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1دورية أكاديمية
المؤلفون: Kristinn P Magnusson, Shan Duan, Haraldur Sigurdsson, Hjorvar Petursson, Zhenglin Yang, Yu Zhao, Paul S Bernstein, Jian Ge, Fridbert Jonasson, Einar Stefansson, Gudleif Helgadottir, Norman A Zabriskie, Thorlakur Jonsson, Asgeir Björnsson, Theodora Thorlacius, Palmi V Jonsson, Gudmar Thorleifsson, Augustine Kong, Hreinn Stefansson, Kang Zhang, Kari Stefansson, Jeffrey R Gulcher
المصدر: PLoS Medicine, Vol 3, Iss 1, p e5 (2006)
مصطلحات موضوعية: Medicine
وصف الملف: electronic resource
العلاقة: http://europepmc.org/articles/PMC1288033?pdf=renderTest; https://doaj.org/toc/1549-1277Test; https://doaj.org/toc/1549-1676Test
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المؤلفون: Aarno Palotie, Daniel F. Gudbjartsson, Stacy Steinberg, Thorlakur Jonsson, Augustine Kong, Kari Stefansson, Jon Snaedal, Ryan J. Watts, Timothy W. Behrens, Patrick Sulem, Palmi V. Jonsson, Kwame Hoyte, Unnur Thorsteinsdottir, Yichin Liu, Gyda Bjornsdottir, Sigurbjorn Bjornsson, Ole A. Andreassen, Olafur T. Magnusson, Johanna Huttenlocher, Robert R. Graham, Erik G. Jönsson, Amy Gustafson, Janice A. Maloney, Yanmei Lu, Jasvinder K. Atwal, Hreinn Stefansson, Tushar Bhangale
المصدر: Nature. 488:96-99
مصطلحات موضوعية: Aging, Age-related cognitive decline, Plaque, Amyloid, Disease, Amyloid beta-Protein Precursor, 03 medical and health sciences, Cognition, 0302 clinical medicine, Alzheimer Disease, Amyloid precursor protein, Aspartic Acid Endopeptidases, Humans, Medicine, Dementia, Genetic Predisposition to Disease, Cognitive decline, Allele, Gene, Alleles, 030304 developmental biology, 0303 health sciences, Multidisciplinary, biology, business.industry, medicine.disease, HEK293 Cells, Mutation, Immunology, biology.protein, Verubecestat, Amyloid Precursor Protein Secretases, Cognition Disorders, business, 030217 neurology & neurosurgery
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7408df1fc876b3360c1866a2f5d5ee26Test
https://doi.org/10.1038/nature11283Test -
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المؤلفون: Neill R. Graff-Radford, Caroline S. Widdowson, John Hardy, Simon Lovestone, Stefan Schreiber, Ana Frank-García, Amy Gerrish, Kevin Mayo, Alexandra Stretton, Michael John Owen, Minerva M. Carrasquillo, Seth Love, Jade Chapman, Vincent Chouraki, Monique M.B. Breteler, Francesco Panza, Emma R L C Vardy, Ronald C. Petersen, Harald Hampel, S. Nicolhaus, Lenore J. Launer, Michelle K. Lupton, Eckart Rüther, A. David Smith, David C. Rubinsztein, Rebecca Sims, Gill Livingston, Diana Zelenika, Simon Mead, Martin N. Rossor, Hilkka Soininen, Christine Van Broeckhoven, Kristel Sleegers, Thorlakur Jonsson, M. Arfan Ikram, Helen Beaumont, Michael Conlon O'Donovan, Federico Licastro, Sudha Seshadri, Alexander Richards, Nick C. Fox, Markus M. Nöthen, Claudine Berr, T. Feulner, Benedetta Nacmias, Carlos Cruchaga, Peter Passmore, Oscar L. Lopez, Julie Williams, Matthias Riemenschneider, Florence Pasquier, John Gallacher, Didier Hannequin, Sigrid Botne Sando, Jens Wiltfang, Charlene Thomas, Gabriele Siciliano, Maria Barcikowska, Mikko Hiltunen, Carol Brayne, Dobril Ivanov, Anita L. DeStefano, Bernadette McGuinness, Norman Klopp, Gordon K. Wilcock, Aoibhinn Lynch, Wolfgang Maier, Peter Holmans, H.