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Material Type: Artigo
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Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21Spencer, Chris C A ; Plagnol, Vincent ; Strange, Amy ; Gardner, Michelle ; Paisan-Ruiz, Coro ; Band, Gavin ; Barker, Roger A ; Bellenguez, Celine ; Bhatia, Kailash ; Blackburn, Hannah ; Blackwell, Jennie M ; Bramon, Elvira ; Brown, Martin A ; Brown, Matthew A ; Burn, David ; Casas, Juan-Pablo ; Chinnery, Patrick F ; Clarke, Carl E ; Corvin, Aiden ; Craddock, Nicholas ; Deloukas, Panos ; Edkins, Sarah ; Evans, Jonathan ; Freeman, Colin ; Gray, Emma ; Hardy, John ; Hudson, Gavin ; Hunt, Sarah ; Jankowski, Janusz ; Langford, Cordelia ; Lees, Andrew J ; Markus, Hugh S ; Mathew, Christopher G ; McCarthy, Mark I ; Morrison, Karen E ; Palmer, Colin N A ; Pearson, Justin P ; Peltonen, Leena ; Pirinen, Matti ; Plomin, Robert ; Potter, Simon ; Rautanen, Anna ; Sawcer, Stephen J ; Su, Zhan ; Trembath, Richard C ; Viswanathan, Ananth C ; Williams, Nigel W ; Morris, Huw R ; Donnelly, Peter ; Wood, Nicholas WHuman molecular genetics, 2011-01, Vol.20 (2), p.345-353 [Periódico revisado por pares]Oxford: Oxford University PressTexto completo disponível |
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Material Type: Artigo
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Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studiesNalls, Michael A ; Plagnol, Vincent ; Hernandez, Dena G ; Sharma, Manu ; Sheerin, Una-Marie ; Saad, Mohamad ; Simón-Sánchez, J ; Schulte, Claudia ; Lesage, Suzanne ; Sveinbjörnsdóttir, Sigurlaug ; Stefánsson, Kári ; Martinez, Maria ; Hardy, John ; Heutink, Peter ; Brice, Alexis ; Gasser, Thomas ; Singleton, Andrew B ; Wood, Nicholas WThe Lancet (British edition), 2011-02, Vol.377 (9766), p.641-649 [Periódico revisado por pares]Kidlington: Elsevier LtdTexto completo disponível |
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Material Type: Artigo
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A systematic review of physicians' survival predictions in terminally ill cancer patientsGlare, Paul ; Virik, Kiran ; Jones, Mark ; Hudson, Malcolm ; Eychmuller, Steffen ; Simes, John ; Christakis, NicholasBMJ, 2003-07, Vol.327 (7408), p.195-198 [Periódico revisado por pares]London: British Medical Journal Publishing GroupTexto completo disponível |
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Material Type: Artigo
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Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's diseaseKELLER, Margaux F ; SAAD, Mohamad ; SCHULTE, Claudia ; MOSKVINA, Valentina ; DURR, Alexandra ; HOLMANS, Peter ; KILARSKI, Laura L ; GUERREIRO, Rita ; HERNANDEZ, Dena G ; BRICE, Alexis ; YLIKOTILA, Pauli ; STEFANSSON, Hreinn ; BRAS, Jose ; MAJAMAA, Kari ; MORRIS, Huw R ; WILLIAMS, Nigel ; GASSER, Thomas ; HEUTINK, Peter ; WOOD, Nicholas W ; HARDY, John ; MARTINEZ, Maria ; SINGLETON, Andrew B ; NALLS, Michael A ; BETTELLA, Francesco ; NICOLAOU, Nayia ; SIMON-SANCHEZ, Javier ; MITTAG, Florian ; BÜCHEL, Finja ; SHARMA, Manu ; RAPHAEL GIBBS, JHuman molecular genetics, 2012-11, Vol.21 (22), p.4996-5009 [Periódico revisado por pares]Oxford: Oxford University PressTexto completo disponível |
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Material Type: Artigo
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Famotidine for the Prevention of Gastric and Duodenal Ulcers Caused by Nonsteroidal Antiinflammatory DrugsTaha, Ali S ; Hudson, Nicholas ; Hawkey, Christopher J ; Swannell, Anthony J ; Trye, Penelope N ; Cottrell, Jeremy ; Mann, Stephen G ; Simon, Thomas J ; Sturrock, Roger D ; Russell, Robin IThe New England journal of medicine, 1996-05, Vol.334 (22), p.1435-1439 [Periódico revisado por pares]Boston, MA: Massachusetts Medical SocietyTexto completo disponível |