Spectral Effects of Varying Texture and Composition in Two-component “Mudpie” Simulations: Insights for Asteroid (101955) Bennu by Sen, Antara, Clark, Beth E., Cloutis, Edward A., DellaGiustina, Daniella N., Hendrix, Amanda R., Simon, Amy A., Applin, Daniel M., Parkinson, Alexis, Turenne, Nathalie, Connell, Stephanie, Ferrone, Salvatore M., Li, Jian-Yang, Lim, Lucy F., Lauretta, Dante S.

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Spectral reflectance properties of minerals exposed to martian surface conditions: Implications for spectroscopy-based mineral detection on Mars by Turenne, Nathalie, Parkinson, Alexis, Applin, Daniel M., Mann, Paul, Cloutis, Edward A., Mertzman, Stanley A.

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A simulated rover exploration of a long-lived hypersaline spring environment: The East German Creek (MB, Canada) Mars analogue site by Cloutis, Ed, Applin, Daniel, Connell, Stephanie, Kubanek, Krista, Kuik, Jesse, Parkinson, Alexis, Ramirez, Mary, Turenne, Nathalie, Mertzman, Stanley

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The Lake St. Martin impact structure (Manitoba, Canada): A simulated rover exploration of a sulfate-bearing impact crater by Cloutis, Ed, Stromberg, Jessica, Applin, Daniel, Connell, Stephanie, Kubanek, Krista, Kuik, Jesse, Lechowicz, Adam, Parkinson, Alexis, Ramirez, Mary, Turenne, Nathalie, Cieszecki, Jeff, Germinario, Matteo, Kum, Ryan, Parson, Rachel, Walker, Ryan, Wiens, Edward, Wiens, James, Mertzman, Stanley

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Biosignature detection by Mars rover equivalent instruments in samples from the CanMars Mars Sample Return Analogue Deployment by Stromberg, Jessica M., Parkinson, Alexis, Morison, Matthew, Cloutis, Edward, Casson, Nora, Applin, Daniel, Poitras, Jordan, Marti, Arola Moreras, Maggiori, Catherine, Cousins, Claire, Whyte, Lyle, Kruzelecky, Roman, Das, Debarati, Leveille, Richard, Berlo, Kim, Sharma, Shiv K., Acosta-Maeda, Tayro, Daly, Michael, Lalla, Emmanuel

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Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database by 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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Global, regional, and national burden of Parkinson's disease, 1990–2016: a systematic analysis for the Global Burden of Disease Study 2016 by Dorsey, E. Ray, Elbaz, Alexis, Nichols, Emma, Abbasi, Nooshin, Abd-Allah, Foad, Abdelalim, Ahmed, Adsuar, Jose C., Ansha, Mustafa Geleto, Brayne, Carol, Choi, Jee-Young J, Collado-Mateo, Daniel, Dahodwala, Nabila, Do, Huyen Phuc, Edessa, Dumessa, Endres, Matthias, Fereshtehnejad, Seyed-Mohammad, Foreman, Kyle J, Gankpe, Fortune Gbetoho, Gupta, Rahul, Hamidi, Samer, Hankey, Graeme J., Hay, Simon I., Hegazy, Mohamed I, Hibstu, Desalegn T., Kasaeian, Amir, Khader, Yousef, Khalil, Ibrahim, Khang, Young-Ho, Kim, Yun Jin, Kokubo, Yoshihiro, Logroscino, Giancarlo, Massano, João, Mohamed Ibrahim, Norlinah, Mohammed, Mohammed A., Mohammadi, Alireza, Moradi-Lakeh, Maziar, Naghavi, Mohsen, Nguyen, Binh Thanh, Nirayo, Yirga Legesse, Ogbo, Felix Akpojene, Owolabi, Mayowa Ojo, Pereira, David M., Postma, Maarten J, Qorbani, Mostafa, Rahman, Muhammad Aziz, Roba, Kedir T., Safari, Hosein, Safiri, Saeid, Satpathy, Maheswar, Sawhney, Monika, Shafieesabet, Azadeh, Shiferaw, Mekonnen Sisay, Smith, Mari, Szoeke, Cassandra E I, Tabarés-Seisdedos, Rafael, Truong, Nu Thi, Ukwaja, Kingsley Nnanna, Venketasubramanian, Narayanaswamy, Villafaina, Santos, weldegwergs, Kidu gidey, Westerman, Ronny, Wijeratne, Tissa, Winkler, Andrea S., Xuan, Bach Tran, Yonemoto, Naohiro, Feigin, Valery L, Vos, Theo, Murray, Christopher J L

