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Abundant quantitative trait loci exist for DNA methylation and gene expression in human brain
Abundant quantitative trait loci exist for DNA methylation and gene expression in human brain
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Abundant quantitative trait loci exist for DNA methylation and gene expression in human brain

Gibbs, J Raphael ; van der Brug, Marcel P ; Hernandez, Dena G ; Traynor, Bryan J ; Nalls, Michael A ; Lai, Shiao-Lin ; Arepalli, Sampath ; Dillman, Allissa ; Rafferty, Ian P ; Troncoso, Juan ; Johnson, Robert ; Zielke, H Ronald ; Ferrucci, Luigi ; Longo, Dan L ; Cookson, Mark R ; Singleton, Andrew B Flint, Jonathan

PLoS genetics, 2010-05, Vol.6 (5), p.e1000952-e1000952 [Periódico revisado por pares]

United States: Public Library of Science

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2
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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3
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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4
Genetics of early onset Parkinson’s disease in Finland: exome sequencing and genome-wide association study
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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5
Race-specific alterations in DNA methylation among middle-aged African Americans and Whites with metabolic syndrome
Race-specific alterations in DNA methylation among middle-aged African Americans and Whites with metabolic syndrome
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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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6
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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7
Trans-ethnic meta-analysis identifies new loci associated with longitudinal blood pressure traits
Trans-ethnic meta-analysis identifies new loci associated with longitudinal blood pressure traits
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Trans-ethnic meta-analysis identifies new loci associated with longitudinal blood pressure traits

Gouveia, Mateus H ; Bentley, Amy R ; Leonard, Hampton ; Meeks, Karlijn A C ; Ekoru, Kenneth ; Chen, Guanjie ; Nalls, Michael A ; Simonsick, Eleanor M ; Tarazona-Santos, Eduardo ; Lima-Costa, Maria Fernanda ; Adeyemo, Adebowale ; Shriner, Daniel ; Rotimi, Charles N

Scientific reports, 2021-02, Vol.11 (1), p.4075-4075, Article 4075 [Periódico revisado por pares]

England: Nature Publishing Group

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8
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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9
Measures of autozygosity in decline: globalization, urbanization, and its implications for medical genetics
Measures of autozygosity in decline: globalization, urbanization, and its implications for medical genetics
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Measures of autozygosity in decline: globalization, urbanization, and its implications for medical genetics

Nalls, Michael A ; Simon-Sanchez, Javier ; Gibbs, J Raphael ; Paisan-Ruiz, Coro ; Bras, Jose Tomas ; Tanaka, Toshiko ; Matarin, Mar ; Scholz, Sonja ; Weitz, Charles ; Harris, Tamara B ; Ferrucci, Luigi ; Hardy, John ; Singleton, Andrew B Visscher, Peter M.

PLoS genetics, 2009-03, Vol.5 (3), p.e1000415-e1000415 [Periódico revisado por pares]

United States: Public Library of Science

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10
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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