المؤلفون: Salpietro, Vincenzo, Malintan, Nancy T., Llano-Rivas, Isabel, Spaeth, Christine G., Efthymiou, Stephanie, Striano, Pasquale, Vandrovcova, Jana, Cutrupi, Maria C., Chimenz, Roberto, David, Emanuele, Di Rosa, Gabriella, Marce-Grau, Anna, Raspall-Chaure, Miquel, Martin-Hernandez, Elena, Zara, Federico, Minetti, Carlo, Kriouile, Yamna, El Khorassani, Mohamed, Aguennouz, Mhammed, Karashova, Blagovesta, Avdjieva, Daniela, Kathom, Hadil, Tincheva, Radka, Van Maldergem, Lionel, Nachbauer, Wolfgang, Boesch, Sylvia, Arning, Larissa, Timmann, Dagmar, Cormand, Bru, Pérez-Dueñas, Belen, Pironti, Erica, Goraya, Jatinder S., Sultan, Tipu, Kirmani, Salman, Ibrahim, Shahnaz, Jan, Farida, Mine, Jun, Banu, Selina, Veggiotti, Pierangelo, Ferrari, Michel D., Verrotti, Alberto, Marseglia, Gian Luigi, Savasta, Salvatore, Garavaglia, Barbara, Scuderi, Carmela, Borgione, Eugenia, Dipasquale, Valeria, Cutrupi, Maria Concetta, Portaro, Simona, Sanchez, Benigno Monteagudo, Pineda-Marfa, Mercedes, Munell, Francina, Macaya, Alfons, Boles, Richard, Heimer, Gali, Papacostas, Savvas, Manole, Andreea, Malintan, Nancy, Zanetti, Maria Natalia, Hanna, Michael G., Rothman, James E., Kullmann, Dimitri M., Houlden, Henry, Bello, Oscar D., De Zorzi, Rita, Fortuna, Sara, Dauber, Andrew, Alkhawaja, Mariam, Mankad, Kshitij, Vitobello, Antonio, Thomas, Quentin, Mau-Them, Frederic Tran, Faivre, Laurence, Martinez-Azorin, Francisco, Prada, Carlos E., Krishnakumar, Shyam S.

المساهمون: Salpietro, Vincenzo, Malintan, Nancy T., Llano-Rivas, Isabel, Spaeth, Christine G., Efthymiou, Stephanie, Striano, Pasquale, Vandrovcova, Jana, Cutrupi, Maria C., Chimenz, Roberto, David, Emanuele, Di Rosa, Gabriella, Marce-Grau, Anna, Raspall-Chaure, Miquel, Martin-Hernandez, Elena, Zara, Federico, Minetti, Carlo, Kriouile, Yamna, El Khorassani, Mohamed, Aguennouz, Mhammed, Karashova, Blagovesta, Avdjieva, Daniela, Kathom, Hadil, Tincheva, Radka, Van Maldergem, Lionel, Nachbauer, Wolfgang, Boesch, Sylvia, Arning, Larissa, Timmann, Dagmar, Cormand, Bru, Pérez-Dueñas, Belen, Pironti, Erica, Goraya, Jatinder S., Sultan, Tipu, Kirmani, Salman, Ibrahim, Shahnaz, Jan, Farida, Mine, Jun, Banu, Selina, Veggiotti, Pierangelo, Ferrari, Michel D., Verrotti, Alberto, Marseglia, Gian Luigi, Savasta, Salvatore, Garavaglia, Barbara, Scuderi, Carmela, Borgione, Eugenia, Dipasquale, Valeria, Cutrupi, Maria Concetta, Portaro, Simona, Sanchez, Benigno Monteagudo, Pineda-Marfa, Mercede, Munell, Francina, Macaya, Alfon, Boles, Richard, Heimer, Gali, Papacostas, Savva, Manole, Andreea, Malintan, Nancy, Zanetti, Maria Natalia, Hanna, Michael G., Rothman, James E., Kullmann, Dimitri M., Houlden, Henry, Bello, Oscar D., De Zorzi, Rita, Fortuna, Sara, Dauber, Andrew, Alkhawaja, Mariam, Mankad, Kshitij, Vitobello, Antonio, Thomas, Quentin, Mau-Them, Frederic Tran, Faivre, Laurence, Martinez-Azorin, Francisco, Prada, Carlos E., Krishnakumar, Shyam S.

