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Material Type: Artigo
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ABCA7 p.G215S as potential protective factor for Alzheimer’s diseaseSassi, C ; Nalls, M.A ; Ridge, P.G ; Gibbs, R ; Ding, J ; Lupton, M.K ; Troakes, C ; Lunnon, K ; Al-Sarraj, S ; Brown, K.S ; Medway, C ; Clement, N ; Lord, J ; Turton, J ; Bras, J ; Almeida, M.R ; Holstege, H ; Louwersheimer, E ; van der Flier, W ; Scheltens, P ; Van Swieten, J.C ; Santana, I ; Oliveira, C ; Morgan, K ; Powell, J.F ; Kauwe, J.S ; Cruchaga, C ; Goate, A.M ; Singleton, A.B ; Guerreiro, R ; Hardy, JNeurobiology of aging, 2016-10, Vol.46, p.235.e1-235.e9 [Periódico revisado por pares]United States: Elsevier IncTexto completo disponível |
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Material Type: Artigo
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Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource studyFOX, Ervin R ; HUNTER YOUNG, J ; RAMACHANDRAN, VasanS ; POLAK, JosefF ; FABSITZ, Richard R ; DRIES, Daniel L ; FARLOW, Deborah N ; REDLINE, Susan ; ADEYEMO, Adebowale ; HIRSCHORN, Joel N ; SUN, Yan V ; WYATT, Sharon B ; YALI LI ; PENMAN, Alan D ; PALMAS, Walter ; ROTTER, Jerome I ; TOWNSEND, Raymond R ; DOUMATEY, Ayo P ; TAYO, Bamidele O ; MOSLEY, Thomas H ; LYON, Helen N ; KANG, Sun J ; ROTIMI, Charles N ; DREISBACH, Albert W ; COOPER, Richard S ; FRANCESCHINI, Nora ; CURB, J. David ; MARTIN, Lisa W ; EATON, Charles B ; KARDIA, Sharon L. R ; TAYLOR, Herman A ; CAULFIELD, Mark J ; EHRET, Georg B ; JOHNSON, Toby ; KEATING, Brendan J ; CHAKRAVARTI, Aravinda ; XIAOFENG ZHU ; LEVY, Daniel ; MUSANI, Solomon K ; KIANG LIU ; MORRISON, Alanna C ; GANESH, Santhi ; KUTLAR, AbdullahHuman molecular genetics, 2011-06, Vol.20 (11), p.2273-2284 [Periódico revisado por pares]Oxford: Oxford University PressTexto completo disponível |
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Material Type: Artigo
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Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association studyLaaksovirta, Hannu, MD ; Peuralinna, Terhi, MSc ; Schymick, Jennifer C, PhD ; Scholz, Sonja W, MD ; Lai, Shaoi-Lin, MD ; Myllykangas, Liisa, MD ; Sulkava, Raimo, MD ; Jansson, Lilja ; Hernandez, Dena G, MSc ; Gibbs, J Raphael, BS ; Nalls, Michael A, PhD ; Heckerman, David, MD ; Tienari, Pentti J, MD ; Traynor, Bryan J, DrLancet neurology, 2010-10, Vol.9 (10), p.978-985 [Periódico revisado por pares]England: Elsevier LtdTexto completo disponível |
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Material Type: Artigo
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Common Variants Within Oxidative Phosphorylation Genes Influence Risk of Ischemic Stroke and Intracerebral HemorrhageANDERSON, Christopher D ; BIFFI, Alessandro ; VISWANATHAN, Anand ; WORRALL, Bradford B ; BROTT, Thomas G ; GOLDSTEIN, Joshua N ; BROWN, Devin ; BRODERICK, Joseph P ; NORRVING, Bo ; GREENBERG, Steven M ; SILLIMAN, Scott L ; HANSEN, Björn M ; NALLS, Michael A ; TIRSCHWELL, David L ; LINDGREN, Arne ; SLOWIK, Agnieszka ; SCHMIDT, Reinhold ; SELIM, Magdy ; ROQUER, Jaume ; MONTANER, Joan ; SINGLETON, Andrew B ; KIDWELL, Chelsea S ; WOO, Daniel ; DEVAN, William J ; FURIE, Karen L ; MESCHIA, James F ; ROSAND, Jonathan ; SCHWAB, Kristin ; AYRES, Alison M ; VALANT, Valerie ; ROSS, Owen A ; ROST, Natalia S ; SAXENA, RichaStroke (1970), 2013-03, Vol.44 (3), p.612-619 [Periódico revisado por pares]Hagerstown, MD: Lippincott Williams & WilkinsTexto completo disponível |
