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1. Tilmann Riemenschneider
: die Werke im Bayerischen Nationalmuseum
by Riemenschneider, Tilman, -1531 and Weniger, Matthias and Eikelmann, Renate
2017, ISBN 9783731904755, 208
Riemenschneider, Tilman, -1531 | Bayerisches Nationalmuseum
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2. Full Text The "DGPPN-Cohort": a national collaboration initiative by the German Association for Psychiatry and Psychotherapy (DGPPN) for establishing a large-scale cohort of psychiatric patients
by Anderson-Schmidt, Heike and Adler, Lothar and Aly, Chadiga and Anghelescu, Ion-George and Bauer, Michael and Baumgaertner, Jessica and Becker, Joachim and Bianco, Roswitha and Becker, Thomas and Bitter, Cosima and Boensch, Dominikus and Buckow, Karoline and Budde, Monika and Buehrig, Martin and Deckert, Juergen and Demiroglu, Sara Y and Dietrich, Detlef and Duempelmann, Michael and Engelhardt, Uta and Fallgatter, Aneas J and Feldhaus, Daniel and Figge, Christian and Folkerts, Here and Franz, Michael and Gade, Katrin and Gaebel, Wolfgang and Grabe, Hans-Joergen and Gruber, Oliver and Gullatz, Verena and Gusky, Linda and Heilbronner, Urs and Helbing, Krister and Hegerl, Ulrich and Heinz, Aneas and Hensch, Tilman and Hiemke, Christoph and Jaeger, Markus and Jahn-Brodmann, Anke and Juckel, Georg and Kandulski, Franz and Kaschka, Wolfgang P and Kircher, Tilo and Koller, Manfred and Konrad, Carsten and Kornhuber, Johannes and Krause, Marina and Krug, Axel and Lee, Mahsa and Leweke, Markus and Lieb, Klaus and Mammes, Mechthild and Meyer-Lindenberg, Aneas and Muehlbacher, Moritz and Mueller, Matthias J and Nieratschker, Vanessa and Nierste, Barbara and Ohle, Jacqueline and Pfennig, Anea and Pieper, Marlenna and Quade, Matthias and Reich-Erkelenz, Daniela and Reif, Aneas and Reitt, Markus and Reininghaus, Bernd and Reininghaus, Eva Z and Riemenschneider, Matthias and Rienhoff, Otto and Roser, Patrik and Rujescu, Dan and Schennach, Rebecca and Scherk, Harald and Schmauss, Max and Schneider, Frank and Schosser, Alexana and Schott, Bjoern H and Schwab, Sybille G and Schwanke, Jens and Skrowny, Daniela and Spitzer, Carsten and Stierl, Sebastian and Stoeckel, Judith and Stuebner, Susanne and Thiel, Aneas and Volz, Hans-Peter and von Hagen, Martin and Walter, Henrik and Witt, Stephanie H and Wobrock, Thomas and Zielasek, Juergen and Zimmermann, Joerg and Zitzelsberger, Antje and Maier, Wolfgang and Falkai, Peter G and Rietschel, Marcella and Schulze, Thomas G
European Archives of Psychiatry and Clinical Neuroscience, ISSN 0940-1334, 12/2013, Volume 263, Issue 8, pp. 695 - 701
The German Association for Psychiatry and Psychotherapy (DGPPN) has committed itself to establish a prospective national cohort of patients with major... 
Schizophrenia | Bipolar disorder | Anxiety disorders | Major depression | Biobank | PSYCHOSES | GWAS | PSYCHIATRY | GENES | CLINICAL NEUROLOGY | Mental Disorders - therapy | Humans | Cooperative Behavior | Male | Mental Disorders - psychology | Psychotherapy - standards | Societies, Medical | Psychotherapy - methods | Female | Mental Disorders - diagnosis | Psychiatry | Germany | Cohort Studies | Psychotherapy | Index Medicus
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3. Full Text Analysis of shared heritability in common disorders of the brain
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
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4. Gustav Heinemann, Christ und Politiker
by Thierfelder, Jörg, 1938 and Riemenschneider, Matthias, 1959
1999, 1. Aufl., Edition Zeitzeugen, ISBN 9783872971395, 256
Biography | Presidents | Heinemann, Gustav Walter, 1899-1976
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5. Full Text MRI Plaque Imaging Detects Carotid Plaques with a High Risk for Future Cerebrovascular Events in Asymptomatic Patients
by Esposito-Bauer, Lorena and Saam, Tobias and Ghodrati, Iman and Pelisek, Jaroslav and Heider, Peter and Bauer, Matthias and Wolf, Petra and Bockelbrink, Angelina and Feurer, Regina and Sepp, Dominik and Winkler, Claudia and Zepper, Peter and Boeckh-Behrens, Tobias and Riemenschneider, Matthias and Hemmer, Bernhard and Poppert, Holger
PLoS ONE, ISSN 1932-6203, 07/2013, Volume 8, Issue 7, pp. e67927 - e67927
Purpose: The aim of this study was to investigate prospectively whether MRI plaque imaging can identify patients with asymptomatic carotid artery stenosis who... 
