Genetics in Parkinson disease: Mendelian versus non‐Mendelian inheritance von Hernandez, Dena G., Reed, Xylena, Singleton, Andrew B.

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Menopause accelerates biological aging von Levine, Morgan E., Lu, Ake T., Chen, Brian H., Hernandez, Dena G., Singleton, Andrew B., Ferrucci, Luigi, Bandinelli, Stefania, Salfati, Elias, Manson, JoAnn E., Quach, Austin, Kusters, Cynthia D. J., Kuh, Diana, Wong, Andrew, Teschendorff, Andrew E., Widschwendter, Martin, Ritz, Beate R., Absher, Devin, Assimes, Themistocles L., Horvath, Steve

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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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DNA Methylation of Lipid-Related Genes Affects Blood Lipid Levels von Pfeiffer, Liliane, Wahl, Simone, Pilling, Luke C, Reischl, Eva, Sandling, Johanna K, Kunze, Sonja, Holdt, Lesca M, Kretschmer, Anja, Schramm, Katharina, Adamski, Jerzy, Klopp, Norman, Illig, Thomas, Hedman, Åsa K, Roden, Michael, Hernandez, Dena G, Singleton, Andrew B, Thasler, Wolfgang E, Grallert, Harald, Gieger, Christian, Herder, Christian, Teupser, Daniel, Meisinger, Christa, Spector, Timothy D, Kronenberg, Florian, Prokisch, Holger, Melzer, David, Peters, Annette, Deloukas, Panos, Ferrucci, Luigi, Waldenberger, Melanie

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Mutations in GBA2 Cause Autosomal-Recessive Cerebellar Ataxia with Spasticity von Hammer, Monia B., Eleuch-Fayache, Ghada, Schottlaender, Lucia V., Nehdi, Houda, Gibbs, J. Raphael, Arepalli, Sampath K., Chong, Sean B., Hernandez, Dena G., Sailer, Anna, Liu, Guoxiang, Mistry, Pramod K., Cai, Huaibin, Shrader, Ginamarie, Sassi, Celeste, Bouhlal, Yosr, Houlden, Henry, Hentati, Fayçal, Amouri, Rim, Singleton, Andrew B.

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Next-generation sequencing reveals substantial genetic contribution to dementia with Lewy bodies von Geiger, Joshua T, Ding, Jinhui, Crain, Barbara, Pletnikova, Olga, Letson, Christopher, Dawson, Ted M, Rosenthal, Liana S, Pantelyat, Alexander, Gibbs, J. Raphael, Albert, Marilyn S, Hernandez, Dena G, Hillis, Argye E, Stone, David J, Singleton, Andrew B, Hardy, John A, Troncoso, Juan C, Scholz, Sonja W

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Exome sequencing reveals riboflavin transporter mutations as a cause of motor neuron disease von JOHNSON, Janel O, RAPHAEL GIBBS, J, REILLY, Mary M, MUNTONI, Francesco, ABRAMZON, Yevgeniya, HOULDEN, Henry, SINGLETON, Andrew B, MEGARBANE, Andre, ANDONI URTIZBEREA, J, HERNANDEZ, Dena G, REGHAN FOLEY, A, AREPALLI, Sampath, PANDRAUD, Amelie, SIMON-SANCHEZ, Javier, CLAYTON, Peter

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SLC25A46 Mutations Associated with Autosomal Recessive Cerebellar Ataxia in North African Families von Hammer, Monia B., Ding, Jinhui, Mochel, Fanny, Eleuch-Fayache, Ghada, Charles, Perrine, Coutelier, Marie, Gibbs, J. Raphael, Arepalli, Sampath K., Chong, Sean B., Hernandez, Dena G., Majounie, Elisa, Clipman, Steven, Bouhlal, Yosr, Nehdi, Houda, Brice, Alexis, Hentati, Faycal, Stevanin, Giovanni, Amouri, Rim, Durr, Alexandra, Singleton, Andrew B.

