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Lancet neurology, ISSN 1474-4422, 2015, Volume 14, Issue 4, pp. 388 - 405
Summary Increasing evidence suggests that Alzheimer's disease pathogenesis is not restricted to the neuronal compartment, but includes strong interactions with... 
Neurology | CEREBRAL AMYLOID ANGIOPATHY | POSITRON-EMISSION-TOMOGRAPHY | TRAUMATIC BRAIN-INJURY | NITRIC-OXIDE SYNTHASE | ANTIINFLAMMATORY PREVENTION TRIAL | CENTRAL-NERVOUS-SYSTEM | RANDOMIZED CONTROLLED-TRIAL | MILD COGNITIVE IMPAIRMENT | TRANSGENIC MOUSE MODEL | CLINICAL NEUROLOGY | GENOME-WIDE ASSOCIATION | Humans | Astrocytes - pathology | Brain Injuries - complications | Brain Injuries - metabolism | Alzheimer Disease - pathology | Inflammation - metabolism | Microglia - immunology | Astrocytes - immunology | Alzheimer Disease - prevention & control | Inflammation Mediators - metabolism | Microglia - pathology | Inflammation - diagnosis | Alzheimer Disease - immunology | Disease Models, Animal | Inflammation Mediators - immunology | Severity of Illness Index | Immunization | Obesity - complications | Locus Coeruleus - pathology | Risk Factors | Clinical Trials as Topic | Inflammation - immunology | Biomarkers - blood | Immunity, Innate | Disease Progression | Protein Folding | Obesity - metabolism | Animals | Anti-Inflammatory Agents, Non-Steroidal - therapeutic use | Nootropic Agents - administration & dosage | Alzheimer Disease - metabolism | Biomarkers - cerebrospinal fluid | Alzheimer Disease - genetics | Phagocytosis | Alzheimer's disease | Analysis | Genotype & phenotype | Neurosciences | Brain research | Pathogenesis | Cognitive ability | Ligands | Physiology | Mutation | Alzheimers disease | Gene expression | Immune system
Journal Article
by Su, Zhan and Gay, Laura J and Strange, Amy and Palles, Claire and Band, Gavin and Whiteman, David C and Lescai, Francesco and Langford, Cordelia and Nanji, Manoj and Edkins, Sarah and van der Winkel, Anouk and Levine, David and Sasieni, Peter and Bellenguez, Céline and Howarth, Kimberley and Freeman, Colin and Trudgill, Nigel and Tucker, Art T and Pirinen, Matti and Peppelenbosch, Maikel P and van der Laan, Luc J W and Kuipers, Ernst J and Drenth, Joost P H and Peters, Wilbert H and Reynolds, John V and Kelleher, Dermot P and McManus, Ross and Grabsch, Heike and Prenen, Hans and Bisschops, Raf and Krishnadath, Kausila and Siersema, Peter D and van Baal, Jantine W P M and Middleton, Mark and Petty, Russell and Gillies, Richard and Burch, Nicola and Bhandari, Pradeep and Paterson, Stuart and Edwards, Cathryn and Penman, Ian and Vaidya, Kishor and Ang, Yeng and Murray, Iain and Patel, Praful and Ye, Weimin and Mullins, Paul and Wu, Anna H and Bird, Nigel C and Dallal, Helen and Shaheen, Nicholas J and Murray, Liam J and Koss, Konrad and Bernstein, Leslie and Romero, Yvonne and Hardie, Laura J and Zhang, Rui and Winter, Helen and Corley, Douglas A and Panter, Simon and Risch, Harvey A and Reid, Brian J and Sargeant, Ian and Gammon, Marilie D and Smart, Howard and Dhar, Anjan and McMurtry, Hugh