Reduced serum lipoprotein(a) levels in patients with primary biliary cirrhosis von Gregory, Wendy L., Game, Frances L., Farrer, Martin, Idle, Jeffrey R., Laker, Michael F., James, Oliver F.W.

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Genomic and Molecular Identification of Genes Contributing to the Caspofungin Paradoxical Effect in Aspergillus fumigatus von Zhao, Shu, Martin-Vicente, Adela, Colabardini, Ana Cristina, Pereira Silva, Lilian, Rinker, David C, Fortwendel, Jarrod R, Goldman, Gustavo Henrique, Gibbons, John G

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Caspase-8, association with Alzheimer's Disease and functional analysis of rare variants von Rehker, Jan, Rodhe, Johanna, Nesbitt, Ryan R, Boyle, Evan A, Martin, Beth K, Lord, Jenny, Karaca, Ilker, Naj, Adam, Jessen, Frank, Helisalmi, Seppo, Soininen, Hilkka, Hiltunen, Mikko, Ramirez, Alfredo, Scherer, Martin, Farrer, Lindsay A, Haines, Jonathan L, Pericak-Vance, Margaret A, Raskind, Wendy H, Cruchaga, Carlos, Schellenberg, Gerard D, Joseph, Bertrand, Brkanac, Zoran

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Head circumference, atrophy, and cognition: Implications for brain reserve in Alzheimer disease von PERNECZKY, R, WAGENPFEIL, S, LUNETTA, K. L, CUPPLES, L. A, GREEN, R. C, DECARLI, C, FARRER, L. A, KURZ, A

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Evidence for fibroblast growth factor-2 as a mediator of amphetamine-enhanced motor improvement following stroke von Wolf, William A, Martin, Jody L, Kartje, Gwendolyn L, Farrer, Robert G

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Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database von Lill, Christina M, Roehr, Johannes T, McQueen, Matthew B, Kavvoura, Fotini K, Bagade, Sachin, Schjeide, Brit-Maren M, Schjeide, Leif M, Meissner, Esther, Zauft, Ute, Allen, Nicole C, Liu, Tian, Schilling, Marcel, Anderson, Kari J, Beecham, Gary, Berg, Daniela, Biernacka, Joanna M, Brice, Alexis, DeStefano, Anita L, Do, Chuong B, Eriksson, Nicholas, Factor, Stewart A, Farrer, Matthew J, Foroud, Tatiana, Gasser, Thomas, Hamza, Taye, Hardy, John A, Heutink, Peter, Hill-Burns, Erin M, Klein, Christine, Latourelle, Jeanne C, Maraganore, Demetrius M, Martin, Eden R, Martinez, Maria, Myers, Richard H, Nalls, Michael A, Pankratz, Nathan, Payami, Haydeh, Satake, Wataru, Scott, William K, Sharma, Manu, Singleton, Andrew B, Stefansson, Kari, Toda, Tatsushi, Tung, Joyce Y, Vance, Jeffery, Wood, Nick W, Zabetian, Cyrus P, Young, Peter, Tanzi, Rudolph E, Khoury, Muin J, Zipp, Frauke, Lehrach, Hans, Ioannidis, John P A, Bertram, Lars

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A phased SNP-based classification of sickle cell anemia HBB haplotypes von Shaikho, Elmutaz M, Farrell, John J, Alsultan, Abdulrahman, Qutub, Hatem, Al-Ali, Amein K, Figueiredo, Maria Stella, Chui, David H K, Farrer, Lindsay A, Murphy, George J, Mostoslavsky, Gustavo, Sebastiani, Paola, Steinberg, Martin H

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The Alzheimer's Disease Sequencing Project: Study design and sample selection von Beecham, Gary W, Bis, J C, Martin, E R, Choi, S-H, DeStefano, A L, van Duijn, C M, Fornage, M, Gabriel, S B, Koboldt, D C, Larson, D E, Naj, A C, Psaty, B M, Salerno, W, Bush, W S, Foroud, T M, Wijsman, E, Farrer, L A, Goate, A, Haines, J L, Pericak-Vance, Margaret A, Boerwinkle, E, Mayeux, R, Seshadri, S, Schellenberg, G

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Blood-derived mitochondrial DNA copy number is associated with Alzheimer disease, Alzheimer-related biomarkers and serum metabolites von Tong, Tong, Zhu, Congcong, Farrell, John J, Khurshid, Zainab, Martin, Eden R, Pericak-Vance, Margaret A, Wang, Li-San, Bush, William S, Schellenberg, Gerard D, Haines, Jonathan L, Qiu, Wei Qiao, Lunetta, Kathryn L, Farrer, Lindsay A, Zhang, Xiaoling

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Hemolysis-associated priapism in sickle cell disease von Nolan, Vikki G., Wyszynski, Diego F., Farrer, Lindsay A., Steinberg, Martin H.