-Erich Wichmann, Giorgio Annoni, Beatrice Arosio, Alison Goate, Sigurbjorn Bjornsson, Karl-Heinz Jöckel, Dan Rujescu, Hugh Gurling, Nigel M. Hooper, Clive Holmes, Andrew McQuillin, Patricia Friedrich, John Powell, Rhian Gwilliam, R. Heun, Jacques Epelbaum, Isabella Heuser, Magda Tsolaki, Dennis W. Dickson, Alberto Pilotto, Stephen Todd, Dominique Campion, Michael Krawczak, Jan O. Aasly, Olivier Hanon, Patrick G. Kehoe, Johannes Kornhuber, Marc Delepine, Peter Paul De Deyn, Britta Schürmann, Brian A. Lawlor, Christophe Tzourio, Richard Abraham, Petra Nowotny, Jean-François Dartigues, Heike Kölsch, Michelangelo Mancuso, Marian L. Hamshere, Zbigniew K. Wszolek, Paola Piccardi, Paolo Bosco, Jean-Charles Lambert, Denise Harold, Frank Jessen, Palmi V. Jonsson, Paola Bossù, Paul Hollingworth, Jon Snaedal, Michael Gill, Onofre Combarros, David M. A. Mann, John C. Morris, Annette L. Fitzpatrick, Christopher Shaw, Alexis Brice, Philippe Amouyel, Elio Scarpini, Lesley Jones, Sebastiaan Engelborghs, Daniela Galimberti, Vincenzo Solfrizzi, V. Shane Pankratz, John Collinge, María J. Bullido, Kristelle Brown, Nicholas Bass, Andrew B. Singleton, Jaspreet Singh Pahwa, Kari Stefansson, Lutz Frölich, Steven G. Younkin, Ignacio Mateo, Annick Alpérovitch, Benjamin Genier-Boley, Ina Giegling, Caterina Riehle, Kimberley Dowzell, Mark Lathrop, Hreinn Stefansson, Sandro Sorbi, Rita Guerreiro, Thomas W. Mühleisen, Karolien Bettens, Michael Hüll, Martin Dichgans, Petroula Proitsi, Panagiotis Deloukas, Valentina Moskvina, Cornelia M. van Duijn, Donald Warden, Victoria Alvarez, Eliecer Coto, Kevin Morgan, Susanne Moebus, Ammar Al-Chalabi, Elisa Porcellini, Stefan Wagenpfeil, Hendrik van den Bussche, John S. K. Kauwe, Stacy Steinberg, David Craig, Nicola Jones, Manuel Mayhaus, Davide Seripa
المساهمون: Neurology, NCA - Neurodegeneration, HOLLINGWORTH P, HAROLD D, SIMS R, GERRISH A, LAMBERT JC, CARRASQUILLO MM, ABRAHAM R, HAMSHERE ML, PAHWA JS, MOSKVINA V, DOWZELL K, JONES N, STRETTON A, THOMAS C, RICHARDS A, IVANOV D, WIDDOWSON C, CHAPMAN J, LOVESTONE S, POWELL J, PROITSI P, LUPTON MK, BRAYNE C, RUBINSZTEIN DC, GILL M, LAWLOR B, LYNCH A, BROWN KS, PASSMORE PA, CRAIG D, MCGUINNESS B, TODD S, HOLMES C, MANN D, SMITH AD, BEAUMONT H, WARDEN D, WILCOCK G, LOVE S, KEHOE PG, HOOPER NM, VARDY ER, HARDY J, MEAD S, FOX NC, ROSSOR M, COLLINGE J, MAIER W, JESSEN F, RÜTHER E, SCHÜRMANN B, HEUN R, KÖLSCH H, VAN DEN BUSSCHE H, HEUSER I, KORNHUBER J, WILTFANG J, DICHGANS M, FRÖLICH L, HAMPEL H, GALLACHER J, HÜLL M, RUJESCU D, GIEGLING I, GOATE AM, KAUWE JS, CRUCHAGA C, NOWOTNY P, MORRIS JC, MAYO K, SLEEGERS K, BETTENS K, ENGELBORGHS S, DE DEYN PP, VAN BROECKHOVEN C, LIVINGSTON G, BASS NJ, GURLING H, MCQUILLIN A, GWILLIAM R, DELOUKAS P, AL-CHALABI A, SHAW CE, TSOLAKI M, SINGLETON AB, GUERREIRO R, MÜHLEISEN TW, NÖTHEN MM, MOEBUS S, JÖCKEL KH, KLOPP N, WICHMANN HE, PANKRATZ VS, SANDO SB, AASLY JO, BARCIKOWSKA M, WSZOLEK ZK, DICKSON DW, GRAFF-RADFORD NR, PETERSEN RC, ALZHEIMER'S DISEASE NEUROIMAGING