المؤلفون: Bryois, Julien, Skene, Nathan G, Hansen, Thomas Folkmann, Kogelman, Lisette JA, Watson, Hunna J, Liu, Zijing, Brueggeman, Leo, Breen, Gerome, Bulik, Cynthia M, Arenas, Ernest, Hjerling-Leffler, Jens, Sullivan, Patrick F

المصدر: Nature Genetics. 52(5)

مصطلحات موضوعية: Human Genome, Genetics, Aging, Parkinson's Disease, Brain Disorders, Neurodegenerative, Neurosciences, 2.1 Biological and endogenous factors, Underpinning research, 1.1 Normal biological development and functioning, Aetiology, Neurological, Animals, Brain, Genome-Wide Association Study, Humans, Mice, Neurons, Parkinson Disease, Transcriptome, Eating Disorders Working Group of the Psychiatric Genomics Consortium, International Headache Genetics Consortium, 23andMe Research Team, Biological Sciences, Medical and Health Sciences, Developmental Biology

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/0qn87155

المؤلفون: Srinivasan, Saurabh, Bettella, Francesco, Mattingsdal, Morten, Wang, Yunpeng, Witoelar, Aree, Schork, Andrew J, Thompson, Wesley K, Zuber, Verena, Schizophrenia Working Group of the Psychiatric Genomics Consortium, The International Headache Genetics Consortium, Winsvold, Bendik S, Zwart, John-Anker, Collier, David A, Desikan, Rahul S, Melle, Ingrid, Werge, Thomas, Dale, Anders M, Djurovic, Srdjan, Andreassen, Ole A

المصدر: Biological psychiatry. 80(4)

مصطلحات موضوعية: Schizophrenia Working Group of the Psychiatric Genomics Consortium, The International Headache Genetics Consortium, Brain, Humans, Genetic Predisposition to Disease, Genetic Markers, Schizophrenia, Multifactorial Inheritance, Polymorphism, Single Nucleotide, Genome-Wide Association Study, Biological Evolution, Evolution, GWAS, Human, Neanderthal, Polygenic, Schizophrenia Working Group of the Psychiatric Genomics Consortium, The International Headache Genetics Consortium, Polymorphism, Single Nucleotide, Clinical Research, Biotechnology, Human Genome, Prevention, Genetics, Brain Disorders, Mental Health, 2.1 Biological and endogenous factors, Psychiatry, Biological Sciences, Psychology and Cognitive Sciences, Medical and Health Sciences

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/5615t7wn

المؤلفون: Winsvold, Bendik S, Bettella, Francesco, Witoelar, Aree, Anttila, Verneri, Gormley, Padhraig, Kurth, Tobias, Terwindt, Gisela M, Freilinger, Tobias M, Frei, Oleksander, Shadrin, Alexey, Wang, Yunpeng, Dale, Anders M, van den Maagdenberg, Arn MJM, Chasman, Daniel I, Nyholt, Dale R, Palotie, Aarno, Andreassen, Ole A, Zwart, John-Anker, International Headache Genetics Consortium

المصدر: PloS one. 12(9)

مصطلحات موضوعية: International Headache Genetics Consortium, Humans, Genetic Predisposition to Disease, Phenotype, Polymorphism, Single Nucleotide, Female, Male, Migraine Disorders, Coronary Artery Disease, Genome-Wide Association Study, General Science & Technology

