X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (571) 571
Conference Proceeding (224) 224
Publication (176) 176
Book Review (46) 46
Book / eBook (10) 10
Book Chapter (4) 4
Dissertation (2) 2
Magazine Article (2) 2
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
clinical neurology (461) 461
index medicus (328) 328
humans (327) 327
male (236) 236
female (235) 235
peripheral vascular disease (222) 222
aged (208) 208
middle aged (182) 182
article (152) 152
stroke (142) 142
intracerebral hemorrhage (126) 126
risk factors (125) 125
aged, 80 and over (122) 122
neurosciences (100) 100
abridged index medicus (98) 98
neurology (91) 91
risk (80) 80
genetics (79) 79
magnetic resonance imaging (72) 72
cohort studies (70) 70
adult (68) 68
prospective studies (62) 62
cerebral amyloid angiopathy (60) 60
cerebral hemorrhage - diagnostic imaging (55) 55
mortality (54) 54
retrospective studies (53) 53
genotype (51) 51
metaanalysis (49) 49
genome-wide association study (48) 48
hemorrhage (48) 48
brain (47) 47
genome-wide association (46) 46
association (45) 45
disease (44) 44
critical care medicine (43) 43
polymorphism, single nucleotide (43) 43
risk-factors (42) 42
stroke - genetics (42) 42
prognosis (38) 38
research (38) 38
cerebral hemorrhage - pathology (36) 36
cerebral hemorrhage - genetics (35) 35
medical and health sciences (35) 35
medicin och hälsovetenskap (35) 35
case-control studies (34) 34
cerebral hemorrhage (34) 34
ischemic-stroke (34) 34
clinical medicine (33) 33
klinisk medicin (32) 32
mri (32) 32
dementia (31) 31
internal medicine (31) 31
alzheimers-disease (30) 30
cerebral hemorrhage - complications (30) 30
intracranial hemorrhage (30) 30
medicine & public health (30) 30
population (30) 30
warfarin (30) 30
atrial-fibrillation (29) 29
cerebral amyloid angiopathy - complications (29) 29
cerebral hemorrhage - epidemiology (29) 29
cerebral hemorrhage - mortality (29) 29
genetic predisposition to disease (29) 29
predictive value of tests (29) 29
neurologi (28) 28
epidemiology (27) 27
genetics & heredity (27) 27
studies (27) 27
tomography, x-ray computed (27) 27
treatment outcome (27) 27
brain - pathology (26) 26
prevalence (26) 26
small vessel disease (26) 26
diagnosis (25) 25
genomes (25) 25
longitudinal studies (25) 25
volume (25) 25
disease progression (24) 24
hematoma expansion (24) 24
analysis (23) 23
anticoagulants - adverse effects (23) 23
hypertension (23) 23
polymorphism, single nucleotide - genetics (23) 23
cerebral hemorrhage - chemically induced (22) 22
genetic aspects (22) 22
genomics (22) 22
multivariate analysis (22) 22
neuroimaging (22) 22
patients (22) 22
score (22) 22
traumatic brain injury (22) 22
white-matter lesions (22) 22
cerebral hemorrhage - diagnosis (21) 21
cerebral hemorrhage - therapy (21) 21
medical research (21) 21
warfarin - adverse effects (21) 21
brain ischemia - genetics (20) 20
cerebral amyloid angiopathy - pathology (20) 20
cerebral hemorrhage - physiopathology (20) 20
follow-up studies (20) 20
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Robarts - Stacks (9) 9
Art - Library use only (2) 2
Collection Dvlpm't (Acquisitions) - Vendor file (1) 1
Trinity College (John W Graham) - Stacks (1) 1
UofT at Mississauga - Stacks (1) 1
UofT at Scarborough - Stacks (1) 1
Victoria University E.J. Pratt - Stacks (1) 1
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


