Publications by authors named "Pilar Gómez-Garre"

40Publications

The role of RHOT1 and RHOT2 genetic variation on Parkinson disease risk and onset.

Neurobiol Aging 2020 Jul 14. Epub 2020 Jul 14.

Molecular Genetics Section, Laboratory of Neurogenetics, NIA, NIH, Bethesda, MD, USA. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.neurobiolaging.2020.07.003DOI Listing
July 2020

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

Mov Disord 2020 Sep 11. Epub 2020 Sep 11.

Unidad de Trastornos del Movimiento, Servicio de Neurología y Neurofisiología Clínica, Instituto de Biomedicina de Sevilla, Hospital Universitario Virgen del, Rocío/Consejo Superior de Investigaciones Científicas (CSIC)/Universidad de Sevilla, Seville, Spain.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/mds.28283DOI Listing
September 2020

Analysis of p.Tyr307Asn variant in the LRP10 gene in Parkinson's disease in southern Spain.

Neurobiol Aging 2020 Sep 15;93:142.e1-142.e3. Epub 2020 Apr 15.

Unidad de Trastornos del Movimiento, Servicio de Neurología y Neurofisiología Clínica, Instituto de Biomedicina de Sevilla, Hospital Universitario Virgen del Rocío/CSIC/Universidad de Sevilla, Seville, Spain; Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED), Madrid, Spain. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.neurobiolaging.2020.04.007DOI Listing
September 2020

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

Authors:
Sara Bandres-Ciga Sarah Ahmed Marya S Sabir Cornelis Blauwendraat Astrid D Adarmes-Gómez Inmaculada Bernal-Bernal Marta Bonilla-Toribio Dolores Buiza-Rueda Fátima Carrillo Mario Carrión-Claro Pilar Gómez-Garre Silvia Jesús Miguel A Labrador-Espinosa Daniel Macias Carlota Méndez-Del-Barrio Teresa Periñán-Tocino Cristina Tejera-Parrado Laura Vargas-González Monica Diez-Fairen Ignacio Alvarez Juan Pablo Tartari Mariateresa Buongiorno Miquel Aguilar Ana Gorostidi Jesús Alberto Bergareche Elisabet Mondragon Ana Vinagre-Aragon Ioana Croitoru Javier Ruiz-Martínez Oriol Dols-Icardo Jaime Kulisevsky Juan Marín-Lahoz Javier Pagonabarraga Berta Pascual-Sedano Mario Ezquerra Ana Cámara Yaroslau Compta Manel Fernández Rubén Fernández-Santiago Esteban Muñoz Eduard Tolosa Francesc Valldeoriola Isabel Gonzalez-Aramburu Antonio Sanchez Rodriguez María Sierra Manuel Menéndez-González Marta Blazquez Ciara Garcia Esther Suarez-San Martin Pedro García-Ruiz Juan Carlos Martínez-Castrillo Lydia Vela-Desojo Clara Ruz Francisco Javier Barrero Francisco Escamilla-Sevilla Adolfo Mínguez-Castellanos Debora Cerdan Cesar Tabernero Maria Jose Gomez Heredia Francisco Perez Errazquin Manolo Romero-Acebal Cici Feliz Jose Luis Lopez-Sendon Marina Mata Irene Martínez Torres Jonggeol Jeffrey Kim Clifton L Dalgard Janet Brooks Sara Saez-Atienzar J Raphael Gibbs Rafael Jorda Juan A Botia Luis Bonet-Ponce Karen E Morrison Carl Clarke Manuela Tan Huw Morris Connor Edsall Dena Hernandez Javier Simon-Sanchez Mike A Nalls Sonja W Scholz Adriano Jimenez-Escrig Jacinto Duarte Francisco Vives Raquel Duran Janet Hoenicka Victoria Alvarez Jon Infante Maria José Marti Jordi Clarimón Adolfo López de Munain Pau Pastor Pablo Mir Andrew Singleton

Mov Disord 2019 12 29;34(12):1851-1863. Epub 2019 Oct 29.

Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/mds.27864DOI Listing
December 2019

A replication study of GWAS-genetic risk variants associated with Parkinson's disease in a Spanish population.

Neurosci Lett 2019 11 17;712:134425. Epub 2019 Aug 17.

Unidad de Trastornos del Movimiento, Servicio de Neurología y Neurofisiología Clínica, Instituto de Biomedicina de Sevilla (IBiS), Hospital Universitario Virgen del Rocío/CSIC/Universidad de Sevilla, Sevilla, Spain; Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED), Madrid, Spain. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.neulet.2019.134425DOI Listing
November 2019

Increased bilirubin levels in Parkinson's disease.

