Works matching AU Clarimon, Jordi

Results: 106

HSP70-2 (HSPA1B) is associated with noncognitive symptoms in late-onset Alzheimer's disease.

Published in:

2003

By:

Clarimón, Jordi;
Bertranpetit, Jaume;
Boada, Mercè;
Tàrraga, Lluís;
Comas, David;
Clarimón, Jordi;
Boada, Mercè;
Tàrraga, Lluís

Publication type:

journal article

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

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

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

Distinct Clinical Features and Outcomes in Motor Neuron Disease Associated with Behavioural Variant Frontotemporal Dementia.

Published in:

Dementia & Geriatric Cognitive Disorders, 2018, v. 45, n. 3/4, p. 220, doi. 10.1159/000488528

By:

Cortés-Vicente, Elena;
Turon-Sans, Janina;
Illa, Isabel;
Rojas-García, Ricard;
Gelpi, Ellen;
Clarimón, Jordi;
Dols-Icardo, Oriol;
Illán-Gala, Ignacio;
Lleó, Alberto;
Blesa, Rafael;
Borrego-Écija, Sergi;
Al-Chalabi, Ammar

Publication type:

Article

Early diagnosis of amyotrophic lateral sclerosis mimic syndromes: pros and cons of current clinical diagnostic criteria.

Published in:

Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration, 2017, v. 18, n. 5/6, p. 333, doi. 10.1080/21678421.2017.1316408

By:

Cortés-Vicente, Elena;
Pradas, Jesús;
Marín-lahoz, Juan;
De Luna, Noemi;
Clarimón, Jordi;
Turon-Sans, Janina;
Gelpí, Ellen;
Díaz-Manera, Jordi;
Illa, Isabel;
Rojas-Garcia, Ricard

Publication type:

Article

Genetic structure of north-west Africa revealed by STR analysis.

Published in:

European Journal of Human Genetics, 2000, v. 8, n. 5, p. 360, doi. 10.1038/sj.ejhg.5200464

By:

Bosch, Elena;
Calafell, Francesc;
Pérez-Lezaun, Anna;
Clarimón, Jordi;
Comas, David;
Mateu, Eva;
Martínez-Arias, Rosa;
Morera, Bernal;
Brakez, Zahra;
Akhayat, Omar;
Sefiani, Abdelaziz;
Hariti, Ghania;
Cambon-Thomsen, Anne;
Bertranpetit, Jaume

Publication type:

Article

Correction: Absence of pathogenic mutations in CD59 in chronic inflammatory demyelinating polyradiculoneuropathy.

Published in:

PLoS ONE, 2019, v. 14, n. 4, p. 1, doi. 10.1371/journal.pone.0215784

By:

Duchateau, Lena;
Martín-Aguilar, Lorena;
Lleixà, Cinta;
Cortese, Andrea;
Dols-Icardo, Oriol;
Cervera-Carles, Laura;
Pascual-Goñi, Elba;
Diaz-Manera, Jordi;
Callegari, Ilaria;
Franciotta, Diego;
Rojas-Garcia, Ricard;
Illa, Isabel;
Clarimon, Jordi;
Querol, Luis

Publication type:

Article

Absence of pathogenic mutations in CD59 in chronic inflammatory demyelinating polyradiculoneuropathy.

Published in:

PLoS ONE, 2019, v. 14, n. 2, p. 1, doi. 10.1371/journal.pone.0212647

By:

Duchateau, Lena;
Martín-Aguilar, Lorena;
Lleixà, Cinta;
Cortese, Andrea;
Dols-Icardo, Oriol;
Cervera-Carles, Laura;
Pascual-Goñi, Elba;
Diaz-Manera, Jordi;
Calegari, Ilaria;
Franciotta, Diego;
Rojas-Garcia, Ricard;
Illa, Isabel;
Clarimon, Jordi;
Querol, Luis

Publication type:

Article

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

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

Association study between Alzheimer’s disease and genes involved in Aβ biosynthesis, aggregation and degradation: suggestive results with BACE1.

