Miguel Urioste

Spanish National Cancer Research Centre — Spain

Medicine · Health Sciences

40h-index8.9kcitations217works1.12yr avg
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Research Topics

Genetic factors in colorectal cancer(65), Colorectal Cancer Screening and Detection(25), Genomic variations and chromosomal abnormalities(23), Cancer Genomics and Diagnostics(21), DNA Repair Mechanisms(20)

Publications200 total

Data from <i>MAX</i> Mutations Cause Hereditary and Sporadic Pheochromocytoma and Paraganglioma
2023Open Access
Data from <i>MAX</i> Mutations Cause Hereditary and Sporadic Pheochromocytoma and Paraganglioma
2023Open Access
Supplementary Figures 1 - 3 from <i>MAX</i> Mutations Cause Hereditary and Sporadic Pheochromocytoma and Paraganglioma
2023Open Access
Supplementary Figures 1 - 3 from <i>MAX</i> Mutations Cause Hereditary and Sporadic Pheochromocytoma and Paraganglioma
2023Open Access
Supplementary Table 2 from <i>MLH1</i> Founder Mutations with Moderate Penetrance in Spanish Lynch Syndrome Families
2023Open Access
Supplementary Table 1 from <i>MLH1</i> Founder Mutations with Moderate Penetrance in Spanish Lynch Syndrome Families
2023Open Access
Data from <i>MLH1</i> Founder Mutations with Moderate Penetrance in Spanish Lynch Syndrome Families
2023Open Access
Supplementary Methods from <i>MLH1</i> Founder Mutations with Moderate Penetrance in Spanish Lynch Syndrome Families
2023Open Access
Supplementary Methods from <i>MLH1</i> Founder Mutations with Moderate Penetrance in Spanish Lynch Syndrome Families
2023Open Access
Supplementary Table 2 from <i>MLH1</i> Founder Mutations with Moderate Penetrance in Spanish Lynch Syndrome Families
2023Open Access
Data from Association Study of 69 Genes in the Ret Pathway Identifies Low-penetrance Loci in Sporadic Medullary Thyroid Carcinoma
2023Open Access
Supplementary Figure 1 from <i>MLH1</i> Founder Mutations with Moderate Penetrance in Spanish Lynch Syndrome Families
2023Open Access
Data from <i>MLH1</i> Founder Mutations with Moderate Penetrance in Spanish Lynch Syndrome Families
2023Open Access
Supplementary Information and Tables 1-5 from Association Study of 69 Genes in the Ret Pathway Identifies Low-penetrance Loci in Sporadic Medullary Thyroid Carcinoma
2023Open Access
Supplementary Table 1 from <i>MLH1</i> Founder Mutations with Moderate Penetrance in Spanish Lynch Syndrome Families
2023Open Access
Data from Association Study of 69 Genes in the Ret Pathway Identifies Low-penetrance Loci in Sporadic Medullary Thyroid Carcinoma
2023Open Access
Supplementary Information and Tables 1-5 from Association Study of 69 Genes in the Ret Pathway Identifies Low-penetrance Loci in Sporadic Medullary Thyroid Carcinoma
2023Open Access
Supplementary Figure 1 from <i>MLH1</i> Founder Mutations with Moderate Penetrance in Spanish Lynch Syndrome Families
2023Open Access
Functional analysis of PTEN variants of unknown significance from PHTS patients unveils complex patterns of PTEN biological activity in disease
European Journal of Human Genetics·2022· 6 citedOpen Access
Biallelic germline mutations in MAD1L1 induce a syndrome of aneuploidy with high tumor susceptibility
Science Advances·2022· 14 citedOpen Access
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Frequent Co-authors

Javier Benı́tez(30), Mercedes Robledo(10), Ana Osório(10), Juan C. Cigudosa(8), Laura Valle(8), Miguel de la Hoya(8), Alberto Cascón(7), Lucía Inglada‐Pérez(7), Ignacio Blanco(7), Conxi Lázaro(7), Rocío Letón(6), María Victoria Fernández(6), Teresa Ramón y Cajal(6), Manel Esteller(5), Bárbara Rivera(5), Roger L. Milne(5), Beatriz Martı́nez-Delgado(5), José Perea(5), Lorenzo Melchor(5), Ángel Martínez‐Ramírez(5)