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1
Genome-Wide Analysis of the Heritability of Amyotrophic Lateral Sclerosis
Genome-Wide Analysis of the Heritability of Amyotrophic Lateral Sclerosis
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Genome-Wide Analysis of the Heritability of Amyotrophic Lateral Sclerosis

Keller, Margaux F ; Ferrucci, Luigi ; Singleton, Andrew B ; Tienari, Pentti J ; Laaksovirta, Hannu ; Restagno, Gabriella ; Chiò, Adriano ; Traynor, Bryan J ; Nalls, Michael A

JAMA neurology, 2014-09, Vol.71 (9), p.1123-1134 [Periódico revisado por pares]

United States: American Medical Association

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2
Principal-Component Analysis for Assessment of Population Stratification in Mitochondrial Medical Genetics
Principal-Component Analysis for Assessment of Population Stratification in Mitochondrial Medical Genetics
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Principal-Component Analysis for Assessment of Population Stratification in Mitochondrial Medical Genetics

Biffi, Alessandro ; Anderson, Christopher D. ; Nalls, Michael A. ; Rahman, Rosanna ; Sonni, Akshata ; Cortellini, Lynelle ; Rost, Natalia S. ; Matarin, Mar ; Hernandez, Dena G. ; Plourde, Anna ; de Bakker, Paul I.W. ; Ross, Owen A. ; Greenberg, Steven M. ; Furie, Karen L. ; Meschia, James F. ; Singleton, Andrew B. ; Saxena, Richa ; Rosand, Jonathan

American journal of human genetics, 2010-06, Vol.86 (6), p.904-917 [Periódico revisado por pares]

Cambridge, MA: Elsevier Inc

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3
A Genome-wide Association Study of Myasthenia Gravis
A Genome-wide Association Study of Myasthenia Gravis
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A Genome-wide Association Study of Myasthenia Gravis

Renton, Alan E ; Pliner, Hannah A ; Provenzano, Carlo ; Evoli, Amelia ; Ricciardi, Roberta ; Nalls, Michael A ; Marangi, Giuseppe ; Abramzon, Yevgeniya ; Arepalli, Sampath ; Chong, Sean ; Hernandez, Dena G ; Johnson, Janel O ; Bartoccioni, Emanuela ; Scuderi, Flavia ; Maestri, Michelangelo ; Gibbs, J. Raphael ; Errichiello, Edoardo ; Chiò, Adriano ; Restagno, Gabriella ; Sabatelli, Mario ; Macek, Mark ; Scholz, Sonja W ; Corse, Andrea ; Chaudhry, Vinay ; Benatar, Michael ; Barohn, Richard J ; McVey, April ; Pasnoor, Mamatha ; Dimachkie, Mazen M ; Rowin, Julie ; Kissel, John ; Freimer, Miriam ; Kaminski, Henry J ; Sanders, Donald B ; Lipscomb, Bernadette ; Massey, Janice M ; Chopra, Manisha ; Howard, James F ; Koopman, Wilma J ; Nicolle, Michael W ; Pascuzzi, Robert M ; Pestronk, Alan ; Wulf, Charlie ; Florence, Julaine ; Blackmore, Derrick ; Soloway, Aimee ; Siddiqi, Zaeem ; Muppidi, Srikanth ; Wolfe, Gil ; Richman, David ; Mezei, Michelle M ; Jiwa, Theresa ; Oger, Joel ; Drachman, Daniel B ; Traynor, Bryan J

JAMA neurology, 2015-04, Vol.72 (4), p.396-404 [Periódico revisado por pares]

United States: American Medical Association

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4
Association of CR1, CLU and PICALM with Alzheimer's disease in a cohort of clinically characterized and neuropathologically verified individuals
Association of CR1, CLU and PICALM with Alzheimer's disease in a cohort of clinically characterized and neuropathologically verified individuals
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Association of CR1, CLU and PICALM with Alzheimer's disease in a cohort of clinically characterized and neuropathologically verified individuals

Corneveaux, Jason J. ; Myers, Amanda J. ; Allen, April N. ; Pruzin, Jeremy J. ; Ramirez, Manuel ; Engel, Anzhelika ; Nalls, Michael A. ; Chen, Kewei ; Lee, Wendy ; Chewning, Kendria ; Villa, Stephen E. ; Meechoovet, Hunsar B. ; Gerber, Jill D. ; Frost, Danielle ; Benson, Hollie L. ; O'Reilly, Sean ; Chibnik, Lori B. ; Shulman, Joshua M. ; Singleton, Andrew B. ; Craig, David W. ; Van Keuren-Jensen, Kendall R. ; Dunckley, Travis ; Bennett, David A. ; De Jager, Philip L. ; Heward, Christopher ; Hardy, John ; Reiman, Eric M. ; Huentelman, Matthew J.