مصطلحات موضوعية: autism, epilepsy, movement disorders, neurodevelopmental disorders, neuronal exocytosis, SNARE, synaptobrevin, synaptopathy, VAMP2, vesicle fusion, Genetics, Genetics (clinical)

وصف الملف: STAMPA

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/30929742; info:eu-repo/semantics/altIdentifier/wos/WOS:000463474700012; volume:104; issue:4; firstpage:721; lastpage:730; numberofpages:10; journal:AMERICAN JOURNAL OF HUMAN GENETICS; http://hdl.handle.net/11570/3138980Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85063684737; https://www.cell.com/ajhg/fulltext/S0002-9297Test(19)30061-8

الإتاحة: https://doi.org/10.1016/j.ajhg.2019.02.016Test
http://hdl.handle.net/11570/3138980Test
https://www.cell.com/ajhg/fulltext/S0002-9297Test(19)30061-8

المؤلفون: Eising, Else, Huisman, Sjoerd M. H., Mahfouz, Ahmed, Vijfhuizen, Lisanne S., Anttila, Verneri, Winsvold, Bendik S., Kurth, Tobias, Ikram, M. Arfan, Freilinger, Tobias, Kaprio, Jaakko, Boomsma, Dorret I., van Duijn, Cornelia M., Järvelin, Marjo-Riitta R., Zwart, John-Anker, Quaye, Lydia, Strachan, David P., Kubisch, Christian, Dichgans, Martin, Davey Smith, George, Stefansson, Kari, Palotie, Aarno, Chasman, Daniel I., Ferrari, Michel D., Terwindt, Gisela M., de Vries, Boukje, Nyholt, Dale R., Lelieveldt, Boudewijn P. F., van den Maagdenberg, Arn M. J. M., Reinders, Marcel J. T.

المساهمون: Stichting voor de Technische Wetenschappen, Seventh Framework Programme, Nederlandse Organisatie voor Wetenschappelijk Onderzoek

المصدر: Human Genetics ; volume 135, issue 4, page 425-439 ; ISSN 0340-6717 1432-1203

مصطلحات موضوعية: Genetics (clinical), Genetics

الإتاحة: https://doi.org/10.1007/s00439-016-1638-xTest

المؤلفون: Ligthart, Lannie, de Vries, Boukje, Smith, Albert V, Ikram, M Arfan, Amin, Najaf, Hottenga, Jouke-Jan, Koelewijn, Stephany C, Kattenberg, V Mathijs, de Moor, Marleen HM, Janssens, A Cecile JW, Aulchenko, Yurii S, Oostra, Ben A, de Geus, Eco JC, Smit, Johannes H, Zitman, Frans G, Uitterlinden, André G, Hofman, Albert, Willemsen, Gonneke, Nyholt, Dale R, Montgomery, Grant W, Terwindt, Gisela M, Gudnason, Vilmundur, Penninx, Brenda WJH, Breteler, Monique, Ferrari, Michel D, Launer, Lenore J, van Duijn, Cornelia M, van den Maagdenberg, Arn MJM, Boomsma, Dorret I

المصدر: European Journal of Human Genetics ; volume 19, issue 8, page 901-907 ; ISSN 1018-4813 1476-5438

مصطلحات موضوعية: Genetics (clinical), Genetics

الإتاحة: https://doi.org/10.1038/ejhg.2011.48Test
http://www.nature.com/articles/ejhg201148.pdfTest

