Works by Clarimon, Jordi

Results: 106
    1
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    Cognitive decline in amyotrophic lateral sclerosis: Neuropathological substrate and genetic determinants.

    Published in:
    Brain Pathology, 2021, v. 31, n. 3, p. 1, doi. 10.1111/bpa.12942
    By:
    • Borrego‐Écija, Sergi;
    • Turon‐Sans, Janina;
    • Ximelis, Teresa;
    • Aldecoa, Iban;
    • Molina‐Porcel, Laura;
    • Povedano, Mónica;
    • Rubio, Miguel Angel;
    • Gámez, Josep;
    • Cano, Antonio;
    • Paré‐Curell, Martí;
    • Bajo, Lorena;
    • Sotoca, Javier;
    • Clarimón, Jordi;
    • Balasa, Mircea;
    • Antonell, Anna;
    • Lladó, Albert;
    • Sánchez‐Valle, Raquel;
    • Rojas‐García, Ricard;
    • Gelpi, Ellen
    Publication type:
    Article
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    Cerebrospinal fluid β-amyloid and phospho-tau biomarker interactions affecting brain structure in preclinical Alzheimer disease.

    Published in:
    Annals of Neurology, 2014, v. 76, n. 2, p. 223, doi. 10.1002/ana.24186
    By:
    • Fortea, Juan;
    • Vilaplana, Eduard;
    • Alcolea, Daniel;
    • Carmona‐Iragui, María;
    • Sánchez‐Saudinos, María‐Belén;
    • Sala, Isabel;
    • Antón‐Aguirre, Sofía;
    • González, Sofía;
    • Medrano, Santiago;
    • Pegueroles, Jordi;
    • Morenas, Estrella;
    • Clarimón, Jordi;
    • Blesa, Rafael;
    • Lleó, Alberto
    Publication type:
    Article
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    A megalin polymorphism associated with increased Alzheimer's disease risk

    Published in:
    2009
    By:
    • Vargas, Teo;
    • Bullido, Maria J.;
    • Martinez, Ana;
    • Antequera, Desiree;
    • Clarimon, Jordi;
    • Rosich-Estrago, Marcel;
    • Martin-Requero, Angeles;
    • Vilella-Cuadrado, Elisabet;
    • Frank, Ana;
    • Lleo, Alberto;
    • Molina-Porcel, Laura;
    • Blesa, Rafael;
    • Gomez-Isla, Teresa;
    • Bermejo-Pareja, Felix;
    • Valdivieso, Fernando;
    • Carro, Eva
    Publication type:
    Abstract
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    P3-213: Genetic screening in a large cohort of early-onset Alzheimer's disease patients from Spain: Novel mutations in the amyloid precursor protein and presenilines

    Published in:
    2008
    By:
    • Clarimón, Jordi;
    • Guerreiro, Rita;
    • Lleó, Alberto;
    • Guardia, Cristina;
    • Blesa, Rafael;
    • Gómez-Isla, Teresa;
    • Boada, Merce;
    • Bullido, Jesus;
    • Ferrer, Isidre;
    • Martínez-Lage, Pablo;
    • Masdeu, Jose;
    • Molina, Laura;
    • Molinuevo, José Luís;
    • Pastor, Pau;
    • Pérez-Tur, Jordi;
    • Rey, Jesus;
    • Sánchez-Valle, Raquel;
    • Tàrraga, Lluís;
    • Valdivieso, Fernando;
    • Singleton, Andrew
    Publication type:
    Abstract
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    A comprehensive study of the genetic impact of rare variants in SORL1 in European early-onset Alzheimer's disease.

    Published in:
    Acta Neuropathologica, 2016, v. 132, n. 2, p. 213, doi. 10.1007/s00401-016-1566-9
    By:
    • Verheijen, Jan;
    • Bossche, Tobi;
    • Zee, Julie;
    • Engelborghs, Sebastiaan;
    • Sanchez-Valle, Raquel;
    • Lladó, Albert;
    • Graff, Caroline;
    • Thonberg, Håkan;
    • Pastor, Pau;
    • Ortega-Cubero, Sara;
    • Pastor, Maria;
    • Benussi, Luisa;
    • Ghidoni, Roberta;
    • Binetti, Giuliano;
    • Clarimon, Jordi;
    • Lleó, Alberto;
    • Fortea, Juan;
    • Mendonça, Alexandre;
    • Martins, Madalena;
    • Grau-Rivera, Oriol
    Publication type:
    Article
    15

    Cerebrospinal fluid mitochondrial DNA levels in patients with multiple sclerosis.