HIGH-RESOLUTION MRI | ISCHEMIC EVENTS | MULTIDISCIPLINARY SCIENCES | IN-VIVO | VASCULAR-LESIONS | RUPTURE | SYMPTOMS | ATHEROSCLEROTIC PLAQUE | INTRAPLAQUE HEMORRHAGE | ARTERY STENOSIS | ASSOCIATION | Plaque, Atherosclerotic - diagnosis | Carotid Stenosis - diagnosis | Humans | Middle Aged | Aged, 80 and over | Magnetic Resonance Imaging - methods | Female | Male | Aged | Complications and side effects | Usage | Cerebral ischemia | Magnetic resonance imaging | Carotid artery diseases | Diagnosis | Risk factors | Nuclear magnetic resonance--NMR | Stenosis | Psychotherapy | Lipids | Risk | Family medical history | Criteria | Epidemiology | Hemorrhage | Carotid arteries | Cerebrovascular system | Ultrasonic imaging | Ischemia | Atherosclerosis | Electrocardiography | Carotid artery | Thromboembolism | Plaques | Hypertension | Stroke | Vascular surgery | Medical imaging | Risk groups | Angina pectoris | Patients | Survival | Cholesterol | Studies | Image quality | Neurology | Blindness | Index Medicus | Nuclear magnetic resonance | NMR
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6. Full Text Frontotemporal dementia and its subtypes: a genome-wide association study
by Ferrari, Raffaele, PhD and Hernandez, Dena G, MSc and Nalls, Michael A, PhD and Rohrer, Jonathan D, PhD and Ramasamy, Adaikalavan, PhD and Kwok, John B J, PhD and Dobson-Stone, Carol, PhD and Brooks, William S, MBBS and Schofield, Peter R, Prof and Halliday, Glenda M, Prof and Hodges, John R, Prof and Piguet, Olivier, PhD and Bartley, Lauren, MSc and Thompson, Elizabeth, MD and Haan, Eric, Prof and Hernández, Isabel, MD and Ruiz, Agustín, MD and Boada, Mercè, MD and Borroni, Barbara, MD and Padovani, Alessandro, Prof and Cruchaga, Carlos, PhD and Cairns, Nigel J, Prof and Benussi, Luisa, PhD and Binetti, Giuliano, MD and Ghidoni, Roberta, PhD and Forloni, Gianluigi, PhD and Galimberti, Daniela, PhD and Fenoglio, Chiara, PhD and Serpente, Maria, PhD and Scarpini, Elio, MD and Clarimón, Jordi, PhD and Lleó, Alberto, MD and Blesa, Rafael, MD and Waldö, Maria Landqvist, MD and Nilsson, Karin, PhD and Nilsson, Christer, PhD and Mackenzie, Ian R A, Prof and Hsiung, Ging-Yuek R, MD and Mann, David M A, Prof and Grafman, Jordan, Prof and Morris, Christopher M, PhD and Attems, Johannes, Prof and Griffiths, Timothy D, Prof and McKeith, Ian G, Prof and Thomas, Alan J, Prof and Pietrini, P, Prof and Huey, Edward D, MD and Wassermann, Eric M, MD and Baborie, Atik, MD and Jaros, Evelyn, PhD and Tierney, Michael C, MSc and Pastor, Pau, MD and Razquin, Cristina, PhD and Ortega-Cubero, Sara, MD and Alonso, Elena, BSc and Perneczky, Robert, MD and Diehl-Schmid, Janine, MD and Alexopoulos, Panagiotis, MD and Kurz, Alexander, MD and Rainero, Innocenzo, MD and Rubino, Elisa, MD and Pinessi, Lorenzo, Prof and Rogaeva, Ekaterina, PhD and St George-Hyslop, Peter, MD and Rossi, Giacomina, PhD and Tagliavini, Fabrizio, MD and Giaccone, Giorgio, MD and Rowe, James B, PhD and Schlachetzki, Johannes C M, MD and Uphill, James, BSc and Collinge, John, Prof and Mead, Simon, Prof and Danek, Adrian, MD and Van Deerlin, Vivianna M, PhD and Grossman, Murray, Prof and Trojanowski, John Q, Prof and