Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy by Lesage, Suzanne, Deramecourt, Vincent, Jacoupy, Maxime, Hassoun, Sidi Mohamed, Pujol, Claire, Maurage, Claude-Alain, Sahbatou, Mourad, Liebau, Stefan, Bilgic, Basar, Emre, Murat, Erginel-Unaltuna, Nihan, Guven, Gamze, Tison, François, Tranchant, Christine, Corvol, Jean-Christophe, Krack, Paul, Hernandez, Dena G., Gibbs, J. Raphael, Hardy, John, Wood, Nicholas W., Durr, Alexandra, Deleuze, Jean-François, Tazir, Meriem, Destée, Alain, Lohmann, Ebba, Corti, Olga, Brice, Alexis, Lesage, Suzanne, Tison, François, Vidailhet, Marie, Corvol, Jean-Christophe, Agid, Yves, Anheim, Mathieu, Bonnet, Anne-Marie, Borg, Michel, Broussolle, Emmanuel, Durif, Franck, Krack, Paul, Klebe, Stephan, Lohmann, Ebba, Vérin, Marc, Viallet, François, Brice, Alexis, Majounie, Elisa, Corvol, Jean Christophe, Ben-Shlomo, Yoav, Berg, Daniela, Bhatia, Kailash, Bochdanovits, Zoltan, Bonin, Michael, Bras, Jose M., Brockmann, Kathrin, Burn, David J., Chen, Honglei, Clarke, Carl E., Cookson, Mark R., Counsell, Carl, van Dijk, Karin D., Dong, Jing, Escott-Price, Valentina, Evans, Jonathan R., Gray, Emma, Guerreiro, Rita, van Hilten, Jacobus J., Hollenbeck, Albert, Holmans, Peter, Hu, Michèle, Hudson, Gavin, Hunt, Sarah E., Kilarski, Laura L., Jansen, Iris E., Langford, Cordelia, Lees, Andrew, Lorenz, Delia, Lubbe, Steven, Lungu, Codrin, Martinez, María, Mätzler, Walter, McNeill, Alisdair, Moorby, Catriona, O’Sullivan, Sean S., Pearson, Justin, Ravina, Bernard, Rivadeneira, Fernando, Ryten, Mina, Schapira, Anthony, Sharma, Manu, Sheerin, Una-Marie, Sidransky, Ellen, Spencer, Chris C.A., Stefánsson, Kári, Strange, Amy, Talbot, Kevin, Trabzuni, Daniah, Uitterlinden, André G., van de Warrenburg, Bart, Williams-Gray, Caroline H., Winder-Rhodes, Sophie, Hardy, John, Wood, Nicholas W.

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Genome‐Wide Association Studies of Cognitive and Motor Progression in Parkinson's Disease by Tan, Manuela M.X., Lawton, Michael A., Jabbari, Edwin, Reynolds, Regina H., Iwaki, Hirotaka, Blauwendraat, Cornelis, Kanavou, Sofia, Pollard, Miriam I., Hubbard, Leon, Malek, Naveed, Grosset, Katherine A., Marrinan, Sarah L., Bajaj, Nin, Barker, Roger A., Burn, David J., Bresner, Catherine, Foltynie, Thomas, Wood, Nicholas W., Williams‐Gray, Caroline H., Hardy, John, Nalls, Michael A., Singleton, Andrew B., Williams, Nigel M., Ben‐Shlomo, Yoav, Hu, Michele T.M., Grosset, Donald G., Shoai, Maryam, Morris, Huw R.

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Mitochondrial DNA variation in human metabolic rate and energy expenditure by Tranah, Gregory J, Manini, Todd M, Lohman, Kurt K, Nalls, Michael A, Kritchevsky, Stephen, Newman, Anne B, Harris, Tamara B, Miljkovic, Iva, Biffi, Alessandro, Cummings, Steven R, Liu, Yongmei

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Evidence for natural antisense transcript-mediated inhibition of microRNA function by Faghihi, Mohammad Ali, Zhang, Ming, Huang, Jia, Modarresi, Farzaneh, Van der Brug, Marcel P, Nalls, Michael A, Cookson, Mark R, St-Laurent, 3rd, Georges, Wahlestedt, Claes