Published in:

Journal of Neurology, 2003, v. 250, n. 8, p. 956

By:

Clarimón, Jordi;
Bertranpetit, Jaume;
Calafell, Francesc;
Boada, Mercè;
Tàrraga, Lluís;
Comas, David

Publication type:

Article

Detection of genomic rearrangements from targeted resequencing data in Parkinson's disease patients.

Published in:

2017

By:

Spataro, Nino;
Roca‐Umbert, Ana;
Cervera‐Carles, Laura;
Vallès, Mònica;
Anglada, Roger;
Pagonabarraga, Javier;
Pascual‐Sedano, Berta;
Campolongo, Antònia;
Kulisevsky, Jaime;
Casals, Ferran;
Clarimón, Jordi;
Bosch, Elena

Publication type:

journal article

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

Tremor dominant parkinsonism: Clinical description and LRRK2 mutation screening.

Published in:

Movement Disorders, 2008, v. 23, n. 4, p. 518, doi. 10.1002/mds.21771

By:

Clarimón, Jordi;
Pagonabarraga, Javier;
Paisán-Ruíz, Coro;
Campolongo, Antonia;
Pascual-Sedano, Berta;
Martí-Massó, José-Félix;
Singleton, Andrew B.;
Kulisevsky, Jaime

Publication type:

Article

Assessing the role of DRD5 and DYT1 in two different case-control series with primary blepharospasm.

Published in:

Movement Disorders, 2007, v. 22, n. 2, p. 162, doi. 10.1002/mds.21182

By:

Clarimon, Jordi;
Brancati, Francesco;
Peckham, Elizabeth;
Valente, Enza Maria;
Dallapiccola, Bruno;
Abruzzese, Giovanni;
Girlanda, Paolo;
Defazio, Giovanni;
Berardelli, Alfredo;
Hallett, Mark;
Singleton, Andrew B.

Publication type:

Article

Association of the Tau haplotype with Parkinson's disease in the Greek population.

Published in:

2006

By:

Fidani, Liana;
Kalinderi, Kallirhoe;
Bostantjopoulou, Sevasti;
Clarimon, Jordi;
Goulas, Antonis;
Katsarou, Zoe;
Hardy, John;
Kotsis, Alexandros

Publication type:

journal article

Mutation of the Parkin gene in a Persian family: clinical progression over a 40-year period.

Published in:

2005

By:

Clarimon, Jordi;
Johnson, Janel;
Djaldetti, Ruth;
Hernandez, Dena;
Hattori, Nobutaka;
Sroka, Hava;
Barhom, Yael;
Singleton, Andrew

Publication type:

journal article

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

Diagnostic Utility of Measuring Cerebral Atrophy in the Behavioral Variant of Frontotemporal Dementia and Association With Clinical Deterioration.

Published in:

JAMA Network Open, 2021, v. 4, n. 3, p. e211290, doi. 10.1001/jamanetworkopen.2021.1290

By:

Illán-Gala, Ignacio;
Falgàs, Neus;
Friedberg, Adit;
Castro-Suárez, Sheila;
Keret, Ophir;
Rogers, Nicole;
Oz, Didem;
Nigro, Salvatore;
Quattrone, Andrea;
Quattrone, Aldo;
Wolf, Amy;
Younes, Kyan;
Santos-Santos, Miguel;
Borrego-Écija, Sergi;
Cobigo, Yann;
Dols-Icardo, Oriol;
Lladó, Albert;
Sánchez-Valle, Raquel;
Clarimon, Jordi;
Blesa, Rafael

Publication type:

Article

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

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

Heterozygous APOE Christchurch in familial Alzheimer's disease without mutations in other Mendelian genes.

Published in:

Neuropathology & Applied Neurobiology, 2021, v. 47, n. 4, p. 579, doi. 10.1111/nan.12670

By:

Hernandez, Isabel;
Gelpi, Ellen;
Molina‐Porcel, Laura;
Bernal, Sara;
Rodríguez‐Santiago, Benjamín;
Dols‐Icardo, Oriol;
Ruiz, Agustín;
Alcolea, Daniel;
Boada, Mercè;
Lleó, Alberto;
Clarimón, Jordi

Publication type:

Article

A Common BACE1 Polymorphism Is a Risk Factor for Sporadic Creutzfeldt- Jakob Disease.

