Iñaki Comino‐Méndez

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

Assessment of Molecular Relapse Detection in Early-Stage Breast Cancer

Isaac García-Murillas, Neha Chopra, Iñaki Comino‐Méndez et al. · JAMA Oncology · 2019 · 414 citations · Full text

<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

Diverse <i>BRCA1</i> and <i>BRCA2</i> Reversion Mutations in Circulating Cell-Free DNA of Therapy-Resistant Breast or Ovarian Cancer

Britta Weigelt, Iñaki Comino‐Méndez, Ino de Bruijn et al. · Clinical Cancer Research · 2017 · 247 citations

Whole-Exome Sequencing Identifies MDH2 as a New Familial Paraganglioma Gene

Alberto Cascón, Iñaki Comino‐Méndez, María Currás-Freixes et al. · JNCI Journal of the National Cancer Institute · 2015 · 187 citations · Full text

Krebs Cycle, Genetics, Pathology +19