Mercedes Robledo

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

Germline mutations in FH confer predisposition to malignant pheochromocytomas and paragangliomas

Luis Jaime Castro‐Vega, Alexandre Buffet, Aguirre A. de Cubas et al. · Human Molecular Genetics · 2013 · 389 citations

Fh Gene, Tumor Biology, Somatic Variant +13

<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

SDHAF2 mutations in familial and sporadic paraganglioma and phaeochromocytoma

Jean‐Pierre Bayley, Henricus P. M. Kunst, Alberto Cascón et al. · The Lancet Oncology · 2010 · 268 citations

Somatic Variant, Genetic Disorder, Pathology +3

Tumoral and tissue‐specific expression of the major human β‐tubulin isotypes

Luis J. Leandro‐García, Susanna Leskelä, Iñigo Landa et al. · Cytoskeleton · 2010 · 262 citations

Microtubule Dynamics Alteration, Oncology, Medicine +15