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Marta Pineda

Showing results (91-100 of 150) with videos related to

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European Journal of Human Genetics : EJHG|March 17, 2026
Optimizing GRIDSS for clinical use: A targeted NGS filtering strategy for germline structural variant detectionElisabet Munté, Paula Rofes, Miriam Millán-Castillo, et al.
British Journal of Cancer|October 5, 2018
Primary constitutional MLH1 epimutations: a focal epigenetic eventEstela Dámaso, Adela Castillejo, María Del Mar Arias, et al.
Frontiers in Genetics|September 21, 2018
Computational Tools for Splicing Defect Prediction in Breast/Ovarian Cancer Genes: How Efficient Are They at Predicting RNA Alterations?Alejandro Moles-Fernández, Laura Duran-Lozano, Gemma Montalban, et al.
Scientific Data|February 22, 2024
Ethnicity data resource in population-wide health records: completeness, coverage and granularity of diversityMarta Pineda-Moncusí, Freya Allery, Antonella Delmestri, et al.
Clinical Epigenetics|November 30, 2019
Highly sensitive MLH1 methylation analysis in blood identifies a cancer patient with low-level mosaic MLH1 epimutationEstela Dámaso, Júlia Canet-Hermida, Gardenia Vargas-Parra, et al.
Translational Oncology|February 24, 2026
Somatic mutations in cervicovaginal samples: assessing their role in ovarian cancer detection and prognosisBeatriz Pelegrina, Sonia Paytubi, Yolanda Benavente, et al.
Clinical Chemistry|December 6, 2020
A Collaborative Effort to Define Classification Criteria for ATM Variants in Hereditary Cancer PatientsLidia Feliubadaló, Alejandro Moles-Fernández, Marta Santamariña-Pena, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|March 14, 2023
Highly Sensitive Microsatellite Instability and Immunohistochemistry Assessment in Endometrial Aspirates as a Tool for Cancer Risk Individualization in Lynch SyndromeJúlia Canet-Hermida, Fátima Marín, Eduard Dorca, et al.
The Journal of Molecular Diagnostics : JMD|October 21, 2023
A New Set of in Silico Tools to Support the Interpretation of ATM Missense Variants Using Graphical AnalysisLuz-Marina Porras, Natàlia Padilla, Alejandro Moles-Fernández, et al.
Environmental Health Perspectives|February 28, 2024
Total Effective Xenoestrogen Burden in Serum Samples and Risk of Endometrial Cancer in the Spanish Screenwide Case-Control StudyLaura Costas, Jon Frias-Gomez, Francisco M Peinado, et al.
Pageof 15

Showing results (91-100 of 150) with videos related to

Sort By:
Pageof 15
European Journal of Human Genetics : EJHG|March 17, 2026
Optimizing GRIDSS for clinical use: A targeted NGS filtering strategy for germline structural variant detectionElisabet Munté, Paula Rofes, Miriam Millán-Castillo, et al.
British Journal of Cancer|October 5, 2018
Primary constitutional MLH1 epimutations: a focal epigenetic eventEstela Dámaso, Adela Castillejo, María Del Mar Arias, et al.
Frontiers in Genetics|September 21, 2018
Computational Tools for Splicing Defect Prediction in Breast/Ovarian Cancer Genes: How Efficient Are They at Predicting RNA Alterations?Alejandro Moles-Fernández, Laura Duran-Lozano, Gemma Montalban, et al.
Scientific Data|February 22, 2024
Ethnicity data resource in population-wide health records: completeness, coverage and granularity of diversityMarta Pineda-Moncusí, Freya Allery, Antonella Delmestri, et al.
Clinical Epigenetics|November 30, 2019
Highly sensitive MLH1 methylation analysis in blood identifies a cancer patient with low-level mosaic MLH1 epimutationEstela Dámaso, Júlia Canet-Hermida, Gardenia Vargas-Parra, et al.
Translational Oncology|February 24, 2026
Somatic mutations in cervicovaginal samples: assessing their role in ovarian cancer detection and prognosisBeatriz Pelegrina, Sonia Paytubi, Yolanda Benavente, et al.
Clinical Chemistry|December 6, 2020
A Collaborative Effort to Define Classification Criteria for ATM Variants in Hereditary Cancer PatientsLidia Feliubadaló, Alejandro Moles-Fernández, Marta Santamariña-Pena, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|March 14, 2023
Highly Sensitive Microsatellite Instability and Immunohistochemistry Assessment in Endometrial Aspirates as a Tool for Cancer Risk Individualization in Lynch SyndromeJúlia Canet-Hermida, Fátima Marín, Eduard Dorca, et al.
The Journal of Molecular Diagnostics : JMD|October 21, 2023
A New Set of in Silico Tools to Support the Interpretation of ATM Missense Variants Using Graphical AnalysisLuz-Marina Porras, Natàlia Padilla, Alejandro Moles-Fernández, et al.
Environmental Health Perspectives|February 28, 2024
Total Effective Xenoestrogen Burden in Serum Samples and Risk of Endometrial Cancer in the Spanish Screenwide Case-Control StudyLaura Costas, Jon Frias-Gomez, Francisco M Peinado, et al.
Pageof 15