المؤلفون: Wilms, Annelise E., de Boer, I., Pelzer, N., in’t Veld, S. G. J. G., Middelkoop, H. A. M.^{Aff1, Aff3}, Teunissen, C. E., Terwindt, G. M.^{Aff1, IDs00415024122926_cor7}

المصدر: Journal of Neurology. 271(7):4138-4145

المؤلفون: Hautakangas, H, Winsvold, BS, Ruotsalainen, SE, Bjornsdottir, G, Harder, AVE, Kogelman, LJA, Thomas, LF, Noordam, R, Benner, C, Gormley, P, Artto, V, Banasik, K, Bjornsdottir, A, Boomsma, D, Brumpton, B, Burgdorf, KS, Buring, JE, Chalmer, MA, de Boer, I, Dichgans, M, Erikstrup, C, Farkkila, M, Garbrielsen, ME, Ghanbari, M, Hagen, K, Happola, P, Hottenga, JJ, Hrafnsdottir, MG, Hveem, K, Johnsen, MB, Kahonen, M, Kristoffersen, ES, Kurth, T, Lehtimaki, T, Lighart, L, Magnusson, SH, Malik, R, Pedersen, OB, Pelzer, N, Penninx, BWJH, Ran, C, Ridker, PM, Rosendaal, FR, Sigurdardottir, GR, Skogholt, AH, Sveinsson, OA, Thorgeirsson, TE, Ullum, H, Vijfhuizen, LS, Widen, E, van Dijk, KW, Aromaa, A, Belin, AC, Freilinger, T, Ikram, MA, Jarvelin, MR, Raitakari, OT, Terwindt, GM, Kallela, M, Wessman, M, Olesen, J, Chasman, D, Nyholt, DR, Stefansson, H, Stefansson, K, van den Maagdenberg, AMJM, Hansen, TF, Ripatti, S, Zwart, JA, Palotie, A, Pirinen, M

المصدر: Nature genetics. 54(2):152

مصطلحات موضوعية: Medicin och hälsovetenskap

URL الوصول: http://kipublications.ki.se/Default.aspx?queryparsed=id:148678472

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المؤلفون: Hautakangas, H., Winsvold, B.S., Ruotsalainen, S.E., Bjornsdottir, G., Harder, A.V.E., Kogelman, L.J.A., Thomas, L.F., Noordam, R., Benner, C., Gormley, P., Artto, V., Banasik, K., Bjornsdottir, A., Boomsma, D.I., Brumpton, B., Burgdorf, K.S., Buring, J.E., Chalmer, M.A., Boer, I. de, Dichgans, M., Erikstrup, C., Farkkila, M., Garbrielsen, M.E., Ghanbari, M., Hagen, K., Happola, P., Hottenga, J.J., Hrafnsdottir, M.G., Hveem, K., Johnsen, M.B., Kahonen, M., Kristoffersen, E.S., Kurth, T., Lehtimaki, T., Lighart, L., Magnusson, S.H., Malik, R., Pedersen, O.B., Pelzer, N., Penninx, B.W.J.H., Ran, C., Ridker, P.M., Rosendaal, F.R., Sigurdardottir, G.R., Skogholt, A.H., Sveinsson, O.A., Thorgeirsson, T.E., Ullum, H., Vijfhuizen, L.S., Widen, E., Dijk, K.W. van, Aromaa, A., Belin, A.C., Freilinger, T., Ikram, M.A., Jarvelin, M.R., Raitakari, O.T., Terwindt, G.M., Kallela, M., Wessman, M., Olesen, J., Chasman, D.I., Nyholt, D.R., Stefansson, H., Stefansson, K., Maagdenberg, A.M.J.M. van den, Hansen, T.F., Ripatti, S., Zwart, J.A., Palotie, A., Pirinen, M., Int Headache Genetics Consortium, HUNT All-in Headache, Danish Blood Donor Study Genomic C