INITIATIVE, VAN DUIJN CM, BRETELER MM, IKRAM MA, DESTEFANO AL, FITZPATRICK AL, LOPEZ O, LAUNER LJ, SESHADRI S, CHARGE CONSORTIUM, BERR C, CAMPION D, EPELBAUM J, DARTIGUES JF, TZOURIO C, ALPÉROVITCH A, LATHROP M, EADI1 CONSORTIUM, FEULNER TM, FRIEDRICH P, RIEHLE C, KRAWCZAK M, SCHREIBER S, MAYHAUS M, NICOLHAUS S, WAGENPFEIL S, STEINBERG S, STEFANSSON H, STEFANSSON K, SNAEDAL J, BJÖRNSSON S, JONSSON PV, CHOURAKI V, GENIER-BOLEY B, HILTUNEN M, SOININEN H, COMBARROS O, ZELENIKA D, DELEPINE M, BULLIDO MJ, PASQUIER F, MATEO I, FRANK-GARCIA A, PORCELLINI E, HANON O, COTO E, ALVAREZ V, BOSCO P, SICILIANO G, MANCUSO M, PANZA F, SOLFRIZZI V, NACMIAS B, SORBI S, BOSSÙ P, PICCARDI P, AROSIO B, ANNONI G, SERIPA D, PILOTTO A, SCARPINI E, GALIMBERTI D, BRICE A, HANNEQUIN D, LICASTRO F, JONES L, HOLMANS PA, JONSSON T, RIEMENSCHNEIDER M, MORGAN K, YOUNKIN SG, OWEN MJ, O'DONOVAN M, AMOUYEL P, WILLIAMS J, Epidemiology, Radiology & Nuclear Medicine, Clinical sciences, Pathologic Biochemistry and Physiology, Hollingworth, P, Harold, D, Sims, R, Gerrish, A, Lambert, J, Carrasquillo, M, Abraham, R, Hamshere, M, Pahwa, J, Moskvina, V, Dowzell, K, Jones, N, Stretton, A, Thomas, C, Richards, A, Ivanov, D, Widdowson, C, Chapman, J, Lovestone, S, Powell, J, Proitsi, P, Lupton, M, Brayne, C, Rubinsztein, D, Gill, M, Lawlor, B, Lynch, A, Brown, K, Passmore, P, Craig, D, Mcguinness, B, Todd, S, Holmes, C, Mann, D, Smith, A, Beaumont, H, Warden, D, Wilcock, G, Love, S, Kehoe, P, Hooper, N, Vardy, E, Hardy, J, Mead, S, Fox, N, Rossor, M, Collinge, J, Maier, W, Jessen, F, Rüther, E, Schürmann, B, Heun, R, Kölsch, H, van den Bussche, H, Heuser, I, Kornhuber, J, Wiltfang, J, Dichgans, M, Frölich, L, Hampel, H, Gallacher, J, Hüll, M, Rujescu, D, Giegling, I, Goate, A, Kauwe, J, Cruchaga, C, Nowotny, P, Morris, J, Mayo, K, Sleegers, K, Bettens, K, Engelborghs, S, De Deyn, P, Van Broeckhoven, C, Livingston, G, Bass, N, Gurling, H, Mcquillin, A, Gwilliam, R, Deloukas, P, Al Chalabi, A, Shaw, C, Tsolaki, M, Singleton, A, Guerreiro, R, Mühleisen, T, Nöthen, M, Moebus, S, Jöckel, K, Klopp, N, Wichmann, H, Pankratz, V, Sando, S, Aasly, J, Barcikowska, M, Wszolek, Z, Dickson, D, Graff Radford, N, Petersen, R, van Duijn, C, Breteler, M, Ikram, M, Destefano, A, Fitzpatrick, A, Lopez, O, Launer, L, Seshadri, S, Berr, C, Campion, D, Epelbaum, J, Dartigues, J, Tzourio, C, Alpérovitch, A, Lathrop, M, Feulner, T, Friedrich, P, Riehle, C, Krawczak, M, Schreiber, S, Mayhaus, M, Nicolhaus, S, Wagenpfeil, S, Steinberg, S, Stefansson, H, Stefansson, K, Snædal, J, Björnsson, S, Jonsson, P, Chouraki, V, Genier Boley, B, Hiltunen, M, Soininen, H, Combarros, O, Zelenika, D, Delepine, M, Bullido, M, Pasquier, F, Mateo, I, Frank Garcia, A, Porcellini, E, Hanon, O, Coto, E, Alvarez, V, Bosco, P, Siciliano, G, Mancuso, M, Panza, F, Solfrizzi, V, Nacmias, B, Sorbi, S, Bossù, P, Piccardi, P, Arosio, B, Annoni, G, Seripa, D, Pilotto, A, Scarpini, E, Galimberti, D, Brice, A, Hannequin, D, Licastro, F, Jones, L, Holmans, P, Jonsson, T, Riemenschneider, M, Morgan, K, Younkin, S, Owen, M, O'Donovan, M, Amouyel, P, Williams, J
المصدر: Nature genetics 43(5), 429-435 (2011). doi:10.1038/ng.803
