Miguel Urioste - Concepedia

Author

Miguel Urioste

Spanish National Cancer Research Centre ORCID

Also Known As

Angela Toss, Damián García-Olmo, J García, Jesús Troya, Jesús Troya, Karla S. C. Souza, M Urioste, M. Urioste, MIGUEL URIOSTE, Ma’en Obeidat

217

Publications

8.9K

Citations

H-Index

Concepts

All Affiliations

Spanish National Cancer Research Centre Centre for Biomedical Network Research on Rare Diseases Hospital Clínico San Carlos Centro de Investigación del Cáncer Instituto de Salud Carlos III

About

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

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	26	44	5.4K
2	Health Sciences	5	5	283
3	Public Health	3	3	3.7K
4	Engineering	2	2	119
5	Biostatistics	1	1	79

Miguel Urioste

Publications

7.5K

Citations

H-Index

Page 1

	Year	Citations
Epigenetic differences arise during the lifetime of monozygotic twins Mario F. Fraga, Esteban Ballestar, Maria F. Paz, Proceedings of the National Academy of Sciences ChromatinDevelopmental BiologyGenetic DisorderMedicineGenetics	2005	3.6K
<i>MAX</i> Mutations Cause Hereditary and Sporadic Pheochromocytoma and Paraganglioma Nelly Burnichon, Alberto Cascón, Francesca Schiavi, Clinical Cancer Research	2012	321
Whole-Exome Sequencing Identifies MDH2 as a New Familial Paraganglioma Gene Alberto Cascón, Iñaki Comino‐Méndez, María Currás-Freixes, JNCI Journal of the National Cancer Institute Krebs CycleGeneticsPathologyGliomaTumor Biology	2015	187
A mutation in the POT1 gene is responsible for cardiac angiosarcoma in TP53-negative Li–Fraumeni-like families Oriol Calvete, Paula Martínez, Pablo García‐Pavía, Nature Communications	2015	161
Short rib‐polydactyly syndrome and pericentric inversion of chromosome 4 Miguel Urioste, María Luisa Martínez‐Frías, Eva Bermejo, American Journal of Medical Genetics	1994	108
Germline Mutations in FAN1 Cause Hereditary Colorectal Cancer by Impairing DNA Repair Núria Seguí, Leonardo Mina, Conxi Lázaro, Gastroenterology	2015	104
Analysis of FANCB and FANCN/PALB2 Fanconi Anemia genes in BRCA1/2-negative Spanish breast cancer families María J. García, María Victoria Fernández, Ana Osório, Breast Cancer Research and Treatment Breast OncologyGeneticsMolecular GeneticsBreast CancerCancer Genetics	2008	102
Genetic Anticipation Is Associated with Telomere Shortening in Hereditary Breast Cancer Beatriz Martı́nez-Delgado, Kira Yanowsky, Lucía Inglada‐Pérez, PLoS Genetics Genome InstabilityEngineeringCancer PathologySomatic VariantGenetic Disorder	2011	93
The Average Cumulative Risks of Breast and Ovarian Cancer for Carriers of Mutations in <i>BRCA1</i> and <i>BRCA2</i> Attending Genetic Counseling Units in Spain Roger L. Milne, Ana Osório, Teresa Ramón y Cajal, Clinical Cancer Research	2008	93
Recurrent Germline DLST Mutations in Individuals with Multiple Pheochromocytomas and Paragangliomas Laura Remacha, David Pirman, Christopher E. Mahoney, The American Journal of Human Genetics Neuro-oncologyGenetic DisorderGeneticsPathologyMedicine	2019	91

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