Works by Garre, Pilar

Results: 67

Reply to: "Increased Stroke Risk in Patients with Parkinson's Disease with LRRK2 Mutations".

Published in:

2022

By:

Macías‐García, Daniel;
Periñán, María Teresa;
Muñoz‐Delgado, Laura;
Jesús, Silvia;
Jimenez‐Jaraba, María Valle;
Buiza‐Rueda, Dolores;
Bonilla‐Toribio, Marta;
Adarmes‐Gómez, Astrid;
Carrillo, Fátima;
Gómez‐Garre, Pilar;
Mir, Pablo;
Macías-García, Daniel;
Muñoz-Delgado, Laura;
Jimenez-Jaraba, María Valle;
Buiza-Rueda, Dolores;
Bonilla-Toribio, Marta;
Adarmes-Gómez, Astrid;
Gómez-Garre, Pilar

Publication type:

Letter

Association of PICALM with Cognitive Impairment in Parkinson's Disease.

Published in:

2021

By:

Periñán, María Teresa;
Macías‐García, Daniel;
Labrador‐Espinosa, Miguel Ángel;
Jesús, Silvia;
Buiza‐Rueda, Dolores;
Adarmes‐Gómez, Astrid D.;
Muñoz‐Delgado, Laura;
Gómez‐Garre, Pilar;
Mir, Pablo;
Macías-García, Daniel;
Labrador-Espinosa, Miguel Ángel;
Buiza-Rueda, Dolores;
Adarmes-Gómez, Astrid D;
Muñoz-Delgado, Laura;
Gómez-Garre, Pilar

Publication type:

journal article

Durable benefit and change in TCR clonality with nivolumab in a Lynch syndrome–associated glioma.

Published in:

Therapeutic Advances in Medical Oncology, 2022, p. 1, doi. 10.1177/17588359221100863

By:

Cabezas-Camarero, Santiago;
Pérez-Alfayate, Rebeca;
García-Barberán, Vanesa;
Polidura, María Carmen;
Gómez-Ruiz, María Natividad;
Casado-Fariñas, Isabel;
Subhi-Issa, Issa Ahmad;
Hernández, José Carlos Plaza;
Garre, Pilar;
Díaz-Millán, Isabel;
Pérez-Segura, Pedro

Publication type:

Article

PSMC1 Gene in Parkinson's Disease.

Published in:

European Neurology, 2012, v. 68, n. 4, p. 193, doi. 10.1159/000339003

By:

Gómez-Garre, Pilar;
Jesús, Silvia;
Carrillo, Fátima;
Cáceres-Redondo, Maria Teresa;
Bernal-Bernal, Inmaculada;
Carballo, Manuel;
Gao, Lin;
Mir, Pablo

Publication type:

Article

Familial partial epilepsy with variable foci: A new family with suggestion of linkage to chromosome 22q12.

Published in:

Epilepsia (Series 4), 2010, v. 51, n. 9, p. 1910, doi. 10.1111/j.1528-1167.2010.02680.x

By:

Morales-Corraliza, Jos;
Gómez-Garre, Pilar;
Sanz, Raúl;
Díaz-Otero, Fernando;
Gutiérrez-Delicado, Eva;
Serratosa, José M.

Publication type:

Article

Autosomal dominant nocturnal frontal lobe epilepsy with a mutation in the CHRNB2 gene.

Published in:

Epilepsia (Series 4), 2008, v. 49, n. 3, p. 516, doi. 10.1111/j.1528-1167.2007.01328.x

By:

Díaz-Otero, Fernando;
Quesada, Mar;
Morales-Corraliza, José;
Martínez-Parra, Carlos;
Gómez-Garre, Pilar;
Serratosa, José M.

Publication type:

Article

Increased Stroke Risk in Patients with Parkinson's Disease with LRRK2 Mutations.

Published in:

Movement Disorders, 2022, v. 37, n. 1, p. 225, doi. 10.1002/mds.28863

By:

Macías‐García, Daniel;
Periñán, María Teresa;
Muñoz‐Delgado, Laura;
Jesús, Silvia;
Jimenez‐Jaraba, María Valle;
Buiza‐Rueda, Dolores;
Bonilla‐Toribio, Marta;
Adarmes‐Gómez, Astrid;
Carrillo, Fátima;
Gómez‐Garre, Pilar;
Mir, Pablo

Publication type:

Article

The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population-Specific Risk, Differential Haplotype Structures, and Providing Etiologic Insight.