Human molecular genetics, 2010-08, Vol.19 (16), p.3295-3301 [Periódico revisado por pares]

Oxford: Oxford University Press

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5
Genome-wide association study for serum urate concentrations and gout among African Americans identifies genomic risk loci and a novel URAT1 loss-of-function allele
Genome-wide association study for serum urate concentrations and gout among African Americans identifies genomic risk loci and a novel URAT1 loss-of-function allele
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Genome-wide association study for serum urate concentrations and gout among African Americans identifies genomic risk loci and a novel URAT1 loss-of-function allele

Tin, Adrienne ; Woodward, Owen M ; Kao, Wen Hong Linda ; Liu, Ching-Ti ; Lu, Xiaoning ; Nalls, Michael A ; Shriner, Daniel ; Semmo, Mariam ; Akylbekova, Ermeg L ; Wyatt, Sharon B ; Hwang, Shih-Jen ; Yang, Qiong ; Zonderman, Alan B ; Adeyemo, Adebowale A ; Palmer, Cameron ; Meng, Yan ; Reilly, Muredach ; Shlipak, Michael G ; Siscovick, David ; Evans, Michele K ; Rotimi, Charles N ; Flessner, Michael F ; Köttgen, Michael ; Cupples, L. Adrienne ; Fox, Caroline S ; Köttgen, Anna

Human molecular genetics, 2011-10, Vol.20 (20), p.4056-4068 [Periódico revisado por pares]

Oxford: Oxford University Press

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6
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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7
A meta-analysis and genome-wide association study of platelet count and mean platelet volume in african americans
A meta-analysis and genome-wide association study of platelet count and mean platelet volume in african americans
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A meta-analysis and genome-wide association study of platelet count and mean platelet volume in african americans

Qayyum, Rehan ; Snively, Beverly M ; Ziv, Elad ; Nalls, Michael A ; Liu, Yongmei ; Tang, Weihong ; Yanek, Lisa R ; Lange, Leslie ; Evans, Michele K ; Ganesh, Santhi ; Austin, Melissa A ; Lettre, Guillaume ; Becker, Diane M ; Zonderman, Alan B ; Singleton, Andrew B ; Harris, Tamara B ; Mohler, Emile R ; Logsdon, Benjamin A ; Kooperberg, Charles ; Folsom, Aaron R ; Wilson, James G ; Becker, Lewis C ; Reiner, Alexander P Visscher, Peter M.

PLoS genetics, 2012-03, Vol.8 (3), p.e1002491-e1002491 [Periódico revisado por pares]

United States: Public Library of Science

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8
Analysis of Genome-Wide Association Studies of Alzheimer Disease and of Parkinson Disease to Determine If These 2 Diseases Share a Common Genetic Risk
Analysis of Genome-Wide Association Studies of Alzheimer Disease and of Parkinson Disease to Determine If These 2 Diseases Share a Common Genetic Risk
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Analysis of Genome-Wide Association Studies of Alzheimer Disease and of Parkinson Disease to Determine If These 2 Diseases Share a Common Genetic Risk

Moskvina, Valentina ; Harold, Denise ; Russo, GianCarlo ; Vedernikov, Alexey ; Sharma, Manu ; Saad, Mohamad ; Holmans, Peter ; Bras, Jose M ; Bettella, Francesco ; Keller, Margaux F ; Nicolaou, Nayia ; Simón-Sánchez, Javier ; Gibbs, J. Raphael ; Schulte, Claudia ; Durr, Alexandra ; Guerreiro, Rita ; Hernandez, Dena ; Brice, Alexis ; Stefánsson, Hreinn ; Majamaa, Kari ; Gasser, Thomas ; Heutink, Peter ; Wood, Nick ; Martinez, Maria ; Singleton, Andrew B ; Nalls, Michael A ; Hardy, John ; Owen, Michael J ; O’Donovan, Michael C ; Williams, Julie ; Morris, Huw R ; Williams, Nigel M

JAMA neurology, 2013-10, Vol.70 (10), p.1268-1276 [Periódico revisado por pares]

United States: American Medical Association

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9
Allelic heterogeneity and more detailed analyses of known loci explain additional phenotypic variation and reveal complex patterns of association
Allelic heterogeneity and more detailed analyses of known loci explain additional phenotypic variation and reveal complex patterns of association
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Allelic heterogeneity and more detailed analyses of known loci explain additional phenotypic variation and reveal complex patterns of association

Wood, Andrew R ; Hernandez, Dena G ; Nalls, Michael A ; Yaghootkar, Hanieh ; Gibbs, J. Raphael ; Harries, Lorna W ; Chong, Sean ; Moore, Matthew ; Weedon, Michael N ; Guralnik, Jack M ; Bandinelli, Stefania ; Murray, Anna ; Ferrucci, Luigi ; Singleton, Andrew B ; Melzer, David ; Frayling, Timothy M

Human molecular genetics, 2011-10, Vol.20 (20), p.4082-4092 [Periódico revisado por pares]

Oxford: Oxford University Press

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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
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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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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