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1
Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study
Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study
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Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study

Laaksovirta, Hannu, MD ; Peuralinna, Terhi, MSc ; Schymick, Jennifer C, PhD ; Scholz, Sonja W, MD ; Lai, Shaoi-Lin, MD ; Myllykangas, Liisa, MD ; Sulkava, Raimo, MD ; Jansson, Lilja ; Hernandez, Dena G, MSc ; Gibbs, J Raphael, BS ; Nalls, Michael A, PhD ; Heckerman, David, MD ; Tienari, Pentti J, MD ; Traynor, Bryan J, Dr

Lancet neurology, 2010-10, Vol.9 (10), p.978-985 [Periódico revisado por pares]

England: Elsevier Ltd

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2
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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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
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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5
Head injury, potential interaction with genes, and risk for Parkinson's disease
Head injury, potential interaction with genes, and risk for Parkinson's disease
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Head injury, potential interaction with genes, and risk for Parkinson's disease

Gao, Jianjun ; Liu, Rui ; Zhao, Edward ; Huang, Xuemei ; Nalls, Michael A ; Singleton, Andrew B ; Chen, Honglei

Parkinsonism & related disorders, 2015-03, Vol.21 (3), p.292-296 [Periódico revisado por pares]

England: Elsevier Ltd

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6
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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7
Mitochondrial DNA sequence associations with dementia and amyloid-β in elderly African Americans
Mitochondrial DNA sequence associations with dementia and amyloid-β in elderly African Americans
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Mitochondrial DNA sequence associations with dementia and amyloid-β in elderly African Americans

Tranah, Gregory J ; Yokoyama, Jennifer S ; Katzman, Shana M ; Nalls, Michael A ; Newman, Anne B ; Harris, Tamara B ; Cesari, Matteo ; Manini, Todd M ; Schork, Nicholas J ; Cummings, Steven R ; Liu, Yongmei ; Yaffe, Kristine

Neurobiology of aging, 2014-02, Vol.35 (2), p.442.e1-442.e8 [Periódico revisado por pares]

United States: Elsevier Inc

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8
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study
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Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study

Majounie, Elisa, PhD ; Renton, Alan E, PhD ; Mok, Kin, MSc ; Dopper, Elise GP ; Waite, Adrian, PhD ; Rollinson, Sara, PhD ; Chiò, Adriano, MD ; Restagno, Gabriella, MD ; Nicolaou, Nayia, MSc ; Simon-Sanchez, Javier, PhD ; van Swieten, John C, Prof ; Abramzon, Yevgeniya ; Johnson, Janel O, PhD ; Sendtner, Michael, Prof ; Pamphlett, Roger, MD ; Orrell, Richard W, MD ; Mead, Simon, MD ; Sidle, Katie C, MD ; Houlden, Henry, Prof ; Rohrer, Jonathan D, MD ; Morrison, Karen E, Prof ; Pall, Hardev, MD ; Talbot, Kevin, Prof ; Ansorge, Olaf, MD ; Hernandez, Dena G, MSc ; Arepalli, Sampath, MS ; Sabatelli, Mario, MD ; Mora, Gabriele, MD ; Corbo, Massimo, MD ; Giannini, Fabio, MD ; Calvo, Andrea, MD ; Englund, Elisabet, MD ; Borghero, Giuseppe, MD ; Floris, Gian Luca, MD ; Remes, Anne M, Prof ; Laaksovirta, Hannu, MD ; McCluskey, Leo, MD ; Trojanowski, John Q, Prof ; Van Deerlin, Vivianna M, MD ; Schellenberg, Gerard D, Prof ; Nalls, Michael A, PhD ; Drory, Vivian E, MD ; Lu, Chin-Song, Prof ; Yeh, Tu-Hsueh, MD ; Ishiura, Hiroyuki, MD ; Takahashi, Yuji, MD ; Tsuji, Shoji, Prof ; Le Ber, Isabelle, MD ; Brice, Alexis, Prof ; Drepper, Carsten, PhD ; Williams, Nigel, PhD ; Kirby, Janine, PhD ; Shaw, Pamela, Prof ; Hardy, John, Prof ; Tienari, Pentti J, MD ; Heutink, Peter, Prof ; Morris, Huw R, MD ; Pickering-Brown, Stuart, Prof ; Traynor, Bryan J, Dr