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/04m6g4fj

المؤلفون: Kai-How Farh, Caleb Webber, Albert Hofman, George McMahon, Nicholas G. Martin, Paul M. Ridker, Lynn Cherkas, Mart Kals, Dorret I. Boomsma, George Davey Smith, Verneri Anttila, Tune H. Pers, Bertram Müller-Myhsok, Ville Artto, Benjamin M. Neale, Ester Cuenca-León, Anine H. Stam, Christopher Sivert Nielsen, Hieab H.H. Adams, Guntram Borck, Andres Metspalu, Maria Gudlaug Hrafnsdottir, Martin Dichgans, Reedik Mägi, Hailiang Huang, Daniel I. Chasman, Elizabeth Loehrer, John-Anker Zwart, Thomas Meitinger, Markus Färkkilä, Cornelia M. van Duijn, Arn M. J. M. van den Maagdenberg, Evie Stergiakouli, Johan G. Eriksson, Kauko Heikkilä, Hreinn Stefansson, Nicholas A. Furlotte, Minna Männikkö, Nicholas Eriksson, Jaakko Kaprio, David P. Strachan, Juho Wedenoja, Zameel M. Cader, Scott G. Gordon, Brenda W.J.H. Penninx, Linda M. Pedersen, Olli T. Raitakari, Phil Lee, André G. Uitterlinden, Ann-Louise Esserlind, Tobias Kurth, Arpo Aromaa, Priit Palta, Jes Olesen, Audun Stubhaug, Antti-Pekka Sarin, Andres Ingason, Stefan Schreiber, Salli Vepsäläinen, Hartmut Göbel, Kalle Pärn, Jouke-Jan Hottenga, Kari Stefansson, Bendik S. Winsvold, Markku Koiranen, Tim D. Spector, Evelin Mihailov, Mikko Muona, Marjo-Riitta Järvelin, Cynthia Sandor, Anne Francke Christensen, Lude Franke, Grant W. Montgomery, Tobias Freilinger, Caroline Ran, Thomas Werge, Maija Wessman, David A. Hinds, Lannie Ligthart, Terho Lehtimäki, Lili Milani, Mari A. Kaunisto, Lydia Quaye, Andrea Carmine Belin, Eija Hamalainen, M. Arfan Ikram, Veikko Salomaa, Mark J. Daly, Dale R. Nyholt, Pamela A. F. Madden, Andrew C. Heath, Tõnu Esko, Rainer Malik, Gisela M. Terwindt, Mitja I. Kurki, Aarno Palotie, Thomas Hansen, Padhraig Gormley, Michel D. Ferrari, Susan M. Ring, Julie E. Buring, Christian Kubisch, Mikko Kallela, Andrea Byrnes, Stacy Steinberg, Jie Huang, Markus Schürks

المساهمون: Groningen Institute for Gastro Intestinal Genetics and Immunology (3GI), Stem Cell Aging Leukemia and Lymphoma (SALL), Amsterdam Neuroscience - Complex Trait Genetics, Psychiatry, EMGO - Mental health, Internal Medicine, Epidemiology, Neurology, Amsterdam Neuroscience - Mood, Anxiety, Psychosis, Stress & Sleep, APH - Mental Health, Biological Psychology, Complex Trait Genetics

