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.803Test

مصطلحات 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

المؤلفون: Maria Paola Piccardi, Alessio Squassina, Donatella Congiu, Maria Del Zompo, Maria Erminia Stochino, Francesca Manconi, Carlo Asuni, A. Cherchi, Mirko Manchia

المصدر: Journal of Neurology. 256:194-197

مصطلحات موضوعية: Adult, Genetic Markers, Male, Linkage disequilibrium, Genotype, Aura, Migraine Disorders, DNA Mutational Analysis, Human leukocyte antigen, Linkage Disequilibrium, Pathogenesis, Gene Frequency, HLA Antigens, Polymorphism (computer science), Humans, Medicine, Genetic Predisposition to Disease, Genetic Testing, Lymphotoxin-alpha, Polymorphism, Genetic, Tumor Necrosis Factor-alpha, business.industry, Middle Aged, medicine.disease, Italy, Neurology, Migraine, Immunology, Chromosomes, Human, Pair 6, Female, Tumor necrosis factor alpha, Neurology (clinical), Gene polymorphism, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::759440d8ae45d78bd2cd844395f91c66Test
https://doi.org/10.1007/s00415-009-0961-8Test

المؤلفون: Giovanni Severino, Vincenzo De Luca, Donatella Congiu, Maria Paola Piccardi, Stefania Mulas, Xingqun Ni, Maria Del Zompo, James L. Kennedy

المصدر: American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. :237-241

مصطلحات موضوعية: Adult, Male, Proband, Canada, Candidate gene, Bipolar Disorder, Single-nucleotide polymorphism, Biology, Polymorphism, Single Nucleotide, Cellular and Molecular Neuroscience, Risk Factors, medicine, Humans, Genetic Predisposition to Disease, Bipolar disorder, Gene, Alleles, Genetics (clinical), Genetic association, Genetics, Receptors, Dopamine D1, Haplotype, Control subjects, medicine.disease, Psychiatry and Mental health, Haplotypes, Italy, Case-Control Studies, Female

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::801c457f7fcb503621b2c7c366a36e9bTest
https://doi.org/10.1002/ajmg.b.30445Test

المؤلفون: Paolo Stratta, Antonio Vita, Giovanni Severino, Paolo Cassano, Mario Maj, Alessandro Rossi, Giordano Invernizzi, Paola Piccardi, Armida Mucci, Maria Del Zompo, Silvana Galderisi, Stefano Pini, Brian Kirkpatrick

المساهمون: Galderisi, Silvana, Maj, Mario, Kirkpatrick, B, Piccardi, P, Mucci, Armida, Invernizzi, G, Rossi, A, Pini, S, Vita, A, Cassano, P, Stratta, P, Severino, G, DEL ZOMPO, M.

المصدر: Università degli Studi di Brescia-IRIS

مصطلحات موضوعية: Psychosis, medicine.medical_specialty, Genotype, Genetic Linkage, Nerve Tissue Proteins, Catechol-O-methyl transferase gene, Catechol O-Methyltransferase, behavioral disciplines and activities, Polymorphism (computer science), Neurotrophic factors, Internal medicine, mental disorders, medicine, Humans, Alleles, Biological Psychiatry, Genetics, Brain-derived neurotrophic factor, Polymorphism, Genetic, Catechol-O-methyl transferase, Brain-Derived Neurotrophic Factor, Case-control study, medicine.disease, Diagnostic and Statistical Manual of Mental Disorders, Psychiatry and Mental health, Endocrinology, nervous system, Schizophrenia, Psychology, Brain-derived neurotrophic factor gene

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32a6dcb52fbbbf9e19fa83fc3d5068c7Test
https://doi.org/10.1016/j.schres.2004.06.017Test

المؤلفون: Paola Piccardi, Stefano Pini, Maria Del Zompo, Mario Maj, Silvana Galderisi, Antonio Vita, Giovanni Severino, Paolo Cassano, Brian Kirkpatrick, Alessandro Rossi, Paolo Stratta, Armida Mucci, Giordano Invernizzi