and Ali, Haythem and Liu, Geoffrey and Casson, Alan G and Chow, Wong-Ho and Rutter, Matt and Tawil, Ashref and Morris, Danielle and Nwokolo, Chuka and Isaacs, Peter and Rodgers, Colin and Ragunath, Krish and MacDonald, Chris and Haigh, Chris and Monk, David and Davies, Gareth and Wajed, Saj and Johnston, David and Gibbons, Michael and Cullen, Sue and Church, Nicholas and Langley, Ruth and Griffin, Michael and Alderson, Derek and Deloukas, Panos and Hunt, Sarah E and Gray, Emma and Dronov, Serge and Potter, Simon C and Tashakkori-Ghanbaria, Avazeh and Anderson, Mark and Brooks, Claire and Blackwell, Jenefer M and Bramon, Elvira and ... and Wellcome Trust Case Control Consor and Esophageal Adenocarcinoma Genetics and Wellcome Trust Case Control Consortium 2 and Esophageal Adenocarcinoma Genetics Consortium and The Wellcome Trust Case Control Consortium 2 and The Esophageal Adenocarcinoma Genetics Consortium
Nature genetics, ISSN 1061-4036, 2012, Volume 44, Issue 10, pp. 1131 - 1136
Journal Article
by Helgadottir, Anna and Gretarsdottir, Solveig and Thorleifsson, Gudmar and Holm, Hilma and Patel, Riyaz S and Gudnason, Thorarinn and Jones, Gregory T and van Rij, Andre M and Eapen, Danny J and Baas, Annette F and Tregouet, David-Alexandre and Morange, Pierre-Emmanuel and Emmerich, Joseph and Lindblad, Bengt and Gottsäter, Anders and Kiemeny, Lambertus A and Lindholt, Jes S and Sakalihasan, Natzi and Ferrell, Robert E and Carey, David J and Elmore, James R and Tsao, Philip S and Grarup, Niels and Jørgensen, Torben and Witte, Daniel R and Hansen, Torben and Pedersen, Oluf and Pola, Roberto and Gaetani, Eleonora and Magnadottir, Hulda B and Wijmenga, Cisca and Tromp, Gerard and Ronkainen, Antti and Ruigrok, Ynte M and Blankensteijn, Jan D and Mueller, Thomas and Wells, Philip S and Corral, Javier and Soria, Jose Manuel and Souto, Juan Carlos and Peden, John F and Jalilzadeh, Shapour and Mayosi, Bongani M and Keavney, Bernard and Strawbridge, Rona J and Sabater-Lleal, Maria and Gertow, Karl and Baldassarre, Damiano and Nyyssönen, Kristiina and Rauramaa, Rainer and Smit, Andries J and Mannarino, Elmo and Giral, Philippe and Tremoli, Elena and de Faire, Ulf and Humphries, Steve E and Hamsten, Anders and Haraldsdottir, Vilhelmina and Olafsson, Isleifur and Magnusson, Magnus K and Samani, Nilesh J and Levey, Allan I and Markus, Hugh S and Kostulas, Konstantinos and Dichgans, Martin and Berger, Klaus and Kuhlenbäumer, Gregor and Ringelstein, E. Bernd and Stoll, Monika and Seedorf, Udo and Rothwell, Peter M and Powell, Janet T and Kuivaniemi, Helena and Onundarson, Pall T and Valdimarsson, Einar and Matthiasson, Stefan E and Gudbjartsson, Daniel F and Thorgeirsson, Guðmundur and Quyyumi, Arshed A and Watkins, Hugh and Farrall, Martin and Thorsteinsdottir, Unnur and Stefansson, Kari
Journal of the American College of Cardiology, ISSN 0735-1097, 2012, Volume 60, Issue 8, pp. 722 - 729
Objectives The purpose of this study is investigate the effects of variants in the apolipoprotein(a) gene ( LPA ) on vascular diseases with different... 
