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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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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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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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Genomic analysis of the 8p11‐12 amplicon in familial breast cancer

International journal of cancer, 2007-02, Vol.120 (3), p.714-717

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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Recurrent Germline DLST Mutations in Individuals with Multiple Pheochromocytomas and Paragangliomas

American journal of human genetics, 2019-04, Vol.104 (4), p.651-664

2019

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Histopathology of BRCA1- and BRCA2-associated breast cancer

Critical reviews in oncology/hematology, 2006-07, Vol.59 (1), p.27-39

2006

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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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Recurrent Germline DLST Mutations in Individuals with Multiple Pheochromocytomas and Paragangliomas

American journal of human genetics, 2019-05, Vol.104 (5), p.1008-1010

2019

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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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Phenotypic characterization of BRCA1 and BRCA2 tumors based in a tissue microarray study with 37 immunohistochemical markers

Breast cancer research and treatment, 2005-03, Vol.90 (1), p.5-14

2005

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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

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

Splenic Lesions and Other Findings in Kaposiform Lymphangiomatosis

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

Genomic analysis of the 8p11‐12 amplicon in familial 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

Recurrent Germline DLST Mutations in Individuals with Multiple Pheochromocytomas and Paragangliomas

Histopathology of BRCA1- and BRCA2-associated breast cancer

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

Recurrent Germline DLST Mutations in Individuals with Multiple Pheochromocytomas and Paragangliomas

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

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

Phenotypic characterization of BRCA1 and BRCA2 tumors based in a tissue microarray study with 37 immunohistochemical markers

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