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1
Genetics of early onset Parkinson’s disease in Finland: exome sequencing and genome-wide association study
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Genetics of early onset Parkinson’s disease in Finland: exome sequencing and genome-wide association study

Siitonen, A ; Nalls, M.A ; Hernández, D ; Gibbs, J.R ; Ding, J ; Ylikotila, P ; Edsall, C ; Singleton, A ; Majamaa, K

Neurobiology of aging, 2017-05, Vol.53, p.195.e7-195.e10 [Periódico revisado por pares]

United States: Elsevier Inc

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2
Race-specific alterations in DNA methylation among middle-aged African Americans and Whites with metabolic syndrome
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Artigo
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Race-specific alterations in DNA methylation among middle-aged African Americans and Whites with metabolic syndrome

Chitrala, Kumaraswamy Naidu ; Hernandez, Dena G. ; Nalls, Michael A. ; Mode, Nicolle A. ; Zonderman, Alan B. ; Ezike, Ngozi ; Evans, Michele K.

Epigenetics, 2020-05, Vol.15 (5), p.462-482 [Periódico revisado por pares]

United States: Taylor & Francis

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3
Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy
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Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy

Lesage, Suzanne ; Deramecourt, Vincent ; Jacoupy, Maxime ; Hassoun, Sidi Mohamed ; Pujol, Claire ; Maurage, Claude-Alain ; Sahbatou, Mourad ; Liebau, Stefan ; Bilgic, Basar ; Emre, Murat ; Erginel-Unaltuna, Nihan ; Guven, Gamze ; Tison, François ; Tranchant, Christine ; Corvol, Jean-Christophe ; Krack, Paul ; Hernandez, Dena G. ; Gibbs, J. Raphael ; Hardy, John ; Wood, Nicholas W. ; Durr, Alexandra ; Deleuze, Jean-François ; Tazir, Meriem ; Destée, Alain ; Lohmann, Ebba ; Corti, Olga ; Brice, Alexis ; Lesage, Suzanne ; Tison, François ; Vidailhet, Marie ; Corvol, Jean-Christophe ; Agid, Yves ; Anheim, Mathieu ; Bonnet, Anne-Marie ; Borg, Michel ; Broussolle, Emmanuel ; Durif, Franck ; Krack, Paul ; Klebe, Stephan ; Lohmann, Ebba ; Vérin, Marc ; Viallet, François ; Brice, Alexis ; Majounie, Elisa ; Corvol, Jean Christophe ; Ben-Shlomo, Yoav ; Berg, Daniela ; Bhatia, Kailash ; Bochdanovits, Zoltan ; Bonin, Michael ; Bras, Jose M. ; Brockmann, Kathrin ; Burn, David J. ; Chen, Honglei ; Clarke, Carl E. ; Cookson, Mark R. ; Counsell, Carl ; van Dijk, Karin D. ; Dong, Jing ; Escott-Price, Valentina ; Evans, Jonathan R. ; Gray, Emma ; Guerreiro, Rita ; van Hilten, Jacobus J. ; Hollenbeck, Albert ; Holmans, Peter ; Hu, Michèle ; Hudson, Gavin ; Hunt, Sarah E. ; Kilarski, Laura L. ; Jansen, Iris E. ; Langford, Cordelia ; Lees, Andrew ; Lorenz, Delia ; Lubbe, Steven ; Lungu, Codrin ; Martinez, María ; Mätzler, Walter ; McNeill, Alisdair ; Moorby, Catriona ; O’Sullivan, Sean S. ; Pearson, Justin ; Ravina, Bernard ; Rivadeneira, Fernando ; Ryten, Mina ; Schapira, Anthony ; Sharma, Manu ; Sheerin, Una-Marie ; Sidransky, Ellen ; Spencer, Chris C.A. ; Stefánsson, Kári ; Strange, Amy ; Talbot, Kevin ; Trabzuni, Daniah ; Uitterlinden, André G. ; van de Warrenburg, Bart ; Williams-Gray, Caroline H. ; Winder-Rhodes, Sophie ; Hardy, John ; Wood, Nicholas W.

