The genetics of Parkinson's disease: Progress and therapeutic implications von Singleton, Andrew B., Farrer, Matthew J., Bonifati, Vincenzo

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Insights from late-onset familial parkinsonism on the pathogenesis of idiopathic Parkinson's disease von Volta, Mattia, PhD, Milnerwood, Austen J, PhD, Farrer, Matthew J, Prof

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Alpha-synuclein p.H50Q, a novel pathogenic mutation for Parkinson's disease von Appel-Cresswell, Silke, Vilarino-Guell, Carles, Encarnacion, Mary, Sherman, Holly, Yu, Irene, Shah, Brinda, Weir, David, Thompson, Christina, Szu-Tu, Chelsea, Trinh, Joanne, Aasly, Jan O., Rajput, Alex, Rajput, Ali H., Jon Stoessl, A., Farrer, Matthew J.

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PSEN1 p.Met233Val in a Complex Neurodegenerative Movement and Neuropsychiatric Disorder von Appel-Cresswell, Silke, Guella, Ilaria, Lehman, Anna, Foti, Dean, Farrer, Matthew J.

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Dynamic control of the dopamine transporter in neurotransmission and homeostasis von Bu, Mengfei, Farrer, Matthew J., Khoshbouei, Habibeh

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VPS35 Mutations in Parkinson Disease von Vilariño-Güell, Carles, Wider, Christian, Ross, Owen A., Dachsel, Justus C., Kachergus, Jennifer M., Lincoln, Sarah J., Soto-Ortolaza, Alexandra I., Cobb, Stephanie A., Wilhoite, Greggory J., Bacon, Justin A., Behrouz, Bahareh, Melrose, Heather L., Hentati, Emna, Puschmann, Andreas, Evans, Daniel M., Conibear, Elizabeth, Wasserman, Wyeth W., Aasly, Jan O., Burkhard, Pierre R., Djaldetti, Ruth, Ghika, Joseph, Hentati, Faycal, Krygowska-Wajs, Anna, Lynch, Tim, Melamed, Eldad, Rajput, Alex, Rajput, Ali H., Solida, Alessandra, Wu, Ruey-Meei, Uitti, Ryan J., Wszolek, Zbigniew K., Vingerhoets, François, Farrer, Matthew J.

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A Meta-Analysis of α-Synuclein Multiplication in Familial Parkinsonism von Book, Adam, Guella, Ilaria, Candido, Tara, Brice, Alexis, Hattori, Nobutaka, Jeon, Beomseok, Farrer, Matthew J

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DNM3 and genetic modifiers of age of onset in LRRK2 Gly2019Ser parkinsonism: a genome-wide linkage and association study von Trinh, Joanne, BSc, Gustavsson, Emil K, MSc, Vilariño-Güell, Carles, PhD, Bortnick, Stephanie, BSc, Latourelle, Jeanne, PhD, McKenzie, Marna B, BSc, Tu, Chelsea Szu, MSc, Nosova, Ekaterina, PhD, Khinda, Jaskaran, BSc, Milnerwood, Austen, PhD, Lesage, Suzanne, PhD, Brice, Alexis, MD, Tazir, Meriem, MD, Aasly, Jan O, MD, Parkkinen, Laura, PhD, Haytural, Hazal, MSc, Foroud, Tatiana, PhD, Myers, Richard H, PhD, Sassi, Samia Ben, MD, Hentati, Emna, MD, Nabli, Fatma, MD, Farhat, Emna, MD, Amouri, Rim, PhD, Hentati, Fayçal, MD, Farrer, Matthew J, Dr

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Homozygous alpha-synuclein p.A53V in familial Parkinson’s disease von Yoshino, Hiroyo, PhD, Hirano, Makito, MD, PhD, Stoessl, A. Jon, MD, Imamichi, Yoko, BS, Ikeda, Aya, MD, Li, Yuanzhe, MD, PhD, Funayama, Manabu, PhD, Yamada, Ikuko, MD, PhD, Nakamura, Yusaku, MD, PhD, Sossi, Vesna, PhD, Farrer, Matthew J., PhD, Nishioka, Kenya, MD, PhD, Hattori, Nobutaka, MD, PhD

