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Enfermedad de Caffey en una familia y trastornos relacionados con el colageno tipo 1

Universitas Medica, 2019-04, Vol.60 (2), p.67-76

2019

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Polimorfismos genéticos en pacientes con fisuras labio y/o palatinas no sindrómicos

Ciencia en desarrollo, 2019-12, Vol.10 (2), p.59-92

2019

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Human ESCs predisposition to karyotypic instability: Is a matter of culture adaptation or differential vulnerability among hESC lines due to inherent properties?

Molecular cancer, 2008-10, Vol.7 (1), p.76-76, Article 76

2008

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Salivary MicroRNAs for Early Detection of Head and Neck Squamous Cell Carcinoma: A Case-Control Study in the High Altitude Mestizo Ecuadorian Population

BioMed research international, 2018-01, Vol.2018, p.9792730-9

2018

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A quick guide for using Microsoft OneNote as an electronic laboratory notebook

PLoS computational biology, 2019-05, Vol.15 (5), p.e1006918-e1006918

2019

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Homozygous Deletion Mapping in Myeloma Samples Identifies Genes and an Expression Signature Relevant to Pathogenesis and Outcome

Clinical cancer research, 2010-03, Vol.16 (6), p.1856-1864

2010

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Integration of global SNP-based mapping and expression arrays reveals key regions, mechanisms, and genes important in the pathogenesis of multiple myeloma

Blood, 2006-09, Vol.108 (5), p.1733-1743

2006

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Oncology and Pharmacogenomics Insights in Polycystic Ovary Syndrome: An Integrative Analysis

Frontiers in endocrinology (Lausanne), 2020-10, Vol.11, p.585130

2020

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Clinical, genomics and networking analyses of a high-altitude native American Ecuadorian patient with congenital insensitivity to pain with anhidrosis: a case report

BMC medical genomics, 2020-08, Vol.13 (1), p.113-113, Article 113

2020

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Gene mapping and expression analysis of 16q loss of heterozygosity identifies WWOX and CYLD as being important in determining clinical outcome in multiple myeloma

Blood, 2007-11, Vol.110 (9), p.3291-3300

2007

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Post-transcriptional Regulation of Colorectal Cancer: A Focus on RNA-Binding Proteins

Frontiers in molecular biosciences, 2019-08, Vol.6, p.65

2019

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Positive Association of the Cathepsin D Ala224Val Gene Polymorphism With the Risk of Alzheimer's Disease

The American journal of the medical sciences, 2015-10, Vol.350 (4), p.296-301

2015

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Clinical, cytogenetic, and molecular findings in a patient with ring chromosome 4: case report and literature review

BMC medical genomics, 2019-11, Vol.12 (1), p.167-167, Article 167

2019

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Deletions of CDKN2C in Multiple Myeloma: Biological and Clinical Implications

Clinical cancer research, 2008-10, Vol.14 (19), p.6033-6041

2008

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Ring chromosome 15 - cytogenetics and mapping arrays: a case report and review of the literature

Journal of medical case reports, 2018-11, Vol.12 (1), p.340-340, Article 340

2018

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A deep analysis using panel-based next-generation sequencing in an Ecuadorian pediatric patient with anaplastic astrocytoma: a case report

Journal of medical case reports, 2020-08, Vol.14 (1), p.136-136, Article 136

2020

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Analysis of Racial/Ethnic Representation in Select Basic and Applied Cancer Research Studies

Scientific reports, 2018-09, Vol.8 (1), p.13978-8, Article 13978

2018

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Cytogenetic and genomic analysis of a patient with turner syndrome and t(2;12): a case report

Molecular cytogenetics, 2020-11, Vol.13 (1), p.1-46, Article 46

2020

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A compendium of myeloma-associated chromosomal copy number abnormalities and their prognostic value

Blood, 2010-10, Vol.116 (15), p.e56-e65

2010

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Enfermedad de Caffey en una familia y expansión del espectro de trastornos relacionados con el colágeno tipo 1