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Cooperative genome-wide analysis shows increased homozygosity in early onset Parkinson's disease by Simón-Sánchez, Javier, Kilarski, Laura L, Nalls, Michael A, Martinez, Maria, Schulte, Claudia, Holmans, Peter, Gasser, Thomas, Hardy, John, Singleton, Andrew B, Wood, Nicholas W, Brice, Alexis, Heutink, Peter, Williams, Nigel, Morris, Huw R

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Distinct DNA methylation changes highly correlated with chronological age in the human brain by HERNANDEZ, Dena G, NALLS, Michael A, SINGLETON, Andrew B, RAPHAEL GIBBS, J, AREPALLI, Sampath, VAN DER BRUG, Marcel, CHONG, Sean, MOORE, Matthew, LONGO, Dan L, COOKSON, Mark R, TRAYNOR, Bryan J

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Principal-Component Analysis for Assessment of Population Stratification in Mitochondrial Medical Genetics by Biffi, Alessandro, Anderson, Christopher D., Nalls, Michael A., Rahman, Rosanna, Sonni, Akshata, Cortellini, Lynelle, Rost, Natalia S., Matarin, Mar, Hernandez, Dena G., Plourde, Anna, de Bakker, Paul I.W., Ross, Owen A., Greenberg, Steven M., Furie, Karen L., Meschia, James F., Singleton, Andrew B., Saxena, Richa, Rosand, Jonathan

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Phosphorylation of LRRK2 by casein kinase 1α regulates trans-Golgi clustering via differential interaction with ARHGEF7 by Chia, Ruth, Haddock, Sara, Beilina, Alexandra, Rudenko, Iakov N., Mamais, Adamantios, Kaganovich, Alice, Li, Yan, Kumaran, Ravindran, Nalls, Michael A., Cookson, Mark R.

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Genomic risk profiling of ischemic stroke: results of an international genome-wide association meta-analysis by Meschia, James F, Singleton, Andrew, Nalls, Michael A, Rich, Stephen S, Sharma, Pankaj, Ferrucci, Luigi, Matarin, Mar, Hernandez, Dena G, Pearce, Kerra, Brott, Thomas G, Brown, Jr, Robert D, Hardy, John, Worrall, Bradford B

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Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodies by Bras, Jose, Guerreiro, Rita, Darwent, Lee, Parkkinen, Laura, Ansorge, Olaf, Escott-Price, Valentina, Hernandez, Dena G, Nalls, Michael A, Clark, Lorraine N, Honig, Lawrence S, Marder, Karen, Van Der Flier, Wiesje M, Lemstra, Afina, Scheltens, Philip, Rogaeva, Ekaterina, St George-Hyslop, Peter, Londos, Elisabet, Zetterberg, Henrik, Ortega-Cubero, Sara, Pastor, Pau, Ferman, Tanis J, Graff-Radford, Neill R, Ross, Owen A, Barber, Imelda, Braae, Anne, Brown, Kristelle, Morgan, Kevin, Maetzler, Walter, Berg, Daniela, Troakes, Claire, Al-Sarraj, Safa, Lashley, Tammaryn, Compta, Yaroslau, Revesz, Tamas, Lees, Andrew, Cairns, Nigel, Halliday, Glenda M, Mann, David, Pickering-Brown, Stuart, Dickson, Dennis W, Singleton, Andrew, Hardy, John

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Genome-wide analysis of genetic correlation in dementia with Lewy bodies, Parkinson's and Alzheimer's diseases by Guerreiro, Rita, Escott-Price, Valentina, Darwent, Lee, Parkkinen, Laura, Ansorge, Olaf, Hernandez, Dena G, Nalls, Michael A, Clark, Lorraine, Honig, Lawrence, Marder, Karen, van der Flier, Wiesje, Holstege, Henne, Louwersheimer, Eva, Lemstra, Afina, Scheltens, Philip, Rogaeva, Ekaterina, St George-Hyslop, Peter, Londos, Elisabet, Zetterberg, Henrik, Ortega-Cubero, Sara, Pastor, Pau, Ferman, Tanis J, Graff-Radford, Neill R, Ross, Owen A, Barber, Imelda, Braae, Anne, Brown, Kristelle, Morgan, Kevin, Maetzler, Walter, Berg, Daniela, Troakes, Claire, Al-Sarraj, Safa, Lashley, Tammaryn, Compta, Yaroslau, Revesz, Tamas, Lees, Andrew, Cairns, Nigel J, Halliday, Glenda M, Mann, David, Pickering-Brown, Stuart, Powell, John, Lunnon, Katie, Lupton, Michelle K, Dickson, Dennis, Hardy, John, Singleton, Andrew, Bras, Jose