Published in:

PLoS ONE, 2012, v. 7, n. 8, p. 1, doi. 10.1371/journal.pone.0043926

By:

Calero, Olga;
Bullido, Mariá J.;
Clarimón, Jordi;
Frank-García, Ana;
Martínez-Martín, Pablo;
Lleó, Alberto;
Rey, Mariá Jesús;
Sastre, Isabel;
Rábano, Alberto;
De Pedro-Cuesta, Jesús;
Ferrer, Isidro;
Calero, Miguel

Publication type:

Article

Tau Enhances α-Synuclein Aggregation and Toxicity in Cellular Models of Synucleinopathy.

Published in:

PLoS ONE, 2011, v. 6, n. 10, p. 1, doi. 10.1371/journal.pone.0026609

By:

Badiola, Nahuai;
de Oliveira, Rita Machado;
Herrera, Federico;
Guardia-Laguarta, Cristina;
Gonçalves, Susana A.;
Pera, Marta;
Suárez-Calvet, Marc;
Clarimon, Jordi;
Outeiro, Tiago Fleming;
Lleó, Alberto

Publication type:

Article

Genetic Cross-Interaction between APOE and PRNP in Sporadic Alzheimer's and Creutzfeldt-Jakob Diseases.

Published in:

PLoS ONE, 2011, v. 6, n. 7, p. 1, doi. 10.1371/journal.pone.0022090

By:

Calero, Olga;
Bullido, María J.;
Clarimón, Jordi;
Frank-García, Ana;
Martínez-Martín, Pablo;
Lleó, Alberto;
Rey, María Jesús;
Rábano, Alberto;
Blesa, Rafael;
Gómez-Isla, Teresa;
Valdivieso, Fernando;
de Pedro-Cuesta, Jesús;
Ferrer, Isidro;
Calero, Miguel

Publication type:

Article

Activation of PKR Causes Amyloid ß-Peptide Accumulation via De-Repression of BACE1 Expression.

Published in:

PLoS ONE, 2011, v. 6, n. 6, p. 1, doi. 10.1371/journal.pone.0021456

By:

Ill-Raga, Gerard;
Palomer, Ernest;
Wozniak, Matthew A.;
Ramos-Fernández, Eva;
Bosch-Morató, Mònica;
Tajes, Marta;
Guix, Francesc X.;
Galán, José J.;
Clarimón, Jordi;
Antúnez, Carmen;
Real, Luis M.;
Boada, Mercé;
Itzhaki, Ruth F.;
Fandos, César;
Muñoz, Francisco J.

Publication type:

Article

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

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

Missense mutations in TENM4, a regulator of axon guidance and central myelination, cause essential tremor.

Published in:

Human Molecular Genetics, 2015, v. 24, n. 20, p. 5677, doi. 10.1093/hmg/ddv281

By:

Hyun Hor;
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.

Publication type:

Article

Mendelian genes for Parkinson's disease contribute to the sporadic forms of the disease.

Published in:

Human Molecular Genetics, 2015, v. 24, n. 7, p. 2023, doi. 10.1093/hmg/ddu616

By:

Spataro, Nino;
Calafell, Francesc;
Cervera-Carles, Laura;
Casals, Ferran;
Pagonabarraga, Javier;
Pascual-Sedano, Berta;
Campolongo, Antònia;
Kulisevsky, Jaime;
Lleó, Alberto;
Navarro, Arcadi;
Clarimón, Jordi;
Bosch, Elena

Publication type:

Article

Lack of Association of the PICALM rs3851179 Polymorphism With Parkinson's Disease in the Greek Population.