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Variants in saposin D domain of prosaposin gene linked to Parkinson's disease von Oji, Yutaka, Hatano, Taku, Ueno, Shin-Ichi, Funayama, Manabu, Ishikawa, Kei-Ichi, Okuzumi, Ayami, Noda, Sachiko, Sato, Shigeto, Satake, Wataru, Toda, Tatsushi, Li, Yuanzhe, Hino-Takai, Tomoko, Kakuta, Soichiro, Tsunemi, Taiji, Yoshino, Hiroyo, Nishioka, Kenya, Hattori, Tatsuya, Mizutani, Yasuaki, Mutoh, Tatsuro, Yokochi, Fusako, Ichinose, Yuta, Koh, Kishin, Shindo, Kazumasa, Takiyama, Yoshihisa, Hamaguchi, Tsuyoshi, Yamada, Masahito, Farrer, Matthew J, Uchiyama, Yasuo, Akamatsu, Wado, Wu, Yih-Ru, Matsuda, Junko, Hattori, Nobutaka

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Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy von Müller, Ulrich, Schellenberg, Gerard D, Höglinger, Günter U, Melhem, Nadine M, Dickson, Dennis W, Sleiman, Patrick M A, Wang, Li-San, Klei, Lambertus, Rademakers, Rosa, de Silva, Rohan, Litvan, Irene, Riley, David E, van Swieten, John C, Heutink, Peter, Wszolek, Zbigniew K, Uitti, Ryan J, Vandrovcova, Jana, Hurtig, Howard I, Gross, Rachel G, Maetzler, Walter, Goldwurm, Stefano, Tolosa, Eduardo, Borroni, Barbara, Pastor, Pau, Cantwell, Laura B, Han, Mi Ryung, Dillman, Allissa, van der Brug, Marcel P, Gibbs, J Raphael, Cookson, Mark R, Hernandez, Dena G, Singleton, Andrew B, Farrer, Matthew J, Yu, Chang-En, Golbe, Lawrence I, Revesz, Tamas, Hardy, John, Lees, Andrew J, Devlin, Bernie, Hakonarson, Hakon

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DNAJC13 mutations in Parkinson disease von Vilariño-Güell, Carles, Rajput, Alex, Milnerwood, Austen J, Shah, Brinda, Szu-Tu, Chelsea, Trinh, Joanne, Yu, Irene, Encarnacion, Mary, Munsie, Lise N, Tapia, Lucia, Gustavsson, Emil K, Chou, Patrick, Tatarnikov, Igor, Evans, Daniel M, Pishotta, Frederick T, Volta, Mattia, Beccano-Kelly, Dayne, Thompson, Christina, Lin, Michelle K, Sherman, Holly E, Han, Heather J, Guenther, Bruce L, Wasserman, Wyeth W, Bernard, Virginie, Ross, Colin J, Appel-Cresswell, Silke, Stoessl, A Jon, Robinson, Christopher A, Dickson, Dennis W, Ross, Owen A, Wszolek, Zbigniew K, Aasly, Jan O, Wu, Ruey-Meei, Hentati, Faycal, Gibson, Rachel A, McPherson, Peter S, Girard, Martine, Rajput, Michele, Rajput, Ali H, Farrer, Matthew J

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The emerging role of Rab GTPases in the pathogenesis of Parkinson's disease von Gao, Yujing, Wilson, Gabrielle R., Stephenson, Sarah E. M., Bozaoglu, Kiymet, Farrer, Matthew J., Lockhart, Paul J.

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LRRK2 in Parkinson's disease: protein domains and functional insights von Mata, Ignacio F., Wedemeyer, William J., Farrer, Matthew J., Taylor, Julie P., Gallo, Kathleen A.

