Automated Neuromelanin Imaging as a Diagnostic Biomarker for Parkinson's Disease von Castellanos, Gabriel, Fernández-Seara, María A., Lorenzo-Betancor, Oswaldo, Ortega-Cubero, Sara, Puigvert, Marc, Uranga, Javier, Vidorreta, Marta, Irigoyen, Jaione, Lorenzo, Elena, Muñoz-Barrutia, Arrate, Ortiz-de-Solorzano, Carlos, Pastor, Pau, Pastor, María A.

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Volumetric growth rate of incidental asymptomatic meningiomas: a single-center prospective cohort study von Delgado-López, Pedro David, Montalvo-Afonso, Antonio, Martín-Alonso, Javier, Martín-Velasco, Vicente, Castilla-Díez, José Manuel, Galacho-Harriero, Ana María, Ortega-Cubero, Sara, Sánchez-Rodríguez, Antonio, Rodríguez-Salazar, Antonio

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No evidence of association between common European mitochondrial DNA variants in Alzheimer, Parkinson, and migraine in the Spanish population von Fachal, Laura, Mosquera-Miguel, Ana, Pastor, Pau, Ortega-Cubero, Sara, Lorenzo, Elena, Oterino-Durán, Agustín, Toriello, María, Quintáns, Beatriz, Camiña-Tato, Montse, Sesar, Angel, Vega, Ana, Sobrido, María-Jesús, Salas, Antonio

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Pleiotropic Effects of Variants in Dementia Genes in Parkinson Disease von Ibanez, Laura, Dube, Umber, Davis, Albert A, Fernandez, Maria V, Budde, John, Cooper, Breanna, Diez-Fairen, Monica, Ortega-Cubero, Sara, Pastor, Pau, Perlmutter, Joel S, Cruchaga, Carlos, Benitez, Bruno A

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Thr105Ile (rs11558538) polymorphism in the histamine-1-methyl-transferase (HNMT) gene and risk for restless legs syndrome von Jiménez-Jiménez, Félix Javier, García-Martín, Elena, Alonso-Navarro, Hortensia, Martínez, Carmen, Zurdo, Martín, Turpín-Fenoll, Laura, Millán-Pascual, Jorge, Adeva-Bartolomé, Teresa, Cubo, Esther, Navacerrada, Francisco, Rojo-Sebastián, Ana, Rubio, Lluisa, Ortega-Cubero, Sara, Pastor, Pau, Calleja, Marisol, Plaza-Nieto, José Francisco, Pilo-de-la-Fuente, Belén, Arroyo-Solera, Margarita, García-Albea, Esteban, Agúndez, José A. G.

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Delta‐amino‐levulinic acid dehydratase gene and essential tremor von Agúndez, José A. G., García‐Martín, Elena, Alonso‐Navarro, Hortensia, Ayuso, Pedro, Esguevillas, Gara, Benito‐León, Julián, Ortega‐Cubero, Sara, Pastor, Pau, López‐Alburquerque, Tomás, Jiménez‐Jiménez, Félix Javier

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Effect of deep brain stimulation of the subthalamic nucleus on non-motor fluctuations in Parkinson's disease: Two-year' follow-up von Ortega-Cubero, Sara, Clavero, Pedro, Irurzun, Cecilia, Gonzalez-Redondo, Rafael, Guridi, Jorge, Obeso, Jose A, Rodriguez-Oroz, Maria C

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Missense mutations in TENM4, a regulator of axon guidance and central myelination, cause essential tremor von Hor, Hyun, Francescatto, Ludmila, Bartesaghi, Luca, Ortega-Cubero, Sara, Kousi, Maria, Lorenzo-Betancor, Oswaldo, Jiménez-Jiménez, Felix J, Gironell, Alexandre, Clarimón, Jordi, Drechsel, Oliver, Agúndez, José A G, Kenzelmann Broz, Daniela, Chiquet-Ehrismann, Ruth, Lleó, Alberto, Coria, Francisco, García-Martin, Elena, Alonso-Navarro, Hortensia, Martí, Maria J, Kulisevsky, Jaume, Hor, Charlotte N, Ossowski, Stephan, Chrast, Roman, Katsanis, Nicholas, Pastor, Pau, Estivill, Xavier

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Molecular interactions of the neuronal GPI-anchored lipocalin Lazarillo von Sanchez, Diego, Ortega-Cubero, Sara, Åkerström, Bo, Herrera, Macarena, Bastiani, Michael J., Ganfornina, Maria D.