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Assessment of APOE in atypical parkinsonism syndromes von Sabir, Marya S., Blauwendraat, Cornelis, Ahmed, Sarah, Serrano, Geidy E., Beach, Thomas G., Perkins, Matthew, Rice, Ann C., Masliah, Eliezer, Morris, Christopher M., Pihlstrom, Lasse, Pantelyat, Alexander, Resnick, Susan M., Cookson, Mark R., Hernandez, Dena G., Albert, Marilyn, Dawson, Ted M., Rosenthal, Liana S., Houlden, Henry, Pletnikova, Olga, Troncoso, Juan, Scholz, Sonja W.

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Exome Sequencing Reveals VCP Mutations as a Cause of Familial ALS von Johnson, Janel O., Mandrioli, Jessica, Benatar, Michael, Abramzon, Yevgeniya, Van Deerlin, Vivianna M., Trojanowski, John Q., Gibbs, J. Raphael, Brunetti, Maura, Gronka, Susan, Wuu, Joanne, Ding, Jinhui, McCluskey, Leo, Martinez-Lage, Maria, Falcone, Dana, Hernandez, Dena G., Arepalli, Sampath, Chong, Sean, Schymick, Jennifer C., Rothstein, Jeffrey, Landi, Francesco, Wang, Yong-Dong, Calvo, Andrea, Mora, Gabriele, Sabatelli, Mario, Monsurrò, Maria Rosaria, Battistini, Stefania, Salvi, Fabrizio, Spataro, Rossella, Sola, Patrizia, Borghero, Giuseppe, Galassi, Giuliana, Scholz, Sonja W., Taylor, J. Paul, Restagno, Gabriella, Chiò, Adriano, Traynor, Bryan J.

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High-resolution inference of genetic relationships among Jewish populations von Kopelman, Naama M, Stone, Lewi, Hernandez, Dena G, Gefel, Dov, Singleton, Andrew B, Heyer, Evelyne, Feldman, Marcus W, Hillel, Jossi, Rosenberg, Noah A

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Integration of GWAS SNPs and tissue specific expression profiling reveal discrete eQTLs for human traits in blood and brain von Hernandez, Dena G, Nalls, Mike A, Moore, Matthew, Chong, Sean, Dillman, Allissa, Trabzuni, Daniah, Gibbs, J. Raphael, Ryten, Mina, Arepalli, Sampath, Weale, Michael E, Zonderman, Alan B, Troncoso, Juan, O'Brien, Richard, Walker, Robert, Smith, Colin, Bandinelli, Stefania, Traynor, Bryan J, Hardy, John, Singleton, Andrew B, Cookson, Mark R

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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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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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Genetic risk of Parkinson disease and progression von Iwaki, Hirotaka, Blauwendraat, Cornelis, Leonard, Hampton L, Liu, Ganqiang, Maple-Grødem, Jodi, Corvol, Jean-Christophe, Pihlstrøm, Lasse, van Nimwegen, Marlies, Hutten, Samantha J, Nguyen, Khanh-Dung H, Rick, Jacqueline, Eberly, Shirley, Faghri, Faraz, Auinger, Peggy, Scott, Kirsten M, Wijeyekoon, Ruwani, van Deerlin, Vivianna M, Hernandez, Dena G, Day-Williams, Aaron G, Brice, Alexis, Alves, Guido, Noyce, Alastair J, Tysnes, Ole-Bjørn, Evans, Jonathan R, Breen, David P, Estrada, Karol, Wegel, Claire E, Danjou, Fabrice, Simon, David K, Ravina, Bernard, Toft, Mathias, Heutink, Peter, Bloem, Bastiaan R, Weintraub, Daniel, Barker, Roger A, Williams-Gray, Caroline H, van de Warrenburg, Bart P, van Hilten, Jacobus J, Scherzer, Clemens R, Singleton, Andrew B, Nalls, Mike A

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An exploratory analysis on gene-environment interactions for Parkinson disease von Gao, Jianjun, Nalls, Michael A, Shi, Min, Joubert, Bonnie R, Hernandez, Dena G, Huang, Xuemei, Hollenbeck, Albert, Singleton, Andrew B, Chen, Honglei

