Multi-modality machine learning predicting Parkinson’s disease von Makarious, Mary B., Leonard, Hampton L., Vitale, Dan, Iwaki, Hirotaka, Sargent, Lana, Dadu, Anant, Violich, Ivo, Hutchins, Elizabeth, Saffo, David, Bandres-Ciga, Sara, Kim, Jonggeol Jeff, Song, Yeajin, Maleknia, Melina, Bookman, Matt, Nojopranoto, Willy, Campbell, Roy H., Hashemi, Sayed Hadi, Botia, Juan A., Carter, John F., Craig, David W., Van Keuren-Jensen, Kendall, Morris, Huw R., Hardy, John A., Blauwendraat, Cornelis, Singleton, Andrew B., Faghri, Faraz, Nalls, Mike A.

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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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The contribution of Neanderthal introgression and natural selection to neurodegenerative diseases von Chen, Zhongbo, Reynolds, Regina H., Pardiñas, Antonio F., Gagliano Taliun, Sarah A., van Rheenen, Wouter, Lin, Kuang, Shatunov, Aleksey, Gustavsson, Emil K., Fogh, Isabella, Jones, Ashley R., Robberecht, Wim, Corcia, Philippe, Chiò, Adriano, Shaw, Pamela J., Morrison, Karen E., Veldink, Jan H., van den Berg, Leonard H., Shaw, Christopher E., Powell, John F., Silani, Vincenzo, Hardy, John A., Houlden, Henry, Owen, Michael J., Turner, Martin R., Ryten, Mina, Al-Chalabi, Ammar

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SNCA variants are associated with increased risk for multiple system atrophy von Scholz, Sonja W., Houlden, Henry, Schulte, Claudia, Sharma, Manu, Li, Abi, Berg, Daniela, Melchers, Anna, Paudel, Reema, Gibbs, J. Raphael, Simon-Sanchez, Javier, Paisan-Ruiz, Coro, Bras, Jose, Ding, Jinhui, Chen, Honglei, Traynor, Bryan J., Arepalli, Sampath, Zonozi, Ryan R., Revesz, Tamas, Holton, Janice, Wood, Nick, Lees, Andrew, Oertel, Wolfgang, Wüllner, Ullrich, Goldwurm, Stefano, Pellecchia, Maria Teresa, Illig, Thomas, Riess, Olaf, Fernandez, Hubert H., Rodriguez, Ramon L., Okun, Michael S., Poewe, Werner, Wenning, Gregor K., Hardy, John A., Singleton, Andrew B., Gasser, Thomas

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A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release von Matarín, Mar, PhD, Brown, W Mark, MA, Scholz, Sonja, MD, Simón-Sánchez, Javier, BS, Fung, Hon-Chung, MD, Hernandez, Dena, MS, Gibbs, J Raphael, BS, De Vrieze, Fabienne Wavrant, PhD, Crews, Cynthia, Britton, Angela, MS, Langefeld, Carl D, PhD, Brott, Thomas G, MD, Brown, Robert D, MD, Worrall, Bradford B, MD, Frankel, Michael, MD, Silliman, Scott, MD, Case, L Douglas, PhD, Singleton, Andrew, Dr, Hardy, John A, PhD, Rich, Stephen S, PhD, Meschia, James F, MD

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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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Comparing Spatial Maps of Human Population-Genetic Variation Using Procrustes Analysis von Wang, Chaolong, Szpiech, Zachary A, Degnan, James H, Jakobsson, Mattias, Pemberton, Trevor J, Hardy, John A, Singleton, Andrew B, Rosenberg, Noah A

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Identification of Stk25 as a genetic modifier of Tau phosphorylation in Dab1-mutant mice von Matsuki, Tohru, Zaka, Mariam, Guerreiro, Rita, van der Brug, Marcel P, Cooper, Jonathan A, Cookson, Mark R, Hardy, John A, Howell, Brian W

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Support for association between ADHD and two candidate genes: NET1 and DRD1 von Bobb, Aaron J., Addington, Anjene M., Sidransky, Ellen, Gornick, Michele C., Lerch, Jason P., Greenstein, Deanna K., Clasen, Liv S., Sharp, Wendy S., Inoff-Germain, Gale, Wavrant-De Vrièze, Fabienne, Arcos-Burgos, Mauricio, Straub, Richard E., Hardy, John A., Castellanos, F. Xavier, Rapoport, Judith L.

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Differential DJ-1 gene expression in Parkinson's disease von Kumaran, Ravindran, Vandrovcova, Jana, Luk, Connie, Sharma, Simone, Renton, Alan, Wood, Nicholas W, Hardy, John A, Lees, Andrew J, Bandopadhyay, Rina

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Assessing clinical progression measures in Alzheimer's disease trials: A systematic review and meta-analysis von McLaughlin, Jonathan, Scotton, William J, Ryan, Natalie S, Hardy, John A, Shoai, Maryam

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Parkin variants in North American Parkinson's disease: Cases and controls von Lincoln, Sarah J., Maraganore, Demetrius M., Lesnick, Timothy G., Bounds, Rebecca, de Andrade, Mariza, Bower, James H., Hardy, John A., Farrer, Matthew J.