van der Zee, Julie, PhD and Deschamps, William, MSc and Van Langenhove, Tim, MD and Cruts, Marc, PhD and Van Broeckhoven, Christine, Prof and Cappa, Stefano F, Prof and Le Ber, Isabelle, MD and Hannequin, Didier, Prof and Golfier, Véronique, MD and Vercelletto, Martine, MD and Brice, Alexis, MD and Nacmias, Benedetta, PhD and Sorbi, Sandro, Prof and Bagnoli, Silvia, PhD and Piaceri, Irene, PhD and Nielsen, Jørgen E, MD and Hjermind, Lena E, MD and Riemenschneider, Matthias, Prof and Mayhaus, Manuel, PhD and Ibach, Bernd, PhD and Gasparoni, Gilles, PhD and Pichler, Sabrina, MSc and Gu, Wei, PhD and Rossor, Martin N, Prof and ... and Lund University and Psychiatry (Lund) and MultiPark: Multidisciplinary research focused on Parkinson´s disease and Psykiatri, Lund and Lunds universitet
Lancet Neurology, The, ISSN 1474-4422, 2014, Volume 13, Issue 7, pp. 686 - 699
Summary Background Frontotemporal dementia (FTD) is a complex disorder characterised by a broad range of clinical manifestations, differential pathological... 
Neurology | GENETIC-VARIATION | COMMON VARIANTS | PROTEIN | LOBAR DEGENERATION | DISEASE | SUSCEPTIBILITY LOCI | RISK | MUTATIONS | HEXANUCLEOTIDE REPEAT | BRAIN | CLINICAL NEUROLOGY | Frontotemporal Dementia - genetics | Humans | Middle Aged | Aged, 80 and over | Adult | Female | Genotype | Male | Aged | Frontotemporal Dementia - diagnosis | Genome-Wide Association Study - methods | Frontotemporal Dementia - classification | Genetic research | Genomics | Dementia | Genealogy | Principal components analysis | Genomes | Patients | Proteins | Studies | Pathology | Semantics | Consent | Quality control | Aging | Aphasia | DNA methylation | Mutation | Genetic testing | Chromosomes | Deoxyribonucleic acid--DNA | Index Medicus | Neurologi | Clinical Medicine | Medical and Health Sciences | Klinisk medicin | Medicin och hälsovetenskap
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7. Full Text Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease
by Lambert, Jean-Charles and Ibrahim-Verbaas, Carla A and Harold, Denise and Naj, Adam C and Sims, Rebecca and Bellenguez, Céline and Jun, Gyungah and DeStefano, Anita L and Bis, Joshua C and Beecham, Gary W and Grenier-Boley, Benjamin and Russo, Giancarlo and Thornton-Wells, Tricia A and Jones, Nicola and Smith, Albert V and Chouraki, Vincent and Thomas, Charlene and Ikram, M. Arfan and Zelenika, Diana and Vardarajan, Badri N and Kamatani, Yoichiro and Lin, Chiao-Feng and Gerrish, Amy and Schmidt, Helena and Kunkle, Brian and Fiévet, Nathalie and Amouyel, Philippe and Pasquier, Florence and Deramecourt, Vincent and De Bruijn, Renee F.A.G and Amin, Najaf and Hofman, Albert and Van Duijn, Cornelia M and Dunstan, Melanie L and Hollingworth, Paul and Owen, Michael J and O'Donovan, Michael C and Jones, Lesley and Holmans, Peter A and Moskvina, Valentina and Williams, Julie and Baldwin, Clinton and Farrer, Lindsay A and Choi, Seung-Hoan and Lunetta, Kathryn L and Fitzpatrick, Annette L and Harris, Tamara B and Psaty, Bruce M and Gilbert, John R and Hamilton-Nelson, Kara L and Martin, Eden R and Kunkle, Brian and Haines, Jonathan L and Gudnason, Vilmundur and Jonsson, Palmi V and