المصدر: Neuropsychobiology. 52:83-89

مصطلحات موضوعية: Psychosis, Catechol-O-methyl transferase, Cognitive disorder, Case-control study, Cognition, Neurological disorder, medicine.disease, Bioinformatics, Psychiatry and Mental health, Neuropsychology and Physiological Psychology, Polymorphism (computer science), Schizophrenia, medicine, Psychology, Neuroscience, Biological Psychiatry

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::3d91bd3c906981944aca62e6a0a84158Test
https://doi.org/10.1159/000087096Test

المؤلفون: Donatella Congiu, Jacques Mallet, Giovanni Severino, Michele Bayorek, Rolando Meloni, Maria Del Zompo, Maria Paola Piccardi, Caterina Chillotti, Antonio Oi, Raffaella Ardau, Jean-François Deleuze

المصدر: Psychiatric Genetics. 12:23-27

مصطلحات موضوعية: Adult, Male, Parents, Candidate gene, medicine.medical_specialty, Bipolar Disorder, Phosphatase, Nerve Tissue Proteins, Neurotransmission, chemistry.chemical_compound, Internal medicine, mental disorders, Genetics, medicine, Humans, Inositol, Bipolar disorder, Age of Onset, Gene, Alleles, Biological Psychiatry, Genetics (clinical), Serotonin transporter, Genetic association, Serotonin Plasma Membrane Transport Proteins, Membrane Glycoproteins, biology, business.industry, Membrane Transport Proteins, DNA, medicine.disease, Phosphoric Monoester Hydrolases, Psychiatry and Mental health, Endocrinology, chemistry, biology.protein, Female, sense organs, Carrier Proteins, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c56bdbc168d2823d8ee89cd9b38301b8Test
https://doi.org/10.1097/00041444-200203000-00003Test

المؤلفون: Alessio Squassina, Paola Piccardi, Antonio Vita, Maria Del Zompo, Armida Mucci, Alessandro Rossi, Stefano Pini, Silvana Galderisi

المساهمون: Squassina, A, Piccardi, P, DEL ZOMPO, M, Rossi, A, Vita, A, Pini, S, Mucci, Armida, Galderisi, Silvana

المصدر: Psychiatry Research. 176:82-84

مصطلحات موضوعية: Adult, Male, Genotype, Neuregulin-1, Single-nucleotide polymorphism, Biology, Gene Frequency, mental disorders, Genetic variation, Haplotype, medicine, Humans, Genetic Predisposition to Disease, Allele, Neuregulin 1, Gene-gene interaction, Gene, Biological Psychiatry, Genetics, Polymorphism, Genetic, Brain-Derived Neurotrophic Factor, Middle Aged, medicine.disease, Psychiatry and Mental health, Italy, Schizophrenia, Case-Control Studies, biology.protein, Female, Neurotrophin, Genome-Wide Association Study

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ac4c89f7adb6095bd410a11847023dbTest
https://doi.org/10.1016/j.psychres.2009.03.017Test

المؤلفون: Maria Paola Piccardi, M. A. Palmas, Antonio Oi, Caterina Chillotti, Alberto Bocchetta, Maria Del Zompo

المصدر: American Journal of Medical Genetics. 88:522-526

مصطلحات موضوعية: Proband, Genetics, Candidate gene, Linkage disequilibrium, Transmission disequilibrium test, Biology, medicine.disease, mental disorders, biology.protein, medicine, Bipolar disorder, Allele, Genetics (clinical), Serotonin transporter, Genetic association

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::2d2d157b2eed2eac467e7da94e61bb50Test
https://doi.org/10.1002Test/(sici)1096-8628(19991015)88:5<522::aid-ajmg16>3.0.co;2-m

المؤلفون: M. Del Zompo, Paola Piccardi, M. A. Palmas, C. Severino, S. Ruiu

المصدر: European Neuropsychopharmacology. 6:S4-112

مصطلحات موضوعية: Pharmacology, medicine.medical_specialty, business.industry, medicine.disease, Psychiatry and Mental health, Endocrinology, Neurology, Dopamine receptor D3, Internal medicine, Medicine, Pharmacology (medical), Neurology (clinical), Bipolar disorder, business, Association (psychology), Gene, Biological Psychiatry