Published in:

2019

By:

Bandres‐Ciga, Sara;
Ahmed, Sarah;
Sabir, Marya S.;
Blauwendraat, Cornelis;
Adarmes‐Gómez, Astrid D.;
Bernal‐Bernal, Inmaculada;
Bonilla‐Toribio, Marta;
Buiza‐Rueda, Dolores;
Carrillo, Fátima;
Carrión‐Claro, Mario;
Gómez‐Garre, Pilar;
Jesús, Silvia;
Labrador‐Espinosa, Miguel A.;
Macias, Daniel;
Méndez‐del‐Barrio, Carlota;
Periñán‐Tocino, Teresa;
Tejera‐Parrado, Cristina;
Vargas‐González, Laura;
Diez‐Fairen, Monica;
Alvarez, Ignacio

Publication type:

journal article

Low serum uric acid levels in progressive supranuclear palsy.

Published in:

2016

By:

Oropesa‐Ruiz, Juan Manuel;
Huertas‐Fernández, Ismael;
Jesús, Silvia;
Cáceres‐Redondo, María Teresa;
Vargas‐Gonzalez, Laura;
Carrillo, Fátima;
Carballo, Manuel;
Gómez‐Garre, Pilar;
Mir, Pablo

Publication type:

journal article

GDNF gene is associated with tourette syndrome in a family study.

Published in:

Movement Disorders, 2015, v. 30, n. 8, p. 1115, doi. 10.1002/mds.26279

By:

Huertas-Fernández, Ismael;
Gómez-Garre, Pilar;
Madruga-Garrido, Marcos;
Bernal-Bernal, Inmaculada;
Bonilla-Toribio, Marta;
Martín-Rodríguez, Juan Francisco;
Cáceres-Redondo, María Teresa;
Vargas-González, Laura;
Carrillo, Fátima;
Pascual, Alberto;
Tischfield, Jay A.;
King, Robert A.;
Heiman, Gary A.;
Mir, Pablo

Publication type:

Article

Lack of validation of variants associated with cervical dystonia risk: A GWAS replication study.

Published in:

Movement Disorders, 2014, v. 29, n. 14, p. 1825, doi. 10.1002/mds.26044

By:

Gómez‐Garre, Pilar;
Huertas‐Fernández, Ismael;
Cáceres‐Redondo, María Teresa;
Alonso‐Canovas, Araceli;
Bernal‐Bernal, Inmaculada;
Blanco‐Ollero, Alberto;
Bonilla‐Toribio, Marta;
Burguera, Juan Andrés;
Carballo, Manuel;
Carrillo, Fatima;
José Catalán‐Alonso, M.;
Escamilla‐Sevilla, Francisco;
Espinosa‐Rosso, Raul;
Carmen Fernández‐Moreno, María;
García‐Caldentey, Juan;
García‐Moreno, José Manuel;
Giacometti‐Silveira, Sandra;
Gutiérrez‐García, Javier;
Jesús‐Maestre, Silvia;
López‐Valdés, Eva

Publication type:

Article

BDNF Val66Met polymorphism in primary adult-onset dystonia: A case-control study and meta-analysis.

Published in:

Movement Disorders, 2014, v. 29, n. 8, p. 1083, doi. 10.1002/mds.25938

By:

Gómez‐Garre, Pilar;
Huertas‐Fernández, Ismael;
Cáceres‐Redondo, María Teresa;
Alonso‐Canovas, Araceli;
Bernal‐Bernal, Inmaculada;
Blanco‐Ollero, Alberto;
Bonilla‐Toribio, Marta;
Burguera, Juan Andrés;
Carballo, Manuel;
Carrillo, Fátima;
Catalán‐Alonso, María José;
Escamilla‐Sevilla, Francisco;
Espinosa‐Rosso, Raúl;
Fernández‐Moreno, María Carmen;
García‐Caldentey, Juan;
García‐Moreno, José Manuel;
García‐Ruiz, Pedro José;
Giacometti‐Silveira, Sandra;
Gutiérrez‐García, Javier;
Jesús, Silvia

Publication type:

Article

Genome-wide association study in musician's dystonia: A risk variant at the arylsulfatase G locus?

