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Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21
Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21
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Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21

Spencer, 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 W

Human molecular genetics, 2011-01, Vol.20 (2), p.345-353 [Periódico revisado por pares]

Oxford: Oxford University Press

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2
A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease
A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease
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A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease

Holmans, Peter ; Moskvina, Valentina ; Jones, Lesley ; Sharma, Manu ; Vedernikov, Alexey ; Buchel, Finja ; Saad, Mohamad ; Sadd, Mohamad ; Bras, Jose M ; Bettella, Francesco ; Nicolaou, Nayia ; Simón-Sánchez, Javier ; Mittag, Florian ; Gibbs, J Raphael ; Schulte, Claudia ; Durr, Alexandra ; Guerreiro, Rita ; Hernandez, Dena ; Brice, Alexis ; Stefánsson, Hreinn ; Majamaa, Kari ; Gasser, Thomas ; Heutink, Peter ; Wood, Nicholas W ; Martinez, Maria ; Singleton, Andrew B ; Nalls, Michael A ; Hardy, John ; Morris, Huw R ; Williams, Nigel M

Human molecular genetics, 2013-03, Vol.22 (5), p.1039-1049 [Periódico revisado por pares]

England: Oxford University Press

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3
Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease
Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease
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Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease

KELLER, 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, J

Human molecular genetics, 2012-11, Vol.21 (22), p.4996-5009 [Periódico revisado por pares]

Oxford: Oxford University Press

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4
Genetic comorbidities in Parkinson's disease
Genetic comorbidities in Parkinson's disease
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Genetic comorbidities in Parkinson's disease

Nalls, Mike A ; Saad, Mohamad ; Noyce, Alastair J ; Keller, Margaux F ; Schrag, Anette ; Bestwick, Jonathan P ; Traynor, Bryan J ; Gibbs, J Raphael ; Hernandez, Dena G ; Cookson, Mark R ; Morris, Huw R ; Williams, Nigel ; Gasser, Thomas ; Heutink, Peter ; Wood, Nick ; Hardy, John ; Martinez, Maria ; Singleton, Andrew B

Human molecular genetics, 2014-02, Vol.23 (3), p.831-841 [Periódico revisado por pares]

England: Oxford University Press

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5
Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21
Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21
Material Type:
Artigo 		Adicionar ao Meu Espaço

Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21

UK Parkinson's Disease Consortium ; Wellcome Trust Case Control Consortium 2 ; Spencer, Chris CA ; 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 NA ; 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 W

Human molecular genetics, 2011, Vol.20 (2), p.345-353 [Periódico revisado por pares]

Oxford University Press (OUP)

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6
Dinucleotide repeat polymorphism at the D9S126 locus (9p21)
Dinucleotide repeat polymorphism at the D9S126 locus (9p21)
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Dinucleotide repeat polymorphism at the D9S126 locus (9p21)

Fountain, Jane W. ; Hudson, Thomas J. ; Engelstein, Marcy ; Housman, David E. ; Dracopoli, Nicholas C.

Human molecular genetics, 1993-06, Vol.2 (6), p.823-823 [Periódico revisado por pares]

Oxford: Oxford University Press

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