    Published in:
    Multiple Sclerosis Journal, 2019, v. 25, n. 11, p. 1535, doi. 10.1177/1352458518786055
    By:
    • Fissolo, Nicolas;
    • Cervera-Carles, Laura;
    • Villar Guimerans, Luisa María;
    • Lleó, Alberto;
    • Clarimón, Jordi;
    • Drulovic, Jelena;
    • Dujmovic, Irena;
    • Voortman, Margarete;
    • Khalil, Michael;
    • Gil, Elia;
    • Navarro, Laura;
    • Álvarez-Cermeño, Jose Carlos;
    • Montalban, Xavier;
    • Comabella, Manuel
    Publication type:
    Article
    16

    A POGLUT1 mutation causes a muscular dystrophy with reduced Notch signaling and satellite cell loss.

    Published in:
    EMBO Molecular Medicine, 2016, v. 8, n. 11, p. 1289, doi. 10.15252/emmm.201505815
    By:
    • Servián‐Morilla, Emilia;
    • Takeuchi, Hideyuki;
    • Lee, Tom V;
    • Clarimon, Jordi;
    • Mavillard, Fabiola;
    • Area‐Gómez, Estela;
    • Rivas, Eloy;
    • Nieto‐González, Jose L;
    • Rivero, Maria C;
    • Cabrera‐Serrano, Macarena;
    • Gómez‐Sánchez, Leonardo;
    • Martínez‐López, Jose A;
    • Estrada, Beatriz;
    • Márquez, Celedonio;
    • Morgado, Yolanda;
    • Suárez‐Calvet, Xavier;
    • Pita, Guillermo;
    • Bigot, Anne;
    • Gallardo, Eduard;
    • Fernández‐Chacón, Rafael
    Publication type:
    Article
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    Neuropathology of a patient with Alzheimer disease treated with low doses of verubecestat.

    Published in:
    Neuropathology & Applied Neurobiology, 2022, v. 48, n. 3, p. 1, doi. 10.1111/nan.12781
    By:
    • Querol‐Vilaseca, Marta;
    • Sirisi, Sònia;
    • Molina‐Porcel, Laura;
    • Molina, Beatriu;
    • Pegueroles, Jordi;
    • Ferrer‐Raventós, Paula;
    • Nuñez‐Llaves, Raúl;
    • Dols‐Icardo, Oriol;
    • Balasa, Mircea;
    • Iulita, Maria Florencia;
    • Blesa, Rafael;
    • Belbin, Olivia;
    • Clarimon, Jordi;
    • Fortea, Juan;
    • Gelpi, Ellen;
    • Sánchez‐Valle, Raquel;
    • Lleó, Alberto
    Publication type:
    Article
    21
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    Brain hypometabolism in non‐demented microtubule‐associated protein tau H1 carriers with Parkinson's disease.

    Published in:
    Journal of Neuroimaging, 2023, v. 33, n. 6, p. 953, doi. 10.1111/jon.13156
    By:
    • Gasca‐Salas, Carmen;
    • Trompeta, Clara;
    • López‐Aguirre, Miguel;
    • Rodríguez Rojas, Rafael;
    • Clarimon, Jordi;
    • Dols‐Icardo, Oriol;
    • El Bounasri, Shaimaa;
    • Guida, Pasqualina;
    • Mata‐Marín, David;
    • Hernández‐Fernández, Frida;
    • Marras, Connie;
    • García‐Cañamaque, Lina;
    • Plaza de las Heras, Isabel;
    • Obeso, Ignacio;
    • Vela, Lydia;
    • Fernández‐Rodríguez, Beatriz
    Publication type:
    Article
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    Myelin loss in C9orf72 hexanucleotide expansion carriers.