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Loss-of-Function and Gain-of-Function Mutations in KCNQ5 Cause Intellectual Disability or Epileptic Encephalopathy von Lehman, Anna, Thouta, Samrat, Mancini, Grazia M.S., Naidu, Sakkubai, van Slegtenhorst, Marjon, McWalter, Kirsty, Person, Richard, Mwenifumbo, Jill, Salvarinova, Ramona, Adam, Shelin, du Souich, Christèle, Elliott, Alison M., Lehman, Anna, Mwenifumbo, Jill, Nelson, Tanya N., van Karnebeek, Clara, Friedman, Jan M., Boelman, Cyrus, Bolbocean, Corneliu, Buerki, Sarah E., Candido, Tara, Eydoux, Patrice, Evans, Daniel M., Gibson, William, Horvath, Gabriella, Huh, Linda, Sinclair, Graham, Tarling, Tamsin, Toyota, Eric B., Townsend, Katelin N., Van Allen, Margot I., Vercauteren, Suzanne, Guella, Ilaria, McKenzie, Marna B., Datta, Anita, Connolly, Mary B., Kalkhoran, Somayeh Mojard, Poburko, Damon, Friedman, Jan M., Farrer, Matthew J., Demos, Michelle, Desai, Sonal, Claydon, Thomas

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DNAJC12 and dopa‐responsive nonprogressive parkinsonism von Straniero, Letizia, Guella, Ilaria, Cilia, Roberto, Parkkinen, Laura, Rimoldi, Valeria, Young, Alexander, Asselta, Rosanna, Soldà, Giulia, Sossi, Vesna, Stoessl, A. Jon, Priori, Alberto, Nishioka, Kenya, Hattori, Nobutaka, Follett, Jordan, Rajput, Alex, Blau, Nenad, Pezzoli, Gianni, Farrer, Matthew J., Goldwurm, Stefano, Rajput, Ali H., Duga, Stefano

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Experimental procedures for flow cytometry of wild-type mouse brain: a systematic review von Sharp, Robert C, Guenther, Dylan T, Farrer, Matthew J

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De Novo Mutations in YWHAG Cause Early-Onset Epilepsy von Guella, Ilaria, McKenzie, Marna B., Evans, Daniel M., Buerki, Sarah E., Toyota, Eric B., Van Allen, Margot I., Adam, Shelin, Boelman, Cyrus, Bolbocean, Corneliu, Candido, Tara, Eydoux, Patrice, Horvath, Gabriella, Huh, Linda, Nelson, Tanya N., Sinclair, Graham, van Karnebeek, Clara, Vercauteren, Suzanne, Suri, Mohnish, Elmslie, Frances, Simon, Marleen E.H., van Gassen, Koen L.I., Héron, Delphine, Keren, Boris, Nava, Caroline, Connolly, Mary B., Demos, Michelle, Farrer, Matthew J.

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High-Resolution Whole-Genome Association Study of Parkinson Disease von Maraganore, Demetrius M., de Andrade, Mariza, Lesnick, Timothy G., Strain, Kari J., Farrer, Matthew J., Rocca, Walter A., Pant, P.V. Krishna, Frazer, Kelly A., Cox, David R., Ballinger, Dennis G.

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Age- and disease-dependent increase of the mitophagy marker phospho-ubiquitin in normal aging and Lewy body disease von Hou, Xu, Fiesel, Fabienne C., Truban, Dominika, Castanedes Casey, Monica, Lin, Wen-lang, Soto, Alexandra I., Tacik, Pawel, Rousseau, Linda G., Diehl, Nancy N., Heckman, Michael G., Lorenzo-Betancor, Oswaldo, Ferrer, Isidre, Arbelo, José M., Steele, John C., Farrer, Matthew J., Cornejo-Olivas, Mario, Torres, Luis, Mata, Ignacio F., Graff-Radford, Neill R., Wszolek, Zbigniew K., Ross, Owen A., Murray, Melissa E., Dickson, Dennis W., Springer, Wolfdieter

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