المصدر: 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, Ran, C, Gordon, S G, Stam, A H, Steinberg, S, Borck, G, Koiranen, M, Quaye, L, Adams, H H H, Lehtimäki, T, Sarin, A P, Wedenoja, J, Hinds, D A, Buring, J E, Schürks, M, Ridker, P M, Gudlaug Hrafnsdottir, M, Stefansson, H, Ring, S M, Hottenga, J J, Penninx, B W J H, Färkkilä, M, Artto, V, Kaunisto, M A, Vepsäläinen, S, Malik, R, Heath, A C, Madden, P A F, Martin, N G, Montgomery, G W, Kurki, M I, Kals, M, Mägi, R, Pärn, K, Hämaläinen, E, Huang, H, Byrnes, A E, Franke, L, Huang, J, Stergiakouli, E, Lee, P H, Sandor, C, Webber, C, Cader, Z, Müller-Myhsok, B, Schreiber, S, Meitinger, T, Eriksson, J G, Salomaa, V, Heikkilä, K, Loehrer, A G, Uitterlinden, A G, Hofman, A, van Duijn, C M, Cherkas, L, Pedersen, L, Stubhaug, A, Nielsen, C S, Männikkö, M, Mihailov, E, Milani, L, Göbel, H, Esserlind, A L, Francke Christensen, A, Folkmann Hansen, T, Werge, T, Kaprio, J, Aromaa, A, Raitakari, O, Ikram, M A, Spector, T D, Järvelin, M R, Metspalu, A, Kubisch, C, Strachan, D P, Ferrari, M D, Belin, A C, Dichgans, M, Wessman, M, van den Maagdenberg, A M J M, Zwart, J A, Boomsma, D I, Davey Smith, G, Stefansson, K, Eriksson, N, Daly, M J, Neale, B M, Olesen, J, Chasman, D I, Nyholt, DR, Palotie, A & Posthuma, D 2016, ' Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine ', Nature Genetics, vol. 48, no. 8, pp. 856-866 . https://doi.org/10.1038/ng.3598
Nature Genetics
Nature Genetics, 48(8), 856
Nature Genetics, 48(8), 856-869. Nature Publishing Group
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, Steinberg, 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, Farkkila, M, Artto, V, Kaunisto, M, Vepsalainen, S, Malik, R, Heath, A C, Madden, P A F, Martin, N G, Montgomery, G W, Kurki, M I, Kals, M, Magi, R, Parn, K, Hamalainen, E, Huang, H, Byrnes, A E, Franke, L, Huang, J, Stergiakouli, E, Lee, P H, Sandor, C, Webber, C, Cader, Z, Muller-Myhsok, B, Schreiber, S, Meitinger, T, Eriksson, J G, Salomaa, V, Heikkila, K, Loehrer, E, Uitterlinden, A G, Hofman, A, van Duijn, C M, Cherkas, L, Pedersen, L M, Stubhaug, A, Nielsen, C S, Mannikko, M, Mihailov, E, Milani, L, Gobel, H, Esserlind, A-L, Christensen, A F, Hansen, T F, Werge, T, Kaprio, J, Aromaa, A J, Raitakari, O, Ikram, M A, Spector, T, Jarvelin, M-R, Metspalu, A, Kubisch, C, Strachan, D P, Ferrari, M D, Belin, A C, Dichgans, M, Wessman, M, van den Maagdenberg, A M J M, Zwart, J-A, Boomsma, D I, Smith, G D, Stefansson, K, Eriksson, N, Daly, M J, Neale, B M, Olesen, J, Chasman, D I, Nyholt, D R, Palotie, A & Posthuma, D 2016, ' Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine ', Nature Genetics, vol. 48, no. 8, pp. 856-866 . https://doi.org/10.1038/ng.3598
Nature Genetics, 48(8), 856-866. Nature Publishing Group
Dipòsit Digital de la UB
Universidad de Barcelona
Nat. Genet. 48, 856-866 (2016)
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, Steinberg, S, Borck, G, Koiranen, M, Quaye, L, Adams, H H H, Lehtimäki, T, Sarin, A-P, Wedenoja, J, Hinds, D A, Buring, J E, Schürks, 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, Vepsäläinen, S, Malik, R, Heath, A C, Madden, P A F, Martin, N G, Montgomery, G W, Kurki, M I, Kals, M, Stergiakouli, E, Smith, G D 2016, ' Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine ', Nature Genetics, vol. 48, no. 8, pp. 856-66 . https://doi.org/10.1038/ng.3598

مصطلحات موضوعية: 0301 basic medicine, Netherlands Twin Register (NTR), SMOOTH-MUSCLE-CELLS, Medizin, Genome-wide association study, Disease, Bioinformatics, Genome-wide association studies, 0302 clinical medicine, Familial hemiplegic migraine, GENE-EXPRESSION, Genetics, Genetics & Heredity, FAMILIAL HEMIPLEGIC MIGRAINE, International Headache Genetics Consortium, SINGLE-NUCLEOTIDE POLYMORPHISMS, 11 Medical And Health Sciences, Genomics, SDG 10 - Reduced Inequalities, 3. Good health, Migranya, Cortical spreading depression, SPREADING DEPRESSION, Life Sciences & Biomedicine, Gens, Genetic Markers, Migraine Disorders, Locus (genetics), Single-nucleotide polymorphism, Biology, GENOTYPE IMPUTATION, Polymorphism, Single Nucleotide, 03 medical and health sciences, medicine, SYSTEMATIC ANALYSIS, Humans, Genetic Predisposition to Disease, Vascular Diseases, GENOME-WIDE ASSOCIATION, Migraine, Science & Technology, Case-control study, Muscle, Smooth, 06 Biological Sciences, medicine.disease, 030104 developmental biology, Genes, MYOCARDIAL-INFARCTION, Genetic Loci, Case-Control Studies, RECEPTOR-RELATED PROTEIN-1, 030217 neurology & neurosurgery, Developmental Biology, Genome-Wide Association Study

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URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b91b1615fdb6badd6cf24af716bb7404
https://doi.org/10.1038/ng.3598