Cardiovascular | Internal Medicine | atherosclerosis | genetic | association | thrombosis | lipoprotein(a) | INTIMA-MEDIA THICKNESS | RISK-FACTORS | METAANALYSIS | MYOCARDIAL-INFARCTION | UMCG Approved | VASCULAR-DISEASE | WOMEN | PERIPHERAL ARTERIAL-DISEASE | ISCHEMIC-STROKE | SEVERITY | CARDIAC & CARDIOVASCULAR SYSTEMS | Severity of Illness Index | Myocardial Infarction - genetics | European Continental Ancestry Group - genetics | Genetic Predisposition to Disease | Apolipoproteins A - genetics | Angiography | Carotid Intima-Media Thickness | Intracranial Aneurysm - genetics | Atherosclerosis - genetics | Humans | Risk Factors | Brain Ischemia - genetics | African Americans - genetics | Linear Models | Logistic Models | Aortic Aneurysm, Abdominal - genetics | Stroke - genetics | Venous Thromboembolism - genetics | Peripheral Arterial Disease - genetics | Age of Onset | Coronary Artery Disease - genetics | Polymorphism, Single Nucleotide | Odds Ratio | Medical colleges | Neurosciences | Stock options | Genes | Aneurysms | Coronary heart disease | Biometry | Lipoprotein A | Anopheles | Atherosclerosis | Medical genetics | Genetic research | Genetic aspects | Diabetes | Thromboembolism | Cardiology | Public health | Dementia | Stroke | Medical imaging | Values | Cardiovascular disease | Apolipoproteins | Thrombosis | Studies | Confidence intervals | Coronary vessels | Blood pressure | Drug therapy | Age | Methods | Kardiologi | Clinical Medicine | Cardiac and Cardiovascular Systems | Medical and Health Sciences | Medicin och hälsovetenskap | Klinisk medicin
Journal Article
by Traylor, Matthew and Farrall, Martin and Holliday, Elizabeth G and Sudlow, Cathie and Hopewell, Jemma C and Cheng, Yu-Ching and Fornage, Myriam and Ikram, M Arfan and Malik, Rainer and Bevan, Steve and Thorsteinsdottir, Unnur and Nalls, Mike A and Longstreth, WT and Wiggins, Kerri L and Yadav, Sunaina and Parati, Eugenio A and DeStefano, Anita L and Worrall, Bradford B and Kittner, Steven J and Khan, Muhammad Saleem and Reiner, Alex P and Helgadottir, Anna and Achterberg, Sefanja and Fernandez-Cadenas, Israel and Abboud, Sherine and Schmidt, Reinhold and Walters, Matthew and Chen, Wei-Min and Ringelstein, E Bernd and O'Donnell, Martin and Ho, Weang Kee and Pera, Joanna and Lemmens, Robin and Norrving, Bo and Higgins, Peter and Benn, Marianne and Sale, Michele and Kuhlenbäumer, Gregor and Doney, Alexander S F and Vicente, Astrid M and Delavaran, Hossein and Algra, Ale and Davies, Gail and Oliveira, Sofia A and Palmer, Colin N A and Deary, Ian and Schmidt, Helena and Pandolfo, Massimo and Montaner, Joan and Carty, Cara and de Bakker, Paul I W and Kostulas, Konstantinos and Ferro, Jose M and van Zuydam, Natalie R and Valdimarsson, Einar and Nordestgaard, Børge G and Lindgren, Arne and Thijs, Vincent and Slowik, Agnieszka and Saleheen, Danish and Paré, Guillaume and Berger, Klaus and Thorleifsson, Gudmar and Hofman, Albert and Mosley, Thomas H and Mitchell, Braxton D and Furie, Karen and Clarke, Robert and Levi, Christopher and Seshadri, Sudha and Gschwendtner, Andreas and Boncoraglio, Giorgio B and Sharma, Pankaj and Bis, Joshua C and Gretarsdottir, Solveig and Psaty, Bruce M and Rothwell, Peter M and Rosand, Jonathan and Meschia, James F and Stefansson, Kari and Dichgans, Martin and Markus, Hugh S and The Australian Stroke Genetics Collaborative, Wellcome Trust Case Control Consortium 2 (WTCCC2) and on behalf of the International Stroke Genetics Consortium and WTCCC 2 and Australian Stroke Genetics Collabo and Int Stroke Genetics Consortium and International Stroke Genetics Consortium and Australian Stroke Genetics Collaborative, Wellcome Trust Case Control Consortium 2 (WTCCC2)
Lancet neurology, ISSN 1474-4422, 2012, Volume 11, Issue 11, pp. 951 - 962
Journal Article
Lancet neurology, ISSN 1474-4422, 2015, Volume 14, Issue 6, pp. 640 - 654
Journal Article