Published in:

Movement Disorders, 2014, v. 29, n. 7, p. 921, doi. 10.1002/mds.25791

By:

Lohmann, Katja;
Schmidt, Alexander;
Schillert, Arne;
Winkler, Susen;
Albanese, Alberto;
Baas, Frank;
Bentivoglio, Anna Rita;
Borngräber, Friederike;
Brüggemann, Norbert;
Defazio, Giovanni;
Del Sorbo, Francesca;
Deuschl, Günther;
Edwards, Mark J.;
Gasser, Thomas;
Gómez‐Garre, Pilar;
Graf, Julia;
Groen, Justus L.;
Grünewald, Anne;
Hagenah, Johann;
Hemmelmann, Claudia

Publication type:

Article

Genome-Wide Association Study in Musician's Dystonia: A Risk Variant at the Arylsulfatase G Locus?

Published in:

Movement Disorders, 2014, v. 29, p. 921, doi. 10.1002/mds.25791

By:

Lohmann, Katja;
Schmidt, Alexander;
Schillert, Arne;
Winkler, Susen;
Albanese, Alberto;
Baas, Frank;
Bentivoglio, Anna Rita;
Borngräber, Friederike;
Brüggemann, Norbert;
Defazio, Giovanni;
Del Sorbo, Francesca;
Deuschl, Günther;
Edwards, Mark J.;
Gasser, Thomas;
Gómez-Garre, Pilar;
Graf, Julia;
Groen, Justus L.;
Grünewald, Anne;
Hagenah, Johann;
Hemmelmann, Claudia

Publication type:

Article

Genetic variability related to serum uric acid concentration and risk of Parkinson's disease.

Published in:

Movement Disorders, 2013, v. 28, n. 12, p. 1737, doi. 10.1002/mds.25507

By:

González‐Aramburu, Isabel;
Sánchez‐Juan, Pascual;
Jesús, Silvia;
Gorostidi, Ana;
Fernández‐Juan, Eduardo;
Carrillo, Fátima;
Sierra, María;
Gómez‐Garre, Pilar;
Cáceres‐Redondo, María T.;
Berciano, José;
Ruiz‐Martínez, Javier;
Combarros, Onofre;
Mir, Pablo;
Infante, Jon

Publication type:

Article

Novel Lrrk2-p.S1761R mutation is not a common cause of Parkinson's disease in Spain.

Published in:

2013

By:

Mata, Ignacio F;
Alvarez, Victoria;
Ribacoba, Renee;
Infante, Jon;
Sierra, María;
Gómez-Garre, Pilar;
Mir, Pablo;
Waldherr, Sarah;
Yearout, Dora;
Zabetian, Cyrus P

Publication type:

Letter

Novel Lrrk2-p. S1761R mutation is not a common cause of Parkinson's disease in Spain.

Published in:

Movement Disorders, 2013, v. 28, n. 2, p. 248, doi. 10.1002/mds.25293

By:

Mata, Ignacio F.;
Alvarez, Victoria;
Ribacoba, Renee;
Infante, Jon;
Sierra, María;
Gómez‐Garre, Pilar;
Mir, Pablo;
Waldherr, Sarah;
Yearout, Dora;
Zabetian, Cyrus P.

Publication type:

Article

Common variation in the LRRK2 gene is a risk factor for Parkinson's disease.

Published in:

Movement Disorders, 2012, v. 27, n. 14, p. 1823, doi. 10.1002/mds.25226

By:

Mata, Ignacio F.;
Checkoway, Harvey;
Hutter, Carolyn M.;
Samii, Ali;
Roberts, John W.;
Kim, Hojoong M.;
Agarwal, Pinky;
Alvarez, Victoria;
Ribacoba, Renee;
Pastor, Pau;
Lorenzo-Betancor, Oswaldo;
Infante, Jon;
Sierra, María;
Gómez-Garre, Pilar;
Mir, Pablo;
Ritz, Beate;
Rhodes, Shannon L.;
Colcher, Amy;
Van Deerlin, Vivianna;
Chung, Kathryn A.

Publication type:

Article

Lack of sequence variations in THAP1 gene and THAP1-binding sites in TOR1A promoter of DYT1 patients.

Published in:

Movement Disorders, 2012, v. 27, n. 7, p. 917, doi. 10.1002/mds.24974

By:

Palada, Vinko;
Stiern, Sandra;
Glöckle, Nicola;
Gómez-Garre, Pilar;
Carrillo, Fatima;
Mir, Pablo;
Szczaluba, Krzysztof;
Tinazzi, Michele;
Ajena, Domenico;
Romani, Marta;
Valente, Enza Maria;
Müller, Ulrich;
Bauer, Peter;
Riess, Olaf;
Ott, Thomas;
Grundmann, Kathrin

Publication type:

Article

The effect of BDNF val66met polymorphism on visuomotor adaptation.