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Genome-wide Association Analysis of Blood-Pressure Traits in African-Ancestry Individuals Reveals Common Associated Genes in African and Non-African Populations by Fox, Ervin, Edwards, Todd L., Nalls, Michael A., Tayo, Bamidele O., Adeyemo, Adebawole, Young, J. Hunter, Duan, Qing, Chen, Fang, Li, Yun, Fornage, Myriam, Keene, Keith L., Andrews, Jeanette S., Smith, Jennifer A., Faul, Jessica D., Liu, Yu, Murray, Sarah S., Musani, Solomon K., Srinivasan, Sathanur, Velez Edwards, Digna R., Wang, Heming, Bovet, Pascal, Bochud, Murielle, Broeckel, Ulrich, Burnier, Michel, Chasman, Daniel I., Ehret, Georg, Chen, Wei-Min, Chen, Wei, Dreisbach, Albert W., Evans, Michele K., Guo, Xiuqing, Garcia, Melissa E., Jensen, Rich, Lettre, Guillaume, Lotay, Vaneet, Martin, Lisa W., Moore, Jason H., Morrison, Alanna C., Mosley, Thomas H., Penman, Alan, Polak, Joseph F., Ridker, Paul M., Salako, Babatunde, Singleton, Andrew B., Shriner, Daniel, Taylor, Kent D., Wiggins, Kerri, Williams, Scott M., Yanek, Lisa R., Zonderman, Alan B., Becker, Diane M., Berenson, Gerald, Boerwinkle, Eric, Bottinger, Erwin, Nyberg, Fredrik, Heiss, Gerardo, Howard, Virginia J., Liu, Kiang, Liu, Yongmei, Loos, Ruth, Snyder, Michael, Go, Min Jin, Kim, Young Jin, Lee, Jong-Young, Jeon, Jae-Pil, Han, Bok-Ghee, Cho, Yoon Shin, Tay, Wan Ting, Ong, Rick Twee Hee, Seielstad, Mark, Aung, Tin, Wong, Tien Yin, Tai, E. Shyong, Chang, Li-ching, Wu, Jer-Yuarn, Kelly, Tanika N., Hixson, James E., Sung, Yun Ju, Kato, Norihiro, Takeuchi, Fumihiko, Sugiyama, Takao, Zhang, Yi, Huang, Wei, Zhou, Xueya, Jin, Li, Zhu, Dingliang, Schork, Nicholas J., Weir, David R., Harris, Tamara, Hunt, Steven C., Arnett, Donna, Redline, Susan, Cooper, Richard S., Risch, Neil J., Rotter, Jerome I., Chakravarti, Aravinda, Reiner, Alex P., Levy, Daniel, Keating, Brendan J., Zhu, Xiaofeng

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Genetic analysis of amyotrophic lateral sclerosis identifies contributing pathways and cell types by Saez-Atienzar, Sara, Bandres-Ciga, Sara, Langston, Rebekah G, Kim, Jonggeol J, Choi, Shing Wan, Reynolds, Regina H, Abramzon, Yevgeniya, Dewan, Ramita, Ahmed, Sarah, Landers, John E, Chia, Ruth, Ryten, Mina, Cookson, Mark R, Nalls, Michael A, Chiò, Adriano, Traynor, Bryan J

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Reduced neutrophil count in people of African descent is due to a regulatory variant in the Duffy antigen receptor for chemokines gene by Reich, David, Nalls, Michael A, Kao, W H Linda, Akylbekova, Ermeg L, Tandon, Arti, Patterson, Nick, Mullikin, James, Hsueh, Wen-Chi, Cheng, Ching-Yu, Coresh, Josef, Boerwinkle, Eric, Li, Man, Waliszewska, Alicja, Neubauer, Julie, Li, Rongling, Leak, Tennille S, Ekunwe, Lynette, Files, Joe C, Hardy, Cheryl L, Zmuda, Joseph M, Taylor, Herman A, Ziv, Elad, Harris, Tamara B, Wilson, James G