المساهمون: Biological Psychology, APH - Mental Health, APH - Methodology, APH - Health Behaviors & Chronic Diseases, APH - Personalized Medicine, Sociology and Social Gerontology, Institute for Molecular Medicine Finland, Statistical and population genetics, Complex Disease Genetics, Clinicum, HUS Helsinki and Uusimaa Hospital District, HUS Neurocenter, Neurologian yksikkö, Genomics of Neurological and Neuropsychiatric Disorders, Centre of Excellence in Complex Disease Genetics, Genomic Discoveries and Clinical Translation, Biosciences, Faculty Common Matters (Faculty of Social Sciences), Department of Public Health, Biostatistics Helsinki, Research Programs Unit, Research Programme of Molecular Medicine, Department of Mathematics and Statistics, Helsinki Institute for Information Technology, Tampere University, Department of Clinical Physiology and Nuclear Medicine, Clinical Medicine, Department of Clinical Chemistry, Epidemiology, Psychiatry, Amsterdam Neuroscience - Complex Trait Genetics, Amsterdam Neuroscience - Mood, Anxiety, Psychosis, Stress & Sleep, APH - Digital Health

المصدر: Nature genetics, 54(2), 152-160. Nature Publishing Group
Nature Genetics
International Headache Genetics Consortium, HUNT All-in Headache & Danish Blood Donor Study Genomic Cohort 2022, ' Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles ', Nature Genetics, vol. 54, no. 2, pp. 152-160 . https://doi.org/10.1038/s41588-021-00990-0
Nature Genetics, 54, 152-160. NATURE PORTFOLIO
Hautakangas, H, Winsvold, B S, Ruotsalainen, S E, Bjornsdottir, G, Harder, A V E, Kogelman, L J A, Thomas, L F, Noordam, R, Benner, C, Gormley, P, Artto, V, Banasik, K, Bjornsdottir, A, Boomsma, D I, Brumpton, B M, Burgdorf, K S, Buring, J E, Chalmer, M A, de Boer, I, Dichgans, M, Erikstrup, C, Farkkila, M, Garbrielsen, M E, Ghanbari, M, Hagen, K, Happola, P, Hottenga, J-J, Hrafnsdottir, M G, Hveem, K, Johnsen, M B, Kahonen, M, Kristoffersen, E S, Kurth, T, Lehtimaki, T, Lighart, L, Magnusson, S H, Malik, R, Pedersen, O B, Pelzer, N, Penninx, B W J H, Ran, C, Ridker, P M, Rosendaal, F R, Sigurdardottir, G R, Skogholt, A H, Sveinsson, O A, Thorgeirsson, T E, Ullum, H, Vijfhuizen, L S, Widen, E, van Dijk, K W, Aromaa, A, Belin, A C, Freilinger, T, Ikram, M A, Jarvelin, M-R, Raitakari, O T, Terwindt, G M, Kallela, M, Wessman, M, Olesen, J, Chasman, D I, Nyholt, D R, Stefansson, H, Stefansson, K, van den Maagdenberg, A M J M, Hansen, T F, Ripatti, S, Zwart, J-A, Palotie, A & Pirinen, M 2022, ' Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles ', Nature Genetics, vol. 54, pp. 152-160 . https://doi.org/10.1038/s41588-021-00990-0
Hautakangas, H, Winsvold, B S, Ruotsalainen, S E, Bjornsdottir, G, Harder, A V E, Kogelman, L J A, Thomas, L F, Noordam, R, Benner, C, Gormley, P, Artto, V, Banasik, K, Bjornsdottir, A, Boomsma, D I, Brumpton, B M, Burgdorf, K S, Buring, J E, Chalmer, M A, de Boer, I, Dichgans, M, Erikstrup, C, Färkkilä, M, Garbrielsen, M E, Ghanbari, M, Hagen, K, Häppölä, P, Hottenga, J J, Hrafnsdottir, M G, Hveem, K, Johnsen, M B, Kähönen, M, Kristoffersen, E S, Kurth, T, Lehtimäki, T, Lighart, L, Magnusson, S H, Malik, R, Pedersen, O B, Pelzer, N, Penninx, B W J H, Ran, C, Ridker, P M, Rosendaal, F R, Sigurdardottir, G R, Skogholt, A H, Sveinsson, O A, Thorgeirsson, T E, Ullum, H, Vijfhuizen, L S, Widen, E, van Dijk, K W, International Headache Genetics Consortium, HUNT All-in Headache, Danish Blood Donor Study Genomic Cohort, Aromaa, A, Belin, A C, Freilinger, T, Ikram, M A, Järvelin, M-R, Raitakari, O T, Terwindt, G M, Kallela, M, Wessman, M, Olesen, J, Chasman, D I, Nyholt, D R, Stefansson, H, Stefansson, K, van den Maagdenberg, A M J M, Hansen, T F, Ripatti, S, Zwart, J-A, Palotie, A & Pirinen, M 2022, ' Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles ', Nature Genetics, vol. 54, no. 2, pp. 152-160 . https://doi.org/10.1038/s41588-021-00990-0
Nature Genetics, 54(2), 152-160. Nature Publishing Group
Hautakangas, H, Winsvold, B S, Boomsma, D I, Hottenga, J-J, Ligthart, L, Penninx, B W J H, Palotie, A, Pirinen, M & International Headache Genetics Consortium 2022, ' Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles ', Nature genetics, vol. 54, no. 2, pp. 152-160 . https://doi.org/10.1038/s41588-021-00990-0

