Rocío Letón

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 · 527 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

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 · 391 citations

Life Sciences, Genetics, Oncology +13

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

Nelly Burnichon, Alberto Cascón, Francesca Schiavi et al. · Clinical Cancer Research · 2012 · 327 citations · Full text

Life Sciences, Genetics, Oncology +14

Identification of a Frameshift Mutation in Osterix in a Patient with Recessive Osteogenesis Imperfecta

Pablo Lapunzina, Mona Aglan, Samia A. Temtamy et al. · The American Journal of Human Genetics · 2010 · 289 citations · Full text

Medicine, Genetics, Molecular Genetics +13

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

Luis J. Leandro‐García, Susanna Leskelä, Iñigo Landa et al. · Cytoskeleton · 2010 · 268 citations

Medicine, Molecular Biology, Oncology +13