Universitas médica, 2019-04, Vol.60 (2), p.1-10

2019

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The three-hybrid genetic composition of an Ecuadorian population using AIMs-InDels compared with autosomes, mitochondrial DNA and Y chromosome data

Scientific reports, 2019-06, Vol.9 (1), p.9247-8, Article 9247

2019

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Mutational Analysis of Oncogenic AKT1 Gene Associated with Breast Cancer Risk in the High Altitude Ecuadorian Mestizo Population

BioMed research international, 2018-01, Vol.2018, p.7463832-10

2018

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Deficiency in p53 but not Retinoblastoma Induces the Transformation of Mesenchymal Stem Cells In vitro and Initiates Leiomyosarcoma In vivo

Cancer research (Chicago, Ill.), 2010-05, Vol.70 (10), p.4185-4194

2010

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NF2 gene mutations and allelic status of 1p, 14q and 22q in sporadic meningiomas

Oncogene, 1999-04, Vol.18 (13), p.2231-2239

1999

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Pharmacogenomics, biomarker network, and allele frequencies in colorectal cancer

The pharmacogenomics journal, 2020-02, Vol.20 (1), p.136-158

2020

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Enfermedad de Caffey en una familia y trastornos relacionados con el colageno tipo 1

Polimorfismos genéticos en pacientes con fisuras labio y/o palatinas no sindrómicos

Human ESCs predisposition to karyotypic instability: Is a matter of culture adaptation or differential vulnerability among hESC lines due to inherent properties?

Salivary MicroRNAs for Early Detection of Head and Neck Squamous Cell Carcinoma: A Case-Control Study in the High Altitude Mestizo Ecuadorian Population

A quick guide for using Microsoft OneNote as an electronic laboratory notebook

Homozygous Deletion Mapping in Myeloma Samples Identifies Genes and an Expression Signature Relevant to Pathogenesis and Outcome

Integration of global SNP-based mapping and expression arrays reveals key regions, mechanisms, and genes important in the pathogenesis of multiple myeloma

Oncology and Pharmacogenomics Insights in Polycystic Ovary Syndrome: An Integrative Analysis

Clinical, genomics and networking analyses of a high-altitude native American Ecuadorian patient with congenital insensitivity to pain with anhidrosis: a case report

Gene mapping and expression analysis of 16q loss of heterozygosity identifies WWOX and CYLD as being important in determining clinical outcome in multiple myeloma

Post-transcriptional Regulation of Colorectal Cancer: A Focus on RNA-Binding Proteins

Positive Association of the Cathepsin D Ala224Val Gene Polymorphism With the Risk of Alzheimer's Disease

Clinical, cytogenetic, and molecular findings in a patient with ring chromosome 4: case report and literature review

Deletions of CDKN2C in Multiple Myeloma: Biological and Clinical Implications

Ring chromosome 15 - cytogenetics and mapping arrays: a case report and review of the literature

A deep analysis using panel-based next-generation sequencing in an Ecuadorian pediatric patient with anaplastic astrocytoma: a case report

Analysis of Racial/Ethnic Representation in Select Basic and Applied Cancer Research Studies

Cytogenetic and genomic analysis of a patient with turner syndrome and t(2;12): a case report

A compendium of myeloma-associated chromosomal copy number abnormalities and their prognostic value

Enfermedad de Caffey en una familia y expansión del espectro de trastornos relacionados con el colágeno tipo 1

The three-hybrid genetic composition of an Ecuadorian population using AIMs-InDels compared with autosomes, mitochondrial DNA and Y chromosome data

Mutational Analysis of Oncogenic AKT1 Gene Associated with Breast Cancer Risk in the High Altitude Ecuadorian Mestizo Population

Deficiency in p53 but not Retinoblastoma Induces the Transformation of Mesenchymal Stem Cells In vitro and Initiates Leiomyosarcoma In vivo

NF2 gene mutations and allelic status of 1p, 14q and 22q in sporadic meningiomas

Pharmacogenomics, biomarker network, and allele frequencies in colorectal cancer

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