مصطلحات موضوعية: Central Nervous System, SUSCEPTIBILITY LOCI, Migraine Disorders, Migraine with Aura, Quantitative Trait Loci, PATHOPHYSIOLOGY, Genome-wide association studies, Cardiovascular System, Polymorphism, Single Nucleotide, Genetics, Humans, Genetic Predisposition to Disease, TRANSCRIPTOME, AURA, Migraine, Alleles, METAANALYSIS, GENE-EXPRESSION, ARCHITECTURE, MUTATIONS, HERITABILITY, 1184 Genetics, developmental biology, physiology, Molecular Sequence Annotation, ASSOCIATION, 3142 Public health care science, environmental and occupational health, Genetic Loci, Case-Control Studies, 3111 Biomedicine, Genome-Wide Association Study

وصف الملف: application/pdf; fulltext

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::271e89f31a913a67875ee7088a9a1e7c
https://research.vu.nl/en/publications/dad00511-8fd1-468a-a806-7f8306e18447

المؤلفون: Pelzer, N., Vandersteene, J., Bekooij, T. J. S., Schoonman, G. G., Wirtz, P. W., Vanopdenbosch, L. J., Koppen, H.

المصدر: Neurological Sciences: Official Journal of the Italian Neurological Society. December 2014 35(12):1997-1999

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المؤلفون: Pelzer, N., de Vries, B., Boon, E. M. J., Kruit, M. C., Haan, J., Ferrari, M. D., van den Maagdenberg, A. M. J. M., Terwindt, G. M.

المصدر: Journal of Neurology: Official Journal of the European Neurological Society. August 2013 260(8):2188-2190

المؤلفون: Pelzer, N.

المساهمون: Ferrari, M.D., Maagdenberg, A.M.J.M. van den, Terwindt, G.M., Verschuren, J.J.G.M., Duijn, C.M. van, Eikenboom, H.C.J., Reinders, M.E.J., Haren - Maassen van den Brink, A. van, Leiden University

المصدر: None

مصطلحات موضوعية: Channelopathy, Neurogenetics, Endotheliopathy, Migraine, Hemiplegic migraine, Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::07a7eeabb6e602d236b414df823882b4
https://hdl.handle.net/1887/67103

المؤلفون: Boer, I. de, Pelzer, N., Hoogeveen, E.S., Steenmeijer, S.R., Notting, I.C., Middelkoop, H.A., Kruit, M.C., Terwindt, G.M.

URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::b2aa5b27d6cfc3c40ed8af297bc47026
https://hdl.handle.net/1887/121566

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