Nature Genetics, 43(5), 429-435. Nature Publishing Group
Hollingworth, P, Harold, D, Sims, R, Gerrish, A, Lambert, J-C, Carrasquillo, M M, Abraham, R, Hamshere, M L, Pahwa, J S, Moskvina, V, Dowzell, K, Jones, N, Stretton, A, Thomas, C, Richards, A, Ivanov, D, Widdowson, C, Chapman, J, Lovestone, S, Powell, J, Proitsi, P, Lupton, M K, Brayne, C, Rubinsztein, D C, Gill, M, Lawlor, B, Lynch, A, Brown, K S, Passmore, P A, Craig, D, McGuinness, B, Todd, S, Holmes, C, Mann, D, Smith, A D, Beaumont, H, Warden, D, Wilcock, G, Love, S, Kehoe, P G, Hooper, N M, Vardy, E R L C, Hardy, J, Mead, S, Fox, N C, Rossor, M, Collinge, J, Maier, W, Jessen, F, Ruether, E, Schuermann, B, Heun, R, Koelsch, H, van den Bussche, H, Heuser, I, Kornhuber, J, Wiltfang, J, Dichgans, M, Froelich, L, Hampel, H, Gallacher, J, Huell, M, Rujescu, D, Giegling, I, Goate, A M, Kauwe, J S K, Cruchaga, C, Nowotny, P, Morris, J C, Mayo, K, Sleegers, K, Bettens, K, Engelborghs, S, De Deyn, P P, Van Broeckhoven, C, Livingston, G, Bass, N J, Gurling, H, McQuillin, A, Gwilliam, R, Deloukas, P, Al-Chalabi, A, Shaw, C E, Tsolaki, M, Singleton, A B, Guerreiro, R, Muehleisen, T W, Noethen, M M, Moebus, S, Joeckel, K-H, Klopp, N, Wichmann, H-E, Pankratz, V S, Sando, S B, Aasly, J O, Barcikowska, M, Wszolek, Z K, Dickson, D W, Graff-Radford, N R, Petersen, R C, van Duijn, C M, Breteler, M M B, Ikram, M A, DeStefano, A L, Fitzpatrick, A L, Lopez, O, Launer, L J, Seshadri, S, Berr, C, Campion, D, Epelbaum, J, Dartigues, J-F, Tzourio, C, Alperovitch, A, Lathrop, M, Feulner, T M, Friedrich, P, Riehle, C, Krawczak, M, Schreiber, S, Mayhaus, M, Nicolhaus, S, Wagenpfeil, S, Steinberg, S, Stefansson, H, Stefansson, K, Snaedal, J, Bjornsson, S, Jonsson, P V, Chouraki, V, Genier-Boley, B, Hiltunen, M, Soininen, H, Combarros, O, Zelenika, D, Delepine, M, Bullido, M J, Pasquier, F, Mateo, I, Frank-Garcia, A, Porcellini, E, Hanon, O, Coto, E, Alvarez, V, Bosco, P, Siciliano, G, Mancuso, M, Panza, F, Solfrizzi, V, Nacmias, B, Sorbi, S, Bossu, P, Piccardi, P, Arosio, B, Annoni, G, Seripa, D, Pilotto, A, Scarpini, E, Galimberti, D, Brice, A, Hannequin, D, Licastro, F, Jones, L, Holmans, P A, Jonsson, T, Riemenschneider, M, Morgan, K, Younkin, S G, Owen, M J, O'Donovan, M, Amouyel, P & Williams, J 2011, ' Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease ', Nature Genetics, vol. 43, no. 5, pp. 429-435 . https://doi.org/10.1038/ng.803Test
Nature genetics
Hollingworth, P, Harold, D, Sims, R, Gerrish, A, Lambert, J C, Carrasquillo, M M, Abraham, R, Hamshere, M L, Pahwa, J S, Moskvina, V, Dowzell, K, Jones, N, Stretton, A, Thomas, C, Richards, A, Ivanov, D, Widdowson, C, Chapman, J, Lovestone, S, Powell, J, Proitsi, P, Lupton, M K, Brayne, C, Rubinsztein, D C, Gill, M, Lawlor, B, Lynch, A, Brown, K S, Passmore, P, Craig, D, McGuinness, B, Todd, S, Holmes, C, Mann, D, Smith, A D, Beaumont, H, Warden, D, Wilcock, G, Love, S, Kehoe, P G, Hooper, N M, Vardy, E R L C, Hardy, J, Mead, S, Fox, N C, Rossor, M, Collinge, J, Maier, W, Jessen, F, Ruther, E, Schurmann, B, Heun, R, Kolsch, H, Van Den