Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytomaIñaki Comino‐Méndez, Alberto Cascón, Mercedes Gómez‐Morales et al.|Nature Genetics|2011Cited by 528
Research Resource: Transcriptional Profiling Reveals Different Pseudohypoxic Signatures in SDHB and VHL-Related PheochromocytomasElena López‐Jiménez, Alberto Cascón, Gonzalo Goméz-López et al.|Molecular Endocrinology|2010Cited by 211
Regulatory Polymorphisms in β-Tubulin IIa Are Associated with Paclitaxel-Induced Peripheral NeuropathyLuis J. Leandro‐García, Cristina Rodríguez‐Antona, Susanna Leskelä et al.|Clinical Cancer Research|2012Cited by 77
Integrative analysis of miRNA and mRNA expression profiles in pheochromocytoma and paraganglioma identifies genotype-specific markers and potentially regulated pathwaysAguirre A. de Cubas, Mercedes Robledo, Luis J. Leandro‐García et al.|Endocrine Related Cancer|2013Cited by 55
Rationalization of Genetic Testing in Patients with Apparently Sporadic Pheochromocytoma/ParagangliomaAlberto Cascón, Mercedes Robledo, Elena López‐Jiménez et al.|Hormone and Metabolic Research|2009Cited by 44