Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease von Nalls, Mike A, Pankratz, Nathan, Lill, Christina M, Do, Chuong B, Hernandez, Dena G, Saad, Mohamad, DeStefano, Anita L, Kara, Eleanna, Bras, Jose, Sharma, Manu, Schulte, Claudia, Keller, Margaux F, Arepalli, Sampath, Letson, Christopher, Edsall, Connor, Stefansson, Hreinn, Liu, Xinmin, Pliner, Hannah, Lee, Joseph H, Cheng, Rong, Ikram, M Arfan, Ioannidis, John P A, Hadjigeorgiou, Georgios M, Bis, Joshua C, Martinez, Maria, Perlmutter, Joel S, Goate, Alison, Marder, Karen, Fiske, Brian, Sutherland, Margaret, Xiromerisiou, Georgia, Myers, Richard H, Clark, Lorraine N, Stefansson, Kari, Hardy, John A, Heutink, Peter, Chen, Honglei, Wood, Nicholas W, Houlden, Henry, Payami, Haydeh, Brice, Alexis, Scott, William K, Gasser, Thomas, Bertram, Lars, Eriksson, Nicholas, Foroud, Tatiana, Singleton, Andrew B

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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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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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MAPT expression and splicing is differentially regulated by brain region: relation to genotype and implication for tauopathies von TRABZUNI, Daniah, WRAY, Selina, AREPALLI, Sampath, SINGLETON, Andrew B, COOKSON, Mark R, PITTMAN, Alan M, DE SILVA, Rohan, WEALE, Michael E, HARDY, John, RYTEN, Mina, VANDROVCOVA, Jana, RAMASAMY, Adaikalavan, WALKER, Robert, SMITH, Colin, LUK, Connie, RAPHAEL GIBBS, J, DILLMAN, Allissa, HERNANDEZ, Dena G

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Epigenetic signature of human immune aging in the GESTALT study von Roy, Roshni, Kuo, Pei-Lun, Candia, Julián, Sarantopoulou, Dimitra, Ubaida-Mohien, Ceereena, Hernandez, Dena, Kaileh, Mary, Arepalli, Sampath, Singh, Amit, Bektas, Arsun, Kim, Jaekwan, Moore, Ann Z, Tanaka, Toshiko, McKelvey, Julia, Zukley, Linda, Nguyen, Cuong, Wallace, Tonya, Dunn, Christopher, Wood, William, Piao, Yulan, Coletta, Christopher, De, Supriyo, Sen, Jyoti, Weng, Nan-ping, Sen, Ranjan, Ferrucci, Luigi

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A genome-wide association study identifies protein quantitative trait loci (pQTLs) von Melzer, David, Perry, John R B, Hernandez, Dena, Corsi, Anna-Maria, Stevens, Kara, Rafferty, Ian, Lauretani, Fulvio, Murray, Anna, Gibbs, J Raphael, Paolisso, Giuseppe, Rafiq, Sajjad, Simon-Sanchez, Javier, Lango, Hana, Scholz, Sonja, Weedon, Michael N, Arepalli, Sampath, Rice, Neil, Washecka, Nicole, Hurst, Alison, Britton, Angela, Henley, William, van de Leemput, Joyce, Li, Rongling, Newman, Anne B, Tranah, Greg, Harris, Tamara, Panicker, Vijay, Dayan, Colin, Bennett, Amanda, McCarthy, Mark I, Ruokonen, Aimo, Jarvelin, Marjo-Riitta, Guralnik, Jack, Bandinelli, Stefania, Frayling, Timothy M, Singleton, Andrew, Ferrucci, Luigi

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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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Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data von Schymick, Jennifer C, BS, Scholz, Sonja W, MD, Fung, Hon-Chung, MD, Britton, Angela, MS, Arepalli, Sampath, MS, Gibbs, J Raphael, BS, Lombardo, Federica, PhD, Matarin, Mar, PhD, Kasperaviciute, Dalia, PhD, Hernandez, Dena G, MSc, Crews, Cynthia, Bruijn, Lucie, PhD, Rothstein, Jeffrey, MD, Mora, Gabriele, MD, Restagno, Gabriella, MD, Chiò, Adriano, MD, Singleton, Andrew, PhD, Hardy, John, PhD, Traynor, Bryan J, MD

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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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Genome-wide association study confirms extant PD risk loci among the Dutch von SIMON-SANCHEZ, Javier, VAN HILTEN, Jacobus J, BLOEM, Bas, VAN DIJK, Karin D, RIVADENEIRA, Fernando, HOFMAN, Albert, UITTERLINDEN, André G, RIZZU, Patrizia, BOCHDANOVITS, Zoltan, SINGLETON, Andrew B, HEUTINK, Peter, VAN DE WARRENBURG, Bart, POST, Bart, BERENDSE, Henk W, AREPALLI, Sampath, HERNANDEZ, Dena G, DE BIE, Rob Ma, VELSEBOER, Daan, SCHEFFER, Hans

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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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Canine hereditary ataxia in old english sheepdogs and gordon setters is associated with a defect in the autophagy gene encoding RAB24 von Agler, Caryline, Nielsen, Dahlia M, Urkasemsin, Ganokon, Singleton, Andrew, Tonomura, Noriko, Sigurdsson, Snaevar, Tang, Ruqi, Linder, Keith, Arepalli, Sampath, Hernandez, Dena, Lindblad-Toh, Kerstin, van de Leemput, Joyce, Motsinger-Reif, Alison, O'Brien, Dennis P, Bell, Jerold, Harris, Tonya, Steinberg, Steven, Olby, Natasha J