Bussche, H, Heuser, I, Kornhuber, J, Wiltfang, J, Dichgans, M, Frolich, L, Hampel, H, Gallacher, J, Hull, M, Rujescu, D, Giegling, I, Goate, A M, Kauwe, J S K, Cruchaga, C, Nowotny, P, Morris, J C, Mayo, K, Sleegers, K, Bettens, K, Engelborghs, S, De Deyn, P P, Van Broeckhoven, C, Livingston, G, Bass, N J, Gurling, H, McQuillin, A, Gwilliam, R, Deloukas, P, Al-Chalabi, A, Shaw, C E, Tsolaki, M, Singleton, A B, Guerreiro, R, Muhleisen, T W, Nothen, M M, Moebus, S, Jockel, K H, Klopp, N, Wichmann, H E, Pankratz, V S, Sando, S B, Aasly, J O, Barcikowska, M, Wszolek, Z K, Dickson, D W, Graff-Radford, N R, Petersen, R C, Van Duijn, C M, Breteler, M M B, Ikram, M A, DeStefano, A L, Fitzpatrick, A L, Lopez, O, Launer, L J, Seshadri, S, Berr, C, Campion, D, Epelbaum, J, Dartigues, J F, Tzourio, C, Alperovitch, A, Lathrop, M, Feulner, T M, Friedrich, P, Riehle, C, Krawczak, M, Schreiber, S, Mayhaus, M, Nicolhaus, S, Wagenpfeil, S, Steinberg, S, Stefansson, H, Stefansson, K, Snaedal, J, Bjornsson, S, Jonsson, P V, Chouraki, V, Genier-Boley, B, Hiltunen, M, Soininen, H, Combarros, O, Zelenika, D, Delepine, M, Bullido, M J, Pasquier, F, Mateo, I, Frank-Garcia, A, Porcellini, E, Hanon, O, Coto, E, Alvarez, V, Bosco, P, Siciliano, G, Mancuso, M, Panza, F, Solfrizzi, V, Nacmias, B, Sorbi, S, Bossu, P, Piccardi, P, Arosio, B, Annoni, G, Seripa, D, Pilotto, A, Scarpini, E, Galimberti, D, Brice, A, Hannequin, D, Licastro, F, Jones, L, Holmans, P A, Jonsson, T, Riemenschneider, M, Morgan, K, Younkin, S G, Owen, M J, O'Donovan, M, Amouyel, P & Williams, J 2011, ' Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease ', Nature Genetics, vol. 43, no. 5, pp. 429-35 . https://doi.org/10.1038/ng.803Test
Hollingworth, P, Harold, D, Sims, R, Gerrish, A, Lambert, J C, Carrasquillo, M M, Abraham, R, Hamshere, M L, Pahwa, J S, Moskvina, V, Dowzell, K, Jones, N, Stretton, A, Thomas, C, Richards, A, Ivanov, D, Widdowson, C, Chapman, J, Lovestone, S, Powell, J, Proitsi, P, Lupton, M K, Brayne, C, Rubinsztein, D C, Gill, M, Lawlor, B, Lynch, A, Brown, K S, Passmore, P A, Craig, D, McGuinness, B, Todd, S, Holmes, C, Mann, D, Smith, A D, Beaumont, H, Warden, D, Wilcock, G, Love, S, Kehoe, P G, Hooper, N M, Vardy, E R L C, Hardy, J, Mead, S, Fox, N C, Rossor, M, Collinge, J, Maier, W, Jessen, F, Ruther, E, Schurmann, B, Heun, R, Kolsch, H, van den Bussche, H, Heuser, I, Kornhuber, J, Wiltfang, J, Dichgans, M, Frolich, L, Hampel, H, Gallacher, J, Hull, M, Rujescu, D, Giegling, I, Goate, A M, Kauwe, J S K, Cruchaga, C, Nowotny, P, Morris, J C, Mayo, K, Sleegers, K, Bettens, K, Engelborghs, S, de Deyn, P P, Van Broeckhoven, C, Livingston, G, Bass, N J, Gurling, H, McQuillin, A, Gwilliam, R, Deloukas, P, Al-Chalabi, A, Shaw, C E, Tsolaki, M, Singleton, A B, Guerreiro, R, Muhleisen, T W, Nothen, M M, Moebus, S, Jockel, K H, Klopp, N, Wichmann, H E, Pankratz, V S, Sando, S B, Aasly, J O, Barcikowska, M, Wszolek, Z K, Dickson, D W & Graff-Radford, N R A O 2011, ' Common Variants at Abca7, Ms4A6A/Ms4A4E, Epha1, Cd33 and Cd2Ap Are Associated with Alzheimer'S Disease ', Nature Genetics, vol. 43, no. 5, pp. 429-435 . https://doi.org/10.1038/ng.803Testمصطلحات موضوعية: Male, ABCA7 