by Ellinor, Patrick T and Lunetta, Kathryn L and Albert, Christine M and Glazer, Nicole L and Ritchie, Marylyn D and Smith, Albert V and Arking, Dan E and Müller-Nurasyid, Martina and Krijthe, Bouwe P and Lubitz, Steven A and Bis, Joshua C and Chung, Mina K and Dörr, Marcus and Ozaki, Kouichi and Roberts, Jason D and Smith, J Gustav and Pfeufer, Arne and Sinner, Moritz F and Lohman, Kurt and Ding, Jingzhong and Smith, Nicholas L and Smith, Jonathan D and Rienstra, Michiel and Rice, Kenneth M and Van Wagoner, David R and Magnani, Jared W and Wakili, Reza and Clauss, Sebastian and Rotter, Jerome I and Steinbeck, Gerhard and Launer, Lenore J and Davies, Robert W and Borkovich, Matthew and Harris, Tamara B and Lin, Honghuang and Völker, Uwe and Völzke, Henry and Milan, David J and Hofman, Albert and Boerwinkle, Eric and Chen, Lin Y and Soliman, Elsayed Z and Voight, Benjamin F and Li, Guo and Chakravarti, Aravinda and Kubo, Michiaki and Teow, Usha B and Rose, Lynda M and Ridker, Paul M and Conen, David and Tsunoda, Tatsuhiko and Furukawa, Tetsushi and Sotoodehnia, Nona and Xu, Siyan and Kamatani, Naoyuki and Levy, Daniel and Nakamura, Yusuke and Parvez, Babar and Mahida, Saagar and Furie, Karen L and Rosand, Jonathan and Muhammad, Raafia and Psaty, Bruce M and Meitinger, Thomas and Perz, Siegfried and Wichmann, H-Erich and Witteman, Jacqueline C M and Kao, W H Linda and Kathiresan, Sekar and Roden, Dan M and Uitterlinden, Ane G and Rivadeneira, Fernando and McKnight, Barbara and Sjögren, Marketa and Newman, Anne B and Liu, Yongmei and Gollob, Michael H and Melander, Olle and Tanaka, Toshihiro and Stricker, Bruno H Ch and Felix, Stephan B and Alonso, Alvaro and Darbar, Dawood and Barnard, John and Chasman, Daniel I and Heckbert, Susan R and Benjamin, Emelia J and Gudnason, Vilmundur and Kääb, Stefan
Nature Genetics, ISSN 1061-4036, 06/2012, Volume 44, Issue 6, pp. 670 - 5
Journal Article
by Anttila, Verneri and Bulik-Sullivan, Brendan and Finucane, Hilary K and Walters, Raymond K and Bras, Jose and Duncan, Laramie and Escott-Price, Valentina and Falcone, Guido J and Gormley, Padhraig and Malik, Rainer and Patsopoulos, Nikolaos A and Ripke, Stephan and Wei, Zhi and Yu, Dongmei and Lee, Phil H and Turley, Patrick and Grenier-Boley, Benjamin and Chouraki, Vincent and Kamatani, Yoichiro and Berr, Claudine and Letenneur, Luc and Hannequin, Didier and Amouyel, Philippe and Boland, Anne and Deleuze, Jean-François and Duron, Emmanuelle and Vardarajan, Badri N and Reitz, Christiane and Goate, Alison M and Huentelman, Matthew J and Ilyas Kamboh, M and Larson, Eric B and Rogaeva, Ekaterina and George-Hyslop, Peter St and Hakonarson, Hakon and Kukull, Walter A and Farrer, Lindsay A and Barnes, Lisa L and Beach, Thomas G and Yesim Demirci, F and Head, Elizabeth and Hulette, Christine M and Jicha, Gregory A and Kauwe, John S.K and Kaye, Jeffrey A and Leverenz, James B and Levey, Allan I and Lieberman, Andrew P and Pankratz, Vernon S and Poon, Wayne W and Quinn, Joseph F and Saykin, Andrew J and Schneider, Lon S and Smith, Amanda G and Sonnen, Joshua A and Stern, Robert A and Van Deerlin, Vivianna M and Van Eldik, Linda J and Harold, Denise and Russo, Giancarlo and Rubinsztein, David C and Bayer, Anthony and Tsolaki, Magda and Proitsi, Petra and Fox, Nick C and Hampel, Harald and Owen, Michael J and Mead, Simon and Passmore, Peter and Morgan, Kevin and Nöthen, Markus M and Rossor, Martin and Lupton, Michelle K and Hoffmann, Per and Kornhuber, Johannes and Lawlor, Brian and McQuillin, Andrew and Al-Chalabi, Ammar and Bis, Joshua C and Ruiz, Agustin and Boada, Mercè and Seshadri, Sudha and Beiser, Alexa and Rice, Kenneth and Van Der Lee, Sven J and De Jager, Philip L and Geschwind, Daniel H and Riemenschneider, Matthias and Riedel-Heller, Steffi and Rotter, Jerome I and Ransmayr, Gerhard and Hyman, Bradley T and Cruchaga, Carlos and Alegret, Montserrat and Winsvold, Bendik and Palta, Priit and Farh, Kai-How and Cuenca-Leon, Ester and Furlotte, Nicholas and Kurth, Tobias and ... and Brainstorm Consortium and The Brainstorm Consortium
Science, ISSN 0036-8075, 06/2018, Volume 360, Issue 6395, pp. 1313 - 1313
Disorders of the brain can exhibit considerable epidemiological comorbidity and often share symptoms, provoking debate about their etiologic overlap. We... 