Parkinsonism Relat Disord 2019 06 14;63:213-216. Epub 2019 Jan 14.

Unidad de Trastornos del Movimiento, Servicio de Neurología y Neurofisiología Clínica, Instituto de Biomedicina de Sevilla, Hospital Universitario Virgen del Rocío/CSIC/Universidad de Sevilla, Seville, Spain; Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED), Spain. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.parkreldis.2019.01.012DOI Listing
June 2019

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

PLoS One 2018 17;13(5):e0197271. Epub 2018 May 17.

Unidad de Trastornos del Movimiento, Servicio de Neurología y Neurofisiología Clínica, Instituto de Biomedicina de Sevilla (IBiS), Hospital Universitario Virgen del Rocío/CSIC/Universidad de Sevilla, Sevilla, España.

View Article

Download full-text PDF

Source
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0197271PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5957438PMC
November 2018

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

PLoS One 2017 11;12(4):e0175560. Epub 2017 Apr 11.

Unidad de Trastornos del Movimiento, Servicio de Neurología y Neurofisiología Clínica, Instituto de Biomedicina de Sevilla (IBiS), Hospital Universitario Virgen del Rocío/CSIC/Universidad de Sevilla, Seville, Spain.

View Article

Download full-text PDF

Source
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0175560PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5388496PMC
September 2017

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

PLoS One 2017 30;12(3):e0174644. Epub 2017 Mar 30.

Unidad de Trastornos del Movimiento, Servicio de Neurología y Neurofisiología Clínica, Instituto de Biomedicina de Sevilla (IBiS), Hospital Universitario Virgen del Rocío/CSIC/Universidad de Sevilla, Seville, Spain.

View Article

Download full-text PDF

Source
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0174644PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5373593PMC
August 2017

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

PLoS One 2016 28;11(12):e0167749. Epub 2016 Dec 28.

Unidad de Trastornos del Movimiento, Servicio de Neurología y Neurofisiología Clínica, Instituto de Biomedicina de Sevilla, Hospital Universitario Virgen del Rocío/CSIC/Universidad de Sevilla, Seville, Spain.

View Article

Download full-text PDF

Source
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0167749PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5193380PMC
July 2017

Genetic analysis of CHCHD2 in a southern Spanish population.

Neurobiol Aging 2017 02 21;50:169.e1-169.e2. Epub 2016 Oct 21.

Unidad de Trastornos del Movimiento, Servicio de Neurología y Neurofisiología Clínica, Instituto de Biomedicina de Sevilla (IBiS), Hospital Universitario Virgen del Rocío/CSIC/Universidad de Sevilla, Sevilla, Spain; Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED), Madrid, Spain. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.neurobiolaging.2016.10.019DOI Listing
February 2017

Low serum uric acid levels in progressive supranuclear palsy.

Mov Disord 2016 Mar 21;31(3):402-5. Epub 2015 Dec 21.

Unidad de Trastornos del Movimiento, Servicio de Neurología y Neurofisiología Clínica, Instituto de Biomedicina de Sevilla (IBiS), Hospital Universitario Virgen del Rocío/CSIC/Universidad de Sevilla, Seville, Spain.

View Article

Download full-text PDF

Source
http://doi.wiley.com/10.1002/mds.26466
Publisher Site
http://dx.doi.org/10.1002/mds.26466DOI Listing
March 2016

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

Mov Disord 2015 Jul 12;30(8):1115-20. Epub 2015 Jun 12.

Unidad de Trastornos del Movimiento, Servicio de Neurología y Neurofisiología Clínica, Instituto de Biomedicina de Sevilla (IBiS), Hospital Universitario Virgen del Rocío/CSIC/Universidad de Sevilla, Seville, Spain.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/mds.26279DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5036394PMC
July 2015

Atypical course in individuals from Spanish families with benign familial infantile seizures and mutations in the PRRT2 gene.

Epilepsy Res 2014 Oct 7;108(8):1274-8. Epub 2014 Jul 7.

Neurology Lab and Epilepsy Unit, Department of Neurology, IIS - Fundación Jiménez Díaz, UAM, Madrid, Spain; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Madrid, Spain. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.eplepsyres.2014.06.011DOI Listing
October 2014

Analysis of c.801-2A>G mutation in the DNAJC6 gene in Parkinson's disease in southern Spain.

Parkinsonism Relat Disord 2014 Feb 31;20(2):248-9. Epub 2013 Oct 31.

Unidad de Trastornos del Movimiento, Servicio de Neurología y Neurofisiología Clínica, Instituto de Biomedicina de Sevilla, Hospital Universitario Virgen del Rocío/CSIC/Universidad de Sevilla, Seville, Spain; Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED), Spain. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.parkreldis.2013.10.018DOI Listing
February 2014

Systematic mutational analysis of FBXO7 in a Parkinson's disease population from southern Spain.

