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A Previously Unrecognized Molecular Landscape of Lynch Syndrome in the Mexican Population

International journal of molecular sciences, 2022-09, Vol.23 (19), p.11549

2022

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Familial erythrocytosis 2 and von Hippel-Lindau disease in the same pediatric patient

Boletín médico del Hospital Infantil de México, 2021-07, Vol.78 (4), p.341-345

2021

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Gastric cancer in Latin America

Scandinavian journal of gastroenterology, 2018-02, Vol.53 (2), p.124-129

2018

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Deep DNA sequencing of MGMT, TP53 and AGT in Mexican astrocytoma patients identifies an excess of genetic variants in women and a predictive biomarker

Journal of neuro-oncology, 2023, Vol.161 (1), p.165-174

2023

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Clinical prognostic factors in adults with astrocytoma: Historic cohort

Clinical neurology and neurosurgery, 2016-07, Vol.146, p.116-122

2016

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Expression Levels of Human Equilibrative Nucleoside Transporter 1 and Deoxycytidine Kinase Enzyme as Prognostic Factors in Patients with Acute Myeloid Leukemia Treated with Cytarabine

Chemotherapy (Basel), 2016, Vol.61 (6), p.313-318

2016

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G80A Single Nucleotide Polymorphism in Reduced Folate Carrier-1 Gene in a Mexican Population and its Impact on Survival in Patients with Acute Lymphoblastic Leukemia

Revista de investigacion clinica, 2016-05, Vol.68 (3), p.154-162

2016

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Thiopurine S-methyltransferase Gene (TMPT) polymorphisms in a Mexican population of healthy individuals and leukemic patients

Medical oncology (Northwood, London, England), 2008-03, Vol.25 (1), p.56-62

2008

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Case report: Benign and malignant tumors in adult patients with neurofibromatosis type 1: a comprehensive case series from a large oncologic reference center

Frontiers in oncology, 2024-01, Vol.13, p.1291286

2024

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Full-exon pyrosequencing screening of BRCA germline mutations in Mexican women with inherited breast and ovarian cancer

PloS one, 2012-05, Vol.7 (5), p.e37432-e37432

2012

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A Molecular Characterization of the Allelic Expression of the BRCA1 Founder Δ9–12 Pathogenic Variant and Its Potential Clinical Relevance in Hereditary Cancer

International journal of molecular sciences, 2024-06, Vol.25 (12), p.6773

2024

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Familial erythrocytosis 2 and von Hippel-Lindau disease in the same pediatric patient

Boletín médico del Hospital Infantil de México (Spanish edition), 2021-05, Vol.78 (4)

2021

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Polymorphisms of the thiopurine methyl transferase gene in healthy and acute lymphoblastic leukemia mestizos

BMC cancer, 2007-02, Vol.7 (S1), p.A39-A39, Article A39

2007

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Importancia del asesoramiento genético en familiascon alta susceptibilidad a cáncerque serán sometidas a pruebas moleculares

Cirugia y cirujanos, 2006, Vol.74 (2)

2006

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Genetic determinants of cancer drug efficacy and toxicity: practical considerations and perspectives

Anti-cancer drugs, 2005-10, Vol.16 (9), p.923-933

2005

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Search of the p.M918T Mutation in the RET Oncogene in Mexican Adult Patients with Medullary Thyroid Carcinoma

Experimental and clinical endocrinology & diabetes, 2017-04, Vol.125 (4), p.218

2017

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Importance of genetic counseling and molecular diagnosis testing in families at high risk for cancer

Cirugia y cirujanos, 2006-03, Vol.74 (2), p.137-142

2006

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Acetylator status and N-acetyltransferase 2 gene polymorphisms; phenotype–genotype correlation with the sulfamethazine test

Pharmacogenetics and genomics, 2011-12, Vol.21 (12), p.894-901

2011

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Case report: Benign and malignant tumors in adult patients with neurofibromatosis type 1: a comprehensive case series from a large oncologic reference center

Frontiers in oncology, 2023, Vol.13, p.1291286-1291286

2023

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Molecular characterization of BRCA1 and BRCA2 genes in breast cancer patients under 40 years-old or with familiar cancer history

BMC cancer, 2007-02, Vol.7 (S1), p.A5-A5, Article A5

2007

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A Previously Unrecognized Molecular Landscape of Lynch Syndrome in the Mexican Population

Familial erythrocytosis 2 and von Hippel-Lindau disease in the same pediatric patient

Gastric cancer in Latin America

Deep DNA sequencing of MGMT, TP53 and AGT in Mexican astrocytoma patients identifies an excess of genetic variants in women and a predictive biomarker

Angiotensinogen rs5050 germline genetic variant as potential biomarker of poor prognosis in astrocytoma

Clinical prognostic factors in adults with astrocytoma: Historic cohort

Expression Levels of Human Equilibrative Nucleoside Transporter 1 and Deoxycytidine Kinase Enzyme as Prognostic Factors in Patients with Acute Myeloid Leukemia Treated with Cytarabine

G80A Single Nucleotide Polymorphism in Reduced Folate Carrier-1 Gene in a Mexican Population and its Impact on Survival in Patients with Acute Lymphoblastic Leukemia

Thiopurine S-methyltransferase Gene (TMPT) polymorphisms in a Mexican population of healthy individuals and leukemic patients

Case report: Benign and malignant tumors in adult patients with neurofibromatosis type 1: a comprehensive case series from a large oncologic reference center

Full-exon pyrosequencing screening of BRCA germline mutations in Mexican women with inherited breast and ovarian cancer

A Molecular Characterization of the Allelic Expression of the BRCA1 Founder Δ9–12 Pathogenic Variant and Its Potential Clinical Relevance in Hereditary Cancer

Landscape of Germline Genetic Variants in AGT, MGMT, and TP53 in Mexican Adult Patients with Astrocytoma

Familial erythrocytosis 2 and von Hippel-Lindau disease in the same pediatric patient

Polymorphisms of the thiopurine methyl transferase gene in healthy and acute lymphoblastic leukemia mestizos

Importancia del asesoramiento genético en familiascon alta susceptibilidad a cáncerque serán sometidas a pruebas moleculares

Genetic determinants of cancer drug efficacy and toxicity: practical considerations and perspectives

Search of the p.M918T Mutation in the RET Oncogene in Mexican Adult Patients with Medullary Thyroid Carcinoma

Importance of genetic counseling and molecular diagnosis testing in families at high risk for cancer

Acetylator status and N-acetyltransferase 2 gene polymorphisms; phenotype–genotype correlation with the sulfamethazine test

Case report: Benign and malignant tumors in adult patients with neurofibromatosis type 1: a comprehensive case series from a large oncologic reference center

Molecular characterization of BRCA1 and BRCA2 genes in breast cancer patients under 40 years-old or with familiar cancer history

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