ANOREXIA-NERVOSA | POPULATION-BASED TWIN | DEFICIT HYPERACTIVITY DISORDER | LONG-TERM SURVIVAL | ALZHEIMERS-DISEASE | MULTIDISCIPLINARY SCIENCES | GENETIC CORRELATIONS | BODY-MASS INDEX | MAJOR DEPRESSIVE DISORDER | BIPOLAR DISORDER | GENOME-WIDE ASSOCIATION | Genetic Variation | Mental Disorders - genetics | Genome-Wide Association Study | Phenotype | Brain Diseases - classification | Quantitative Trait, Heritable | Brain Diseases - diagnosis | Humans | Mental Disorders - classification | Risk Factors | Brain Diseases - genetics | Mental Disorders - diagnosis | Anorexia | Disorders | Cognitive ability | Bipolar disorder | Posttraumatic stress disorder | Mental depression | Epidemiology | Risk factors | Consortia | Proteins | Ischemia | Etiology | Classification | Gilles de la Tourette syndrome | Alzheimer's disease | Neurological disorders | Neurodegenerative diseases | Comorbidity | Behavior disorders | Anorexia nervosa | Risk analysis | Patients | Neurological diseases | Correlation analysis | Heritability | Attention deficit disorder | Headache | Mental disorders | Medical services | Schizophrenia | Risk sharing | Genomes | Heterogeneity | Biological effects | Risk assessment | Stroke | Phenotypes | Migraine | Attention deficit hyperactivity disorder | Eating disorders | Personality | Genetic diversity | Statistics | Activity patterns | Crohn's Disease | Population (statistical) | Scaffolding | Diagnostic systems | Alzheimers disease | Index Medicus | Life Sciences | Human health and pathology | Mental Disorders | Neurons and Cognition | Brain Diseases | Genetics
Journal Article
by Malik, Rainer and Chauhan, Ganesh and Traylor, Matthew and Sargurupremraj, Muralidharan and Okada, Yukinori and Mishra, Aniket and Rutten-Jacobs, Loes and Giese, Anne-Katrin and Van Der Laan, Sander W and Gretarsdottir, Solveig and Anderson, Christopher D and Chong, Michael and Adams, Hieab H. H and Ago, Tetsuro and Almgren, Peter and Amouyel, Philippe and Ay, Hakan and Bartz, Traci M and Benavente, Oscar R and Bevan, Steve and Boncoraglio, Giorgio B and Brown, Robert D and Butterworth, Adam S and Carrera, Caty and Carty, Cara L and Chasman, Daniel I and Chen, Wei-Min and Cole, John W and Correa, Adolfo and Cotlarciuc, Ioana and Cruchaga, Carlos and Danesh, John and De Bakker, Paul I. W and Destefano, Anita L and Den Hoed, Marcel and Duan, Qing and Engelter, Stefan T and Falcone, Guido J and Gottesman, Rebecca F and Grewal, Raji P and Gudnason, Vilmundur and Gustafsson, Stefan and Haessler, Jeffrey and Harris, Tamara B and Hassan, Ahamad and Havulinna, Aki S and Heckbert, Susan R and Holliday, Elizabeth G and Howard, George and Hsu, Fang-Chi and Hyacinth, Hyacinth I and Ikram, M. Arfan and Ingelsson, Erik and Irvin, Marguerite R and Jian, Xueqiu and Jiménez-Conde, Jordi and Johnson, Julie A and Jukema, J. Wouter and Kanai, Masahiro and Keene, Keith L and Kissela, Brett M and Kleindorfer, Dawn O and Kooperberg, Charles and Kubo, Michiaki and Lange, Leslie A and Langefeld, Carl D and Langenberg, Claudia and Launer, Lenore J and Lee, Jin-Moo and Lemmens, Robin and Leys, Didier and Lewis, Cathryn M and Lin, Wei-Yu and Lindgren, Arne G and Lorentzen, Erik and Magnusson, Patrik K and Maguire, Jane and Manichaikul, Ani and McArdle, Patrick F and Meschia, James F and Mitchell, Braxton D and Mosley, Thomas