Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytomaIñaki Comino‐Méndez, Alberto Cascón, Giuseppe Pica et al.|Nature Genetics|2011Cited by 528
Germline mutations in FH confer predisposition to malignant pheochromocytomas and paragangliomasLuis Jaime Castro‐Vega, Anne‐Paule Gimenez‐Roqueplo, Alexandre Buffet et al.|Human Molecular Genetics|2013Cited by 394
<i>MAX</i> Mutations Cause Hereditary and Sporadic Pheochromocytoma and ParagangliomaNelly Burnichon, Elisa Taschin, Alberto Cascón et al.|Clinical Cancer Research|2012Cited by 330
Whole-Exome Sequencing Identifies MDH2 as a New Familial Paraganglioma GeneAlberto Cascón, Mercedes Robledo, Iñaki Comino‐Méndez et al.|JNCI Journal of the National Cancer Institute|2015Cited by 189
Tumoral EPAS1 (HIF2A) mutations explain sporadic pheochromocytoma and paraganglioma in the absence of erythrocytosisIñaki Comino‐Méndez, Alberto Cascón, Aguirre A. de Cubas et al.|Human Molecular Genetics|2013Cited by 168