Neurobiol Aging 2014 Mar 8;35(3):727.e5-7. Epub 2013 Oct 8.

Unidad de Trastornos del Movimiento, Servicio de Neurología y Neurofisiología, Instituto de Biomedicina de Sevilla (IBiS), Hospital Universitario Virgen del Rocío/CSIC/Universidad de Sevilla, Seville, Spain; Centro de Investigación en Red sobre Enfermedades Neurodegenerativas (CIBERNED), Madrid, Spain.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.neurobiolaging.2013.09.011DOI Listing
March 2014

Genetic association of sirtuin genes and Parkinson's disease.

J Neurol 2013 Sep 30;260(9):2237-41. Epub 2013 May 30.

Unidad de Trastornos del Movimiento, Servicio de Neurología y Neurofisiología Clínica, Hospital Universitario Virgen del Rocío/CSIC/Universidad de Sevilla/Instituto de Biomedicina de Sevilla, Av. Manuel Siurot s/n, 41013 Seville, Spain.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s00415-013-6970-7DOI Listing
September 2013

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

Mov Disord 2013 Oct 27;28(12):1737-40. Epub 2013 May 27.

Service of Neurology, Universitary Hospital Marqués de Valdecilla (IFIMAV), University of Cantabria (UC), Santander, Spain.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/mds.25507DOI Listing
October 2013

PSMC1 Gene in Parkinson's Disease.

Eur Neurol 2012 29;68(4):193-8. Epub 2012 Aug 29.

Unidad de Trastornos del Movimiento, Servicio de Neurología y Neurofisiología, Hospital Universitario Virgen del Rocío/CSIC/Universidad de Sevilla, Seville, Spain.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1159/000339003DOI Listing
June 2013

The effect of BDNF val66met polymorphism on visuomotor adaptation.

Exp Brain Res 2012 Nov 1;223(1):43-50. Epub 2012 Sep 1.

Nuffield Department of Clinical Neurosciences, University of Oxford, Level 6, West Wing, John Radcliffe Hospital, Oxford, OX3 9DU, UK.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s00221-012-3239-9DOI Listing
November 2012

A PTG variant contributes to a milder phenotype in Lafora disease.

PLoS One 2011 30;6(6):e21294. Epub 2011 Jun 30.

Laboratorio de Neurología-Unidad de Epilepsia, Servicio de Neurología, Instituto Investigación Sanitaria Fundación Jiménez Díaz, and Centro de Investigación Biomédica en Red de Enfermedades Raras, Madrid, Spain.

View Article

Download full-text PDF

Source
http://digital.csic.es/bitstream/10261/37651/1/Plos%20One%20
Web Search
http://dx.plos.org/10.1371/journal.pone.0021294
Publisher Site
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0021294PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3127956PMC
December 2011

Intermediate alleles at the FRAXA and FRAXE loci in Parkinson's disease.

Parkinsonism Relat Disord 2011 May 22;17(4):281-4. Epub 2011 Jan 22.

Departamento de Bioquímica Médica y Biología Molecular, Servicio de Biología Molecular, Hospital Universitario Virgen Macarena, Universidad de Sevilla, Av. Sánchez Pizjuán 4, Seville, Spain.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.parkreldis.2010.12.013DOI Listing
May 2011

Variability of age at onset in siblings with familial Alzheimer disease.

Arch Neurol 2007 Dec;64(12):1743-8

Department of Neurology, Fundación Jiménez Díaz, Avda Reyes Católicos 2, 28040, Madrid, Spain.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1001/archneur.64.12.1743DOI Listing
December 2007

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

Epilepsia 2008 Mar 26;49(3):516-20. Epub 2007 Sep 26.

Epilepsy Unit, Neurology Service, Fundación Jiménez Díaz, Madrid, Spain.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/j.1528-1167.2007.01328.xDOI Listing
March 2008

MRI volumetry and proton MR spectroscopy of the brain in Lafora disease.

Epilepsia 2006 Apr;47(4):788-92

Epilepsy Unit, Neurology Service, Fundación Jiménez Díaz, Madrid, Spain.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/j.1528-1167.2006.00526.xDOI Listing
April 2006

Characterization of a 6p21 translocation breakpoint in a family with idiopathic generalized epilepsy.

Epilepsy Res 2003 Oct;56(2-3):155-63

Laboratorio de Neurología, Fundación Jiménez Díaz, Avda. Reyes Católicos 2, Madrid 28040, Spain.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.eplepsyres.2003.09.002DOI Listing
October 2003