Erasmus University Medical Center-ko ikertzaileekin lankidetzan egindako argitalpenak (14)

2021

  1. Genetic variants associated with methotrexate-induced mucositis in cancer treatment: A systematic review and meta-analysis

    Critical Reviews in Oncology/Hematology, Vol. 161

  2. Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1

    Autophagy, Vol. 17, Núm. 1, pp. 1-382

2020

  1. Recommendations for Diagnosis and Treatment of Pseudohypoparathyroidism and Related Disorders: An Updated Practical Tool for Physicians and Patients

    Hormone Research in Paediatrics, Vol. 93, Núm. 3, pp. 182-196

2018

  1. Diagnosis and management of pseudohypoparathyroidism and related disorders: First international Consensus Statement

    Nature Reviews Endocrinology, Vol. 14, Núm. 8, pp. 476-500

2017

  1. Epigenetic identity in AML depends on disruption of nonpromoter regulatory elements and is affected by antagonistic effects of mutations in epigenetic modifiers

    Cancer Discovery, Vol. 7, Núm. 8, pp. 868-883

  2. Stem cell-like transcriptional reprogramming mediates metastatic resistance to mTOR inhibition

    Oncogene, Vol. 36, Núm. 19, pp. 2737-2749

2015

  1. C8-glycosphingolipids preferentially insert into tumor cell membranes and promote chemotherapeutic drug uptake

    Biochimica et Biophysica Acta - Biomembranes, Vol. 1848, Núm. 8, pp. 1656-1670

  2. Genetic and metabolic determinants of methotrexate-induced mucositis in pediatric acute lymphoblastic leukemia

    Pharmacogenomics Journal, Vol. 15, Núm. 3, pp. 248-254

  3. Genome-wide significant association with seven novel multiple sclerosis risk loci

    Journal of Medical Genetics, Vol. 52, Núm. 12, pp. 848-855

2013

  1. MANBA, CXCR5, SOX8, RPS6KB1 and ZBTB46 are genetic risk loci for multiple sclerosis

    Brain, Vol. 136, Núm. 6, pp. 1778-1782

2010

  1. CTCF regulates the local epigenetic state of ribosomal DNA repeats

    Epigenetics and Chromatin, Vol. 3, Núm. 1

2009

  1. United Europeans for development of pharmacogenomics in multiple sclerosis network

    Pharmacogenomics, Vol. 10, Núm. 5, pp. 885-894

2008

  1. Refining genetic associations in multiple sclerosis

    The Lancet Neurology

2000

  1. Molecular cytogenetic analysis of eight inversion duplications of human chromosome 13q that each contain a neocentromere

    American Journal of Human Genetics, Vol. 66, Núm. 6, pp. 1794-1806