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Germline MC1R status influences somatic mutation burden in melanoma

Nature communications, 2016-07, Vol.7 (1), p.12064-7, Article 12064

2016

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Cross-species genomic landscape comparison of human mucosal melanoma with canine oral and equine melanoma

Nature communications, 2019-01, Vol.10 (1), p.353-14, Article 353

2019

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The genome that fuelled a Mexican scientific revolution

Nature reviews. Genetics, 2022-06, Vol.23 (6), p.322-323

Robles-Espinoza, Carla Daniela

2022

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Somatic Mutational Landscape in Mexican Patients: CDH1 Mutations and chr20q13.33 Amplifications Are Associated with Diffuse-Type Gastric Adenocarcinoma

International journal of molecular sciences, 2022-10, Vol.23 (19), p.11116

2022

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Melanoma: a global perspective

Nature reviews. Cancer, 2017-07, Vol.17 (7), p.393-394

2017

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More than just acral melanoma: the controversies of defining the disease

The journal of pathology. Clinical research, 2021-11, Vol.7 (6), p.531-541

2021

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RSAT 2018: regulatory sequence analysis tools 20th anniversary

Nucleic acids research, 2018-07, Vol.46 (W1), p.W209-W214

2018

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RSAT 2018: regulatory sequence analysis tools 20th anniversary

Nucleic acids research, 2018-07, Vol.46 (W1), p.W209

2018

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Allele-specific expression: applications in cancer and technical considerations

Current opinion in genetics & development, 2021-02, Vol.66, p.10-19

2021

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Respiratory syncytial virus A genotype classification based on systematic intergenotypic and intragenotypic sequence analysis

Scientific reports, 2019-12, Vol.9 (1), p.20097-12, Article 20097

2019

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Virtual meetings promise to eliminate geographical and administrative barriers and increase accessibility, diversity and inclusivity

Nature biotechnology, 2022-01, Vol.40 (1), p.133-137

2022

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Variant ranking pipeline for complex familial disorders

Scientific reports, 2024-06, Vol.14 (1), p.13599-14

2024

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BRN2 suppresses apoptosis, reprograms DNA damage repair, and is associated with a high somatic mutation burden in melanoma

Genes & development, 2019-03, Vol.33 (5-6), p.310-332

2019

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A Genome-Wide Association Study for Regulators of Micronucleus Formation in Mice

G3 : genes - genomes - genetics, 2016-08, Vol.6 (8), p.2343-2354

2016

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Population-based analysis of POT1 variants in a cutaneous melanoma case-control cohort

Journal of medical genetics, 2023-07, Vol.60 (7), p.692-696

2023

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An Overview of Strategies for Detecting Genotype-Phenotype Associations Across Ancestrally Diverse Populations

Frontiers in genetics, 2021-11, Vol.12, p.703901-703901

2021

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VCF/Plotein: visualization and prioritization of genomic variants from human exome sequencing projects

Bioinformatics, 2019-11, Vol.35 (22), p.4803-4805

2019

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Rare Variant, Gene-Based Association Study of Hereditary Melanoma Using Whole-Exome Sequencing

JNCI : Journal of the National Cancer Institute, 2017-12, Vol.109 (12)

2017

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A chromoanagenesis-driven ultra-complex t(5;7;21)dn truncates neurodevelopmental genes in a disabled boy as revealed by whole-genome sequencing

European journal of medical genetics, 2022-10, Vol.65 (10), p.104579-104579, Article 104579

2022

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Going home: the challenges and rewards of genetics research in Mexico

Nature genetics, 2021-07, Vol.53 (7), p.937-939

Robles-Espinoza, Carla Daniela

2021

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Multiomics subtyping for clinically prognostic cancer subtypes and personalized therapy: A systematic review and meta-analysis

Genetics in medicine, 2022-01, Vol.24 (1), p.15-25

2022

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The protective effect of time-caloric restriction in liver fibrosis induced by nitrosamines in rat model

Journal of hepatology, 2022-07, Vol.77, p.S476

2022

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Germline MC1R status influences somatic mutation burden in melanoma

Cross-species genomic landscape comparison of human mucosal melanoma with canine oral and equine melanoma

The genome that fuelled a Mexican scientific revolution

Somatic Mutational Landscape in Mexican Patients: CDH1 Mutations and chr20q13.33 Amplifications Are Associated with Diffuse-Type Gastric Adenocarcinoma

Melanoma: a global perspective

More than just acral melanoma: the controversies of defining the disease

RSAT 2018: regulatory sequence analysis tools 20th anniversary

RSAT 2018: regulatory sequence analysis tools 20th anniversary

Allele-specific expression: applications in cancer and technical considerations

Respiratory syncytial virus A genotype classification based on systematic intergenotypic and intragenotypic sequence analysis

Virtual meetings promise to eliminate geographical and administrative barriers and increase accessibility, diversity and inclusivity

Variant ranking pipeline for complex familial disorders

BRN2 suppresses apoptosis, reprograms DNA damage repair, and is associated with a high somatic mutation burden in melanoma

A Genome-Wide Association Study for Regulators of Micronucleus Formation in Mice

Population-based analysis of POT1 variants in a cutaneous melanoma case-control cohort

An Overview of Strategies for Detecting Genotype-Phenotype Associations Across Ancestrally Diverse Populations

VCF/Plotein: visualization and prioritization of genomic variants from human exome sequencing projects

Rare Variant, Gene-Based Association Study of Hereditary Melanoma Using Whole-Exome Sequencing

Genome-wide chemical mutagenesis screens allow unbiased saturation of the cancer genome and identification of drug resistance mutations

A chromoanagenesis-driven ultra-complex t(5;7;21)dn truncates neurodevelopmental genes in a disabled boy as revealed by whole-genome sequencing

Going home: the challenges and rewards of genetics research in Mexico

Melanoma models for the next generation of therapies

Multiomics subtyping for clinically prognostic cancer subtypes and personalized therapy: A systematic review and meta-analysis

The protective effect of time-caloric restriction in liver fibrosis induced by nitrosamines in rat model

High-resolution functional mapping of RAD51C by saturation genome editing

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