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A comprehensive study of the genetic impact of rare variants in SORL1 in European early-onset Alzheimer’s disease von Verheijen, Jan, Van den Bossche, Tobi, van der Zee, Julie, Engelborghs, Sebastiaan, Sanchez-Valle, Raquel, Lladó, Albert, Graff, Caroline, Thonberg, Håkan, Pastor, Pau, Ortega-Cubero, Sara, Pastor, Maria A., Benussi, Luisa, Ghidoni, Roberta, Binetti, Giuliano, Clarimon, Jordi, Lleó, Alberto, Fortea, Juan, de Mendonça, Alexandre, Martins, Madalena, Grau-Rivera, Oriol, Gelpi, Ellen, Bettens, Karolien, Mateiu, Ligia, Dillen, Lubina, Cras, Patrick, De Deyn, Peter P., Van Broeckhoven, Christine, Sleegers, Kristel

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Frontobasal gray matter loss is associated with the TREM2 p.R47H variant von Luis, Elkin O, Ortega-Cubero, Sara, Lamet, Isabel, Razquin, Cristina, Cruchaga, Carlos, Benitez, Bruno A, Lorenzo, Elena, Irigoyen, Jaione, Pastor, Maria A, Pastor, Pau

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Heterozygous STUB1 mutation causes familial ataxia with cognitive affective syndrome (SCA48) von Genis, David, Ortega-Cubero, Sara, San Nicolás, Hector, Corral, Jordi, Gardenyes, Josep, de Jorge, Laura, López, Eva, Campos, Berta, Lorenzo, Elena, Tonda, Raúl, Beltran, Sergi, Negre, Montserrat, Obón, María, Beltran, Brigitte, Fàbregas, Laura, Alemany, Berta, Márquez, Fabián, Ramió-Torrentà, Lluís, Gich, Jordi, Volpini, Víctor, Pastor, Pau

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Experiencia clínica del tratamiento con onabotulinumtoxin A en pacientes con migraña refractaria von Palma Carazo, José Alberto, Irimia Sieira, Pablo, Fernández Torrón, Roberto, Ortega Cubero, Sara, Riverol Fernández, Mario, Luquin Piudo, Mª Rosario, Martínez Vila, Eduardo

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Clinicopathological contribution of rare deleterious ABCA7 mutations to early-onset Alzheimer disease (P6.101) von Van den Bossche, Tobi, De Roeck, Arne, Sanchez-Valle, Raquel, Lladó, Albert, Graff, Caroline, Thonberg, Håkan, Pastor, Pau, Ortega-Cubero, Sara, Pastor, Maria A., Benussi, Luisa, Ghidoni, Roberta, Binetti, Giuliano, Clarimon, Jordi, Lleo, Alberto, Fortea, Juan, de Mendonça, Alexandre, Martins, Madalena, Gelpi, Ellen, Grau-Rivera, Oriol, Gomez-Tortosa, Estrella, Nacmias, Benedetta, Sorbi, Sandro, Borroni, Barbara, Padovani, Alessandro, Almeida, Maria Rosario, Santana, Isabel, Diehl-Schmid, Janine, Alexopoulos, Panagiotis, Koutroumani, Maria, Tsolaki, Magda, Cras, Patrick, van der Zee, Julie, Sleegers, Kristel, Van Broeckhoven, Christine