protein, human, ATP-Binding Cassette Transporters/genetics, Sialic Acid Binding Ig-like Lectin 3, CD33, SORL1, Medizin, genetics [Alzheimer Disease], Adaptor Proteins, Signal Transducing/genetics, Disease, PICALM, ABCA7, Disease susceptibility, 0302 clinical medicine, genetics [Adaptor Proteins, Signal Transducing], Databases, Genetic, GWAS, GENE-EXPRESSION, Medicine(all), Aged, 80 and over, Genetics, 0303 health sciences, Alzheimer's disease, genetic predisposition, Receptor, EphA1, ALZHEIMER’S DISEASE, Antigens, CD/genetics, genetics [Receptor, EphA1], genetics [Membrane Proteins], Multigene Family, Female, genetics [Antigens, Differentiation, Myelomonocytic], APOE, Antigens, Differentiation, Myelomonocytic, Single-nucleotide polymorphism, Case-control studies, Cytoskeletal Proteins/genetics, Biology, Polymorphism, Single Nucleotide, Article, 03 medical and health sciences, CD33 protein, human, Alzheimer Disease, Antigens, CD, ddc:570, Humans, Genetic Predisposition to Disease, Membrane Proteins/genetics, CLUSTERIN, Aged, genetics [Cytoskeletal Proteins], Adaptor Proteins, Signal Transducing, 030304 developmental biology, Alzheimer Disease/genetics, Antigens, Differentiation, Myelomonocytic/genetics, Genetic Variation, Membrane Proteins, CD2-associated protein, genetics [Antigens, CD], Cytoskeletal Proteins, MS4A4E protein, human, Case-Control Studies, Susceptibility locus, biology.protein, ATP-Binding Cassette Transporters, Human medicine, genetics [ATP-Binding Cassette Transporters], aged, 80 and over, Receptor, EphA1/genetics, 030217 neurology & neurosurgery, Genome-Wide Association Study
وصف الملف: STAMPA; application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dfea33b035eebd8e655803794b897217Test
https://doi.org/10.1038/ng.803Test -
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المؤلفون: Arsaell Arnarsson, Thorlakur Jonsson, Daniel F. Gudbjartsson, Adalbjorg Jonasdottir, Gudmundur A. Hardarson, Jeffrey R. Gulcher, Kristinn P. Magnusson, Unnur Thorsteinsdottir, Fridbert Jonasson, Hreinn Stefansson, Mehdi Motallebipour, Kari Stefansson, Aslaug Jonasdottir, Augustine Kong, Ola Wallerman, Gudmar Thorleifsson, Gisli Masson, G. Bragi Walters, Claes Wadelius, Gerdur Stefansdottir, H. Petursson, Patrick Sulem
المصدر: Science. 317:1397-1400
مصطلحات موضوعية: Male, Genotype, Population, Iceland, Pseudoexfoliation syndrome, Gene Expression, Glaucoma, Single-nucleotide polymorphism, Biology, Exfoliation Syndrome, Polymorphism, Single Nucleotide, Exon, medicine, Humans, Genetic Predisposition to Disease, Risk factor, education, Genetics, education.field_of_study, Chi-Square Distribution, Multidisciplinary, Haplotype, medicine.disease, eye diseases, Adipose Tissue, Case-Control Studies, Female, Amino Acid Oxidoreductases, Glaucoma, Open-Angle
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d36d1c4f8c42174e6416de6c0ef84eddTest
https://doi.org/10.1126/science.1146554Test -