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G51D α-synuclein mutation causes a novel Parkinsonian-pyramidal syndrome by Lesage, Suzanne, Anheim, Mathieu, Letournel, Franck, Bousset, Luc, Honoré, Aurélie, Rozas, Nelly, Pieri, Laura, Madiona, Karine, Dürr, Alexandra, Melki, Ronald, Verny, Christophe, Brice, Alexis

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GP2: The Global Parkinson's Genetics Program

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Specifically neuropathic Gaucher's mutations accelerate cognitive decline in Parkinson's by Liu, Ganqiang, Boot, Brendon, Locascio, Joseph J., Jansen, Iris E., Winder-Rhodes, Sophie, Eberly, Shirley, Elbaz, Alexis, Brice, Alexis, Ravina, Bernard, van Hilten, Jacobus J., Cormier-Dequaire, Florence, Corvol, Jean-Christophe, Barker, Roger A., Heutink, Peter, Marinus, Johan, Williams-Gray, Caroline H., Scherzer, Clemens R.

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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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Loss-of-function mutations in RAB39B are associated with typical early-onset Parkinson disease by Lesage, Suzanne, Bras, Jose, Cormier-Dequaire, Florence, Condroyer, Christel, Nicolas, Aude, Darwent, Lee, Guerreiro, Rita, Majounie, Elisa, Federoff, Monica, Heutink, Peter, Wood, Nicholas W, Gasser, Thomas, Hardy, John, Tison, François, Singleton, Andrew, Brice, Alexis

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Long-term disease progression in spinocerebellar ataxia types 1, 2, 3, and 6: a longitudinal cohort study by Jacobi, Heike, MD, du Montcel, Sophie Tezenas, PhD, Bauer, Peter, MD, Giunti, Paola, PhD, Cook, Arron, MBBS, Labrum, Robyn, MD, Parkinson, Michael H, MBBS, Durr, Alexandra, PhD, Brice, Alexis, Prof, Charles, Perrine, MD, Marelli, Cecilia, MD, Mariotti, Caterina, MD, Nanetti, Lorenzo, MD, Panzeri, Marta, MD, Rakowicz, Maria, MD, Sulek, Anna, PhD, Sobanska, Anna, MD, Schmitz-Hübsch, Tanja, MD, Schöls, Ludger, MD, Hengel, Holger, MD, Baliko, Laszlo, MD, Melegh, Bela, Prof, Filla, Alessandro, Prof, Antenora, Antonella, MD, Infante, Jon, MD, Berciano, José, Prof, van de Warrenburg, Bart P, PhD, Timmann, Dagmar, MD, Szymanski, Sandra, MD, Boesch, Sylvia, MD, Kang, Jun-Suk, MD, Pandolfo, Massimo, Prof, Schulz, Jörg B, Prof, Molho, Sonia, MSc, Diallo, Alhassane, MD, Klockgether, Thomas, Prof

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Characterization of Recessive Parkinson Disease in a Large Multicenter Study by Lesage, Suzanne, Lunati, Ariane, Houot, Marion, Romdhan, Sawssan Ben, Clot, Fabienne, Tesson, Christelle, Mangone, Graziella, Toullec, Benjamin Le, Courtin, Thomas, Larcher, Kathy, Benmahdjoub, Mustapha, Arezki, Mohamed, Bouhouche, Ahmed, Anheim, Mathieu, Roze, Emmanuel, Viallet, François, Tison, François, Broussolle, Emmanuel, Emre, Murat, Hanagasi, Hasmet, Bilgic, Basar, Tazir, Meriem, Djebara, Mouna Ben, Gouider, Riadh, Tranchant, Christine, Vidailhet, Marie, Le Guern, Eric, Corti, Olga, Mhiri, Chokri, Lohmann, Ebba, Singleton, Andrew, Corvol, Jean‐Christophe, Brice, Alexis, Lesage, Suzanne, Lunati, Ariane, Houot, Marion, Ben Romdhan, Sawssan, Clot, Fabienne, Tesson, Christelle, Mangone, Graziella, Le Toullec, Benjamin, Courtin, Thomas, Larcher, Kathy, Benmahdjoub, Mustapha, Arezki, Mohammed, Bouhouche, Ahmed, Anheim, Mathieu, Roze, Emmanuel, Viallet, François, Tison, François, Broussolle, Emmanuel, Emre, Murat, Hanagasi, Hasmet, Bilgic, Basar, Ben Djebara, Mouna, Gouider, Riadh, Tazir, Meriem, Tranchant, Christine, Vidailhet, Marie, Le Guern, Eric, Corti, Olga, Mhiri, Chokri, Lohmann, Ebba, Singleton, Andy, Corvol, Jean‐Christophe, Brice, Alexis