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Genome-wide association study reveals genetic risk underlying Parkinson's disease von Singleton, Andrew B, Gasser, Thomas, Simón-Sánchez, Javier, Schulte, Claudia, Bras, Jose M, Sharma, Manu, Gibbs, J Raphael, Berg, Daniela, Paisan-Ruiz, Coro, Lichtner, Peter, Scholz, Sonja W, Hernandez, Dena G, Krüger, Rejko, Federoff, Monica, Klein, Christine, Goate, Alison, Perlmutter, Joel, Bonin, Michael, Nalls, Michael A, Illig, Thomas, Gieger, Christian, Houlden, Henry, Steffens, Michael, Okun, Michael S, Racette, Brad A, Cookson, Mark R, Foote, Kelly D, Fernandez, Hubert H, Traynor, Bryan J, Schreiber, Stefan, Arepalli, Sampath, Zonozi, Ryan, Gwinn, Katrina, van der Brug, Marcel, Lopez, Grisel, Chanock, Stephen J, Schatzkin, Arthur, Park, Yikyung, Hollenbeck, Albert, Gao, Jianjun, Huang, Xuemei, Wood, Nick W, Lorenz, Delia, Deuschl, Günther, Chen, Honglei, Riess, Olaf, Hardy, John A

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MIR-NATs repress MAPT translation and aid proteostasis in neurodegeneration von Simone, Roberto, Javad, Faiza, Emmett, Warren, Wilkins, Oscar G., Almeida, Filipa Lourenço, Barahona-Torres, Natalia, Zareba-Paslawska, Justyna, Ehteramyan, Mazdak, Zuccotti, Paola, Modelska, Angelika, Siva, Kavitha, Virdi, Gurvir S., Mitchell, Jamie S., Harley, Jasmine, Kay, Victoria A., Hondhamuni, Geshanthi, Trabzuni, Daniah, Ryten, Mina, Wray, Selina, Preza, Elisavet, Kia, Demis A., Pittman, Alan, Ferrari, Raffaele, Manzoni, Claudia, Lees, Andrew, Hardy, John A., Denti, Michela A., Quattrone, Alessandro, Patani, Rickie, Svenningsson, Per, Warner, Thomas T., Plagnol, Vincent, Ule, Jernej, de Silva, Rohan

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A genome-wide association study in multiple system atrophy von Sailer, Anna, Scholz, Sonja W, Nalls, Michael A, Schulte, Claudia, Federoff, Monica, Price, T Ryan, Lees, Andrew, Ross, Owen A, Dickson, Dennis W, Mok, Kin, Mencacci, Niccolo E, Schottlaender, Lucia, Chelban, Viorica, Ling, Helen, OʼSullivan, Sean S, Wood, Nicholas W, Traynor, Bryan J, Ferrucci, Luigi, Federoff, Howard J, Mhyre, Timothy R, Morris, Huw R, Deuschl, Günther, Quinn, Niall, Widner, Hakan, Albanese, Alberto, Infante, Jon, Bhatia, Kailash P, Poewe, Werner, Oertel, Wolfgang, Höglinger, Günter U, Wüllner, Ullrich, Goldwurm, Stefano, Pellecchia, Maria Teresa, Ferreira, Joaquim, Tolosa, Eduardo, Bloem, Bastiaan R, Rascol, Olivier, Meissner, Wassilios G, Hardy, John A, Revesz, Tamas, Holton, Janice L, Gasser, Thomas, Wenning, Gregor K, Singleton, Andrew B, Houlden, Henry

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Dissecting the Phenotype and Genotype of PLA2G6‐Related Parkinsonism von Magrinelli, Francesca, Mehta, Sahil, Di Lazzaro, Giulia, Latorre, Anna, Edwards, Mark J., Balint, Bettina, Basu, Purba, Kobylecki, Christopher, Groppa, Sergiu, Hegde, Anaita, Mulroy, Eoin, Estevez‐Fraga, Carlos, Arora, Anshita, Kumar, Hrishikesh, Schneider, Susanne A., Lewis, Patrick A., Jaunmuktane, Zane, Revesz, Tamas, Gandhi, Sonia, Wood, Nicholas W., Hardy, John A., Tinazzi, Michele, Lal, Vivek, Houlden, Henry, Bhatia, Kailash P.

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Abrogation of LRRK2 dependent Rab10 phosphorylation with TLR4 activation and alterations in evoked cytokine release in immune cells von Nazish, Iqra, Arber, Charles, Piers, Thomas M., Warner, Thomas T., Hardy, John A., Lewis, Patrick A., Pocock, Jennifer M., Bandopadhyay, Rina

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Genotype-Imputation Accuracy across Worldwide Human Populations von Huang, Lucy, Li, Yun, Singleton, Andrew B., Hardy, John A., Abecasis, Gonçalo, Rosenberg, Noah A., Scheet, Paul

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Genotype, haplotype and copy-number variation in worldwide human populations von Rosenberg, Noah A, Singleton, Andrew B, Jakobsson, Mattias, Scholz, Sonja W, Scheet, Paul, Gibbs, J. Raphael, VanLiere, Jenna M, Fung, Hon-Chung, Szpiech, Zachary A, Degnan, James H, Wang, Kai, Guerreiro, Rita, Bras, Jose M, Schymick, Jennifer C, Hernandez, Dena G, Traynor, Bryan J, Simon-Sanchez, Javier, Matarin, Mar, Britton, Angela, van de Leemput, Joyce, Rafferty, Ian, Bucan, Maja, Cann, Howard M, Hardy, John A

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Whole Genome Analyses Suggest Ischemic Stroke and Heart Disease Share an Association With Polymorphisms on Chromosome 9p21 von MATARIN, Mar, BROWN, W. Mark, SINGLETON, Andrew, HARDY, John A, MESCHIA, James F

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