المؤلفون: Vanmolkot, Kaate R J, Stam, Anine H, Raman, Ashok, Koenderink, Jan B, de Vries, Boukje, van den Boogerd, Eelke H, van Vark, Judith, van den Heuvel, Jeroen J M W, Bajaj, Nin, Terwindt, Gisela M, Haan, Joost, Frants, Rune R, Ferrari, Michel D, van den Maagdenberg, Arn M J M

المصدر: European Journal of Human Genetics ; volume 15, issue 8, page 884-888 ; ISSN 1018-4813 1476-5438

مصطلحات موضوعية: Genetics (clinical), Genetics

الإتاحة: https://doi.org/10.1038/sj.ejhg.5201841Test
http://www.nature.com/articles/5201841.pdfTest
http://www.nature.com/articles/5201841Test

المؤلفون: Castro, Maria-José, Stam, Anine H., Lemos, Carolina, Barros, José, Gouveia, Raquel G., Martins, Isabel Pavão, Koenderink, Jan B., Vanmolkot, Kaate R. J., Mendes, Alexandre P., Frants, Rune R., Ferrari, Michel D., Sequeiros, Jorge, Pereira-Monteiro, José M., van den Maagdenberg, Arn M. J. M.

المصدر: Journal of Human Genetics ; volume 52, issue 12, page 990-998 ; ISSN 1434-5161 1435-232X

مصطلحات موضوعية: Genetics (clinical), Genetics

الإتاحة: https://doi.org/10.1007/s10038-007-0205-7Test
http://www.nature.com/articles/jhg2007131.pdfTest
http://www.nature.com/articles/jhg2007131Test

المؤلفون: Vanmolkot, Kaate R J, Kors, Esther E, Turk, Ulku, Turkdogan, Dylsad, Keyser, Antoine, Broos, Ludo A M, Kia, Sima Kheradmand, van den Heuvel, Jeroen J M W, Black, David F, Haan, Joost, Frants, Rune R, Barone, Virginia, Ferrari, Michel D, Casari, Giorgio, Koenderink, Jan B, van den Maagdenberg, Arn M J M

المصدر: European Journal of Human Genetics ; volume 14, issue 5, page 555-560 ; ISSN 1018-4813 1476-5438

مصطلحات موضوعية: Genetics (clinical), Genetics

الإتاحة: https://doi.org/10.1038/sj.ejhg.5201607Test
http://www.nature.com/articles/5201607.pdfTest
http://www.nature.com/articles/5201607Test

المؤلفون: Ophoff, Roel A., DeYoung, Joseph, Service, Susan K., Joosse, Marijke, Caffo, Nathan A., Sandkuijl, Lodewijk A., Terwindt, Gisela M., Haan, Joost, van den Maagdenberg, Arn M.J.M., Jen, Joanna, Baloh, Robert W., Barilla-LaBarca, Maria-Louise, Saccone, Nancy L., Atkinson, John P., Ferrari, Michel D., Freimer, Nelson B., Frants, Rune R.

المصدر: The American Journal of Human Genetics ; volume 69, issue 2, page 447-453 ; ISSN 0002-9297

مصطلحات موضوعية: Genetics (clinical), Genetics

الإتاحة: https://doi.org/10.1086/321975Test
https://api.elsevier.com/content/article/PII:S000292970761091X?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S000292970761091X?httpAccept=text/plainTest