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Mitochondrial haplogroups and cognitive progression in Parkinson's disease by Liu, Ganqiang, Ni, Chunming, Zhan, Jiamin, Li, Weimin, Luo, Junfeng, Liao, Zhixiang, Locascio, Joseph J, Xian, Wenbiao, Chen, Ling, Pei, Zhong, Corvol, Jean-Christophe, Maple-Grødem, Jodi, Campbell, Meghan C, Elbaz, Alexis, Lesage, Suzanne, Brice, Alexis, Hung, Albert Y, Schwarzschild, Michael A, Hayes, Michael T, Wills, Anne-Marie, Ravina, Bernard, Shoulson, Ira, Taba, Pille, Kõks, Sulev, Beach, Thomas G, Cormier-Dequaire, Florence, Alves, Guido, Tysnes, Ole-Bjørn, Perlmutter, Joel S, Heutink, Peter, van Hilten, Jacobus J, Barker, Roger A, Williams-Gray, Caroline H, Scherzer, Clemens R

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Diagnosis of Parkinson's disease on the basis of clinical and genetic classification: a population-based modelling study by Nalls, Mike A, PhD, McLean, Cory Y, PhD, Rick, Jacqueline, PhD, Eberly, Shirley, MS, Hutten, Samantha J, PhD, Gwinn, Katrina, MD, Sutherland, Margaret, PhD, Martinez, Maria, PhD, Heutink, Peter, PhD, Williams, Nigel M, PhD, Hardy, John, PhD, Gasser, Thomas, MD, Brice, Alexis, MD, Price, T Ryan, MS, Nicolas, Aude, PhD, Keller, Margaux F, PhD, Molony, Cliona, PhD, Gibbs, J Raphael, MS, Chen-Plotkin, Alice, MD, Suh, Eunran, PhD, Letson, Christopher, BS, Fiandaca, Massimo S, MD, Mapstone, Mark, PhD, Federoff, Howard J, MD, Noyce, Alastair J, MRCP, Morris, Huw, MD, Van Deerlin, Vivianna M, MD, Weintraub, Daniel, MD, Zabetian, Cyrus, MD, Hernandez, Dena G, MS, Lesage, Suzanne, PhD, Mullins, Meghan, BA, Conley, Emily Drabant, PhD, Northover, Carrie A M, PhD, Frasier, Mark, PhD, Marek, Ken, MD, Day-Williams, Aaron G, PhD, Stone, David J, PhD, Ioannidis, John P A, Prof, Singleton, Andrew B, Dr

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Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case–control study by Ross, Owen A, Dr, Soto-Ortolaza, Alexandra I, BSc, Heckman, Michael G, MS, Aasly, Jan O, Prof, Abahuni, Nadine, MD, Annesi, Grazia, Prof, Bacon, Justin A, BSc, Bardien, Soraya, PhD, Bozi, Maria, MD, Brice, Alexis, Prof, Brighina, Laura, MD, Van Broeckhoven, Christine, Prof, Carr, Jonathan, Prof, Chartier-Harlin, Marie-Christine, Prof, Dardiotis, Efthimios, MD, Dickson, Dennis W, Prof, Diehl, Nancy N, BS, Elbaz, Alexis, Prof, Ferrarese, Carlo, Prof, Ferraris, Alessandro, MD, Fiske, Brian, PhD, Gibson, J Mark, Prof, Gibson, Rachel, PhD, Hadjigeorgiou, Georgios M, MD, Hattori, Nobutaka, Prof, Ioannidis, John PA, Prof, Jasinska-Myga, Barbara, MD, Jeon, Beom S, Prof, Kim, Yun Joong, Prof, Klein, Christine, Prof, Kruger, Rejko, MD, Kyratzi, Elli, MD, Lesage, Suzanne, PhD, Lin, Chin-Hsien, MD, Lynch, Timothy, Prof, Maraganore, Demetrius M, Prof, Mellick, George D, PhD, Mutez, Eugénie, MD, Nilsson, Christer, Prof, Opala, Grzegorz, Prof, Park, Sung Sup, Prof, Puschmann, Andreas, MD, Quattrone, Aldo, Prof, Sharma, Manu, PhD, Silburn, Peter A, Prof, Sohn, Young Ho, Prof, Stefanis, Leonidas, MD, Tadic, Vera, MD, Theuns, Jessie, PhD, Tomiyama, Hiroyuki, MD, Uitti, Ryan J, Prof, Valente, Enza Maria, Prof, van de Loo, Simone, PhD, Vassilatis, Demetrios K, PhD, Vilariño-Güell, Carles, PhD, White, Linda R, Prof, Wirdefeldt, Karin, MD, Wszolek, Zbigniew K, Prof, Wu, Ruey-Meei, Prof, Farrer, Matthew J, Prof