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Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodies von 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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TBK1 Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis von der Zee, Julie, Gijselinck, Ilse, Mossevelde, Sara, Perrone, Federica, Dillen, Lubina, Heeman, Bavo, Bäumer, Veerle, Engelborghs, Sebastiaan, Bleecker, Jan, Baets, Jonathan, Gelpi, Ellen, Rojas‐García, Ricardo, Clarimón, Jordi, Lleó, Alberto, Diehl‐Schmid, Janine, Alexopoulos, Panagiotis, Perneczky, Robert, Synofzik, Matthis, Just, Jennifer, Schöls, Ludger, Graff, Caroline, Thonberg, Håkan, Borroni, Barbara, Padovani, Alessandro, Jordanova, Albena, Sarafov, Stayko, Tournev, Ivailo, Mendonça, Alexandre, Miltenberger‐Miltényi, Gabriel, Simões do Couto, Frederico, Ramirez, Alfredo, Jessen, Frank, Heneka, Michael T., Gómez‐Tortosa, Estrella, Danek, Adrian, Cras, Patrick, Vandenberghe, Rik, Jonghe, Peter, Deyn, Peter P., Sleegers, Kristel, Cruts, Marc, Broeckhoven, Christine, Goeman, Johan, Nuytten, Dirk, Smets, Katrien, Robberecht, Wim, Damme, Philip Van, Bleecker, Jan De, Santens, Patrick, Dermaut, Bart, Versijpt, Jan, Michotte, Alex, Ivanoiu, Adrian, Deryck, Olivier, Bergmans, Bruno, Delbeck, Jean, Bruyland, Marc, Willems, Christiana, Salmon, Eric, Pastor, Pau, Ortega‐Cubero, Sara, Benussi, Luisa, Ghidoni, Roberta, Binetti, Giuliano, Hernández, Isabel, Boada, Mercè, Ruiz, Agustín, Sorbi, Sandro, Nacmias, Benedetta, Bagnoli, Silvia, Sorbi, Sandro, Sanchez‐Valle, Raquel, Llado, Albert, Santana, Isabel, Rosário Almeida, Maria, Frisoni, Giovanni B, Maetzler, Walter, Matej, Radoslav, Fraidakis, Matthew J., Kovacs, Gabor G., Fabrizi, Gian Maria, Testi, Silvia

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Genome-wide association study in essential tremor identifies three new loci von Müller, Stefanie H, Girard, Simon L, Hopfner, Franziska, Merner, Nancy D, Bourassa, Cynthia V, Lorenz, Delia, Clark, Lorraine N, Tittmann, Lukas, Soto-Ortolaza, Alexandra I, Klebe, Stephan, Hallett, Mark, Schneider, Susanne A, Hodgkinson, Colin A, Lieb, Wolfgang, Wszolek, Zbigniew K, Pendziwiat, Manuela, Lorenzo-Betancor, Oswaldo, Poewe, Werner, Ortega-Cubero, Sara, Seppi, Klaus, Rajput, Alex, Hussl, Anna, Rajput, Ali H, Berg, Daniela, Dion, Patrick A, Wurster, Isabel, Shulman, Joshua M, Srulijes, Karin, Haubenberger, Dietrich, Pastor, Pau, Vilariño-Güell, Carles, Postuma, Ronald B, Bernard, Geneviève, Ladwig, Karl-Heinz, Dupré, Nicolas, Jankovic, Joseph, Strauch, Konstantin, Panisset, Michel, Winkelmann, Juliane, Testa, Claudia M, Reischl, Eva, Zeuner, Kirsten E, Ross, Owen A, Arzberger, Thomas, Chouinard, Sylvain, Deuschl, Günther, Louis, Elan D, Kuhlenbäumer, Gregor, Rouleau, Guy A

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Resequencing analysis of five Mendelian genes and the top genes from genome-wide association studies in Parkinson's Disease von Benitez, Bruno A, Davis, Albert A, Jin, Sheng Chih, Ibanez, Laura, Ortega-Cubero, Sara, Pastor, Pau, Choi, Jiyoon, Cooper, Breanna, Perlmutter, Joel S, Cruchaga, Carlos

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Genome-wide analysis of genetic correlation in dementia with Lewy bodies, Parkinson's and Alzheimer's diseases von 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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Assessing the role of the TREM2 p.R47H variant as a risk factor for Alzheimer's disease and frontotemporal dementia von Ruiz, Agustín, Dols-Icardo, Oriol, Bullido, María J, Pastor, Pau, Rodríguez-Rodríguez, Eloy, López de Munain, Adolfo, de Pancorbo, Marian M, Pérez-Tur, Jordi, Álvarez, Victoria, Antonell, Anna, López-Arrieta, Jesús, Hernández, Isabel, Tárraga, Lluís, Boada, Mercè, Lleó, Alberto, Blesa, Rafael, Frank-García, Ana, Sastre, Isabel, Razquin, Cristina, Ortega-Cubero, Sara, Lorenzo, Elena, Sánchez-Juan, Pascual, Combarros, Onofre, Moreno, Fermín, Gorostidi, Ana, Elcoroaristizabal, Xabier, Baquero, Miquel, Coto, Eliecer, Sánchez-Valle, Raquel, Clarimón, Jordi

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