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Association of CR1, CLU and PICALM with Alzheimer's disease in a cohort of clinically characterized and neuropathologically verified individuals by Corneveaux, Jason J., Myers, Amanda J., Allen, April N., Pruzin, Jeremy J., Ramirez, Manuel, Engel, Anzhelika, Nalls, Michael A., Chen, Kewei, Lee, Wendy, Chewning, Kendria, Villa, Stephen E., Meechoovet, Hunsar B., Gerber, Jill D., Frost, Danielle, Benson, Hollie L., O'Reilly, Sean, Chibnik, Lori B., Shulman, Joshua M., Singleton, Andrew B., Craig, David W., Van Keuren-Jensen, Kendall R., Dunckley, Travis, Bennett, David A., De Jager, Philip L., Heward, Christopher, Hardy, John, Reiman, Eric M., Huentelman, Matthew J.

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Molecular genetic overlap in bipolar disorder, schizophrenia, and major depressive disorder by Schulze, Thomas G., Akula, Nirmala, Breuer, René, Steele, Jo, Nalls, Michael A., Singleton, Andrew B., Degenhardt, Franziska A., Nöthen, Markus M., Cichon, Sven, Rietschel, Marcella, Mcmahon, Francis J.

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A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease by Holmans, Peter, Moskvina, Valentina, Jones, Lesley, Sharma, Manu, Vedernikov, Alexey, Buchel, Finja, Saad, Mohamad, Sadd, Mohamad, Bras, Jose M, Bettella, Francesco, Nicolaou, Nayia, Simón-Sánchez, Javier, Mittag, Florian, Gibbs, J Raphael, Schulte, Claudia, Durr, Alexandra, Guerreiro, Rita, Hernandez, Dena, Brice, Alexis, Stefánsson, Hreinn, Majamaa, Kari, Gasser, Thomas, Heutink, Peter, Wood, Nicholas W, Martinez, Maria, Singleton, Andrew B, Nalls, Michael A, Hardy, John, Morris, Huw R, Williams, Nigel M

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ABCA7 p.G215S as potential protective factor for Alzheimer’s disease by Sassi, C, Nalls, M.A, Ridge, P.G, Gibbs, R, Ding, J, Lupton, M.K, Troakes, C, Lunnon, K, Al-Sarraj, S, Brown, K.S, Medway, C, Clement, N, Lord, J, Turton, J, Bras, J, Almeida, M.R, Holstege, H, Louwersheimer, E, van der Flier, W, Scheltens, P, Van Swieten, J.C, Santana, I, Oliveira, C, Morgan, K, Powell, J.F, Kauwe, J.S, Cruchaga, C, Goate, A.M, Singleton, A.B, Guerreiro, R, Hardy, J

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Genetic risk factors in Finnish patients with Parkinson's disease by Ylönen, Susanna, Siitonen, Ari, Nalls, Michael A., Ylikotila, Pauli, Autere, Jaana, Eerola-Rautio, Johanna, Gibbs, Raphael, Hiltunen, Mikko, Tienari, Pentti J., Soininen, Hilkka, Singleton, Andrew B., Majamaa, Kari

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The chromosome 9 ALS and FTD locus is probably derived from a single founder by Mok, Kin, Traynor, Bryan J, Schymick, Jennifer, Tienari, Pentti J, Laaksovirta, Hannu, Peuralinna, Terhi, Myllykangas, Liisa, Chiò, Adriano, Shatunov, Aleksey, Boeve, Bradley F, Boxer, Adam L, DeJesus-Hernandez, Mariely, Mackenzie, Ian R, Waite, Adrian, Williams, Nigel, Morris, Huw R, Simón-Sánchez, Javier, van Swieten, John C, Heutink, Peter, Restagno, Gabriella, Mora, Gabriele, Morrison, Karen E, Shaw, Pamela J, Rollinson, Pamela Sara, Al-Chalabi, Ammar, Rademakers, Rosa, Pickering-Brown, Stuart, Orrell, Richard W, Nalls, Michael A, Hardy, John

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