    Published in:
    Journal of Neuroscience Research, 2022, v. 100, n. 10, p. 1862, doi. 10.1002/jnr.25100
    By:
    • Sirisi, Sònia;
    • Querol‐Vilaseca, Marta;
    • Dols‐Icardo, Oriol;
    • Pegueroles, Jordi;
    • Montal, Victor;
    • Muñoz, Laia;
    • Torres, Soraya;
    • Ferrer‐Raventós, Paula;
    • Iulita, Maria Florencia;
    • Sánchez‐Aced, Érika;
    • Blesa, Rafael;
    • Illán‐Gala, Ignacio;
    • Molina‐Porcel, Laura;
    • Borrego‐Ecija, Sergi;
    • Sánchez‐Valle, Raquel;
    • Clarimon, Jordi;
    • Belbin, Olivia;
    • Fortea, Juan;
    • Lleó, Alberto
    Publication type:
    Article
    27

    Synaptic phosphorylated α-synuclein in dementia with Lewy bodies.

    Published in:
    2017
    By:
    • Colom-Cadena, Martí;
    • Pegueroles, Jordi;
    • Herrmann, Abigail G.;
    • Henstridge, Christopher M.;
    • Muñoz, Laia;
    • Querol-Vilaseca, Marta;
    • Martín-Paniello, Carla San;
    • Luque-Cabecerans, Joan;
    • Clarimon, Jordi;
    • Belbin, Olivia;
    • Núñez-Llaves, Raúl;
    • Blesa, Rafael;
    • Smith, Colin;
    • McKenzie, Chris-Anne;
    • Frosch, Matthew P.;
    • Roe, Allyson;
    • Fortea, Juan;
    • Andilla, Jordi;
    • Loza-Alvarez, Pablo;
    • Gelpi, Ellen
    Publication type:
    journal article
    28

    Glucocerebrosidase mutations confer a greater risk of dementia during Parkinson's disease course.

    Published in:
    Movement Disorders, 2012, v. 27, n. 3, p. 393, doi. 10.1002/mds.24045
    By:
    • Setó-Salvia, Núria;
    • Pagonabarraga, Javier;
    • Houlden, Henry;
    • Pascual-Sedano, Berta;
    • Dols-Icardo, Oriol;
    • Tucci, Arianna;
    • Paisán-Ruiz, Coro;
    • Campolongo, Antonia;
    • Antón-Aguirre, Sofía;
    • Martín, Inés;
    • Muñoz, Laia;
    • Bufill, Enric;
    • Vilageliu, Lluïsa;
    • Grinberg, Daniel;
    • Cozar, Mónica;
    • Blesa, Rafael;
    • Lleó, Alberto;
    • Hardy, John;
    • Kulisevsky, Jaime;
    • Clarimón, Jordi
    Publication type:
    Article
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    TBK1 Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis.

    Published in:
    Human Mutation, 2017, v. 38, n. 3, p. 297, doi. 10.1002/humu.23161
    By:
    • 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
    Publication type:
    Article
    34

    PLD3 in non-familial Alzheimer's disease.

    Published in:
    Nature, 2015, v. 520, n. 7545, p. E3, doi. 10.1038/nature14039
    By:
    • Heilmann, Stefanie;
    • Drichel, Dmitriy;
    • Clarimon, Jordi;
    • Fernández, Victoria;
    • Lacour, André;
    • Wagner, Holger;
    • Thelen, Mathias;
    • Hernández, Isabel;
    • Fortea, Juan;
    • Alegret, Montserrat;
    • Blesa, Rafael;
    • Mauleón, Ana;
    • Roca, Maitée Rosende;
    • Kornhuber, Johannes;
    • Peters, Oliver;
    • Heun, Reinhard;
    • Frölich, Lutz;
    • Hüll, Michael;
    • Heneka, Michael T.;
    • Rüther, Eckart
    Publication type:
    Article
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    Author Correction: GBA and APOE ε4 associate with sporadic dementia with Lewy bodies in European genome wide association study.