American journal of human genetics, 2016-03, Vol.98 (3), p.500-513 [Periódico revisado por pares]

United States: Elsevier Inc

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4
A genome-wide association study in multiple system atrophy
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A genome-wide association study in multiple system atrophy

Sailer, Anna ; Scholz, Sonja W ; Nalls, Michael A ; Schulte, Claudia ; Federoff, Monica ; Price, T Ryan ; Lees, Andrew ; Ross, Owen A ; Dickson, Dennis W ; Mok, Kin ; Mencacci, Niccolo E ; Schottlaender, Lucia ; Chelban, Viorica ; Ling, Helen ; OʼSullivan, Sean S ; Wood, Nicholas W ; Traynor, Bryan J ; Ferrucci, Luigi ; Federoff, Howard J ; Mhyre, Timothy R ; Morris, Huw R ; Deuschl, Günther ; Quinn, Niall ; Widner, Hakan ; Albanese, Alberto ; Infante, Jon ; Bhatia, Kailash P ; Poewe, Werner ; Oertel, Wolfgang ; Höglinger, Günter U ; Wüllner, Ullrich ; Goldwurm, Stefano ; Pellecchia, Maria Teresa ; Ferreira, Joaquim ; Tolosa, Eduardo ; Bloem, Bastiaan R ; Rascol, Olivier ; Meissner, Wassilios G ; Hardy, John A ; Revesz, Tamas ; Holton, Janice L ; Gasser, Thomas ; Wenning, Gregor K ; Singleton, Andrew B ; Houlden, Henry

Neurology, 2016-10, Vol.87 (15), p.1591-1598 [Periódico revisado por pares]

United States: American Academy of Neurology

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5
Genome-wide analysis of genetic correlation in dementia with Lewy bodies, Parkinson's and Alzheimer's diseases
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Artigo
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Genome-wide analysis of genetic correlation in dementia with Lewy bodies, Parkinson's and Alzheimer's diseases

Guerreiro, Rita ; Escott-Price, Valentina ; Darwent, Lee ; Parkkinen, Laura ; Ansorge, Olaf ; Hernandez, Dena G ; Nalls, Michael A ; Clark, Lorraine ; Honig, Lawrence ; Marder, Karen ; van der Flier, Wiesje ; Holstege, Henne ; Louwersheimer, Eva ; Lemstra, Afina ; Scheltens, Philip ; Rogaeva, Ekaterina ; St George-Hyslop, Peter ; Londos, Elisabet ; Zetterberg, Henrik ; Ortega-Cubero, Sara ; Pastor, Pau ; Ferman, Tanis J ; Graff-Radford, Neill R ; Ross, Owen A ; Barber, Imelda ; Braae, Anne ; Brown, Kristelle ; Morgan, Kevin ; Maetzler, Walter ; Berg, Daniela ; Troakes, Claire ; Al-Sarraj, Safa ; Lashley, Tammaryn ; Compta, Yaroslau ; Revesz, Tamas ; Lees, Andrew ; Cairns, Nigel J ; Halliday, Glenda M ; Mann, David ; Pickering-Brown, Stuart ; Powell, John ; Lunnon, Katie ; Lupton, Michelle K ; Dickson, Dennis ; Hardy, John ; Singleton, Andrew ; Bras, Jose

Neurobiology of aging, 2016-02, Vol.38, p.214.e7-214.e10 [Periódico revisado por pares]

United States: Elsevier Inc

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6
Trans-ethnic Meta-analysis and Functional Annotation Illuminates the Genetic Architecture of Fasting Glucose and Insulin
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Artigo
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Trans-ethnic Meta-analysis and Functional Annotation Illuminates the Genetic Architecture of Fasting Glucose and Insulin

Liu, Ching-Ti ; Raghavan, Sridharan ; Maruthur, Nisa ; Kabagambe, Edmond Kato ; Hong, Jaeyoung ; Hivert, Marie-France ; Lu, Yingchang ; Bentley, Amy R. ; Drolet, Anne M. ; Gaulton, Kyle J. ; Guo, Xiuqing ; Armstrong, Loren L. ; Irvin, Marguerite R. ; Li, Man ; Rybin, Denis V. ; Agyemang, Charles ; Palmer, Nicholette D. ; Cade, Brian E. ; Chen, Wei-Min ; Dauriz, Marco ; Delaney, Joseph A.C. ; Edwards, Todd L. ; Lange, Leslie A. ; Leong, Aaron ; Liu, Jingmin ; Liu, Yongmei ; Nayak, Uma ; Patel, Sanjay R. ; Rasmussen-Torvik, Laura J. ; Snijder, Marieke B. ; Stallings, Sarah C. ; Tanaka, Toshiko ; Yanek, Lisa R. ; Becker, Diane M. ; Bielak, Lawrence F. ; Biggs, Mary L. ; Chen, Guanjie ; Correa, Adolfo ; Couper, David J. ; Crawford, Dana C. ; Cushman, Mary ; Eicher, John D. ; Fornage, Myriam ; Franceschini, Nora ; Fu, Yi-Ping ; Goodarzi, Mark O. ; Gottesman, Omri ; Harris, Tamara B. ; Jensen, Richard A. ; Jhun, Min A. ; Karter, Andrew J. ; Keller, Margaux F. ; Kho, Abel N. ; Kizer, Jorge R. ; Krauss, Ronald M. ; Langefeld, Carl D. ; Li, Xiaohui ; Liang, Jingling ; Liu, Simin ; Lowe, William L. ; Mosley, Thomas H. ; North, Kari E. ; Pacheco, Jennifer A. ; Peyser, Patricia A. ; Patrick, Alan L. ; Rice, Kenneth M. ; Selvin, Elizabeth ; Sims, Mario ; Tajuddin, Salman M. ; Vaidya, Dhananjay ; Wren, Mary P. ; Yao, Jie ; Ziegler, Julie T. ; Zmuda, Joseph M. ; Zonderman, Alan B. ; Zwinderman, Aeilko H. ; Adeyemo, Adebowale ; Boerwinkle, Eric ; Ferrucci, Luigi ; Hayes, M. Geoffrey ; Kardia, Sharon L.R. ; Miljkovic, Iva ; Pankow, James S. ; Rotimi, Charles N. ; Sale, Michele M. ; Wagenknecht, Lynne E. ; Arnett, Donna K. ; Chen, Yii-Der Ida ; Province, Michael A. ; Kao, W.H. Linda ; Siscovick, David S. ; Psaty, Bruce M. ; Wilson, James G. ; Loos, Ruth J.F. ; Dupuis, Josée ; Rich, Stephen S. ; Florez, Jose C. ; Rotter, Jerome I. ; Morris, Andrew P. ; Meigs, James B.

