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Targeted Exome Sequencing of Krebs Cycle Genes Reveals Candidate Cancer-Predisposing Mutations in Pheochromocytomas and Paragangliomas

Clinical cancer research, 2017-10, Vol.23 (20), p.6315-6324

2017

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The molecular pathology of hereditary breast cancer: genetic testing and therapeutic implications

Modern pathology, 2005-10, Vol.18 (10), p.1305-1320

2005

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Prognostic Significance of Basal-Like Phenotype and Fascin Expression in Node-Negative Invasive Breast Carcinomas

Clinical cancer research, 2006-03, Vol.12 (5), p.1533-1539

2006

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The role of EZH2 in overall survival of colorectal cancer: a meta-analysis

Scientific reports, 2017-10, Vol.7 (1), p.13806-8, Article 13806

2017

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Relationship between Aldehyde Dehydrogenase, PD-L1 and Tumor-Infiltrating Lymphocytes with Pathologic Response and Survival in Breast Cancer

Cancers, 2022-09, Vol.14 (18), p.4418

2022

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Co-occurrence of mutations in NF1 and other susceptibility genes in pheochromocytoma and paraganglioma

Frontiers in endocrinology (Lausanne), 2023-01, Vol.13, p.1070074-1070074

2023

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Identification of a Proliferation Signature Related to Survival in Nodal Peripheral T-Cell Lymphomas

Journal of clinical oncology, 2007-08, Vol.25 (22), p.3321-3329

2007

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Comprehensive characterization of the DNA amplification at 13q34 in human breast cancer reveals TFDP1 and CUL4A as likely candidate target genes

Breast cancer research : BCR, 2009-01, Vol.11 (6), p.R86-R86, Article R86

2009

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A Predictor Based on the Somatic Genomic Changes of the BRCA1/BRCA2 Breast Cancer Tumors Identifies the Non-BRCA1/BRCA2 Tumors with BRCA1 Promoter Hypermethylation

Clinical cancer research, 2005-02, Vol.11 (3), p.1146-1153

2005

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Immunohistochemical Expression of DNA Repair Proteins in Familial Breast Cancer Differentiate BRCA2-Associated Tumors

Journal of clinical oncology, 2005-10, Vol.23 (30), p.7503-7511

2005

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Splenic Lesions and Other Findings in Kaposiform Lymphangiomatosis

The American journal of surgical pathology, 2023-05, Vol.47 (5), p.631-633

2023

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Estrogen Receptor Status Could Modulate the Genomic Pattern in Familial and Sporadic Breast Cancer

Clinical cancer research, 2007-12, Vol.13 (24), p.7305-7313

2007

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The Accumulation of Specific Amplifications Characterizes Two Different Genomic Pathways of Evolution of Familial Breast Tumors

Clinical cancer research, 2005-12, Vol.11 (24), p.8577-8584

2005

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Incidencia hospitalaria, tendencia y distribución municipal del cáncer de próstata en el área de salud de León (1996-2010)

Revista Española de Salud Pública, 2015-12, Vol.89 (6), p.575-583

2015

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Tendencia y distribución municipal de la incidencia de cáncer de mama en el área de salud de León (1996-2010)

Revista española de salud pública, 2014, Vol.88 (2), p.261-269

2014

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Chronic lymphocytic leukemia and Richter transformation skin involvement recruited by herpesvirus infection

Journal of cutaneous pathology, 2021-05, Vol.48 (5), p.713-716

2021

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Caveolin-1 expression is associated with a basal-like phenotype in sporadic and hereditary breast cancer

Breast cancer research and treatment, 2006-09, Vol.99 (1), p.85-90

2006

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Perineurial cells in granular cell tumors and neoplasms with perineural invasion: an immunohistochemical study

The American journal of dermatopathology, 2012-12, Vol.34 (8), p.800-809

2012

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Vimentin and laminin expression is associated with basal-like phenotype in both sporadic and BRCA1-associated breast carcinomas

Journal of clinical pathology, 2007-09, Vol.60 (9), p.1006-1012

2007

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Immunohistochemical characteristics defined by tissue microarray of hereditary breast cancer not attributable to BRCA1 or BRCA2 mutations: Differences from breast carcinomas arising in BRCA1 and BRCA2 mutation carriers

Clinical cancer research, 2003-09, Vol.9 (10), p.3606-3614

2003

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Intraneural hybrid granular cell tumor-perineurioma

APMIS : acta pathologica, microbiologica et immunologica Scandinavica, 2013-07, Vol.121 (7), p.678-680

2013

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The pathology of hereditary breast cancer

Hereditary cancer in clinical practice, 2004-07, Vol.2 (3), p.131-138, Article 131

2004

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Targeted Exome Sequencing of Krebs Cycle Genes Reveals Candidate Cancer-Predisposing Mutations in Pheochromocytomas and Paragangliomas

The molecular pathology of hereditary breast cancer: genetic testing and therapeutic implications

Prognostic Significance of Basal-Like Phenotype and Fascin Expression in Node-Negative Invasive Breast Carcinomas

The role of EZH2 in overall survival of colorectal cancer: a meta-analysis

Relationship between Aldehyde Dehydrogenase, PD-L1 and Tumor-Infiltrating Lymphocytes with Pathologic Response and Survival in Breast Cancer

Co-occurrence of mutations in NF1 and other susceptibility genes in pheochromocytoma and paraganglioma

Identification of a Proliferation Signature Related to Survival in Nodal Peripheral T-Cell Lymphomas

Comprehensive characterization of the DNA amplification at 13q34 in human breast cancer reveals TFDP1 and CUL4A as likely candidate target genes

A Predictor Based on the Somatic Genomic Changes of the BRCA1/BRCA2 Breast Cancer Tumors Identifies the Non-BRCA1/BRCA2 Tumors with BRCA1 Promoter Hypermethylation

Immunohistochemical Expression of DNA Repair Proteins in Familial Breast Cancer Differentiate BRCA2-Associated Tumors

Splenic Lesions and Other Findings in Kaposiform Lymphangiomatosis

Estrogen Receptor Status Could Modulate the Genomic Pattern in Familial and Sporadic Breast Cancer

The Accumulation of Specific Amplifications Characterizes Two Different Genomic Pathways of Evolution of Familial Breast Tumors

Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma

Gain-of-function mutations in DNMT3A in patients with paraganglioma

Incidencia hospitalaria, tendencia y distribución municipal del cáncer de próstata en el área de salud de León (1996-2010)

Tendencia y distribución municipal de la incidencia de cáncer de mama en el área de salud de León (1996-2010)

Chronic lymphocytic leukemia and Richter transformation skin involvement recruited by herpesvirus infection

Caveolin-1 expression is associated with a basal-like phenotype in sporadic and hereditary breast cancer

Perineurial cells in granular cell tumors and neoplasms with perineural invasion: an immunohistochemical study

Vimentin and laminin expression is associated with basal-like phenotype in both sporadic and BRCA1-associated breast carcinomas

Immunohistochemical characteristics defined by tissue microarray of hereditary breast cancer not attributable to BRCA1 or BRCA2 mutations: Differences from breast carcinomas arising in BRCA1 and BRCA2 mutation carriers

Intraneural hybrid granular cell tumor-perineurioma

The pathology of hereditary breast cancer

DLST mutations in pheochromocytoma and paraganglioma cause proteome hyposuccinylation and metabolic remodeling

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