Published in:

Experimental Brain Research, 2012, v. 223, n. 1, p. 43, doi. 10.1007/s00221-012-3239-9

By:

Joundi, Raed;
Lopez-Alonso, Virginia;
Lago, Angel;
Brittain, John-Stuart;
Fernandez-del-Olmo, Miguel;
Gomez-Garre, Pilar;
Mir, Pablo;
Jenkinson, Ned;
Cheeran, Binith;
Brown, Peter

Publication type:

Article

Low prevalence of SLX4 loss-of-function mutations in non-BRCA1/2 breast and/or ovarian cancer families.

Published in:

European Journal of Human Genetics, 2013, v. 21, n. 8, p. 883, doi. 10.1038/ejhg.2012.268

By:

de Garibay, Gorka Ruiz;
Díaz, Avellaneda;
Gaviña, Belén;
Romero, Atocha;
Garre, Pilar;
Vega, Ana;
Blanco, Ana;
Tosar, Alicia;
Díez, Orland;
Pérez-Segura, Pedro;
Díaz-Rubio, Eduardo;
Caldés, Trinidad;
de la Hoya, Miguel

Publication type:

Article

Mutational spectrum of the EPM2A gene in progressive myoclonus epilepsy of Lafora: high degree of allelic heterogeneity and prevalence of deletions.

Published in:

European Journal of Human Genetics, 2000, v. 8, n. 12, p. 946, doi. 10.1038/sj.ejhg.5200571

By:

Gómez-Garre, Pilar;
Sanz, Yolanda;
de Córdoba, Santiago Rodríguez;
Serratosa, José M

Publication type:

Article

Reassessing the TARBP2 mutation rate in hereditary nonpolyposis colorectal cancer.

Published in:

2010

By:

Garre, Pilar;
Pérez-Segura, Pedro;
Díaz-Rubio, Eduardo;
Caldés, Trinidad;
de la Hoya, Miguel

Publication type:

Letter

Transcriptomic analysis reveals an association of FCGBP with Parkinson’s disease.

Published in:

NPJ Parkinson's Disease, 2022, v. 8, n. 1, p. 1, doi. 10.1038/s41531-022-00415-7

By:

Gómez-Garre, Pilar;
Periñán, María Teresa;
Jesús, Silvia;
Bacalini, Maria Giulia;
Garagnani, Paolo;
Mollenhauer, Brit;
Pirazzini, Chiara;
Provini, Federica;
Trenkwalder, Claudia;
Franceschi, Claudio;
Mir, Pablo

Publication type:

Article

Heterogeneity of prodromal Parkinson symptoms in siblings of Parkinson disease patients.

Published in:

NPJ Parkinson's Disease, 2021, v. 7, n. 1, p. 1, doi. 10.1038/s41531-021-00219-1

By:

Baldelli, Luca;
Schade, Sebastian;
Jesús, Silvia;
Schreglmann, Sebastian R.;
Sambati, Luisa;
Gómez-Garre, Pilar;
Halsband, Claire;
Calandra-Buonaura, Giovanna;
Adarmes-Gómez, Astrid Daniela;
Sixel-Döring, Friederike;
Zenesini, Corrado;
Pirazzini, Chiara;
Garagnani, Paolo;
Bacalini, Maria Giulia;
Bhatia, Kailash P.;
Cortelli, Pietro;
Mollenhauer, Brit;
Franceschi, Claudio;
PROPAG-AGEING consortium;
Houlden, Henry

Publication type:

Article

Serum lipid profile among sporadic and familial forms of Parkinson's disease.

Published in:

NPJ Parkinson's Disease, 2021, v. 7, n. 1, p. 1, doi. 10.1038/s41531-021-00206-6

By:

Macías-García, Daniel;
Periñán, María Teresa;
Muñoz-Delgado, Laura;
Jimenez-Jaraba, María Valle;
Labrador-Espinosa, Miguel Ángel;
Jesús, Silvia;
Buiza-Rueda, Dolores;
Méndez-Del Barrio, Carlota;
Adarmes-Gómez, Astrid;
Gómez-Garre, Pilar;
Mir, Pablo

Publication type:

Article

GBA Variants Influence Motor and Non-Motor Features of Parkinson’s Disease.

