Mercedes Robledo - Concepedia

Author

Mercedes Robledo

Spanish National Cancer Research Centre ORCID

Also Known As

Eamonn R. Maher, M Robledo, M. Robledo, M.Mar Robledo, Mario Encinas, María Conchita Robledo, Mercedes Robledo, Mercedes Robledo Batanero, Robledo, Mercedes

476

Publications

14.3K

Citations

H-Index

113

Concepts

All Affiliations

Spanish National Cancer Research Centre Centre for Biomedical Network Research on Rare Diseases Centro de Investigación Biomédica en Red Instituto de Salud Carlos III Technische Universität Dresden

About

Mercedes Robledo is an author at Spanish National Cancer Research Centre specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	41	81	5.9K
2	Natural Sciences	4	4	169
3	Public Health	4	4	284
4	Engineering	3	3	148
5	Health Sciences	2	2	277

Mercedes Robledo

180

Publications

11.6K

Citations

H-Index

Page 1

	Year	Citations
Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma Iñaki Comino‐Méndez, Francisco Javier Gracia-Aznárez, Francesca Schiavi, Nature Genetics Hereditary PheochromocytomaMendelian DisorderGenetic DisorderMedicineGenetics	2011	524
Germline mutations in FH confer predisposition to malignant pheochromocytomas and paragangliomas Luis Jaime Castro‐Vega, Alexandre Buffet, Aguirre A. de Cubas, Human Molecular Genetics Fh GeneTumor BiologySomatic VariantTumor HeterogeneityMedicine	2013	389
<i>MAX</i> Mutations Cause Hereditary and Sporadic Pheochromocytoma and Paraganglioma Nelly Burnichon, Alberto Cascón, Francesca Schiavi, Clinical Cancer Research	2012	321
SDHAF2 mutations in familial and sporadic paraganglioma and phaeochromocytoma Jean‐Pierre Bayley, Henricus P. M. Kunst, Alberto Cascón, The Lancet Oncology Somatic VariantGenetic DisorderPathologySdhaf2 MutationsCancer Genetics	2010	268
Tumoral and tissue‐specific expression of the major human β‐tubulin isotypes Luis J. Leandro‐García, Susanna Leskelä, Iñigo Landa, Cytoskeleton Microtubule Dynamics AlterationOncologyMedicineCancer Cell BiologyPathology	2010	262
SDHB/SDHA immunohistochemistry in pheochromocytomas and paragangliomas: a multicenter interobserver variation analysis using virtual microscopy: a Multinational Study of the European Network for the Study of Adrenal Tumors (ENS@T) Thomas Papathomas, Lindsey Oudijk, Alexandre Persu, Modern Pathology Adrenal GlandSdhb/sdha ImmunohistochemistryVirtual MicroscopySurgical PathologyHistopathology	2015	221
Single nucleotide polymorphism associations with response and toxic effects in patients with advanced renal-cell carcinoma treated with first-line sunitinib: a multicentre, observational, prospective study Jesús García-Donás, Emilio Esteban, Luis J. Leandro‐García, The Lancet Oncology UrologyGenitourinary CancerMedicineToxic EffectsAdvanced Renal-cell Carcinoma	2011	220
Research Resource: Transcriptional Profiling Reveals Different Pseudohypoxic Signatures in SDHB and VHL-Related Pheochromocytomas Elena López‐Jiménez, Gonzalo Goméz-López, Luis J. Leandro‐García, Molecular Endocrinology GeneticsPathologyCancer BiologyTumor BiologyNeuro-oncology	2010	207
The miR-200 family controls -tubulin III expression and is associated with paclitaxel-based treatment response and progression-free survival in ovarian cancer patients Susanna Leskelä, Luis J. Leandro‐García, Marta Mendiola, Endocrine Related Cancer	2010	207
Spectrum and Prevalence of <i>FP/TMEM127</i> Gene Mutations in Pheochromocytomas and Paragangliomas Li Yao, Francesca Schiavi, Alberto Cascón, JAMA	2010	199

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