H and Nalls, Michael A and Ninomiya, Toshiharu and O'Donnell, Martin J and Psaty, Bruce M and Pulit, Sara L and Rannikmäe, Kristiina and Reiner, Alexander P and Rexrode, Kathryn M and Rice, Kenneth and Rich, Stephen S and Ridker, Paul M and Rost, Natalia S and Rothwell, Peter M and Rotter, Jerome I and Rundek, Tatjana and Sacco, Ralph L and Sakaue, Saori and Sale, Michele M and ... and AFGen Consortium and UK Young Lacunar DNA Study and EPIC-CVD Consortium and Int Stroke Genetics Consortium ISG and INVENT Consortium and Int Genomics Blood Pressure iGEN and MEGASTROKE Consortium and COMPASS Consortium and METASTROKE Consortium and EPIC-InterAct Consortium and Cohorts Heart Aging Res Genomic and BioBank Japan Cooperative Hosp Grp and NINDS Stroke Genetics Network Si and STARNET and Neurology Working Grp Charge Con and Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium and International Stroke Genetics Consortium (ISGC) and NINDS Stroke Genetics Network (SiGN) and International Genomics of Blood Pressure (iGEN-BP) Consortium and BioBank Japan Cooperative Hospital Group and Neurology Working Group of the CHARGE Consortium and Science for Life Laboratory, SciLifeLab and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Institutionen för immunologi, genetik och patologi and Medicinsk genetik och genomik and Geriatrik and Kardiovaskulär epidemiologi and Uppsala universitet and Institutionen för medicinska vetenskaper and Molekylär epidemiologi and Institutionen för folkhälso- och vårdvetenskap
Nature Genetics, ISSN 1061-4036, 04/2018, Volume 50, Issue 4, pp. 524 - 537
Journal Article
by Christophersen, Ingrid E and Rienstra, Michiel and Roselli, Carolina and Yin, Xiaoyan and Geelhoed, Bastiaan and Barnard, John and Lin, Honghuang and Arking, Dan E and Smith, Albert V and Albert, Christine M and Chaffin, Mark and Tucker, Nathan R and Li, Molong and Klarin, Derek and Bihlmeyer, Nathan A and Low, Siew-Kee and Weeke, Peter E and Mueller-Nurasyid, Martina and Smith, J. Gustav and Brody, Jennifer A and Niemeijer, Maartje N and Doerr, Marcus and Trompet, Stella and Huffman, Jennifer and Gustafsson, Stefan and Schurmann, Claudia and Kleber, Marcus E and Lyytikainen, Leo-Pekka and Seppala, Ilkka and Malik, Rainer and Horimoto, Anea R. V. R and Perez, Marco and Sinisalo, Juha and Aeschbacher, Stefanie and Theriault, Sebastien and Yao, Jie and Radmanesh, Farid and Weiss, Stefan and Teumer, Alexander and Choi, Seung Hoan and Weng, Lu-Chen and Clauss, Sebastian and Deo, Rajat and Rader, Daniel J and Shah, Svati H and Sun, Albert and Hopewell, Jemma C and Debette, Stephanie and Chauhan, Ganesh and Yang, Qiong and Worrall, Bradford B and Pare, Guillaume and Kamatani, Yoichiro and Hagemeijer, Yanick P and Verweij, Niek and Siland, Joylene E and Kubo, Michiaki and Smith, Jonathan D and Van Wagoner, David R and Bis, Joshua C and Perz, Siegfried and Psaty, Bruce M and Ridker, Paul M and Magnani, Jared W and Harris, Tamara B and Launer, Lenore J and Shoemaker, M. Benjamin and Padmanabhan, Sandosh and Haessler, Jeffrey and Bartz, Traci M and Waldenberger, Melanie and Lichtner, Peter and Arendt, Marina and Krieger, Jose E and Kahonen, Mika and Risch, Lorenz and Mansur, Alfredo J and Peters, Annette and Smith, Blair H and Lind, Lars and Scott, Stuart A and Lu, Yingchang and Bottinger, Erwin B and