Lucía Inglada‐Pérez

Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma

Iñaki Comino‐Méndez, Francisco Javier Gracia-Aznárez, Francesca Schiavi et al. · Nature Genetics · 2011 · 524 citations · Full text

Hereditary Pheochromocytoma, Mendelian Disorder, Genetic Disorder +9

<i>MAX</i> Mutations Cause Hereditary and Sporadic Pheochromocytoma and Paraganglioma

Nelly Burnichon, Alberto Cascón, Francesca Schiavi et al. · Clinical Cancer Research · 2012 · 321 citations · Full text

Tumor MicroRNA Expression Profiling Identifies Circulating MicroRNAs for Early Breast Cancer Detection

Nerea Matamala, María Teresa Vargas, Ricardo González‐Cámpora et al. · Clinical Chemistry · 2015 · 219 citations · Full text

The miR-200 family controls  -tubulin III expression and is associated with paclitaxel-based treatment response and progression-free survival in ovarian cancer patients

Susanna Leskelä, Luis J. Leandro‐García, Marta Mendiola et al. · Endocrine Related Cancer · 2010 · 207 citations · Full text

Spectrum and Prevalence of <i>FP/TMEM127</i> Gene Mutations in Pheochromocytomas and Paragangliomas

Li Yao, Francesca Schiavi, Alberto Cascón et al. · JAMA · 2010 · 199 citations