Publicaciones en colaboración con investigadores/as de Hospital General Universitario de Elche (41)

2024

  1. Discovery of recessive effect of human polymerase δ proofreading deficiency through mutational analysis of POLD1-mutated normal and cancer cells

    European Journal of Human Genetics, Vol. 32, Núm. 7, pp. 837-845

  2. Identification of new targets for glioblastoma therapy based on a DNA expression microarray

    Computers in Biology and Medicine, Vol. 179

  3. SpadaHC: a database to improve the classification of variants in hereditary cancer genes in the Spanish population

    Database : the journal of biological databases and curation, Vol. 2024

  4. Use of multi-gene panels in patients at high risk of hereditary digestive cancer: position statement of AEG, SEOM, AEGH and IMPaCT-GENÓMICA consortium

    Gastroenterologia y Hepatologia, Vol. 47, Núm. 3, pp. 293-318

2022

  1. Cell-free circulating tumor DNA in colorectal cancer: a proof of concept with simplified methodology

    Clinical and Translational Oncology, Vol. 24, Núm. 10, pp. 1924-1931

  2. Considerations on diagnosis and surveillance measures of PTEN hamartoma tumor syndrome: clinical and genetic study in a series of Spanish patients

    Orphanet Journal of Rare Diseases, Vol. 17, Núm. 1

  3. Lynch-like Syndrome: Potential Mechanisms and Management

    Cancers, Vol. 14, Núm. 5

2020

  1. Clinical and Pathological Characterization of Lynch-Like Syndrome

    Clinical Gastroenterology and Hepatology, Vol. 18, Núm. 2, pp. 368-374.e1

  2. Differential effects of IGF-1R small molecule tyrosine kinase inhibitors BMS-754807 and OSI-906 on human cancer cell lines

    Cancers, Vol. 12, Núm. 12, pp. 1-18

  3. Hereditary leiomyomatosis and renal cell cancer syndrome in spain: Clinical and genetic characterization

    Cancers, Vol. 12, Núm. 11, pp. 1-16

  4. Risk of cancer in family members of patients with lynch-like syndrome

    Cancers, Vol. 12, Núm. 8, pp. 1-12

  5. SEOM clinical guideline on hereditary colorectal cancer (2019)

    Clinical and Translational Oncology, Vol. 22, Núm. 2, pp. 201-212

2019

  1. Highly sensitive MLH1 methylation analysis in blood identifies a cancer patient with low-level mosaic MLH1 epimutation

    Clinical Epigenetics, Vol. 11, Núm. 1

  2. Implementation of massive sequencing in the genetic diagnosis of hereditary cancer syndromes: Diagnostic performance in the Hereditary Cancer Programme of the Valencia Community (FamCan-NGS)

    Hereditary Cancer in Clinical Practice, Vol. 17, Núm. 1

  3. Novel molecular characterization of colorectal primary tumors based on mirnas

    Cancers, Vol. 11, Núm. 3

  4. Radiotherapy resistance acquisition in glioblastoma. Role of SOCS1 and SOCS3

    PLoS ONE, Vol. 14, Núm. 2

2018

  1. A phylogenetic approach to the Philippines endemic centipedes of the genus Scolopendra Linnaeus, 1758 (Scolopendromorpha, Scolopendridae), with the description of a new species

    Zootaxa, Vol. 4483, Núm. 3, pp. 401-427

  2. Consensus document on the implementation of next generation sequencing in the genetic diagnosis of hereditary cancer

    Medicina Clinica, Vol. 151, Núm. 2, pp. 80.e1-80.e10

  3. Successful induction therapy with sequential CVD followed by high-dose lanreotide in for metastatic SDHB paraganglioma: Case report

    Journal of Clinical and Translational Endocrinology: Case Reports, Vol. 7, pp. 8-13

2017

  1. Increased Risk of Colorectal Cancer in Patients With Multiple Serrated Polyps and Their First-Degree Relatives

    Gastroenterology, Vol. 153, Núm. 1, pp. 106-112.e2