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Material Type: Artigo
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Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association dataMok, Kin Y ; Sheerin, Una ; Simón-Sánchez, Javier ; Salaka, Afnan ; Chester, Lucy ; Escott-Price, Valentina ; Mantripragada, Kiran ; Doherty, Karen M ; Noyce, Alastair J ; Mencacci, Niccolo E ; Lubbe, Steven J ; International Parkinson's Disease Genomics Consortium (IPDGC) ; Williams-Gray, Caroline H ; Barker, Roger A ; van Dijk, Karin D ; Berendse, Henk W ; Heutink, Peter ; Corvol, Jean-Christophe ; Cormier, Florence ; Lesage, Suzanne ; Brice, Alexis ; Brockmann, Kathrin ; Schulte, Claudia ; Gasser, Thomas ; Foltynie, Thomas ; Limousin, Patricia ; Morrison, Karen E ; Clarke, Carl E ; Sawcer, Stephen ; Warner, Tom T ; Lees, Andrew J ; Morris, Huw R ; Nalls, Mike A ; Singleton, Andrew B ; Hardy, John ; Abramov, Andrey Y ; Plagnol, Vincent ; Williams, Nigel M ; Wood, Nicholas Whttp://dx.doi.org/10.1016/s1474-442200071-5 2016-05Texto 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 |