المؤلفون: Winsvold, Bendik S., Bettella, Francesco, Witoelar, Aree, Anttila, Verneri, Gormley, Padhraig, Kurth, Tobias, Terwindt, Gisela M., Freilinger, Tobias, Frei, Oleksander, Shadrin, Alexey, Wang, Yunpeng, Dale, Anders M., van den Maagdenberg, Arn M.J.M., Nyholt, Dale R., Palotie, Aarno, Andreassen, Ole A., Zwart, John Anker, Artto, Ville, Belin, Andrea Carmine, Boomsma, Dorret I., Børte, Sigrid, Chasman, Daniel I., Cherkas, Lynn, Christensen, Anne Francke, Cormand, Bru, Cuenca-Leon, Ester, Davey-Smith, George, Dichgans, Martin, van Duijn, Cornelia, Eising, Else, Esko, Tonu, Esserlind, Ann Louise, Ferrari, Michel, Frants, Rune R., Furlotte, Nick, Griffiths, Lyn, Hamalainen, Eija, Hansen, Thomas Folkmann, Hiekkala, Marjo, Arfan Ikram, M., Ingason, Andres, Järvelin, Marjo Riitta, Kajanne, Risto, Kallela, Mikko, Kaprio, Jaakko, Kaunisto, Mari, Kubisch, Christian, Kurki, Mitja, Olesen, Jes

المساهمون: Yao, Yong-Gang

المصدر: Winsvold, B S, Bettella, F, Witoelar, A, Anttila, V, Gormley, P, Kurth, T, Terwindt, G M, Freilinger, T, Frei, O, Shadrin, A, Wang, Y, Dale, A M, van den Maagdenberg, A M J M, Nyholt, D R, Palotie, A, Andreassen, O A, Zwart, J A, Artto, V, Belin, A C, Boomsma, D I, Børte, S, Chasman, D I, Cherkas, L, Christensen, A F, Cormand, B, Cuenca-Leon, E, Davey-Smith, G, Dichgans, M, van Duijn, C, Eising, E, Esko, T, Esserlind, A L, Ferrari, M, Frants, R R, Freilinger, T, Furlotte, N, Griffiths, L, Hamalainen, E, Hansen, T F, Hiekkala, M, Arfan Ikram, M, Ingason, A, Järvelin, M R, Kajanne, R, Kallela, M, Kaprio, J, Kaunisto, M, Kubisch, C, Kurki, M, Olesen, J & International Headache Genetics Consortium 2017, ' Shared genetic risk between migraine and coronary artery disease : A genome-wide analysis of common variants ', PLoS ONE, vol. 12, no. 9, e0185663 . https://doi.org/10.1371/journal.pone.0185663
PloS one, vol 12, iss 9
PLoS ONE, 12(9)
PloS one
PLoS ONE, Vol 12, Iss 9, p e0185663 (2017)
Winsvold, BS; Bettella, F; Witoelar, A; Anttila, V; Gormley, P; Kurth, T; et al.(2017). Shared genetic risk between migraine and coronary artery disease: A genome-wide analysis of common variants. PLOS ONE, 12(9). doi: 10.1371/journal.pone.0185663. UC San Diego: Retrieved from: http://www.escholarship.org/uc/item/04m6g4fj
PLoS ONE

مصطلحات موضوعية: 0301 basic medicine, Male, Epidemiology, Genome-wide association study, Disease, Coronary Artery Disease, Pathology and Laboratory Medicine, Bioinformatics, Cardiovascular, Vascular Medicine, Migraines, Medicine and Health Sciences, Coronary Heart Disease, 2.1 Biological and endogenous factors, Aetiology, Genetics, Multidisciplinary, Headaches, Pain Research, International Headache Genetics Consortium, Genomics, Single Nucleotide, Phenotype, Heart Disease, Genetic Epidemiology, Medicine, Medical genetics, Female, Pathogens, Chronic Pain, Research Article, Biotechnology, medicine.medical_specialty, General Science & Technology, Science, Migraine Disorders, Cardiology, Single-nucleotide polymorphism, Biology, Polymorphism, Single Nucleotide, Molecular Genetics, 03 medical and health sciences, Signs and Symptoms, Diagnostic Medicine, Clinical Research, Genome-Wide Association Studies, medicine, SNP, Humans, Genetic Predisposition to Disease, Polymorphism, Molecular Biology, Migraine, Heart Disease - Coronary Heart Disease, Genetic association, Clinical Genetics, Prevention, Human Genome, Biology and Life Sciences, Computational Biology, Human Genetics, Genome Analysis, medicine.disease, Atherosclerosis, Brain Disorders, 030104 developmental biology, Genetic epidemiology, Genetic Loci, Genome-Wide Association Study

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URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4779d5ee71a012df2ca04d6cde6977f1
https://curis.ku.dk/portal/da/publications/shared-genetic-risk-between-migraine-and-coronary-artery-disease(f17c1c28-3856-4f13-a443-37594ac6573c).html