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Evidence of CNIH3 involvement in opioid dependence von Nelson, E C, Agrawal, A, Heath, A C, Bogdan, R, Sherva, R, Zhang, B, Al-Hasani, R, Bruchas, M R, Chou, Y-L, Demers, C H, Carey, C E, Conley, E D, Fakira, A K, Farrer, L A, Goate, A, Gordon, S, Henders, A K, Hesselbrock, V, Kapoor, M, Lynskey, M T, Madden, P A F, Moron, J A, Rice, J P, Saccone, N L, Schwab, S G, Shand, F L, Todorov, A A, Wallace, L, Wang, T, Wray, N R, Zhou, X, Degenhardt, L, Martin, N G, Hariri, A R, Kranzler, H R, Gelernter, J, Bierut, L J, Clark, D J, Montgomery, G W

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Genomewide Association Studies of LRRK2 Modifiers of Parkinson's Disease von Lai, Dongbing, Alipanahi, Babak, Fontanillas, Pierre, Schwantes‐An, Tae‐Hwi, Aasly, Jan, Alcalay, Roy N., Beecham, Gary W., Berg, Daniela, Bressman, Susan, Brice, Alexis, Brockman, Kathrin, Clark, Lorraine, Cookson, Mark, Das, Sayantan, Van Deerlin, Vivianna, Follett, Jordan, Farrer, Matthew J., Trinh, Joanne, Gasser, Thomas, Goldwurm, Stefano, Gustavsson, Emil, Klein, Christine, Lang, Anthony E., Langston, J. William, Latourelle, Jeanne, Lynch, Timothy, Marder, Karen, Marras, Connie, Martin, Eden R., McLean, Cory Y., Mejia‐Santana, Helen, Molho, Eric, Myers, Richard H., Nuytemans, Karen, Ozelius, Laurie, Payami, Haydeh, Raymond, Deborah, Rogaeva, Ekaterina, Rogers, Michael P., Ross, Owen A., Samii, Ali, Saunders‐Pullman, Rachel, Schüle, Birgitt, Schulte, Claudia, Scott, William K., Tanner, Caroline, Tolosa, Eduardo, Tomkins, James E., Vilas, Dolores, Trojanowski, John Q., Uitti, Ryan, Vance, Jeffery M., Visanji, Naomi P., Wszolek, Zbigniew K., Zabetian, Cyrus P., Mirelman, Anat, Giladi, Nir, Orr Urtreger, Avi, Cannon, Paul, Fiske, Brian, Foroud, Tatiana

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Recovery and brain reorganization after stroke in adult and aged rats von Markus, Tiffanie M., Tsai, Shih-Yen, Bollnow, Melanie R., Farrer, Robert G., O'Brien, Timothy E., Kindler-Baumann, Diana R., Rausch, Martin, Rudin, Markus, Wiessner, Christoph, Mir, Anis K., Schwab, Martin E., Kartje, Gwendolyn L.

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An in vitro bioengineered model of the human arterial neurovascular unit to study neurodegenerative diseases von Robert, Jerome, Weilinger, Nicholas L., Cao, Li-Ping, Cataldi, Stefano, Button, Emily B., Stukas, Sophie, Martin, Emma M., Seibler, Philip, Gilmour, Megan, Caffrey, Tara M., Rowe, Elyn M., Fan, Jianjia, MacVicar, Brian, Farrer, Matthew J., Wellington, Cheryl L.

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Genome‐wide association and multi‐omics studies identify MGMT as a novel risk gene for Alzheimer's disease among women von Chung, Jaeyoon, Das, Anjali, Sun, Xinyu, Sobreira, Débora R., Leung, Yuk Yee, Igartua, Catherine, Mozaffari, Sahar, Chou, Yi‐Fan, Thiagalingam, Sam, Mez, Jesse, Zhang, Xiaoling, Jun, Gyungah R., Stein, Thor D., Kunkle, Brian W., Martin, Eden R., Pericak‐Vance, Margaret A., Mayeux, Richard, Haines, Jonathan L., Schellenberg, Gerard D., Nobrega, Marcelo A., Lunetta, Kathryn L., Pinto, Jayant M., Wang, Li‐San, Ober, Carole, Farrer, Lindsay A.