Published in:

International Journal of Neuroscience, 2012, v. 122, n. 10, p. 602, doi. 10.3109/00207454.2012.697083

By:

Kalinderi, Kallirhoe;
Bostantjopoulou, Sevasti;
Katsarou, Zoe;
Clarimón, Jordi;
Fidani, Liana

Publication type:

Article

Cortical microstructure in the behavioural variant of frontotemporal dementia: looking beyond atrophy.

Published in:

2019

By:

Illán-Gala, Ignacio;
Montal, Victor;
Borrego-Écija, Sergi;
Vilaplana, Eduard;
Pegueroles, Jordi;
Alcolea, Daniel;
Sánchez-Saudinós, Belén;
Clarimón, Jordi;
Turón-Sans, Janina;
Bargalló, Nuria;
González-Ortiz, Sofía;
Rosen, Howard J;
Gorno-Tempini, Maria Luisa;
Miller, Bruce L;
Lladó, Albert;
Rojas-García, Ricard;
Blesa, Rafael;
Sánchez-Valle, Raquel;
Lleó, Alberto;
Fortea, Juan

Publication type:

journal article

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

Effect of REST on brain metabolism in the Alzheimer disease continuum.

Published in:

2015

By:

Dols‐Icardo, Oriol;
Vilaplana, Eduard;
Sampedro, Frederic;
Alcolea, Daniel;
Belbin, Olivia;
Camacho, Valle;
Blesa, Rafael;
Lleó, Alberto;
Clarimón, Jordi;
Fortea, Juan

Publication type:

Letter

Cerebrospinal fluid [beta]-amyloid and phospho-tau biomarker interactions affecting brain structure in preclinical Alzheimer disease.

Published in:

2014

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;
Alzheimer's Disease Neuroimaging Initiative

Publication type:

Journal Article

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

Rare missense variant (R251G) on APOE counterbalances the Alzheimer's disease risk associated with APOE‐ε4.

Published in:

Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2022, v. 18, n. 4, p. 1, doi. 10.1002/alz.060114

By:

Guen, Yann Le;
Belloy, Michael E;
Grenier‐Boley, Benjamin;
de Rojas, Itziar;
Castillo, Atahualpa;
Jansen, Iris E;
Nicolas, Aude;
Bellenguez, Céline;
Dalmasso, Carolina;
Küçükali, Fahri;
Eger, Sarah J;
Álvarez‐Martínez, Victoria;
Arosio, Beatrice;
Benussi, Luisa;
Boland, Anne;
Borroni, Barbara;
Bullido, María J.;
Caffarra, Paolo;
Clarimón, Jordi;
Daian, Delphine

Publication type:

Article

Transcriptome wide correlations with neuropathological hallmarks in the frontal cortex of FTLD patients.

Published in:

Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2022, v. 18, n. 4, p. 1, doi. 10.1002/alz.059619

By:

Dols‐Icardo, Oriol;
Dolcet, Sònia Sirisi;
Montal, Victor;
Molina, Laura;
Naganathan, Vikram;
Querol‐Vilaseca, Marta;
Illán‐Gala, Ignacio;
Pegueroles, Jordi;
Tamayo, Natalia Valle;
Sánchez‐Aced, Érika;
Cervantes‐González, Alba;
Iulita, M. Florencia;
Belbin, Olivia;
Blesa, Rafael;
Fortea, Juan;
Lleó, Alberto;
Clarimón, Jordi

Publication type:

Article

Sex differences in the behavioral variant of frontotemporal dementia: A new window to executive and behavioral reserve.

Published in:

Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2021, v. 17, p. 1, doi. 10.1002/alz.049693

By:

Illán‐Gala, Ignacio;
Casaletto, Kaitlin B.;
Borrego‐Écija, Sergi;
Arenaza‐Urquijo, Eider M;
Wolf, Amy;
Cobigo, Yann;
Goh, Sheng‐Yang Matthew;
Staffaroni, Adam M.;
Alcolea, Daniel;
Fortea, Juan;
Blesa, Rafael;
Clarimon, Jordi;
Iulita, M. Florencia;
Brugulat‐Serrat, Anna;
Lladó, Albert;
Grinberg, Lea T.;
Possin, Kate L;
Rankin, Katherine P;
Kramer, Joel H;
Rabinovici, Gil D.