المؤلفون: Yang, Yuanhao, Zhao, Huiying, Boomsma, Dorret I, Smith, George Davey, Esko, Tonu, Hansen, Thomas Folkmann, Ikram, M. Arfan, Paraskevi, Christofidou, Strachan, David P., Wessman, Maija, Gormley, Padhraig, Anttila, Verneri, Winsvold, Bendik S., Palta, Priit, Pers, Tune H., Farh, Kai-How, Cuenca-Leon, Ester, Muona, Mikko, Furlotte, Nicholas A., Kurth, Tobias, Ingason, Andres, McMahon, George, Ligthart, Lannie, Kallela, Mikko, Freilinger, Tobias M., Ran, Caroline, Gordon, Scott G., Stam, Anine H., Steinberg, Stacy, Borck, Guntram, Koiranen, Markku, Quaye, Lydia, Adams, Hieab H. H., 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 W. J. H., 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 I, 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, Werge, Thomas, Kaprio, Jaakko, Aromaa, Arpo J., Raitakari, Olli, Spector, Tim, Järvelin, Marjo-Riitta, Metspalu, Andres, Kubisch, Christian, Ferrari, Michel D., Belin, Andrea C., Dichgans, Martin, Zwart, John-Anker, Stefansson, Kari, Eriksson, Nicholas, Daly, Mark J., Neale, Benjamin M., Olesen, Jes, Chasman, Daniel I., Nyholt, Dale R., Palotie, Aarno, van den Maagdenberg, Arn M. J. M., Terwindt, Gisela M.

المساهمون: Psychiatry, APH - Mental Health, Amsterdam Neuroscience - Mood, Anxiety, Psychosis, Stress & Sleep, APH - Digital Health, Epidemiology, Biological Psychology, APH - Methodology, APH - Personalized Medicine, APH - Health Behaviors & Chronic Diseases

المصدر: European Journal of Human Genetics
Boomsma, D I, Ligthart, L, Hottenga, J J, Penninx, B W J H & The International Headache Genetics Consortium 2018, ' Molecular genetic overlap between migraine and major depressive disorder ', European Journal of Human Genetics, vol. 26, no. 8, pp. 1202-1216 . https://doi.org/10.1038/s41431-018-0150-2Test
The International Headache Genetics Consortium 2018, ' Molecular genetic overlap between migraine and major depressive disorder ', European Journal of Human Genetics, vol. 26, no. 8, pp. 1202-1216 . https://doi.org/10.1038/s41431-018-0150-2Test
the International Headache Genetics Consortium, Yang, Y, Zhao, H, Boomsma, D I, Ligthart, L, Belin, A C, Smith, G D, Esko, T, Freilinger, T M, Hansen, T F, Ikram, M A, Kallela, M, Kubisch, C, Paraskevi, C, Strachan, D P, Wessman, M, 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, Ring, S M, Stergiakouli, E & Smith, G D 2018, ' Molecular genetic overlap between migraine and major depressive disorder ', European Journal of Human Genetics, vol. 26, no. 8, pp. 1202-1216 . https://doi.org/10.1038/s41431-018-0150-2Test
European Journal of Human Genetics, 26(8), 1202-1216. Nature Publishing Group

مصطلحات موضوعية: 0301 basic medicine, Netherlands Twin Register (NTR), Linkage disequilibrium, Migraine Disorders, Medizin, Single-nucleotide polymorphism, Genome-wide association study, Polymorphism, Single Nucleotide, Article, Linkage Disequilibrium, 03 medical and health sciences, 0302 clinical medicine, Potassium Channels, Tandem Pore Domain, SDG 3 - Good Health and Well-being, Genotype, Databases, Genetic, Genetics, medicine, SNP, Humans, Genetics (clinical), Depressive Disorder, Major, business.industry, medicine.disease, Comorbidity, Ankyrin Repeat, 030104 developmental biology, Migraine, Major depressive disorder, business, 030217 neurology & neurosurgery, Genome-Wide Association Study

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::950ea06bbd691cb84376056bc246b2d3Test
https://europepmc.org/articles/PMC6057914Test/

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: de Vries, Boukje, Frants, Rune R., Ferrari, Michel D., van den Maagdenberg, Arn M. J. M.

المصدر: Human Genetics ; volume 126, issue 1, page 115-132 ; ISSN 0340-6717 1432-1203

مصطلحات موضوعية: Genetics (clinical), Genetics

الإتاحة: https://doi.org/10.1007/s00439-009-0684-zTest