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Gender differences in Parkinson's disease depression von Perrin, Andrew J, Nosova, Ekaterina, Co, Kim, Book, Adam, Iu, Oscar, Silva, Vanessa, Thompson, Christina, McKeown, Martin J, Stoessl, A. Jon, Farrer, Matthew J, Appel-Cresswell, Silke

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Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort von Vollstedt, Eva‐Juliane, Padmanabhan, Shalini, Brice, Alexis, Tesson, Christelle, Vidailhet, Marie, Hentati, Faycel, Mirelman, Anat, Fahn, Stanley, Brüggemann, Norbert, Foroud, Tatiana, Tolosa, Eduardo, Garrido, Alicia, Annesi, Grazia, Correia Guedes, Leonor, Petrucci, Simona, Fedotova, Ekaterina Y., Alvarez, Victoria, Menéndez‐González, Manuel, Gómez‐Garre, Pilar, Mir, Pablo, Belin, Andrea Carmine, Jankovic, Joseph, Nishioka, Kenya, Funayama, Manabu, Clarimon, Jordi, Williams‐Gray, Caroline H., Camacho, Marta, Puschmann, Andreas, Carr, Jonathan, Ferese, Rosangela, Gambardella, Stefano, Chase, Bruce, Markopoulou, Katerina, Toda, Tatsushi, Lynch, Timothy, Carvalho Aguiar, Patricia, Saunders‐Pullman, Rachel, Skorvanek, Matej, Garraux, Gaetan, Chung, Sun Ju, Klivényi, Péter, Kostic, Vladimir S., Borges, Vanderci, Spitz, Mariana, Riess, Olaf, Valente, Enza Maria, Corvol, Jean‐Christophe, Klein, Christine, Aasly, Jan O., Abramycheva, Natalya Y., Al‐Mubarak, Bashayer, Ferraz, Henrique Ballalai, Barrett, Matthew J., Başak, A. Nazlı, Boon, Agnita J. W., Borges, Vanderci, Borngräber, Friederike, Bozi, Maria, Bressman, Susan, Brice, Alexis, Belin, Andrea Carmine, Cornejo‐Olivas, Mario, Chung, Sun Ju, Crosiers, David, Carvalho Aguiar, Patricia, Fahn, Stanley, Fedotova, Ekaterina Y., Foroud, Tatiana, Giladi, Nir, Gómez‐Garre, Pilar, Hattori, Nobutaka, Hertz, Jens Michael, Illarioshkin, Sergey N., Kievit, Anneke A., Koziorowski, Dariusz, Krüger, Rejko, Kühn, Andrea A., Kuhlenbäumer, Gregor, Lim, Jia Lun, Lin, Chin‐Hsien, Markopoulou, Katerina, Menéndez‐González, Manuel, Mirelman, Anat, Morris, Huw, Pachchek, Sinthuja, Puschmann, Andreas, Rossi, Malco, Sammler, Esther M., Satake, Wataru, Stefanis, Leonidas, Soto‐Beasley, Alexandra I., Spitz, Mariana, Suchowersky, Oksana, Tan, Eng‐King, Tesson, Christelle, Toda, Tatsushi, Torres‐Ramirez, Luis, Tumas, Vitor, Uyguner, Oya, Wu, Yih‐Ru

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DNAJC13 genetic variants in parkinsonism von Gustavsson, Emil K., Trinh, Joanne, Guella, Ilaria, Vilariño-Güell, Carles, Appel-Cresswell, Silke, Stoessl, A. Jon, Tsui, Joseph K, McKeown, Martin, Rajput, Alex, Rajput, Ali H., Aasly, Jan O., Farrer, Matthew J.

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DNA from multiple viral species is associated with Alzheimer's disease risk von Tejeda, Marlene, Farrell, John, Zhu, Congcong, Wetzler, Lee, Lunetta, Kathryn L., Bush, William S., Martin, Eden R., Wang, Li‐San, Schellenberg, Gerard D., Pericak‐Vance, Margaret A., Haines, Jonathan L., Farrer, Lindsay A., Sherva, Richard

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Largest GWAS of PTSD (N=20 070) yields genetic overlap with schizophrenia and sex differences in heritability von Duncan, L E, Ratanatharathorn, A, Aiello, A E, Almli, L M, Amstadter, A B, Ashley-Koch, A E, Baker, D G, Beckham, J C, Bierut, L J, Bisson, J, Bradley, B, Chen, C-Y, Dalvie, S, Farrer, L A, Galea, S, Garrett, M E, Gelernter, J E, Guffanti, G, Hauser, M A, Johnson, E O, Kessler, R C, Kimbrel, N A, King, A, Koen, N, Kranzler, H R, Logue, M W, Maihofer, A X, Martin, A R, Miller, M W, Morey, R A, Nugent, N R, Rice, J P, Ripke, S, Roberts, A L, Saccone, N L, Smoller, J W, Stein, D J, Stein, M B, Sumner, J A, Uddin, M, Ursano, R J, Wildman, D E, Yehuda, R, Zhao, H, Daly, M J, Liberzon, I, Ressler, K J, Nievergelt, C M, Koenen, K C

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