Hernesniemi, Jussi and Lindgren, Cecilia M and Wong, Jorge A and Huang, Jie and Eskola, Markku and Morris, Anew P and Ford, Ian and Reiner, Alex P and Delgado, Graciela and Chen, Lin Y and Chen, Yii-Der Ida and Sandhu, Roopinder K and Li, Man and Boerwinkle, Eric and Eisele, Lewin and Lannfelt, Lars and Rost, Natalia and ... and Neurology Working Grp CHARGE and AFGen Consortium and METASTROKE Consortium ISGC and METASTROKE Consortium of the ISGC and Neurology Working Group of the CHARGE Consortium and the AFGen Consortium and Science for Life Laboratory, SciLifeLab and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Geriatrik and Kardiovaskulär epidemiologi and Uppsala universitet and Institutionen för medicinska vetenskaper and Molekylär epidemiologi and Institutionen för folkhälso- och vårdvetenskap
Nature Genetics, ISSN 1061-4036, 06/2017, Volume 49, Issue 6, pp. 946 - 952
Journal Article
by Holliday, Elizabeth G and Maguire, Jane M and Evans, Tiffany-Jane and Koblar, Simon A and Jannes, Jim and Sturm, Jonathan W and Hankey, Graeme J and Baker, Ross and Golledge, Jonathan and Parsons, Mark W and Malik, Rainer and McEvoy, Mark and Biros, Erik and Lewis, Martin D and Lincz, Lisa F and Peel, Roseanne and Oldmeadow, Christopher and Smith, Wayne and Moscato, Pablo and Barlera, Simona and Bevan, Steve and Bis, Joshua C and Boerwinkle, Eric and Boncoraglio, Giorgio B and Brott, Thomas G and Brown, Robert D and Cheng, Yu-Ching and Cole, John W and Cotlarciuc, Ioana and Devan, William J and Fornage, Myriam and Furie, Karen L and Grétarsdóttir, Sólveig and Gschwendtner, Andreas and Ikram, M Arfan and Longstreth, W.T and Meschia, James F and Mitchell, Braxton D and Mosley, Thomas H and Nalls, Michael A and Parati, Eugenio A and Psaty, Bruce M and Sharma, Pankaj and Stefansson, Kari and Thorleifsson, Gudmar and Thorsteinsdottir, Unnur and Traylor, Matthew and Verhaaren, Benjamin F. J and Wiggins, Kerri L and Worrall, Bradford B and Sudlow, Cathie and Rothwell, Peter M and Farrall, Martin and Dichgans, Martin and Rosand, Jonathan and Markus, Hugh S and Scott, Rodney J and Levi, Christopher and Attia, John and International Stroke Genetics Cons and Wellcome Trust Case Control Consor and Australian Stroke Genetics Collabo and International Stroke Genetics Consortium and Wellcome Trust Case Control Consortium 2 and Australian Stroke Genetics Collaborative and The Wellcome Trust Case Control Consortium 2 and The Australian Stroke Genetics Collaborative and The International Stroke Genetics Consortium
Nature Genetics, ISSN 1061-4036, 10/2012, Volume 44, Issue 10, pp. 1147 - 1151
Journal Article
by Woo, Daniel and Woo, Jessica G and Falcone, Guido J and Devan, William J and Brown, W. Mark and Brown, Devin L and Biffi, Alessandro and Howard, Timothy D and Anderson, Christopher D and Brouwers, H. Bart and Valant, Valerie and Battey, Thomas W.K and Radmanesh, Farid and Raffeld, Miriam R and Baedorf-Kassis, Sylvia and Deka, Ranjan and Martin, Lisa J and Haverbusch, Mary and Moomaw, Charles J and Sun, Guangyun and Broderick, Joseph P and Flaherty, Matthew L and Martini, Sharyl R and Kleindorfer, Dawn O and Kissela, Brett and Comeau, Mary E and Jagiella, Jeremiasz M and Schmidt, Helena and Schmidt, Reinhold and Freudenberger, Paul and Pichler, Alexander and Enzinger, Christian and Hansen, Björn