Eiriksdottir, Gudny and Bihoreau, Marie-Thérèse and Lathrop, Mark and Valladares, Otto and Cantwell, Laura B and Wang, Li-San and Schellenberg, Gerard D and Ruiz, Agustin and Boada, Mercè and Reitz, Christiane and Mayeux, Richard and Ramirez, Alfredo and Maier, Wolfgang and Hanon, Olivier and Kukull, Walter A and Buxbaum, Joseph D and Campion, Dominique and Wallon, David and Hannequin, Didier and Crane, Paul K and Larson, Eric B and Becker, Tim and Cruchaga, Carlos and Goate, Alison M and Craig, David and Johnston, Janet A and Mc-Guinness, Bernadette and Todd, Stephen and Passmore, Peter and Berr, Claudine and Ritchie, Karen and Lopez, Oscar L and De Jager, Philip L and Evans, Denis and Lovestone, Simon and Proitsi, Petroula and Powell, John F and Letenneur, Luc and Barberger-Gateau, Pascale and Dufouil, Carole and Dartigues, Jean-François and Morón, Francisco J and Rubinsztein, David C and St. George-Hyslop, Peter and Sleegers, Kristel and ... and EADI and CHARGE and ADGC and GERAD and Cohorts for Heart and Aging Research in Genomic Epidemiology and Genetic and Environmental Risk in Alzheimer's Disease and Alzheimer's Disease Genetic Consortium and European Alzheimer's Disease Initiative (EADI) and Alzheimer's Disease Genetic Consortium (ADGC) and Genetic and Environmental Risk in Alzheimer's Disease (GERAD) and Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) and Stockholms universitet and Centrum för forskning om äldre och åldrande (ARC), (tills m KI) and Samhällsvetenskapliga fakulteten
Nature Genetics, ISSN 1061-4036, 12/2013, Volume 45, Issue 12, pp. 1452 - 1458
Eleven susceptibility loci for late-onset Alzheimer's disease (LOAD) were identified by previous studies; however, a large portion of the genetic risk for this... 
GENOTYPES | COMMON VARIANTS | IMPUTATION | GENETIC RISK | SEQUENCE | GENETICS & HEREDITY | NEURONS | RECEPTOR | MUTATIONS | CD33 | GENOME-WIDE ASSOCIATION | Genetic Predisposition to Disease | Humans | Middle Aged | Male | Genetic Loci | Genome-Wide Association Study - statistics & numerical data | Case-Control Studies | Age of Onset | Aged, 80 and over | Alzheimer Disease - epidemiology | Female | Aged | Polymorphism, Single Nucleotide | Alzheimer Disease - genetics | Cohort Studies | Quantitative trait loci | Genetic aspects | Research | Genetic susceptibility | Alzheimer's disease | Identification and classification | Genealogy | Genomics | Genes | Quality control | Aging | Genomes | Alzheimers disease | Health risk assessment | Meta-analysis | Index Medicus | Genetik | Biological Sciences | Genetics | Naturvetenskap | Natural Sciences | Biologiska vetenskaper
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8. Full Text Primary Degenerative Mild Cognitive Impairment: Study Population, Clinical, Brain Imaging and Biochemical Findings
by Lautenschlager, Nicola T and Riemenschneider, Matthias and Drzezga, Alexander and Kurz, Alexander F
Dementia and Geriatric Cognitive Disorders, ISSN 1420-8008, 12/2001, Volume 12, Issue 6, pp. 379 - 386
Mild cognitive impairment (MCI) is a heterogeneous clinical syndrome for which no international diagnostic criteria have yet been established. Longitudinal... 