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Material Type: Artigo
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Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional studyMajounie, Elisa, PhD ; Renton, Alan E, PhD ; Mok, Kin, MSc ; Dopper, Elise GP ; Waite, Adrian, PhD ; Rollinson, Sara, PhD ; Chiò, Adriano, MD ; Restagno, Gabriella, MD ; Nicolaou, Nayia, MSc ; Simon-Sanchez, Javier, PhD ; van Swieten, John C, Prof ; Abramzon, Yevgeniya ; Johnson, Janel O, PhD ; Sendtner, Michael, Prof ; Pamphlett, Roger, MD ; Orrell, Richard W, MD ; Mead, Simon, MD ; Sidle, Katie C, MD ; Houlden, Henry, Prof ; Rohrer, Jonathan D, MD ; Morrison, Karen E, Prof ; Pall, Hardev, MD ; Talbot, Kevin, Prof ; Ansorge, Olaf, MD ; Hernandez, Dena G, MSc ; Arepalli, Sampath, MS ; Sabatelli, Mario, MD ; Mora, Gabriele, MD ; Corbo, Massimo, MD ; Giannini, Fabio, MD ; Calvo, Andrea, MD ; Englund, Elisabet, MD ; Borghero, Giuseppe, MD ; Floris, Gian Luca, MD ; Remes, Anne M, Prof ; Laaksovirta, Hannu, MD ; McCluskey, Leo, MD ; Trojanowski, John Q, Prof ; Van Deerlin, Vivianna M, MD ; Schellenberg, Gerard D, Prof ; Nalls, Michael A, PhD ; Drory, Vivian E, MD ; Lu, Chin-Song, Prof ; Yeh, Tu-Hsueh, MD ; Ishiura, Hiroyuki, MD ; Takahashi, Yuji, MD ; Tsuji, Shoji, Prof ; Le Ber, Isabelle, MD ; Brice, Alexis, Prof ; Drepper, Carsten, PhD ; Williams, Nigel, PhD ; Kirby, Janine, PhD ; Shaw, Pamela, Prof ; Hardy, John, Prof ; Tienari, Pentti J, MD ; Heutink, Peter, Prof ; Morris, Huw R, MD ; Pickering-Brown, Stuart, Prof ; Traynor, Bryan J, DrLancet neurology, 2012-04, Vol.11 (4), p.323-330 [Periódico revisado por pares]England: Elsevier LtdTexto completo disponível |
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Material Type: Artigo
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Gene polymorphisms and gene scores linked to low serum carotenoid status and their associations with metabolic disturbance and depressive symptoms in African-American adultsBeydoun, May A. ; Nalls, Michael A. ; Canas, J. Atilio ; Evans, Michele K. ; Zonderman, Alan B.British journal of nutrition, 2014-09, Vol.112 (6), p.992-1003 [Periódico revisado por pares]Cambridge, UK: Cambridge University PressTexto completo disponível |
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Material Type: Artigo
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Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodiesBras, Jose ; Guerreiro, Rita ; Darwent, Lee ; Parkkinen, Laura ; Ansorge, Olaf ; Escott-Price, Valentina ; Hernandez, Dena G ; Nalls, Michael A ; Clark, Lorraine N ; Honig, Lawrence S ; Marder, Karen ; Van Der Flier, Wiesje M ; Lemstra, Afina ; Scheltens, Philip ; Rogaeva, Ekaterina ; St George-Hyslop, Peter ; Londos, Elisabet ; Zetterberg, Henrik ; Ortega-Cubero, Sara ; Pastor, Pau ; Ferman, Tanis J ; Graff-Radford, Neill R ; Ross, Owen A ; Barber, Imelda ; Braae, Anne ; Brown, Kristelle ; Morgan, Kevin ; Maetzler, Walter ; Berg, Daniela ; Troakes, Claire ; Al-Sarraj, Safa ; Lashley, Tammaryn ; Compta, Yaroslau ; Revesz, Tamas ; Lees, Andrew ; Cairns, Nigel ; Halliday, Glenda M ; Mann, David ; Pickering-Brown, Stuart ; Dickson, Dennis W ; Singleton, Andrew ; Hardy, JohnHuman molecular genetics, 2014-12, Vol.23 (23), p.6139-6146 [Periódico revisado por pares]England: Oxford University PressTexto completo disponível |