Publication type:

Article

Transcriptome‐wide characterization of the frontal cortex in FTLD.

Published in:

Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2021, v. 17, n. 3, p. 1, doi. 10.1002/alz.049569

By:

Dols‐Icardo, Oriol;
Dolcet, Sonia Sirisi;
Montal, Victor;
Molina‐Porcel, Laura;
Blesa, Rafael;
Fortea, Juan;
Lleó, Alberto;
Clarimón, Jordi

Publication type:

Article

Sex differences in the behavioral variant of frontotemporal dementia: A new window to executive and behavioral reserve.

Published in:

Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2021, v. 17, n. 8, p. 1329, doi. 10.1002/alz.12299

By:

Illán‐Gala, Ignacio;
Casaletto, Kaitlin B.;
Borrego‐Écija, Sergi;
Arenaza‐Urquijo, Eider M.;
Wolf, Amy;
Cobigo, Yann;
Goh, Sheng Yang M.;
Staffaroni, Adam M.;
Alcolea, Daniel;
Fortea, Juan;
Blesa, Rafael;
Clarimon, Jordi;
Iulita, Maria Florencia;
Brugulat‐Serrat, Anna;
Lladó, Albert;
Grinberg, Lea T.;
Possin, Katherine;
Rankin, Katherine P.;
Kramer, Joel H.;
Rabinovici, Gil D.

Publication type:

Article

Biphasic cortical macro‐ and microstructural changes in autosomal dominant Alzheimer's disease.

Published in:

Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2021, v. 17, n. 4, p. 618, doi. 10.1002/alz.12224

By:

Montal, Victor;
Vilaplana, Eduard;
Pegueroles, Jordi;
Bejanin, Alexandre;
Alcolea, Daniel;
Carmona‐Iragui, María;
Clarimón, Jordi;
Levin, Johannes;
Cruchaga, Carlos;
Graff‐Radford, Neill R.;
Noble, James M.;
Lee, Jae‐Hong;
Allegri, Ricardo;
Karch, Celeste M.;
Laske, Christoph;
Schofield, Peter R.;
Salloway, Stephen;
Ances, Beau;
Benzinger, Tammie;
McDale, Eric

Publication type:

Article

VAMP2 is a cerebrospinal fluid marker of selective hippocampal synapse loss and episodic memory performance in Alzheimer's disease: Biomarkers (non‐neuroimaging) / Multi‐modal comparisons.

Published in:

Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2020, v. 16, n. 11, p. 1, doi. 10.1002/alz.045268

By:

Belbin, Olivia;
Molina, Beatriu;
Núñez‐Llaves, Raúl;
Goossens, Julie;
Dewit, Nele;
Alcolea, Daniel;
Estellés, Teresa;
Querol‐Vilaseca, Marta;
Dolcet, Sonia Sirisi;
Muñoz, Laia;
Clarimon, Jordi;
Blesa, Rafael;
Fortea, Juan;
Vanmechelen, Eugeen;
Lleó, Alberto

Publication type:

Article

SORL1‐variant carriers in ADES‐ADSP: A higher level of variant pathogenicity associates with earlier age at onset of Alzheimer's disease: Genetics/genetic factors of Alzheimer's disease.

Published in:

Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2020, v. 16, n. 11, p. 1, doi. 10.1002/alz.044492

By:

Holstege, Henne;
Hulsman, Marc;
Charbonnier, Camille;
Grenier‐Boley, Benjamin;
Quenez, Olivier;
Ahmad, Shahzad;
Amin, Najaf;
van Rooij, Jeroen G.J.;
Grozeva, Detelina;
Norsworthy, Penny;
Hummerich, Holger;
Kawalia, Amit;
Mok, Kin Y.;
Shoai, Maryam;
Dols‐Icardo, Oriol;
van Der Flier, Wiesje;
Sims, Rebecca;
Amouyel, Philippe;
Hardy, John;
Clarimon, Jordi

Publication type:

Article

<sup>1</sup>H‐MRS signature in Alzheimer disease in Down syndrome: Neuroimaging / Optimal neuroimaging measures for tracking disease progression.