Published in:

PLoS ONE, 2016, v. 11, n. 12, p. 1, doi. 10.1371/journal.pone.0167749

By:

Jesús, Silvia;
Huertas, Ismael;
Bernal-Bernal, Inmaculada;
Bonilla-Toribio, Marta;
Cáceres-Redondo, María Teresa;
Vargas-González, Laura;
Gómez-Llamas, Myriam;
Carrillo, Fátima;
Calderón, Enrique;
Carballo, Manuel;
Gómez-Garre, Pilar;
Mir, Pablo

Publication type:

Article

Mendelian Randomisation Confirms the Role of Y-Chromosome Loss in Alzheimer's Disease Aetiopathogenesis in Men.

Published in:

International Journal of Molecular Sciences, 2023, v. 24, n. 2, p. 898, doi. 10.3390/ijms24020898

By:

García-González, Pablo;
de Rojas, Itziar;
Moreno-Grau, Sonia;
Montrreal, Laura;
Puerta, Raquel;
Alarcón-Martín, Emilio;
Quintela, Inés;
Orellana, Adela;
Andrade, Victor;
Adami, Pamela V. Martino;
Heilmann-Heimbach, Stefanie;
Gomez-Garre, Pilar;
Periñán, María Teresa;
Alvarez, Ignacio;
Diez-Fairen, Monica;
Nuñez Llaves, Raul;
Olivé Roig, Claudia;
Garcia-Ribas, Guillermo;
Menéndez-González, Manuel;
Martínez, Carmen

Publication type:

Article

Homocysteine levels, genetic background, and cognitive impairment in Parkinson's disease.

Published in:

Journal of Neurology, 2023, v. 270, n. 1, p. 477, doi. 10.1007/s00415-022-11361-y

By:

Periñán, María Teresa;
Macías-García, Daniel;
Jesús, Silvia;
Martín-Rodríguez, Juan Francisco;
Muñoz-Delgado, Laura;
Jimenez-Jaraba, Maria Valle;
Buiza-Rueda, Dolores;
Bonilla-Toribio, Marta;
Adarmes-Gómez, Astrid Daniela;
Gómez-Garre, Pilar;
Mir, Pablo

Publication type:

Article

Genetic association of sirtuin genes and Parkinson's disease.

Published in:

Journal of Neurology, 2013, v. 260, n. 9, p. 2237, doi. 10.1007/s00415-013-6970-7

By:

Jesús, Silvia;
Gómez-Garre, Pilar;
Carrillo, Fátima;
Cáceres-Redondo, María;
Huertas-Fernández, Ismael;
Bernal-Bernal, Inmaculada;
Bonilla-Toribio, Marta;
Vargas-González, Laura;
Carballo, Manuel;
Mir, Pablo

Publication type:

Article

Laforin, the dual-phosphatase responsible for Lafora disease, interacts with R5 (PTG), a regulatory subunit of protein phosphatase-1 that enhances glycogen accumulation.

Published in:

Human Molecular Genetics, 2003, v. 12, n. 23, p. 3161, doi. 10.1093/hmg/ddg340

By:

Fernández-Sánchez, Maria Elena;
Criado-García, Olga;
Heath, Karen E.;
García-Fojeda, Belén;
Medraño-Fernández, Iria;
Gomez-Garre, Pilar;
Sanz, Pascual;
Serratosa, José María;
Rodríguez de Córdoba, Santiago

Publication type:

Article

A novel protein tyrosine phosphatase gene is mutated in progressive myoclonus epilepsy of the Lafora type (EPM2).

Published in:

Human Molecular Genetics, 1999, v. 8, n. 2, p. 345, doi. 10.1093/hmg/8.2.345

By:

Serratosa, José M.;
Gómez-Garre, Pilar;
Gallardo, Ma Esther;
Anta, Berta;
Beltrán-Valero de Bernabé, Daniel;
Lindhout, Dick;
Augustijn, Paul B.;
Tassinari, Carlo A.;
Malafosse, Roberto Michelucci6, Alain;
Topcu, Meral;
Grid, Djamel;
Dravet, Charlotte;
Berkovic, Samuel F.;
Rodríguez de Córdoba, Santiago

Publication type:

Article

Understanding Parkinson disease in Spain: Genetic and clinical insights.

