Estadística e Investigación Operativa
Departament
University of Padua
Padua, ItaliaPublicacions en col·laboració amb investigadors/es de University of Padua (12)
2017
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PheoSeq: A Targeted Next-Generation Sequencing Assay for Pheochromocytoma and Paraganglioma Diagnostics
Journal of Molecular Diagnostics, Vol. 19, Núm. 4, pp. 575-588
2015
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DNA methylation profiling in pheochromocytoma and paraganglioma reveals diagnostic and prognostic markers
Clinical Cancer Research, Vol. 21, Núm. 13, pp. 3020-3030
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Thyroid cancer GWAS identifies 10q26.12 and 6q14.1 as novel susceptibility loci and reveals genetic heterogeneity among populations
International Journal of Cancer, Vol. 137, Núm. 8, pp. 1870-1878
2013
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An Epistatic Interaction between the PAX8 and STK17B Genes in Papillary Thyroid Cancer Susceptibility
PLoS ONE, Vol. 8, Núm. 9
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Differential gene expression of medullary thyroid carcinoma reveals specific markers associated with genetic conditions
American Journal of Pathology, Vol. 182, Núm. 2, pp. 350-362
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Genetics of population exchange along the historical portuguese-spanish border
Journal of Biosocial Science, Vol. 45, Núm. 1, pp. 79-93
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Integrative analysis of miRNA and mRNA expression profiles in pheochromocytoma and paraganglioma identifies genotype-specific markers and potentially regulated pathways
Endocrine-Related Cancer, Vol. 20, Núm. 4, pp. 477-493
2012
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MAX mutations cause hereditary and sporadic pheochromocytoma and paraganglioma
Clinical Cancer Research, Vol. 18, Núm. 10, pp. 2828-2837
2011
2010
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Research resource: Transcriptional profiling reveals different pseudohypoxic signatures in SDHB and VHL-related pheochromocytomas
Molecular Endocrinology, Vol. 24, Núm. 12, pp. 2382-2391
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Spectrum and prevalence of FP/TMEM127 gene mutations in pheochromocytomas and paragangliomas
JAMA - Journal of the American Medical Association, Vol. 304, Núm. 23, pp. 2611-2619