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Resolving the polymorphism-in-probe problem is critical for correct interpretation of expression QTL studies von Ramasamy, Adaikalavan, Trabzuni, Daniah, Gibbs, J Raphael, Dillman, Allissa, Hernandez, Dena G, Arepalli, Sampath, Walker, Robert, Smith, Colin, Ilori, Gigaloluwa Peter, Shabalin, Andrey A, Li, Yun, Singleton, Andrew B, Cookson, Mark R, Hardy, John, Ryten, Mina, Weale, Michael E

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Parkinson's disease age at onset genome‐wide association study: Defining heritability, genetic loci, and α‐synuclein mechanisms von Blauwendraat, Cornelis, Heilbron, Karl, Vallerga, Costanza L., Bandres‐Ciga, Sara, von Coelln, Rainer, Pihlstrøm, Lasse, Simón‐Sánchez, Javier, Schulte, Claudia, Sharma, Manu, Krohn, Lynne, Siitonen, Ari, Iwaki, Hirotaka, Leonard, Hampton, Noyce, Alastair J., Tan, Manuela, Gibbs, J. Raphael, Hernandez, Dena G., Scholz, Sonja W., Jankovic, Joseph, Shulman, Lisa M., Lesage, Suzanne, Corvol, Jean‐Christophe, Brice, Alexis, van Hilten, Jacobus J., Marinus, Johan, Eerola‐Rautio, Johanna, Tienari, Pentti, Majamaa, Kari, Toft, Mathias, Grosset, Donald G., Gasser, Thomas, Heutink, Peter, Shulman, Joshua M., Wood, Nicolas, Hardy, John, Morris, Huw R., Hinds, David A., Gratten, Jacob, Visscher, Peter M., Gan‐Or, Ziv, Nalls, Mike A., Singleton, Andrew B.

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Analysis of repeated leukocyte DNA methylation assessments reveals persistent epigenetic alterations after an incident myocardial infarction von Ward-Caviness, Cavin K, Agha, Golareh, Chen, Brian H, Pfeiffer, Liliane, Wilson, Rory, Wolf, Petra, Gieger, Christian, Schwartz, Joel, Vokonas, Pantel S, Hou, Lifang, Just, Allan C, Bandinelli, Stefania, Hernandez, Dena G, Singleton, Andrew B, Prokisch, Holger, Meitinger, Thomas, Kastenmüller, Gabi, Ferrucci, Luigi, Baccarelli, Andrea A, Waldenberger, Melanie, Peters, Annette

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Blood Leukocyte DNA Methylation Predicts Risk of Future Myocardial Infarction and Coronary Heart Disease von Agha, Golareh, Mendelson, Michael M, Ward-Caviness, Cavin K, Joehanes, Roby, Huan, TianXiao, Gondalia, Rahul, Salfati, Elias, Brody, Jennifer A, Fiorito, Giovanni, Bressler, Jan, Chen, Brian H, Ligthart, Symen, Guarrera, Simonetta, Colicino, Elena, Just, Allan C, Wahl, Simone, Gieger, Christian, Vandiver, Amy R, Tanaka, Toshiko, Hernandez, Dena G, Pilling, Luke C, Singleton, Andrew B, Sacerdote, Carlotta, Krogh, Vittorio, Panico, Salvatore, Tumino, Rosario, Li, Yun, Zhang, Guosheng, Stewart, James D, Floyd, James S, Wiggins, Kerri L, Rotter, Jerome I, Multhaup, Michael, Bakulski, Kelly, Horvath, Steven, Tsao, Philip S, Absher, Devin M, Vokonas, Pantel, Hirschhorn, Joel, Fallin, M Daniele, Liu, Chunyu, Bandinelli, Stefania, Boerwinkle, Eric, Dehghan, Abbas, Schwartz, Joel D, Psaty, Bruce M, Feinberg, Andrew P, Hou, Lifang, Ferrucci, Luigi, Sotoodehnia, Nona, Matullo, Giuseppe, Peters, Annette, Fornage, Myriam, Assimes, Themistocles L, Whitsel, Eric A, Levy, Daniel, Baccarelli, Andrea A

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