M and Norrving, Bo and Jimenez-Conde, Jordi and Giralt-Steinhauer, Eva and Elosua, Roberto and Cuadrado-Godia, Elisa and Soriano, Carolina and Roquer, Jaume and Kraft, Peter and Ayres, Alison M and Schwab, Kristin and McCauley, Jacob L and Pera, Joanna and Urbanik, Andrzej and Rost, Natalia S and Goldstein, Joshua N and Viswanathan, Anand and Stögerer, Eva-Maria and Tirschwell, David L and Selim, Magdy and Silliman, Scott L and Worrall, Bradford B and Meschia, James F and Kidwell, Chelsea S and Montaner, Joan and Fernandez-Cadenas, Israel and Delgado, Pilar and Malik, Rainer and Dichgans, Martin and Greenberg, Steven M and Rothwell, Peter M and Lindgren, Arne and Slowik, Agnieszka and Langefeld, Carl D and Rosand, Jonathan and Int Stroke Genetics Consortium and International Stroke Genetics Consortium and EpiHealth: Epidemiology for Health and Lund University and Neurologi, Lund and Lunds universitet and Neurology, Lund
The American Journal of Human Genetics, ISSN 0002-9297, 04/2014, Volume 94, Issue 4, pp. 511 - 521
Journal Article
by Chauhan, Ganesh and Arnold, Corey R and Chu, Audrey Y and Fornage, Myriam and Reyahi, Azadeh and Bis, Joshua C and Havulinna, Aki S and Sargurupremraj, Muralidharan and Smith, Nicholas L and Smith, Albert Vernon and Adams, Hieab H H and Choi, Seung Hoan and Pulit, Sara L and Trompet, Stella and Garcia, Melissa E and Manichaikul, Ani and Teumer, Alexander and Gustafsson, Stefan and Bartz, Traci M and Bellenguez, Céline and Vidal, Jean Sebastien and Jian, Xueqiu and Kjartansson, Olafur and Wiggins, Kerri L and Satizabal, Claudia L and Xue, Flora and Ripatti, Samuli and Liu, Yongmei and Deelen, Joris and den Hoed, Marcel and Bevan, Steve and Hopewell, Jemma C and Malik, Rainer and Heckbert, Susan R and Rice, Kenneth and Levi, Christopher and Sharma, Pankaj and Sudlow, Cathie LM and Nik, Ali Moussavi and Cole, John W and Schmidt, Reinhold and Schmidt, Carsten Oliver and Meschia, James and Thijs, Vincent and Lindgren, Lars and Lindgren, Arne and Lindgren, Cecilia M and Melander, Olle and Grewal, Raji P and Sacco, Ralph L and Rundek, Tatjana and Rothwell, Peter M and Arnett, Donna K and Jern, Christina and Johnson, Julie A and Johnson, Andrew D and Benavente, Oscar R and Wassertheil-Smoller, Sylvia and Lee, Jin-Moo and Wong, Quenna and Aparicio, Hugo J and Engelter, Stefan T and Kloss, Manja and Leys, Didier and Pezzini, Alessandro and Buring, Julie E and Ridker, Paul M and Berr, Claudine and Dartigues, Jean-François and Hamsten, Anders and Magnusson, Patrik K and Traylor, Matthew and Pedersen, Nancy L and Lannfelt, Lars and Morris, Andrew P and Jimenez-Conde, Jordi and Montaner, Joan and Radmanesh, Farid and Slowik, Agnieszka and Woo, Daniel and Hofman, Albert and Koudstaal, Peter J and Portegies, Marileen L P and Uitterlinden, André G and de Craen, Anton J M and Ford, Ian and Jukema, J Wouter and Stott, David J and Allen, Norrina B and Sale, Michele M and Bennett, David A and De Jager, Philip L and White, Charles C and Grabe, Hans Jörgen and Markus, Marcello Ricardo Paulista and Markus, Hugh S and Schminke, Ulf and Boncoraglio, Giorgio B and Clarke, Robert and Kamatani, Yoichiro and ... and Stroke Genetics Network SiGN and METASTROKE Consortium and Neurology Working Grp Cohorts and Cervical Artery Dissection and Int Stroke Genetics Consortium and