Published in:

European Journal of Neurology, 2025, v. 32, n. 1, p. 1, doi. 10.1111/ene.16499

By:

Gómez‐Garre, Pilar;
Martín‐Bórnez, Miguel;
Muñoz‐Delgado, Laura;
Díaz‐Belloso, Rafael;
Periñán, María Teresa;
Bonilla‐Toribio, Marta;
Buiza‐Rueda, Dolores;
Macías‐García, Daniel;
Jesús, Silvia;
Adarmes‐Gómez, Astrid;
Ojeda, Elena;
Luque‐Ambrosiani, Antonio;
García‐Díaz, Sergio;
Sánchez, Rocío Pineda;
Carrillo, Fátima;
Mir, Pablo

Publication type:

Article

Mutational spectrum of GNAL, THAP1 and TOR1A genes in isolated dystonia: study in a population from Spain and systematic literature review.

Published in:

European Journal of Neurology, 2021, v. 28, n. 4, p. 1188, doi. 10.1111/ene.14638

By:

Gómez‐Garre, Pilar;
Jesús, Silvia;
Periñán, María Teresa;
Adarmes, Astrid;
Alonso‐Canovas, Araceli;
Blanco‐Ollero, Alberto;
Buiza‐Rueda, Dolores;
Carrillo, Fátima;
Catalán‐Alonso, María José;
Val, Javier;
Escamilla‐Sevilla, Francisco;
Espinosa‐Rosso, Raúl;
Fernández‐Moreno, María Carmen;
García‐Moreno, José Manuel;
García‐Ruiz, Pedro José;
Giacometti‐Silveira, Sandra;
Gutiérrez‐García, Javier;
López‐Valdés, Eva;
Macías‐García, Daniel;
Martínez‐Castrillo, Juan Carlos

Publication type:

Article

TMEM230 in Parkinson’s disease in a southern Spanish population.

Published in:

PLoS ONE, 2018, v. 13, n. 5, p. 1, doi. 10.1371/journal.pone.0197271

By:

Tejera-Parrado, Cristina;
Jesús, Silvia;
López-Ruíz, Adrián;
Buiza-Rueda, Dolores;
Bonilla-Toribio, Marta;
Bernal-Bernal, Inmaculada;
Periñán, María Teresa;
Vargas-González, Laura;
Gómez-Garre, Pilar;
Mir, Pablo

Publication type:

Article

Role of GALNT12 in the genetic predisposition to attenuated adenomatous polyposis syndrome.

Published in:

PLoS ONE, 2017, v. 12, n. 11, p. 1, doi. 10.1371/journal.pone.0187312

By:

Lorca, Víctor;
Rueda, Daniel;
Martín-Morales, Lorena;
Poves, Carmen;
Fernández-Aceñero, María Jesús;
Ruiz-Ponte, Clara;
Llovet, Patricia;
Marrupe, David;
García-Barberán, Vanesa;
García-Paredes, Beatriz;
Pérez-Segura, Pedro;
de la Hoya, Miguel;
Díaz-Rubio, Eduardo;
Caldés, Trinidad;
Garre, Pilar

Publication type:

Article

Genetic factors influencing frontostriatal dysfunction and the development of dementia in Parkinson's disease.

Published in:

PLoS ONE, 2017, v. 12, n. 4, p. 1, doi. 10.1371/journal.pone.0175560

By:

Huertas, Ismael;
Jesús, Silvia;
García-Gómez, Francisco Javier;
Lojo, José Antonio;
Bernal-Bernal, Inmaculada;
Bonilla-Toribio, Marta;
Martín-Rodriguez, Juan Francisco;
García-Solís, David;
Gómez-Garre, Pilar;
Mir, Pablo

Publication type:

Article

Lower levels of uric acid and striatal dopamine in non-tremor dominant Parkinson's disease subtype.

Published in:

PLoS ONE, 2017, v. 12, n. 3, p. 1, doi. 10.1371/journal.pone.0174644

By:

Huertas, Ismael;
Jesús, Silvia;
Lojo, José Antonio;
García-Gómez, Francisco Javier;
Cáceres-Redondo, María Teresa;
Oropesa-Ruiz, Juan Manuel;
Carrillo, Fátima;
Vargas-Gonzalez, Laura;
Martín Rodríguez, Juan Francisco;
Gómez-Garre, Pilar;
García-Solís, David;
Mir, Pablo

Publication type:

Article

Genetic linkage of autosomal dominant progressive supranuclear palsy to 1q31.1.