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::a1d69ea02b01ceb20bdde1a8683db339Test
https://doi.org/10.1016/0924-977xTest(96)82937-3

المؤلفون: Anne Boland, Giorgio Annoni, Elisa Porcellini, Gloria Tognoni, Giovanni Ravaglia, Mark Lathrop, Ignacio Mateo, Paola Bossù, Diana Zelenika, Nathalie Fievet, Marc Delepine, Mikko Hiltunen, Ana Frank-García, Hilkka Soininen, Paola Forti, Gianfranco Spalletta, Federico Licastro, Daniela Galimberti, Paola Piccardi, Maria Del Zompo, Seppo Helisalmi, Michelangelo Mancuso, Vincenzo Solfrizzi, Francesco Panza, Davide Seripa, Philippe Amouyel, María J. Bullido, Paolo Bosco, Gabriele Siciliano, Alberto Pilotto, Vincent Chouraki, Beatrice Arosio, Fernando Valdivieso, Jean-Charles Lambert, Elio Scarpini, Victoria Alvarez, Onofre Combarros, Sandro Sorbi, Benedetta Nacmias, Raffaele Ferri, Eliecer Coto

المساهمون: Lambert, J, Zelenika, D, Hiltunen, M, Chouraki, V, Combarros, O, Bullido, M, Tognoni, G, Fiévet, N, Boland, A, Arosio, B, Coto, E, Zompo, M, Mateo, I, Frank Garcia, A, Helisalmi, S, Porcellini, E, Pilotto, A, Forti, P, Ferri, R, Delepine, M, Scarpini, E, Siciliano, G, Solfrizzi, V, Sorbi, S, Spalletta, G, Ravaglia, G, Valdivieso, F, Alvarez, V, Bosco, P, Mancuso, M, Panza, F, Nacmias, B, Bossù, P, Piccardi, P, Annoni, G, Seripa, D, Galimberti, D, Licastro, F, Lathrop, M, Soininen, H, Amouyel, P, Lambert JC, Zelenika D, Hiltunen M, Chouraki V, Combarros O, Bullido MJ, Tognoni G, Fiévet N, Boland A, Arosio B, Coto E, Zompo MD, Mateo I, Frank-Garcia A, Helisalmi S, Porcellini E, Pilotto A, Forti P, Ferri R, Delepine M, Scarpini E, Siciliano G, Solfrizzi V, Sorbi S, Spalletta G, Ravaglia G, Valdivieso F, Alvarez V, Bosco P, Mancuso M, Panza F, Nacmias B, Bossù P, Piccardi P, Annoni G, Seripa D, Galimberti D, Licastro F, Lathrop M, Soininen H, Amouyel P, Universidad de Cantabria

المصدر: Neurobiology of Aging. 2011 Apr;32(4):756.e11-5
UCrea Repositorio Abierto de la Universidad de Cantabria
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مصطلحات موضوعية: Apolipoprotein E, Aging, BIN1, Genotype, Disease, Biology, GWA, Polymorphism, Single Nucleotide, White People, PICALM, Polymorphism (computer science), Alzheimer Disease, Humans, Genetic Predisposition to Disease, Finland, Genetic Association Studies, Genetic association, Adaptor Proteins, Signal Transducing, Genetics, ALZHEIMER’S DISEASE, General Neuroscience, Tumor Suppressor Proteins, Nuclear Proteins, Odds ratio, POLYMORPHISM, Confidence interval, Italy, Spain, Monomeric Clathrin Assembly Proteins, Neurology (clinical), BIN1, PICALM, EXOC3L2, APOE, Alzheimer, Risk, GWA, Association, Polymorphism, Geriatrics and Gerontology, APOE, Developmental Biology

وصف الملف: ELETTRONICO

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::80242a4abe3405397650bb9a912fb567Test
http://hdl.handle.net/11568/151874Test