American journal of human genetics, 2016-07, Vol.99 (1), p.56-75 [Periódico revisado por pares]

United States: Elsevier Inc

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7
Genetic risk factors in Finnish patients with Parkinson's disease
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Artigo
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Genetic risk factors in Finnish patients with Parkinson's disease

Ylönen, Susanna ; Siitonen, Ari ; Nalls, Michael A. ; Ylikotila, Pauli ; Autere, Jaana ; Eerola-Rautio, Johanna ; Gibbs, Raphael ; Hiltunen, Mikko ; Tienari, Pentti J. ; Soininen, Hilkka ; Singleton, Andrew B. ; Majamaa, Kari

Parkinsonism & related disorders, 2017-12, Vol.45, p.39-43 [Periódico revisado por pares]

England: Elsevier Ltd

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8
ABCA7 p.G215S as potential protective factor for Alzheimer’s disease
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Artigo
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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
Influence of Coding Variability in APP-Aβ Metabolism Genes in Sporadic Alzheimer's Disease
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Influence of Coding Variability in APP-Aβ Metabolism Genes in Sporadic Alzheimer's Disease

Sassi, Celeste ; Ridge, Perry G ; Nalls, Michael A ; Gibbs, Raphael ; Ding, Jinhui ; Lupton, Michelle K ; Troakes, Claire ; Lunnon, Katie ; Al-Sarraj, Safa ; Brown, Kristelle S ; Medway, Christopher ; Lord, Jenny ; Turton, James ; Morgan, Kevin ; Powell, John F ; Kauwe, John S ; Cruchaga, Carlos ; Bras, Jose ; Goate, Alison M ; Singleton, Andrew B ; Guerreiro, Rita ; Hardy, John Iijima, Koichi M

PloS one, 2016-06, Vol.11 (6), p.e0150079 [Periódico revisado por pares]

United States: Public Library of Science

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10
Detection of genetic loci associated with plasma fetuin-A: a meta-analysis of genome-wide association studies from the CHARGE Consortium
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Artigo
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Detection of genetic loci associated with plasma fetuin-A: a meta-analysis of genome-wide association studies from the CHARGE Consortium

Jensen, Majken K ; Jensen, Richard A ; Mukamal, Kenneth J ; Guo, Xiuqing ; Yao, Jie ; Sun, Qi ; Cornelis, Marilyn ; Liu, Yongmei ; Chen, Ming-Huei ; Kizer, Jorge R ; Djoussé, Luc ; Siscovick, David S ; Psaty, Bruce M ; Zmuda, Joseph M ; Rotter, Jerome I ; Garcia, Melissa ; Harris, Tamara ; Chen, Ida ; Goodarzi, Mark O ; Nalls, Michael A ; Keller, Margaux ; Arnold, Alice M ; Newman, Anne B ; Hoogeveen, Ron C ; Rexrode, Kathryn M ; Rimm, Eric B ; Hu, Frank B ; Ramachandran, Vasan S ; Katz, Ronit ; Pankow, James S ; Ix, Joachim H

Human molecular genetics, 2017-06, Vol.26 (11), p.2156-2163 [Periódico revisado por pares]

England: Oxford University Press

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