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Material Type: Artigo
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Genetic variability in CLU and its association with Alzheimer's diseaseGuerreiro, Rita J ; Beck, John ; Gibbs, J Raphael ; Santana, Isabel ; Rossor, Martin N ; Schott, Jonathan M ; Nalls, Michael A ; Ribeiro, Helena ; Santiago, Beatriz ; Fox, Nick C ; Oliveira, Catarina ; Collinge, John ; Mead, Simon ; Singleton, Andrew ; Hardy, John Weedon, Michael NicholasPloS one, 2010-03, Vol.5 (3), p.e9510-e9510 [Periódico revisado por pares]United States: Public Library of ScienceTexto completo disponível |
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Material Type: Artigo
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Genome-wide Analyses Identify KIF5A as a Novel ALS GeneNicolas, Aude ; Kenna, Kevin P ; Renton, Alan E ; Ticozzi, Nicola ; Faghri, Faraz ; Chia, Ruth ; Dominov, Janice A ; Kenna, Brendan J ; Nalls, Mike A ; Keagle, Pamela ; Rivera, Alberto M ; van Rheenen, Wouter ; Murphy, Natalie A ; van Vugt, Joke JFA ; Geiger, Joshua T ; Van der Spek, Rick A ; Pliner, Hannah A ; Shankaracharya ; Smith, Bradley N ; Marangi, Giuseppe ; Topp, Simon D ; Abramzon, Yevgeniya ; Gkazi, Athina Soragia ; Eicher, John D ; Kenna, Aoife ; ITALSGEN Consortium ; Mora, Gabriele ; Calvo, Andrea ; Mazzini, Letizia ; Riva, Nilo ; Mandrioli, Jessica ; Caponnetto, Claudia ; Battistini, Stefania ; Volanti, Paolo ; La Bella, Vincenzo ; Conforti, Francesca L ; Borghero, Giuseppe ; Messina, Sonia ; Simone, Isabella L ; Trojsi, Francesca ; Salvi, Fabrizio ; Logullo, Francesco O ; D'Alfonso, Sandra ; Corrado, Lucia ; Capasso, Margherita ; Ferrucci, Luigi ; Genomic Translation for ALS Care (GTAC) Consortium ; Moreno, Cristiane de Araujo Martins ; Kamalakaran, Sitharthan ; Goldstein, David B ; ALS Sequencing Consortium ; Gitler, Aaron D ; Harris, Tim ; Myers, Richard M ; NYGC ALS Consortium ; Phatnani, Hemali ; Musunuri, Rajeeva Lochan ; Evani, Uday Shankar ; Abhyankar, Avinash ; Zody, Michael C ; Answer ALS Foundation ; Kaye, Julia ; Finkbeiner, Steven ; Wyman, Stacia K ; LeNail, Alex ; Lima, Leandro ; Fraenkel, Ernest ; Svendsen, Clive N ; Thompson, Leslie M ; Van Eyk, Jennifer E ; Berry, James D ; Miller, Timothy M ; Kolb, Stephen J ; Cudkowicz, Merit ; Baxi, Emily ; Clinical Research in ALS and Related Disorders for Therapeutic Development (CReATe) Consortium ; Benatar, Michael ; Taylor, J Paul ; Rampersaud, Evadnie ; Wu, Gang ; Wuu, Joanne ; SLAGEN Consortium ; Lauria, Giuseppe ; Verde, Federico ; Fogh, Isabella ; Tiloca, Cinzia ; Comi, Giacomo P ; Sorarù, Gianni ; Cereda, Cristina ; French ALS Consortium ; Corcia, Philippe ; Laaksovirta, Hannu ; Myllykangas, Liisa ; Jansson, Lilja ; Valori, Miko ; Ealing, John ; Hamdalla, Hisham ; Rollinson, Sara ; Pickering-Brown, Stuart ; Orrell, Richard WNeuron, 2018-03, Vol.97 (6), p.1268-1283.e6eScholarship, University of CaliforniaSem texto completo |
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Material Type: Artigo
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Genome-Wide Analysis of the Heritability of Amyotrophic Lateral SclerosisKeller, Margaux F ; Ferrucci, Luigi ; Singleton, Andrew B ; Tienari, Pentti J ; Laaksovirta, Hannu ; Restagno, Gabriella ; Chiò, Adriano ; Traynor, Bryan J ; Nalls, Michael AJAMA neurology, 2014-09, Vol.71 (9), p.1123-1134 [Periódico revisado por pares]United States: American Medical AssociationTexto completo disponível |