Original Research Article | Diagnostic markers | Mild cognitive impairment | Alzheimer's disease | diagnostic markers | HOMOCYSTEINE | DEMENTIA | PSYCHIATRY | CLINICAL NEUROLOGY | MEMORY DECLINE | GERIATRICS & GERONTOLOGY | CONSORTIUM | HIPPOCAMPAL VOLUME | ASYMMETRIES | ESTABLISH | ALZHEIMERS-DISEASE CERAD | mild cognitive impairment | EXPERIENCE | REGISTRY | Memory Disorders - physiopathology | Brain - diagnostic imaging | Follow-Up Studies | Cognition Disorders - diagnostic imaging | Humans | Middle Aged | Dementia - physiopathology | Male | Brain - metabolism | Dementia - cerebrospinal fluid | Female | Memory Disorders - cerebrospinal fluid | Cognition Disorders - cerebrospinal fluid | Dementia - diagnostic imaging | Memory Disorders - diagnostic imaging | Apolipoprotein E4 | Cognition Disorders - physiopathology | Diagnosis, Differential | Genetic Predisposition to Disease | Genotype | Disease Progression | Syndrome | Neuropsychological Tests | Apolipoproteins E - genetics | Aged | Tomography, Emission-Computed | Biomarkers - cerebrospinal fluid | Index Medicus
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9. Full Text Common Variants at Abca7, Ms4A6A/Ms4A4E, Epha1, Cd33 and Cd2Ap Are Associated with Alzheimer'S Disease
by Hollingworth, P and Harold, D and Sims, R and Gerrish, A and Lambert, J.C and Carrasquillo, M.M and Abraham, R and Hamshere, M.L and Pahwa, J.S and Moskvina, V and Dowzell, K and Jones, N and Stretton, A and Thomas, C and Richards, A and Ivanov, D and Widdowson, C and Chapman, J and Lovestone, S and Powell, J and Proitsi, P and Lupton, M.K and Brayne, C and Rubinsztein, D.C and Gill, M and Lawlor, B and Lynch, A and Brown, K.S and Passmore, P.A and Craig, D and McGuinness, B and Todd, S and Holmes, C and Mann, D and Smith, A.D and Beaumont, H and Warden, D and Wilcock, G and Love, S and Kehoe, P.G and Hooper, N.M and Vardy, E.R.L.C and Hardy, J and Mead, S and Fox, N.C and Rossor, M and Collinge, J and Maier, W and Jessen, F and Ruther, E and Schurmann, B and Heun, R and Kolsch, H and van den Bussche, H and Heuser, I and Kornhuber, J and Wiltfang, J and Dichgans, M and Frolich, L and Hampel, H and Gallacher, J and Hull, M and Rujescu, D and Giegling, I and Goate, A.M and Kauwe, J.S.K and Cruchaga, C and Nowotny, P and Morris, J.C and Mayo, K and Sleegers, K and Bettens, K and Engelborghs, S and de Deyn, P.P and Van Broeckhoven, C and Livingston, G and Bass, N.J and Gurling, H and McQuillin, A and Gwilliam, R and Deloukas, P and Al-Chalabi, A and Shaw, C.E and Tsolaki, M and Singleton, A.B and Guerreiro, R and Muhleisen, T. W and Nothen, M. M and Moebus, S and Jockel, K.H and Klopp, N and Wichmann, H. E and Pankratz, V.S and Sando, S.B and Aasly, J.O and Barcikowska, M and Wszolek, Z.K and Dickson, D.W and Graff-Radford, N.R. and others and Alzheimer's Dis Neuroimaging and EADI1 Consortium and CHARGE Consortium and Alzheimer's Disease Neuroimaging Initiative and EADI1 consortium and CHARGE consortium and the Alzheimer's Disease Neuroimaging Initiative
Nature Genetics, ISSN 1061-4036, 2011, Volume 43, Issue 5, pp. 429 - 435
We sought to identify new susceptibility loci for Alzheimer's disease through a staged association study (GERAD+) and by testing suggestive loci reported by... 
IDENTIFIES VARIANTS | GENETICS & HEREDITY | GENE-EXPRESSION | RISK | LOCI | APOE | CR-1 | CLU | RECEPTOR TYROSINE KINASE | GENOME-WIDE ASSOCIATION | PICALM | Genetic Predisposition to Disease | Genome-Wide Association Study | Multigene Family | Cytoskeletal Proteins - genetics | Membrane Proteins - genetics | Humans | Databases, Genetic | Male | Antigens, CD - genetics | Antigens, Differentiation, Myelomonocytic - genetics | Case-Control Studies | Genetic Variation | ATP-Binding Cassette Transporters - genetics | Receptor, EphA1 - genetics | Adaptor Proteins, Signal Transducing - genetics | Aged, 80 and over | Female | Aged | Polymorphism, Single Nucleotide | Sialic Acid Binding Ig-like Lectin 3 | Alzheimer Disease - genetics | Usage | Genetic aspects | Disease susceptibility | Research | Single nucleotide polymorphisms | Drug therapy | Alzheimer's disease | Health aspects | Risk factors | Genomes | Medical imaging | Biomedical research | Alzheimers disease | Genes | Index Medicus
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