Lucia Inglada-Pérez

Lucia Inglada-Pérez

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Lucia Inglada-Pérez

Lucia Inglada-Pérez

Publications by authors named "Lucia Inglada-Pérez"

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42Publications

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MicroRNA deep-sequencing reveals master regulators of follicular and papillary thyroid tumors.

Mod Pathol 2015 Jun 27;28(6):748-57. Epub 2015 Feb 27.

1] Hereditary Endocrine Cancer Group, Spanish National Cancer Research Centre (CNIO), Madrid, Spain [2] ISCIII Center for Biomedical Research on Rare Diseases (CIBERER), Madrid, Spain.

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http://dx.doi.org/10.1038/modpathol.2015.44DOI Listing
June 2015

Whole-exome sequencing identifies MDH2 as a new familial paraganglioma gene.

J Natl Cancer Inst 2015 Mar 11;107(5). Epub 2015 Mar 11.

: Hereditary Endocrine Cancer Group, Spanish National Cancer Research Centre, Madrid, Spain (AC, ICM, MCF, AAdC, VM, LIP, RL, AGG, MAR, CRA, MR); Centro de Investigación Biomédica en Red de Enfermedades Raras, Madrid, Spain (AC, LC, LIP, CRA, JS, MU, MR); Departamento de Biología Molecular, Centro de Biología Molecular Severo Ochoa UAM-CSIC, Universidad Autónoma de Madrid and Instituto de Investigación Sanitaria Fundación Jiménez Díaz, Madrid, Spain (LC, JS); Institute of Clinical Chemistry and Laboratory Medicine, University Hospital Carl Gustav Carus, Medical Faculty Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany (SR, MP, GE); Departments of Pathology (APB) and Endocrinology and Nutrition Service (MC), Hospital 12 de Octubre, Madrid, Spain; Endocrinology Service, Hospital Infanta Sofía, San Sebastián de los Reyes, Spain (SA); Department of Endocrinology and Nutrition Service, Hospital de Fuenlabrada, Madrid, Spain (RVV); Endocrinology Service, Hospital Puerta de Hierro, Majadahonda, Madrid, Spain (JA); Cancer Epigenetics and Biology Program, Bellvitge Biomedical Research Institute, L'Hospitalet, Barcelona, Spain (FS, SM, ME); Department of Pathology, MD Anderson Cancer Center Madrid, Madrid, Spain (JFG); Molecular Cytogenetics Group (ARM), Monoclonal Antibodies Unit, Biotechnology Programme (GR), and Familial Cancer Clinical Unit (MU), Spanish National Cancer Research Centre, Madrid, Spain.

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http://dx.doi.org/10.1093/jnci/djv053DOI Listing
March 2015

Short telomeres are frequent in hereditary breast tumors and are associated with high tumor grade.

Breast Cancer Res Treat 2013 Sep 15;141(2):231-42. Epub 2013 Sep 15.

Human Genetics Group, Spanish National Cancer Research Centre (CNIO) and Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Madrid, Spain,

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http://dx.doi.org/10.1007/s10549-013-2696-6DOI Listing
September 2013

Influence of RET mutations on the expression of tyrosine kinases in medullary thyroid carcinoma.

Endocr Relat Cancer 2013 Aug 12;20(4):611-9. Epub 2013 Jul 12.

Hereditary Endocrine Cancer Group, Human Cancer Genetics Programme, Spanish National Cancer Center (CNIO), Melchor Fernández Almagro 3, Madrid, Spain.

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http://dx.doi.org/10.1530/ERC-12-0316DOI Listing
August 2013

Genetic variation in the SLC19A1 gene and methotrexate toxicity in rheumatoid arthritis patients.

Pharmacogenomics 2012 Nov;13(14):1583-94

Pharmacogenetics Laboratory, Institute of Biochemistry, University of Ljubljana, Vrazov trg 2, 1000 Ljubljana, Slovenia.

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http://dx.doi.org/10.2217/pgs.12.150DOI Listing
November 2012

MAX mutations cause hereditary and sporadic pheochromocytoma and paraganglioma.

Clin Cancer Res 2012 May 27;18(10):2828-37. Epub 2012 Mar 27.

Assistance Publique-Hôpitaux de Paris, Hôpital Européen Georges Pompidou, Paris, France.

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http://clincancerres.aacrjournals.org/content/18/10/2828.ful
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http://clincancerres.aacrjournals.org/cgi/doi/10.1158/1078-0
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http://dx.doi.org/10.1158/1078-0432.CCR-12-0160DOI Listing
May 2012

Genetic anticipation is associated with telomere shortening in hereditary breast cancer.

PLoS Genet 2011 Jul 28;7(7):e1002182. Epub 2011 Jul 28.

Human Genetics Group, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.

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http://dx.doi.org/10.1371/journal.pgen.1002182DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3145621PMC
July 2011