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المؤلفون: Thorlakur Jonsson, Sigurjon A. Gudjonsson, Kari Stefansson, Lars T. Westlye, Sigurbjorn Bjornsson, Ina Giegling, Stacy Steinberg, Seppo Helisalmi, Hrefna Johannsdottir, Hannes Helgason, Harald Hampel, Gun-Peggy Knudsen, Srdjan Djurovic, DemGene, Hilkka Soininen, Augustine Kong, Sigrid Botne Sando, Tormod Fladby, Ingun Ulstein, Palmi V. Jonsson, Unnur Unnsteinsdottir, Geir Selbæk, Dag Aarsland, James J. Lah, Ole A. Andreassen, Mikko Hiltunen, Linda R. White, Olafur T. Magnusson, Patrick Sulem, Hreinn Stefansson, Andres Ingason, Jon Snaedal, Dan Rujescu, Allan I. Levey
مصطلحات موضوعية: Genetics, Risk, Study groups, Genome-wide association study, Disease, Odds ratio, Sequence Analysis, DNA, Biology, humanities, ABCA7, Haplotypes, Alzheimer Disease, Case-Control Studies, Mutation, biology.protein, Humans, ATP-Binding Cassette Transporters, Genetic Predisposition to Disease, Loss function, Genetic Association Studies, Common disease-common variant
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fef0e10e1e49c673e46305b612a606f9Test
http://hdl.handle.net/11250/296499Test -
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المؤلفون: David B. Rye, Finnbogi Jakobsson, John Benedikz, Thorlakur Jonsson, Kari Stefansson, Lisa A Miyatake, Hreinn Stefansson, Theodora Thorlacius, Iris H Gudjonsdottir, Stefan T Palsson, Jona Saemundsdottir, Christoph Hotzy, H. Petursson, Ludger Schöls, Kristleifur Kristleifsson, Martin Dichgans, Jeffrey R. Gulcher, Gyda Bjornsdottir, Friedrich Asmus, Ami Rosen, Claudia M. Testa, Yvonne Böttcher, Omar Gustafsson, Unnur Thorsteinsdottir, Alexander Zimprich, Stacy Steinberg, Gudrun A. Jonsdottir, Dietrich Haubenberger, Eduard Auff, Augustine Kong
المصدر: Nature Genetics. 41:277-279
مصطلحات موضوعية: Essential Tremor, Population, Iceland, Nerve Tissue Proteins, Genome-wide association study, Biology, Polymorphism, Single Nucleotide, Linkage Disequilibrium, Article, Mice, Gene Frequency, Risk Factors, Germany, Genetics, medicine, Animals, Humans, Genetic Predisposition to Disease, Axon, education, Gene, LINGO1, Mice, Knockout, education.field_of_study, Essential tremor, Regeneration (biology), Membrane Proteins, medicine.disease, United States, Oligodendrocyte, Cell biology, Genetics, Population, medicine.anatomical_structure, nervous system, Austria, Genome-Wide Association Study
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c94958f05d0b1d6da6bcbf56237c7627Test
https://doi.org/10.1038/ng.299Test -
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المؤلفون: Sigrún Siguróaróóttir, Ásdís Baldursdóttir, Jeffrey R. Gulcher, Ragnheióur I. Bjarnaóóttir, Reynir Tómas Geirsson, Birgir Palsson, Birkir Thor Bragason, Thorlakur Jonsson, Augustine Kong, Reynir Arngrímsson, Dan L. Nicolae, A. M. A. Lachmeijer, Kari Stefansson, Anna S. Einarsdóttir, Michael L. Frigge, Steinunn Snorradottir, Hreinn Stefansson
المصدر: Human Molecular Genetics. 8:1799-1805
مصطلحات موضوعية: Genetic Markers, Gestational hypertension, medicine.medical_specialty, Genotype, Genetic Linkage, Iceland, Locus (genetics), Prenatal care, Disease, Biology, Preeclampsia, Pre-Eclampsia, Pregnancy, Genetics, medicine, Humans, Genetic Predisposition to Disease, Molecular Biology, reproductive and urinary physiology, Genetics (clinical), Eclampsia, Genome, Human, Obstetrics, Haplotype, Chromosome Mapping, General Medicine, medicine.disease, female genital diseases and pregnancy complications, Pedigree, Haplotypes, Chromosomes, Human, Pair 2, Female, Lod Score