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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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Assessment of nickel oxide substituted bioactive glass-ceramic on in vitro bioactivity and mechanical properties von Vyas, Vikash Kumar, Kumar, Arepalli Sampath, Ali, Akher, Prasad, Sunil, Srivastava, Pradeep, Mallick, Sarada Prasanna, Ershad, Md, Singh, Saryoo Prasad, Pyare, Ram

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Structural characterization and in vitro bioactivity assessment of SiO2–CaO–P2O5–K2O–Al2O3 glass as bioactive ceramic material von Tripathi, Himanshu, Kumar Hira, Sumit, Sampath Kumar, Arepalli, Gupta, Uttam, Pratim Manna, Partha, Singh, S.P.

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Kinesin-associated protein 3 (KIFAP3) has no effect on survival in a population-based cohort of ALS patients von Traynor, Bryan J., Nalls, Michael, Lai, Shiao-Lin, Gibbs, Raphael J., Schymick, Jennifer C., Arepalli, Sampath, Hernandez, Dena, van der Brug, Marcel P., Johnson, Janel O., Dillman, Allissa, Cookson, Mark, Moglia, Cristina, Calvo, Andrea, Restagno, Gabriella, Mora, Gabriele, Chiò, Adriano, Cleveland, Don W.

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The transcriptional landscape of age in human peripheral blood von Peters, Marjolein J., Joehanes, Roby, Pilling, Luke C., Schurmann, Claudia, Conneely, Karen N., Powell, Joseph, Reinmaa, Eva, Sutphin, George L., Zhernakova, Alexandra, Schramm, Katharina, Wilson, Yana A., Kobes, Sayuko, Ramos, Yolande F., Göring, Harald H. H., Fornage, Myriam, Liu, Yongmei, Gharib, Sina A., Stranger, Barbara E., Aviv, Abraham, Levy, Daniel, Murabito, Joanne M., Munson, Peter J., Huan, Tianxiao, Hofman, Albert, Uitterlinden, André G., Rivadeneira, Fernando, van Rooij, Jeroen, Stolk, Lisette, Broer, Linda, Verbiest, Michael M. P. J., Jhamai, Mila, Arp, Pascal, Metspalu, Andres, Milani, Lili, Kasela, Silva, Codd, Veryan, Peters, Annette, Herder, Christian, Waldenberger, Melanie, Roden, Michael, Zeilinger, Sonja, Illig, Thomas, Homuth, Georg, Grabe, Hans-Jörgen, Völzke, Henry, Steil, Leif, Kocher, Thomas, Murray, Anna, Melzer, David, Yaghootkar, Hanieh, Bandinelli, Stefania, Moses, Eric K., Kent, Jack W., Williams-Blangero, Sarah, Westra, Harm-Jan, McRae, Allan F., Smith, Jennifer A., Kardia, Sharon L. R., Hovatta, Iiris, Perola, Markus, Salomaa, Veikko, Henders, Anjali K., Martin, Nicholas G., Smith, Alicia K., Mehta, Divya, Binder, Elisabeth B., Nylocks, K Maria, Kennedy, Elizabeth M., Ding, Jingzhong, Suchy-Dicey, Astrid M., Enquobahrie, Daniel A., Brody, Jennifer, Rotter, Jerome I., Chen, Yii-Der I., Houwing-Duistermaat, Jeanine, Kloppenburg, Margreet, Slagboom, P. Eline, Helmer, Quinta, den Hollander, Wouter, Bean, Shannon, Raj, Towfique, Wang, Qiao Ping, Oyston, Lisa J., Tracy, Russell P., Montgomery, Grant W., Turner, Stephen T., Blangero, John, Meulenbelt, Ingrid, Ressler, Kerry J., Franke, Lude, Kettunen, Johannes, Visscher, Peter M., Neely, G. Gregory, Korstanje, Ron, Hanson, Robert L., Prokisch, Holger, Esko, Tonu, Teumer, Alexander, van Meurs, Joyce B. J., Johnson, Andrew D.

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Genetic variability in the regulation of gene expression in ten regions of the human brain von Ramasamy, Adaikalavan, Trabzuni, Daniah, Guelfi, Sebastian, Varghese, Vibin, Smith, Colin, Walker, Robert, De, Tisham, Coin, Lachlan, de Silva, Rohan, Cookson, Mark R, Singleton, Andrew B, Hardy, John, Ryten, Mina, Weale, Michael E

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Synthesis and characterization of barium-doped bioactive glass with potential anti-inflammatory activity von Majumdar, Shreyasi, Hira, Sumit Kumar, Tripathi, Himanshu, Kumar, Arepalli Sampath, Manna, Partha Pratim, Singh, S.P., Krishnamurthy, Sairam

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Widespread sex differences in gene expression and splicing in the adult human brain von Trabzuni, Daniah, Ramasamy, Adaikalavan, Imran, Sabaena, Walker, Robert, Smith, Colin, Weale, Michael E., Hardy, John, Ryten, Mina

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