Published in:

Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2020, v. 16, n. 11, p. 1, doi. 10.1002/alz.043346

By:

Barroeta, Isabel;
Montal, Victor;
Carmona‐Iragui, Maria;
Pegueroles, Jordi;
Vilaplana, Eduard;
Bejanin, Alexandre;
González‐Ortiz, Sofía;
Altuna, Miren;
Benejam, Bessy;
Alcolea, Daniel;
Videla, Laura;
Valldeneu, Sílvia;
Fernandez, Susana;
Videla, Sebastián;
Blesa, Rafael;
Clarimon, Jordi;
Lleó, Alberto;
Fortea, Juan

Publication type:

Article

Transcriptome characterization of the motor cortex suggests microglial‐related key events due to TDP‐43 aberrant inclusions: Genetics: Molecular genetics of AD and ADRD.

Published in:

Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2020, v. 16, n. 11, p. 1, doi. 10.1002/alz.042953

By:

Dols‐Icardo, Oriol;
Montal, Victor;
Dolcet, Sonia Sirisi;
López‐Pernas, Gema;
Cervera‐Carles, Laura;
Querol‐Vilaseca, Marta;
Muñoz, Laia;
Molina‐Porcel, Laura;
Pegueroles, Jordi;
Turón‐Sans, Janina;
Blesa, Rafael;
Lleó, Alberto;
Fortea, Juan;
Rojas‐García, Ricard;
Clarimon, Jordi

Publication type:

Article

The effect of APOE ɛ4 in Alzheimer's disease biomarkers in Down syndrome: Neuroimaging: Other neurodegenerative disorders.

Published in:

Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2020, v. 16, n. 11, p. 1, doi. 10.1002/alz.042889

By:

Vilaplana, Eduard;
Videla, Laura;
Carmona‐Iragui, Maria;
Benejam, Bessy;
Barroeta, Isabel;
Fernandez, Susana;
Altuna, Miren;
Pegueroles, Jordi;
Montal, Victor;
Bejanin, Alexandre;
Iulita, M. Florencia;
Valldeneu, Sílvia;
González‐Ortiz, Sofía;
Muñoz, Laia;
Camacho, Valle;
Videla, Sebastián;
Alcolea, Daniel;
Blesa, Rafael;
Lleó, Alberto;
Clarimon, Jordi

Publication type:

Article

Exome sequencing identifies three novel AD‐associated genes: Genetics/genetic factors of Alzheimer's disease.

Published in:

Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2020, v. 16, n. 11, p. 1, doi. 10.1002/alz.041592

By:

Holstege, Henne;
Hulsman, Marc;
Charbonnier, Camille;
Grenier‐Boley, Benjamin;
Quenez, Olivier;
Ahmad, Shahzad;
Amin, Najaf;
van Rooij, Jeroen G.J.;
Grozeva, Detelina;
Norsworthy, Penny;
Hummerich, Holger;
Kawalia, Amit;
Mok, Kin Y.;
Shoai, Maryam;
Dols‐Icardo, Oriol;
van Der Flier, Wiesje;
Sims, Rebecca;
Amouyel, Philippe;
Hardy, John;
Clarimon, Jordi

Publication type:

Article

Oligodendroglial alterations in FTD caused by C9orf72 expansion: Human neuropathology: Non‐AD neurodegenerative disease neuropathology.

Published in:

Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2020, v. 16, n. 11, p. 1, doi. 10.1002/alz.040196

By:

Dolcet, Sonia Sirisi;
Querol‐Vilaseca, Marta;
Dols‐Icardo, Oriol;
Pegueroles, Jordi;
Montal, Victor;
Muñoz, Laia;
Torres, Soraya;
Blesa, Rafael;
Belbin, Olivia;
Fortea, Juan;
Clarimon, Jordi;
Lleó, Alberto

Publication type:

Article