Francisco Javier Gracia-Aznárez

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

Whole Exome Sequencing Suggests Much of Non-BRCA1/BRCA2 Familial Breast Cancer Is Due to Moderate and Low Penetrance Susceptibility Alleles

Francisco Javier Gracia-Aznárez, María Victoria Fernández, Guillermo Pita et al. · PLoS ONE · 2013 · 98 citations · Full text

Breast Oncology, Oncology, Medicine +9

Biological and clinical significance of dysplastic hematopoiesis in patients with newly diagnosed multiple myeloma

Catarina Maia, Noemí Puig, María‐Teresa Cedena et al. · Blood · 2020 · 34 citations · Full text

Machine Learning-Based Approach Highlights the Use of a Genomic Variant Profile for Precision Medicine in Ovarian Failure

Ismael Henarejos-Castillo, Alejandro Alemán, Begoña Martinez-Montoro et al. · Journal of Personalized Medicine · 2021 · 13 citations · Full text