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1
Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation
Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation
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Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation

Wood, Andrew R ; Perry, John R B ; Tanaka, Toshiko ; Hernandez, Dena G ; Zheng, Hou-Feng ; Melzer, David ; Gibbs, J Raphael ; Nalls, Michael A ; Weedon, Michael N ; Spector, Tim D ; Richards, J Brent ; Bandinelli, Stefania ; Ferrucci, Luigi ; Singleton, Andrew B ; Frayling, Timothy M Arking, Dan E.

PloS one, 2013-05, Vol.8 (5), p.e64343-e64343 [Periódico revisado por pares]

United States: Public Library of Science

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2
Fine-mapping, gene expression and splicing analysis of the disease associated LRRK2 locus
Fine-mapping, gene expression and splicing analysis of the disease associated LRRK2 locus
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Fine-mapping, gene expression and splicing analysis of the disease associated LRRK2 locus

Trabzuni, Daniah ; Ryten, Mina ; Emmett, Warren ; Ramasamy, Adaikalavan ; Lackner, Karl J ; Zeller, Tanja ; Walker, Robert ; Smith, Colin ; Lewis, Patrick A ; Mamais, Adamantios ; de Silva, Rohan ; Vandrovcova, Jana ; Hernandez, Dena ; Nalls, Michael A ; Sharma, Manu ; Garnier, Sophie ; Lesage, Suzanne ; Simon-Sanchez, Javier ; Gasser, Thomas ; Heutink, Peter ; Brice, Alexis ; Singleton, Andrew ; Cai, Huaibin ; Schadt, Eric ; Wood, Nicholas W ; Bandopadhyay, Rina ; Weale, Michael E ; Hardy, John ; Plagnol, Vincent Dawson, Ted M.

PloS one, 2013-08, Vol.8 (8), p.e70724-e70724 [Periódico revisado por pares]

United States: Public Library of Science

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3
NOTCH3 variants and risk of ischemic stroke
NOTCH3 variants and risk of ischemic stroke
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NOTCH3 variants and risk of ischemic stroke

Ross, Owen A ; Soto-Ortolaza, Alexandra I ; Heckman, Michael G ; Verbeeck, Christophe ; Serie, Daniel J ; Rayaprolu, Sruti ; Rich, Stephen S ; Nalls, Michael A ; Singleton, Andrew ; Guerreiro, Rita ; Kinsella, Emma ; Wszolek, Zbigniew K ; Brott, Thomas G ; Brown, Jr, Robert D ; Worrall, Bradford B ; Meschia, James F Wider, Christian

PloS one, 2013-09, Vol.8 (9), p.e75035-e75035 [Periódico revisado por pares]

United States: Public Library of Science

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4
Genetic variability in CLU and its association with Alzheimer's disease
Genetic variability in CLU and its association with Alzheimer's disease
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Genetic variability in CLU and its association with Alzheimer's disease

Guerreiro, 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 Nicholas

PloS one, 2010-03, Vol.5 (3), p.e9510-e9510 [Periódico revisado por pares]

United States: Public Library of Science

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