicht, Angela; Strom, Tim M.; Lochmuller, Hanns und Senderek, Jan
(2019):
Congenital myasthenic syndrome caused by novel COL13A1 mutations.
In: Journal of Neurology, Bd. 266, Nr. 5: S. 1107-1112
Kogelman, Lisette J. A.; Esserlind, Ann-Louise; Christensen, Anne Francke; Awasthi, Swapnil; Ripke, Stephan; Ingason, Andres; Davidsson, Olafur B.; Erikstrup, Christian; Hjalgrim, Henrik; Ullum, Henrik; Olesen, Jes; Hansen, Thomas Folkmann; Gudbjartsson, Daniel; Gastafsson, Omar; Stefansson, Kari; Stefansson, Hreinn; Porsteinsdottir, Unnur; Andersen, Steffen; Banasik, Karina; Brunak, Soren; Buil, Alfonso; Burgdorf, Kristoffer; Gregor, Jemec; Jennum, Poul; Nielsen, Kasper Rene; Nyegaard, Mette; Paarup, Helene Mariana; Pedersen, Ole Birger; Sorensen, Erik; Werge, Thomas; Anttila, Verneri; Artto, Ville; Belin, Andrea Carmine; de Boer, Irene; Boomsma, Dorret; Borte, Sigrid; Chasman, Daniel; Cherkas, Lynn; Cormand, Bru; Cuenca-Leon, Ester; Davey-Smith, George; Dichgans, Martin; van Duijn, Cornelia; Esko, Tonu; Ferrari, Michel; Frants, Rune R.; Freilinger, Tobias; Furlotte, Nick; Gormley, Padhraig; Griffiths, Lyn; Hamalainen, Eija; Hiekkala, Marjo; Ikram, M. Arfan; Jarvelin, Marjo-Riitta; Kajanne, Risto; Kallela, Mikko; Kaprio, Jaakko; Kaunisto, Mari; Kubisch, Christian; Kurki, Mitja; Kurth, Tobias; Launer, Lenore; Lehtimaki, Terho; Lessel, Davor; Ligthart, Lannie; Litterman, Nadia; van den Maagdenberg, Arn; Macaya, Alfons; Malik, Rainer; Mangino, Massimo; McMahon, George; Muller-Myhsok, Bertram; Neale, Benjamin M.; Northover, Carrie; Nyholt, Dale R.; Palotie, Aarno; Palta, Priit; Pedersen, Linda; Pedersen, Nancy; Posthuma, Danielle; Pozo-Rosich, Patricia; Pressman, Alice; Raitakari, Olli; Schurks, Markus; Sintas, Celia; Steinberg, Stacy; Strachan, David; Terwindt, Gisela; Vila-Pueyo, Marta; Wessman, Maija; Winsvold, Bendik S.; Zhao, Huiying und Zwart, John-Anker
(2019):
Migraine polygenic risk score associates with efficacy of migraine-specific drugs.
In: Neurology-Genetics, Bd. 5, Nr. 6, e364
Kingswood, John C.; Bruzzi, Paolo; Curatolo, Paolo; de Vries, Petrus J.; Fladrowski, Carla; Hertzberg, Christoph; Jansen, Anna C.; Jozwiak, Sergiusz; Nabbout, Rima; Sauter, Matthias; Touraine, Renaud; O'Callaghan, Finbar; Zonnenberg, Bernard; Crippa, Stefania; Comis, Silvia; d'Augeres, Guillaume Beaure; Belousova, Elena; Carter, Tom; Cottin, Vincent; Dahlin, Maria; Ferreira, Jose Carlos; Macaya, Alfons; Benedik, Mirjana Perkovic; Sander, Valentin; Youroukos, Sotirios; Castellana, Ramon; Ulker, Bulent und Feucht, Martha
(2014):
TOSCA - first international registry to address knowledge gaps in the natural history and management of tuberous sclerosis complex.
In: Orphanet Journal of Rare Diseases
9:182
[PDF, 1MB]
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 P. J.; Artto, Ville; Todt, Unda; Hamalainen, Eija; Fernandez-Morales, Jessica; Louter, Mark A.; Kaunisto, Mari A.; Schoenen, Jean; Raitakari, Olli; Lehtimaki, Terho; Vila-Pueyo, Marta; Goebel, Hartmut; Wichmann, Erich; Sintas, Celia; 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; Mueller-Myhsok, Bertram; Zwart, John-Anker; Farkkila, Markus; Macaya, Alfons; Ferrari, Michel D.; Kubisch, Christian; Palotie, Aarno; Dichgans, Martin und van den Maagdenberg, Arn M. J. M.
(2013):
Migraine without aura: genome-wide association analysis identifies several novel susceptibility.
In: The Journal of Headache and Pain, Bd. 14, P18
[PDF, 134kB]
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Sat Nov 16 21:52:36 2024 CET
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