Published in:

Annals of Neurology, 2005, v. 57, n. 5, p. 634

By:

Raquel Ros;
Pilar Gómez Garre;
Michio Hirano;
Yen F. Tai;
Israel Ampuero;
Lídice Vidal;
Ana Rojo;
Aurora Fontan;
Ana Vazquez;
Samira Fanjul;
Jaime Hernandez;
Susana Cantarero;
Janet Hoenicka;
Alison Jones;
R. Laila Ahsan;
Nicola Pavese;
Paola Piccini;
David J. Brooks;
Jordi Perez‐Tur;
Torbjorn Nyggard

Publication type:

Article

Limited family structure and triple-negative breast cancer (TNBC) subtype as predictors of BRCA mutations in a genetic counseling cohort of early-onset sporadic breast cancers.

Published in:

Breast Cancer Research & Treatment, 2014, v. 148, n. 2, p. 415, doi. 10.1007/s10549-014-3167-4

By:

Zugazagoitia, Jon;
Pérez-Segura, Pedro;
Manzano, Arancha;
Blanco, Ignacio;
Vega, Ana;
Custodio, Ana;
Teulé, Alex;
Fachal, Laura;
Martínez, Beatriz;
González-Sarmiento, Rogelio;
Cruz-Hernández, Juan;
Chirivella, Isabel;
Garcés, Vicente;
Garre, Pilar;
Romero, Atocha;
Caldés, Trinidad;
Díaz-Rubio, Eduardo;
Hoya, Miguel

Publication type:

Article

Characterization of four novel BRCA2 large genomic rearrangements in Spanish breast/ovarian cancer families: review of the literature, and reevaluation of the genetic mechanisms involved in their origin.

Published in:

Breast Cancer Research & Treatment, 2012, v. 133, n. 1, p. 273, doi. 10.1007/s10549-011-1909-0

By:

Ruiz de Garibay, Gorka;
Gutiérrez-Enríquez, Sara;
Garre, Pilar;
Bonache, Sandra;
Romero, Atocha;
Palomo, Laura;
Sánchez de Abajo, Ana;
Benítez, Javier;
Balmaña, Judith;
Pérez-Segura, Pedro;
Díaz-Rubio, Eduardo;
Díez, Orland;
Caldés, Trinidad;
Hoya, Miguel

Publication type:

Article

Contribution of New Adenomatous Polyposis Predisposition Genes in an Unexplained Attenuated Spanish Cohort by Multigene Panel Testing.

Published in:

Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-46403-5

By:

Lorca, Víctor;
Rueda, Daniel;
Martín-Morales, Lorena;
Fernández-Aceñero, María Jesús;
Grolleman, Judith;
Poves, Carmen;
Llovet, Patricia;
Tapial, Sandra;
García-Barberán, Vanesa;
Sanz, Julián;
Pérez-Segura, Pedro;
de Voer, Richarda M.;
Díaz-Rubio, Eduardo;
de la Hoya, Miguel;
Caldés, Trinidad;
Garre, Pilar

Publication type:

Article

Novel genetic mutations detected by multigene panel are associated with hereditary colorectal cancer predisposition.

Published in:

PLoS ONE, 2018, v. 13, n. 9, p. 1, doi. 10.1371/journal.pone.0203885

By:

Martin-Morales, Lorena;
Rofes, Paula;
Diaz-Rubio, Eduardo;
Llovet, Patricia;
Lorca, Victor;
Bando, Inmaculada;
Perez-Segura, Pedro;
de la Hoya, Miguel;
Garre, Pilar;
Garcia-Barberan, Vanesa;
Caldes, Trinidad

Publication type:

Article

Differential distribution and enrichment of non-coding RNAs in exosomes from normal and Cancer-associated fibroblasts in colorectal cancer.

Published in:

Molecular Cancer, 2018, v. 17, n. 1, p. N.PAG, doi. 10.1186/s12943-018-0863-4

By:

Herrera, Mercedes;
Llorens, Carlos;
Rodríguez, Marta;
Herrera, Alberto;
Ramos, Ricardo;
Gil, Beatriz;
Candia, Antonio;
Larriba, María Jesús;
Garre, Pilar;
Earl, Julie;
Rodríguez-Garrote, Mercedes;
Caldés, Trinidad;
Bonilla, Félix;
Carrato, Alfredo;
García-Barberán, Vanesa;
Peña, Cristina

Publication type:

Article

A novel TP53 germline inframe deletion identified in a Spanish series of Li-fraumeni syndrome suspected families.

