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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
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
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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4
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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5
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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6
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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7
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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8
A network-based approach to prioritize results from genome-wide association studies
A network-based approach to prioritize results from genome-wide association studies
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A network-based approach to prioritize results from genome-wide association studies

Akula, Nirmala ; Baranova, Ancha ; Seto, Donald ; Solka, Jeffrey ; Nalls, Michael A ; Singleton, Andrew ; Ferrucci, Luigi ; Tanaka, Toshiko ; Bandinelli, Stefania ; Cho, Yoon Shin ; Kim, Young Jin ; Lee, Jong-Young ; Han, Bok-Ghee ; McMahon, Francis J Mailund, Thomas

PloS one, 2011-09, Vol.6 (9), p.e24220-e24220 [Periódico revisado por pares]

United States: Public Library of Science

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9
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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10
Human Obesity Associated with an Intronic SNP in the Brain-Derived Neurotrophic Factor Locus
Human Obesity Associated with an Intronic SNP in the Brain-Derived Neurotrophic Factor Locus
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Human Obesity Associated with an Intronic SNP in the Brain-Derived Neurotrophic Factor Locus

Mou, Zongyang ; Hyde, Thomas M. ; Lipska, Barbara K. ; Martinowich, Keri ; Wei, Peter ; Ong, Chiew-Jen ; Hunter, Lindsay A. ; Palaguachi, Gladys I. ; Morgun, Eva ; Teng, Rujia ; Lai, Chen ; Condarco, Tania A. ; Demidowich, Andrew P. ; Krause, Amanda J. ; Marshall, Leslie J. ; Haack, Karin ; Voruganti, V. Saroja ; Cole, Shelley A. ; Butte, Nancy F. ; Comuzzie, Anthony G. ; Nalls, Michael A. ; Zonderman, Alan B. ; Singleton, Andrew B. ; Evans, Michele K. ; Martin, Bronwen ; Maudsley, Stuart ; Tsao, Jack W. ; Kleinman, Joel E. ; Yanovski, Jack A. ; Han, Joan C.

Cell reports (Cambridge), 2015-11, Vol.13 (6), p.1073-1080 [Periódico revisado por pares]

United States: Elsevier Inc

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