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A large study reveals no association between APOE and Parkinson's disease
A large study reveals no association between APOE and Parkinson's disease
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A large study reveals no association between APOE and Parkinson's disease

Federoff, Monica ; Jimenez-Rolando, Belen ; Nalls, Michael A ; Singleton, Andrew B

Neurobiology of disease, 2012-05, Vol.46 (2), p.389-392 [Periódico revisado por pares]

United States: Elsevier Inc

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2
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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3
Variation in tau isoform expression in different brain regions and disease states
Variation in tau isoform expression in different brain regions and disease states
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Variation in tau isoform expression in different brain regions and disease states

Majounie, Elisa ; Cross, William ; Newsway, Victoria ; Dillman, Allissa ; Vandrovcova, Jana ; Morris, Christopher M ; Nalls, Michael A ; Ferrucci, Luigi ; Owen, Michael J ; O'Donovan, Michael C ; Cookson, Mark R ; Singleton, Andrew B ; de Silva, Rohan ; Morris, Huw R

Neurobiology of aging, 2013-07, Vol.34 (7), p.1922.e7-1922.e12 [Periódico revisado por pares]

United States: Elsevier Inc

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4
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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5
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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6
Cooperative genome-wide analysis shows increased homozygosity in early onset Parkinson's disease
Cooperative genome-wide analysis shows increased homozygosity in early onset Parkinson's disease
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Cooperative genome-wide analysis shows increased homozygosity in early onset Parkinson's disease

Simón-Sánchez, Javier ; Kilarski, Laura L ; Nalls, Michael A ; Martinez, Maria ; Schulte, Claudia ; Holmans, Peter ; Gasser, Thomas ; Hardy, John ; Singleton, Andrew B ; Wood, Nicholas W ; Brice, Alexis ; Heutink, Peter ; Williams, Nigel ; Morris, Huw R Lewin, Alfred

PloS one, 2012-03, Vol.7 (3), p.e28787-e28787 [Periódico revisado por pares]

United States: Public Library of Science

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7
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis
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Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis

Johnson, Janel O ; Pioro, Erik P ; Boehringer, Ashley ; Chia, Ruth ; Feit, Howard ; Renton, Alan E ; Pliner, Hannah A ; Abramzon, Yevgeniya ; Marangi, Giuseppe ; Winborn, Brett J ; Gibbs, J Raphael ; Nalls, Michael A ; Morgan, Sarah ; Shoai, Maryam ; Hardy, John ; Pittman, Alan ; Orrell, Richard W ; Malaspina, Andrea ; Sidle, Katie C ; Fratta, Pietro ; Harms, Matthew B ; Baloh, Robert H ; Pestronk, Alan ; Weihl, Conrad C ; Rogaeva, Ekaterina ; Zinman, Lorne ; Drory, Vivian E ; Borghero, Giuseppe ; Mora, Gabriele ; Calvo, Andrea ; Rothstein, Jeffrey D ; Drepper, Carsten ; Sendtner, Michael ; Singleton, Andrew B ; Taylor, J Paul ; Cookson, Mark R ; Restagno, Gabriella ; Sabatelli, Mario ; Bowser, Robert ; Chiò, Adriano ; Traynor, Bryan J

Nature neuroscience, 2014-05, Vol.17 (5), p.664-666 [Periódico revisado por pares]

United States: Nature Publishing Group

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8
ABCA7 p.G215S as potential protective factor for Alzheimer’s disease
ABCA7 p.G215S as potential protective factor for Alzheimer’s disease
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ABCA7 p.G215S as potential protective factor for Alzheimer’s disease

Sassi, 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, J

Neurobiology of aging, 2016-10, Vol.46, p.235.e1-235.e9 [Periódico revisado por pares]

United States: Elsevier Inc

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9
An exploratory analysis on gene-environment interactions for Parkinson disease
An exploratory analysis on gene-environment interactions for Parkinson disease
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An exploratory analysis on gene-environment interactions for Parkinson disease

Gao, Jianjun ; Nalls, Michael A ; Shi, Min ; Joubert, Bonnie R ; Hernandez, Dena G ; Huang, Xuemei ; Hollenbeck, Albert ; Singleton, Andrew B ; Chen, Honglei

Neurobiology of aging, 2012-10, Vol.33 (10), p.2528.e1-2528.e6 [Periódico revisado por pares]

United States: Elsevier Inc

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10
Genetic variability in the regulation of gene expression in ten regions of the human brain
Genetic variability in the regulation of gene expression in ten regions of the human brain
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Genetic variability in the regulation of gene expression in ten regions of the human brain

Ramasamy, Adaikalavan ; Trabzuni, Daniah ; Guelfi, Sebastian ; Varghese, Vibin ; Smith, Colin ; Walker, Robert ; De, Tisham ; Coin, Lachlan ; de Silva, Rohan ; Cookson, Mark R ; Singleton, Andrew B ; Hardy, John ; Ryten, Mina ; Weale, Michael E

Nature neuroscience, 2014-10, Vol.17 (10), p.1418-1428 [Periódico revisado por pares]

United States: Nature Publishing Group

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