    Published in:
    2019
    By:
    • Rongve, Arvid;
    • Witoelar, Aree;
    • Ruiz, Agustín;
    • Athanasiu, Lavinia;
    • Abdelnour, Carla;
    • Clarimon, Jordi;
    • Heilmann-Heimbach, Stefanie;
    • Hernández, Isabel;
    • Moreno-Grau, Sonia;
    • de Rojas, Itziar;
    • Morenas-Rodríguez, Estrella;
    • Fladby, Tormod;
    • Sando, Sigrid B.;
    • Bråthen, Geir;
    • Blanc, Frédéric;
    • Bousiges, Olivier;
    • Lemstra, Afina W.;
    • van Steenoven, Inger;
    • Londos, Elisabet;
    • Almdahl, Ina S.
    Publication type:
    Correction Notice
    38

    Nanoscale structure of amyloid-β plaques in Alzheimer's disease.

    Published in:
    Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-41443-3
    By:
    • Querol-Vilaseca, Marta;
    • Colom-Cadena, Martí;
    • Pegueroles, Jordi;
    • Nuñez-Llaves, Raúl;
    • Luque-Cabecerans, Joan;
    • Muñoz-Llahuna, Laia;
    • Andilla, Jordi;
    • Belbin, Olivia;
    • Spires-Jones, Tara L.;
    • Gelpi, Ellen;
    • Clarimon, Jordi;
    • Loza-Alvarez, Pablo;
    • Fortea, Juan;
    • Lleó, Alberto
    Publication type:
    Article
    39

    VAMP-2 is a surrogate cerebrospinal fluid marker of Alzheimer-related cognitive impairment in adults with Down syndrome.

    Published in:
    Alzheimer's Research & Therapy, 2021, v. 13, n. 1, p. 1, doi. 10.1186/s13195-021-00861-0
    By:
    • Lleó, Alberto;
    • Carmona-Iragui, Maria;
    • Videla, Laura;
    • Fernández, Susana;
    • Benejam, Bessy;
    • Pegueroles, Jordi;
    • Barroeta, Isabel;
    • Altuna, Miren;
    • Valldeneu, Silvia;
    • Xiao, Mei-Fang;
    • Xu, Desheng;
    • Núñez-Llaves, Raúl;
    • Querol-Vilaseca, Marta;
    • Sirisi, Sònia;
    • Bejanin, Alexandre;
    • Iulita, M. Florencia;
    • Clarimón, Jordi;
    • Blesa, Rafael;
    • Worley, Paul;
    • Alcolea, Daniel
    Publication type:
    Article
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    Distinct patterns of APP processing in the CNS in autosomal-dominant and sporadic Alzheimer disease.

    Published in:
    Acta Neuropathologica, 2013, v. 125, n. 2, p. 201, doi. 10.1007/s00401-012-1062-9
    By:
    • Pera, Marta;
    • Alcolea, Daniel;
    • Sánchez-Valle, Raquel;
    • Guardia-Laguarta, Cristina;
    • Colom-Cadena, Martí;
    • Badiola, Nahuai;
    • Suárez-Calvet, Marc;
    • Lladó, Albert;
    • Barrera-Ocampo, Alvaro;
    • Sepulveda-Falla, Diego;
    • Blesa, Rafael;
    • Molinuevo, José;
    • Clarimón, Jordi;
    • Ferrer, Isidre;
    • Gelpi, Ellen;
    • Lleó, Alberto
    Publication type:
    Article
    43

    APP‐derived peptides reflect neurodegeneration in frontotemporal dementia.

    Published in:
    Annals of Clinical & Translational Neurology, 2019, v. 6, n. 12, p. 2518, doi. 10.1002/acn3.50948
    By:
    • Illán‐Gala, Ignacio;
    • Pegueroles, Jordi;
    • Montal, Victor;
    • Alcolea, Daniel;
    • Vilaplana, Eduard;
    • Bejanin, Alexandre;
    • Borrego‐Écija, Sergi;
    • Sampedro, Frederic;
    • Subirana, Andrea;
    • Sánchez‐Saudinós, María‐Belén;
    • Rojas‐García, Ricard;
    • Vanderstichele, Hugo;
    • Blesa, Rafael;
    • Clarimón, Jordi;
    • Antonell, Anna;
    • Lladó, Albert;
    • Sánchez‐Valle, Raquel;
    • Fortea, Juan;
    • Lleó, Alberto
    Publication type:
    Article
    44

    Agreement of amyloid PET and CSF biomarkers for Alzheimer's disease on Lumipulse.

