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

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

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A large study reveals no association between APOE and Parkinson's disease von Federoff, Monica, Jimenez-Rolando, Belen, Nalls, Michael A, Singleton, Andrew B

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Race-specific alterations in DNA methylation among middle-aged African Americans and Whites with metabolic syndrome von Chitrala, Kumaraswamy Naidu, Hernandez, Dena G., Nalls, Michael A., Mode, Nicolle A., Zonderman, Alan B., Ezike, Ngozi, Evans, Michele K.

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Genetics of early onset Parkinson’s disease in Finland: exome sequencing and genome-wide association study von Siitonen, A, Nalls, M.A, Hernández, D, Gibbs, J.R, Ding, J, Ylikotila, P, Edsall, C, Singleton, A, Majamaa, K

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Genome-Wide Analysis of the Heritability of Amyotrophic Lateral Sclerosis von Keller, Margaux F, Ferrucci, Luigi, Singleton, Andrew B, Tienari, Pentti J, Laaksovirta, Hannu, Restagno, Gabriella, Chiò, Adriano, Traynor, Bryan J, Nalls, Michael A

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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 i... von 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

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Imputation of Exome Sequence Variants into Population-Based Samples and Blood-Cell-Trait-Associated Loci in African Americans: NHLBI GO Exome Sequencing Project von AUER, Paul L, JOHNSEN, Jill M, RICH, Stephen S, O'DONNELL, Christopher J, JACKSON, Rebecca D, WALLACE, Robert B, ZHAO CHEN, GRAUBERT, Timothy A, WILSON, James G, HUA TANG, LETTRE, Guillaume, REINER, Alex P, JOHNSON, Andrew D, GANESH, Santhi K, YUN LI, LOGSDON, Benjamin A, LANGE, Leslie A, NALLS, Michael A, GUOSHENG ZHANG, FRANCESCHINI, Nora, FOX, Keolu, LANGE, Ethan M

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Reduced physical activity increases intermuscular adipose tissue in healthy young adults von MANINI, Todd M, CLARK, Brian C, NALLS, Michael A, GOODPASTER, Bret H, PLOUTZ-SNYDER, Lori L, HARRIS, Tamara B

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Alterations in Muscle Attenuation following Detraining and Retraining in Resistance-Trained Older Adults von Taaffe, Dennis R., Henwood, Tim R., Nalls, Michael A., Walker, Duncan G., Lang, Thomas F., Harris, Tamara B.

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Trans-ethnic meta-analysis identifies new loci associated with longitudinal blood pressure traits von 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.

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Variation in tau isoform expression in different brain regions and disease states von 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

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Fine-mapping, gene expression and splicing analysis of the disease associated LRRK2 locus von 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

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

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A network-based approach to prioritize results from genome-wide association studies von 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

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Human Obesity Associated with an Intronic SNP in the Brain-Derived Neurotrophic Factor Locus von 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.

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Admixture Mapping of White Cell Count: Genetic Locus Responsible for Lower White Blood Cell Count in the Health ABC and Jackson Heart Studies von Nalls, Michael A., Wilson, James G., Patterson, Nick J., Tandon, Arti, Zmuda, Joseph M., Huntsman, Scott, Garcia, Melissa, Hu, Donglei, Li, Rongling, Beamer, Brock A., Patel, Kushang V., Akylbekova, Ermeg L., Files, Joe C., Hardy, Cheryl L., Buxbaum, Sarah G., Taylor, Herman A., Reich, David, Harris, Tamara B., Ziv, Elad

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NOTCH3 variants and risk of ischemic stroke von 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

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Using genetic variation and environmental risk factor data to identify individuals at high risk for age-related macular degeneration von Spencer, Kylee L, Olson, Lana M, Schnetz-Boutaud, Nathalie, Gallins, Paul, Agarwal, Anita, Iannaccone, Alessandro, Kritchevsky, Stephen B, Garcia, Melissa, Nalls, Michael A, Newman, Anne B, Scott, William K, Pericak-Vance, Margaret A, Haines, Jonathan L

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Genome wide assessment of young onset Parkinson's disease from Finland von Hernandez, Dena G, Nalls, Michael A, Ylikotila, Pauli, Keller, Margaux, Hardy, John A, Majamaa, Kari, Singleton, Andrew B

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