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Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association data by Mok, Kin Y, FRCP, Sheerin, Una, MRCP, Simón-Sánchez, Javier, PhD, Salaka, Afnan, PhD, Chester, Lucy, MPharm, Escott-Price, Valentina, PhD, Mantripragada, Kiran, PhD, Doherty, Karen M, MD, Noyce, Alastair J, MRCP, Mencacci, Niccolo E, MD, Lubbe, Steven J, PhD, Williams-Gray, Caroline H, PhD, Barker, Roger A, Prof, van Dijk, Karin D, MD, Berendse, Henk W, Prof, Heutink, Peter, Prof, Corvol, Jean-Christophe, Prof, Cormier, Florence, MD, Lesage, Suzanne, PhD, Brice, Alexis, Prof, Brockmann, Kathrin, MD, Schulte, Claudia, PhD, Gasser, Thomas, Prof, Foltynie, Thomas, PhD, Limousin, Patricia, Prof, Morrison, Karen E, Prof, Clarke, Carl E, Prof, Sawcer, Stephen, Prof, Warner, Tom T, Prof, Lees, Andrew J, Prof, Morris, Huw R, Prof, Nalls, Mike A, PhD, Singleton, Andrew B, PhD, Hardy, John, Prof, Abramov, Andrey Y, Prof, Plagnol, Vincent, PhD, Williams, Nigel M, Dr, Wood, Nicholas W, Prof

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Differences in Survival across Monogenic Forms of Parkinson's Disease by Lanore, Aymeric, Casse, Fanny, Tesson, Christelle, Courtin, Thomas, Menon, Poornima Jayadev, Sambin, Sara, Mangone, Graziella, Mariani, Louise‐Laure, Lesage, Suzanne, Brice, Alexis, Elbaz, Alexis, Corvol, Jean‐Christophe, Agid, Yves, Anheim, Mathieu, Borg, Michel, Brice, Alexis, Broussolle, Emmanuel, Corvol, Jean‐Christophe, Damier, Philippe, Defebvre, Luc, Dürr, Alexandra, Durif, Franck, Houeto, Jean Luc, Krack, Paul, Klebe, Stephan, Lesage, Suzanne, Lohmann, Ebba, Martinez, Maria, Mangone, Graziella, Mariani, Louise‐Laure, Pollak, Pierre, Rascol, Olivier, Tison, François, Tranchant, Christine, Vérin, Marc, Viallet, François, Vidailhet, Marie

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RAB32 Ser71Arg in autosomal dominant Parkinson's disease: linkage, association, and functional analyses by Gustavsson, Emil K, Follett, Jordan, Trinh, Joanne, Barodia, Sandeep K, Real, Raquel, Liu, Zhiyong, Grant-Peters, Melissa, Fox, Jesse D, Appel-Cresswell, Silke, Stoessl, A Jon, Rajput, Alex, Rajput, Ali H, Auer, Roland, Tilney, Russel, Sturm, Marc, Haack, Tobias B, Lesage, Suzanne, Tesson, Christelle, Brice, Alexis, Vilariño-Güell, Carles, Ryten, Mina, Goldberg, Matthew S, West, Andrew B, Hu, Michele T, Morris, Huw R, Sharma, Manu, Gan-Or, Ziv, Samanci, Bedia, Lis, Pawel, Periñan, Maria Teresa, Amouri, Rim, Ben Sassi, Samia, Hentati, Faycel, Tonelli, Francesca, Alessi, Dario R, Farrer, Matthew J

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