Lancet neurology, 2012-04, Vol.11 (4), p.323-330 [Periódico revisado por pares]

England: Elsevier Ltd

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9
Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies
Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies
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Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies

Nalls, 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 W

The Lancet (British edition), 2011-02, Vol.377 (9766), p.641-649 [Periódico revisado por pares]

Kidlington: Elsevier Ltd

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10
Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies
Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies
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Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies

Chauhan, Ganesh ; Arnold, Corey R ; Chu, Audrey Y ; Reyahi, Azadeh ; Bis, Joshua C ; Havulinna, Aki S ; Trompet, Stella ; Manichaikul, Ani ; Teumer, Alexander ; Gustafsson, Stefan ; Bartz, Traci M ; Bellenguez, Céline ; Vidal, Jean Sebastien ; Kjartansson, Olafur ; Satizabal, Claudia L ; Xue, Flora ; Liu, Yongmei ; Bevan, Steve ; Hopewell, Jemma C ; Heckbert, Susan R ; Rice, Kenneth ; Smith, Nicholas L ; Levi, Christopher ; Sharma, Pankaj ; Sudlow, Cathie LM ; Cole, John W ; Schmidt, Reinhold ; Meschia, James ; Thijs, Vincent ; Melander, Olle ; Grewal, Raji P ; Sacco, Ralph L ; Rundek, Tatjana ; Rothwell, Peter M ; Jern, Christina ; Johnson, Julie A ; Benavente, Oscar R ; Lee, Jin-Moo ; Wong, Quenna ; Aparicio, Hugo J ; Engelter, Stefan T ; Kloss, Manja ; Pezzini, Alessandro ; Buring, Julie E ; Ridker, Paul M ; Berr, Claudine ; Dartigues, Jean-François ; Hamsten, Anders ; Traylor, Matthew ; Pedersen, Nancy L ; Lannfelt, Lars ; Morris, Andrew P ; Jimenez-Conde, Jordi ; Montaner, Joan ; Slowik, Agnieszka ; Woo, Daniel ; Hofman, Albert ; Koudstaal, Peter J ; Portegies, Marileen L P ; Uitterlinden, André G ; Ford, Ian ; Jukema, J Wouter ; Stott, David J ; Allen, Norrina B ; Johnson, Andrew D ; De Jager, Philip L ; White, Charles C ; Markus, Marcello Ricardo Paulista ; Schminke, Ulf ; Boncoraglio, Giorgio B ; Clarke, Robert ; Kamatani, Yoichiro ; Dallongeville, Jean ; Rotter, Jerome I ; Nalls, Michael A ; Griswold, Michael E ; Knopman, David S ; Windham, B Gwen ; Beiser, Alexa ; Vartiainen, Erkki ; French, Curtis R ; Pastinen, Tomi ; Gudnason, Vilmundur ; Kurth, Tobias ; Harris, Tamara B ; Rich, Stephen S ; deStefano, Anita L ; Rosand, Jonathan ; Mosley, Thomas H ; Ingelsson, Erik ; van Duijn, Cornelia M ; Tzourio, Christophe ; Rexrode, Kathryn M ; Lehmann, Ordan J ; Launer, Lenore J ; Carlsson, Peter ; Chasman, Daniel I ; Childs, Sarah J ; Seshadri, Sudha ; Debette, Stéphanie

Lancet neurology, 2016-06, Vol.15 (7), p.695-707 [Periódico revisado por pares]

England: Elsevier Ltd

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