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af9b3c3c9610406ef996a5a2a7fb8c3cTest
https://doi.org/10.1093/hmg/8.9.1799Test -
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المؤلفون: Robert T. Sauer, Dionisios Rentzeperis, Thorlakur Jonsson
المصدر: Nature Structural Biology. 6:569-573
مصطلحات موضوعية: Dimer, Kinetics, Repressor, Biochemistry, Folding (chemistry), chemistry.chemical_compound, Crystallography, Monomer, chemistry, Structural Biology, Static electricity, Genetics, Nucleic acid, Protein folding
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::78a78c7800440c4ec63f97abf43b6137Test
https://doi.org/10.1038/9353Test -
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المؤلفون: Thorlakur Jonsson
المصدر: Alzheimer's & Dementia. 9
مصطلحات موضوعية: Genetics, Age-related cognitive decline, Epidemiology, business.industry, Health Policy, Disease, Psychiatry and Mental health, Cellular and Molecular Neuroscience, Developmental Neuroscience, Mutation (genetic algorithm), Medicine, Neurology (clinical), Geriatrics and Gerontology, business, Coding (social sciences)
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::20ebf53ebd51b120dcd02af3bf3e5a68Test
https://doi.org/10.1016/j.jalz.2013.04.464Test -
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المؤلفون: Thorlakur Jonsson, Albert Hofman, Johanna Huttenlocher, Harald Hampel, James J. Lah, Augustine Kong, Knut Engedal, Ingileif Jonsdottir, Cornelia M. van Duijn, Carla A. Ibrahim-Verbaas, Jon Snaedal, M. Arfan Ikram, Ingun Ulstein, Sigurbjorn Bjornsson, Unnur Thorsteinsdottir, Stacy Steinberg, Kari Stefansson, Dan Rujescu, Allan I. Levey, Ina Giegling, Palmi V. Jonsson, Srdjan Djurovic, Hreinn Stefansson, Ole A. Andreassen
المساهمون: Neurology, Epidemiology, Radiology & Nuclear Medicine, Decode, Landspitali University Hospital, Reykjavik, Iceland
المصدر: New England Journal of Medicine, 368(2), 107-116. Massachussetts Medical Society
New England Journal of Medicine; Vol 368مصطلحات موضوعية: Apolipoprotein E, Oncology, medicine.medical_specialty, Heterozygote, Genotyping Techniques, SORL1, Population, Apolipoprotein E4, Iceland, Mutation, Missense, Bioinformatics, Polymorphism, Single Nucleotide, Article, 03 medical and health sciences, 0302 clinical medicine, Cognition, Alzheimer Disease, Risk Factors, Internal medicine, medicine, Humans, Receptors, Immunologic, education, 030304 developmental biology, Aged, 80 and over, 0303 health sciences, education.field_of_study, Membrane Glycoproteins, TREM2, business.industry, Case-control study, Genetic Variation, General Medicine, Odds ratio, Sequence Analysis, DNA, medicine.disease, 3. Good health, Case-Control Studies, Alzheimer's disease, business, 030217 neurology & neurosurgery, Common disease-common variant
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7d540c359d991da3e614fe60ed778b7Test
https://pure.eur.nl/en/publications/8a27fe44-3362-41ee-b817-b615bc0e5c75Test