    Published in:
    Annals of Clinical & Translational Neurology, 2019, v. 6, n. 9, p. 1815, doi. 10.1002/acn3.50873
    By:
    • Alcolea, Daniel;
    • Pegueroles, Jordi;
    • Muñoz, Laia;
    • Camacho, Valle;
    • López‐Mora, Diego;
    • Fernández‐León, Alejandro;
    • Le Bastard, Nathalie;
    • Huyck, Els;
    • Nadal, Alicia;
    • Olmedo, Verónica;
    • Sampedro, Frederic;
    • Montal, Victor;
    • Vilaplana, Eduard;
    • Clarimón, Jordi;
    • Blesa, Rafael;
    • Fortea, Juan;
    • Lleó, Alberto
    Publication type:
    Article
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    Homocysteine and Cognitive Impairment.

    Published in:
    Dementia & Geriatric Cognitive Disorders, 2008, v. 26, n. 6, p. 506, doi. 10.1159/000173710
    By:
    • Sala, Isabel;
    • Sánchez-Saudinós, María Belén;
    • Molina-Porcel, Laura;
    • Lázaro, Estela;
    • Gich, Ignasi;
    • Clarimón, Jordi;
    • Blanco-Vaca, Francisco;
    • Blesa, Rafael;
    • Gómez-Isla, Teresa;
    • Lleó, Alberto
    Publication type:
    Article
    47

    A postzygotic de novo NCDN mutation identified in a sporadic FTLD patient results in neurochondrin haploinsufficiency and altered FUS granule dynamics.

    Published in:
    Acta Neuropathologica Communications, 2022, v. 10, n. 1, p. 1, doi. 10.1186/s40478-022-01314-x
    By:
    • Nicolas, Gaël;
    • Sévigny, Myriam;
    • Lecoquierre, François;
    • Marguet, Florent;
    • Deschênes, Andréanne;
    • del Pelaez, Maria Carment;
    • Feuillette, Sébastien;
    • Audebrand, Anaïs;
    • Lecourtois, Magalie;
    • Rousseau, Stéphane;
    • Richard, Anne-Claire;
    • Cassinari, Kévin;
    • Deramecourt, Vincent;
    • Duyckaerts, Charles;
    • Boland, Anne;
    • Deleuze, Jean-François;
    • Meyer, Vincent;
    • Clarimon Echavarria, Jordi;
    • Gelpi, Ellen;
    • Akiyama, Haruhiko
    Publication type:
    Article
    48

    Copy number variation analysis of the 17q21.31 region and its role in neurodegenerative diseases.

    Published in:
    American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 2, p. 175, doi. 10.1002/ajmg.b.32390
    By:
    • Cervera‐Carles, Laura;
    • Pagonabarraga, Javier;
    • Pascual‐Sedano, Berta;
    • Pastor, Pau;
    • Campolongo, Antonia;
    • Fortea, Juan;
    • Blesa, Rafael;
    • Alcolea, Daniel;
    • Morenas‐Rodríguez, Estrella;
    • Sala, Isabel;
    • Lleó, Alberto;
    • Kulisevsky, Jaime;
    • Clarimón, Jordi
    Publication type:
    Article
    49

    Leveraging large multi-center cohorts of Alzheimer disease endophenotypes to understand the role of Klotho heterozygosity on disease risk.

    Published in:
    PLoS ONE, 2022, v. 17, n. 5, p. 1, doi. 10.1371/journal.pone.0267298
    By:
    • Ali, Muhammad;
    • Sung, Yun Ju;
    • Wang, Fengxian;
    • Fernández, Maria V.;
    • Morris, John C.;
    • Fagan, Anne M.;
    • Blennow, Kaj;
    • Zetterberg, Henrik;
    • Heslegrave, Amanda;
    • Johansson, Per M.;
    • Svensson, Johan;
    • Nellgård, Bengt;
    • Lleó, Alberto;
    • Alcolea, Daniel;
    • Clarimon, Jordi;
    • Rami, Lorena;
    • Molinuevo, José Luis;
    • Suárez-Calvet, Marc;
    • Morenas-Rodríguez, Estrella;
    • Kleinberger, Gernot
    Publication type:
    Article
    50