المؤلفون: Kogelman, Lisette JA, 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 I, Borte, Sigrid, Chasman, Daniel I, 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, Zwart, John-Anker, Consortium, DBDS Genomic, Consortium, Int Headache Genetics

المساهمون: Neurologian yksikkö, HUS Helsinki and Uusimaa Hospital District, HUS Neurocenter, Institute for Molecular Medicine Finland, Genomics of Neurological and Neuropsychiatric Disorders, University of Helsinki, Centre of Excellence in Complex Disease Genetics, Research Programs Unit, Aarno Palotie / Principal Investigator

المصدر: Neurology Genetics
Kogelman, L J A, Esserlind, A-L, Christensen, A F, Awasthi, S, Ripke, S, Ingason, A, Davidsson, O B, Erikstrup, C, Hjalgrim, H, Ullum, H, Olesen, J, Hansen, T F, DBDS Genomic Consortium, The International Headache Genetics Consortium, Gudbjartsson, D, Gastafsson, O, Stefansson, K, Stefansson, H, Porsteinsdottir, U, Andersen, S, Banasik, K, Brunak, S, Buil, A, Burgdorf, K, Gregor, J, Jennum, P, Nielsen, K R, Nyegaard, M, Paarup, H M, Pedersen, O B, Sorensen, E, Werge, T, Anttila, V, Artto, V, Belin, A C, de Boer, I, Boomsma I, D, Borte, S, Chasman I, D, Cherkas, L, Cormand, B, Cuenca-Leon, E, Davey-Smith, G, Dichgans, M, van Duijn, C, Esko, T, Ferrari, M, Frants, R R, Freilinger, T, Furlotte, N, Gormley, P & Pedersen, L 2019, ' Migraine polygenic risk score associates with efficacy of migraine-specific drugs ', Neurology: Genetics, vol. 5, no. 6, e364 . https://doi.org/10.1212/NXG.0000000000000364Test
Kogelman, L J A, Esserlind, A-L, Francke Christensen, A, Awasthi, S, Ripke, S, Ingason, A, Davidsson, O B, Erikstrup, C, Hjalgrim, H, Ullum, H, Olesen, J, Folkmann Hansen, T & DBDS Genomic Consortium, The International Headache Genetics Consortium 2019, ' Migraine polygenic risk score associates with efficacy of migraine-specific drugs ', Neurology: Genetics, vol. 5, no. 6, e364 . https://doi.org/10.1212/NXG.0000000000000364Test
Kogelman, L J A, Esserlind, A-L, Christensen, A F, Awasthi, S, Ripke, S, Ingason, A, Davidsson, O B, Erikstrup, C, Hjalgrim, H, Ullum, H, Olesen, J, Hansen, T F, Gudbjartsson, D, Gastafsson, O, Stefansson, K, Stefansson, H, Porsteinsdottir, U, Andersen, S, Banasik, K, Brunak, S, Buil, A, Burgdorf, K, Gregor, J, Jennum, P, Nielsen, K R, Nyegaard, M, Paarup, H M, Pedersen, O B, Sørensen, E, Werge, T, Anttila, V, Artto, V, Belin, A C, de Boer, I, Boomsma, D I, Borte, S, Chasman, D I, Cherkas, L, Cormand, B, Cuenca-Leon, E, Davey-Smith, G, Dichgans, M, van Duijn, C, Esko, T, Ferrari, M, Frants, R R, Freilinger, T, Furlotte, N, Gormley, P, Griffiths, L, Hamalainen, E, Hiekkala, M, Ikram, M A, Jarvelin, M-R, Kajanne, R, Kallela, M, Kaprio, J, Kaunisto, M, Kubisch, C, Kurki, M, Kurth, T, Launer, L, Lehtimaki, T, Lessel, D, Ligthart, L, Litterman, N, van den Maagdenberg, A, Macaya, A, Malik, R, Mangino, M, McMahon, G, Muller-Myhsok, B, Neale, B M, Northover, C, Nyholt, D R, Palotie, A, Palta, P, Pedersen, L, Pedersen, N, Posthuma, D, Pozo-Rosich, P, Pressman, A, Raitakari, O, Schurks, M, Sintas, C, Steinberg, S, Strachan, D, Terwindt, G, Vila-Pueyo, M, Wessman, M, Winsvold, B S, Zhao, H & Zwart, J-A 2019, ' Migraine polygenic risk score associates with efficacy of migraine-specific drugs ', Neurology: Genetics, vol. 5, no. 6, e364 . https://doi.org/10.1212/NXG.0000000000000364Test
Kogelman, L J A, Esserlind, A-L, Francke Christensen, A, Awasthi, S, Ripke, S, Ingason, A, Davidsson, O B, Erikstrup, C, Hjalgrim, H, Ullum, H, Olesen, J, Folkmann Hansen, T, DBDS Genomic Consortium, Nielsen, K R, Nyegaard, M & The International Headache Genetics Consortium 2019, ' Migraine polygenic risk score associates with efficacy of migraine-specific drugs ', Neurology. Genetics, vol. 5, no. 6, e364, pp. 1-11 . https://doi.org/10.1212/NXG.0000000000000364Test
Neurology: Genetics

مصطلحات موضوعية: 0301 basic medicine, medicine.medical_specialty, SUSCEPTIBILITY LOCI, PHARMACOGENOMICS, Triptans, Logistic regression, Article, 3124 Neurology and psychiatry, 03 medical and health sciences, 0302 clinical medicine, Internal medicine, SCHIZOPHRENIA, Medicine, Migraine treatment, METAANALYSIS, Genetics (clinical), business.industry, 1184 Genetics, developmental biology, physiology, 3112 Neurosciences, Area under the curve, Odds ratio, medicine.disease, Confidence interval, 3. Good health, 030104 developmental biology, Migraine, Cohort, Neurology (clinical), business, 030217 neurology & neurosurgery, medicine.drug

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cfafc8ae11cc8e555481ba9c5defeb8aTest
https://doi.org/10.1212/nxg.0000000000000364Test

المؤلفون: Sintas, Cèlia, Carreño, Oriel, Fernàndez-Castillo, Noèlia, Corominas, Roser, Vila-Pueyo, Marta, Toma, Claudio, Cuenca-León, Ester, Barroeta, Isabel, Roig, Carles, Volpini, Víctor, Macaya Ruiz, Alfons, Cormand, Bru

المساهمون: Universitat de Barcelona

المصدر: Recercat. Dipósit de la Recerca de Catalunya
instname
Scientific Reports, Vol 7, Iss 1, Pp 1-9 (2017)
Dipòsit Digital de la UB
Universidad de Barcelona
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Scientific Reports

مصطلحات موضوعية: Male, Atàxia, Mecànica humana, Science, DNA Mutational Analysis, Medical genetics, Human mechanics, Article, Pedigree, Genètica mèdica, Mutation, Humans, Medicine, Ataxia, Female, Calcium Channels, 3' Untranslated Regions, Gene Deletion, Genetic Association Studies, Sequence Deletion, Gens

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::3d9ca2f7be43de2ecb5784576bfcae18Test
http://hdl.handle.net/2445/119655Test