Published in:

Familial Cancer, 2017, v. 16, n. 4, p. 567, doi. 10.1007/s10689-017-9990-0

By:

Llovet, Patricia;
Illana, Francisco;
Martín-Morales, Lorena;
Hoya, Miguel;
Garre, Pilar;
Ibañez-Royo, M.;
Pérez-Segura, Pedro;
Caldés, Trinidad;
García-Barberán, Vanesa

Publication type:

Article

Cancer risk and overall survival in mismatch repair proficient hereditary non-polyposis colorectal cancer, Lynch syndrome and sporadic colorectal cancer.

Published in:

Familial Cancer, 2014, v. 13, n. 1, p. 109, doi. 10.1007/s10689-013-9683-2

By:

Garre, Pilar;
Martín, Lorena;
Bando, Inmaculada;
Tosar, Alicia;
Llovet, Patricia;
Sanz, Julián;
Romero, Atocha;
Hoya, Miguel;
Díaz-Rubio, Eduardo;
Caldés, Trinidad

Publication type:

Article

Association of MUTYH and MSH6 germline mutations in colorectal cancer patients.

Published in:

Familial Cancer, 2009, v. 8, n. 4, p. 525, doi. 10.1007/s10689-009-9282-4

By:

Giráldez, María;
Balaguer, Francesc;
Caldés, Trinidad;
Sanchez-de-Abajo, Ana;
Gómez-Fernández, Nuria;
Ruiz-Ponte, Clara;
Muñoz, Jenifer;
Garre, Pilar;
Gonzalo, Victoria;
Moreira, Leticia;
Ocaña, Teresa;
Clofent, Joan;
Carracedo, Angel;
Andreu, Montserrat;
Jover, Rodrigo;
Llor, Xavier;
Castells, Antoni;
Castellví-Bel, Sergi

Publication type:

Article

Author Correction: Peripheral inflammatory immune response differs among sporadic and familial Parkinson's disease.

Published in:

2023

By:

Muñoz-Delgado, Laura;
Macías-García, Daniel;
Periñán, María Teresa;
Jesús, Silvia;
Adarmes-Gómez, Astrid D.;
Bonilla Toribio, Marta;
Buiza Rueda, Dolores;
Jiménez-Jaraba, María del Valle;
Benítez Zamora, Belén;
Díaz Belloso, Rafael;
García-Díaz, Sergio;
Martín-Bórnez, Miguel;
Pineda Sánchez, Rocío;
Carrillo, Fátima;
Gómez-Garre, Pilar;
Mir, Pablo

Publication type:

Correction Notice

Peripheral inflammatory immune response differs among sporadic and familial Parkinson's disease.

Published in:

NPJ Parkinson's Disease, 2023, v. 9, n. 1, p. 1, doi. 10.1038/s41531-023-00457-5

By:

Muñoz-Delgado, Laura;
Macías-García, Daniel;
Periñán, María Teresa;
Jesús, Silvia;
Adarmes-Gómez, Astrid D.;
Bonilla Toribio, Marta;
Buiza Rueda, Dolores;
Jiménez-Jaraba, María del Valle;
Benítez Zamora, Belén;
Díaz Belloso, Rafael;
García-Díaz, Sergio;
Martín-Bórnez, Miguel;
Pineda Sánchez, Rocío;
Carrillo, Fátima;
Gómez-Garre, Pilar;
Mir, Pablo

Publication type:

Article

A Large Case-Control Study Performed in Spanish Population Suggests That RECQL5 Is the Only RECQ Helicase Involved in Breast Cancer Susceptibility.

Published in:

Cancers, 2022, v. 14, n. 19, p. 4738, doi. 10.3390/cancers14194738

By:

Marchena-Perea, Erik Michel;
Salazar-Hidalgo, Milton Eduardo;
Gómez-Sanz, Alicia;
Arranz-Ledo, Mónica;
Barroso, Alicia;
Fernández, Victoria;
Tejera-Pérez, Hugo;
Pita, Guillermo;
Núñez-Torres, Rocío;
Pombo, Luz;
Morales-Chamorro, Rafael;
Cano-Cano, Juana María;
Soriano, Maria del Carmen;
Garre, Pilar;
Durán, Mercedes;
Currás-Freixes, María;
de la Hoya, Miguel;
Osorio, Ana

Publication type:

Article