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Timothée Revil

Showing results (11-20 of 27) with videos related to

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Congenital Heart Disease|February 6, 2018
Analysis of DICER1 in familial and sporadic cases of transposition of the great arteriesNelly Sabbaghian, Maria C Digilio, Gillian M Blue, et al.
The Journal of Clinical Endocrinology and Metabolism|July 27, 2016
Deep Sequencing Reveals Spatially Distributed Distinct Hot Spot Mutations in DICER1-Related Multinodular GoiterLeanne de Kock, Ismaël Bah, Timothée Revil, et al.
NPJ Breast Cancer|May 5, 2026
Co-occurring rare germline DNA repair gene variants in BRCA1/BRCA2 implicated hereditary breast cancer familiesWejdan M Alenezi, Neil Recio, Caitlin T Fierheller, et al.
Genes|April 23, 2022
Case Review: Whole-Exome Sequencing Analyses Identify Carriers of a Known Likely Pathogenic Intronic <i>BRCA1</i> Variant in Ovarian Cancer Cases Clinically Negative for Pathogenic <i>BRCA1</i> and <i>BRCA2</i> VariantsWejdan M Alenezi, Caitlin T Fierheller, Timothée Revil, et al.
British Journal of Cancer|May 20, 2017
Sequencing of DICER1 in sarcomas identifies biallelic somatic DICER1 mutations in an adult-onset embryonal rhabdomyosarcomaLeanne de Kock, Barbara Rivera, Timothée Revil, et al.
Scientific Reports|August 21, 2019
Analysis of head and neck carcinoma progression reveals novel and relevant stage-specific changes associated with immortalisation and malignancyRatna Veeramachaneni, Thomas Walker, Timothée Revil, et al.
Journal of Medical Genetics|December 13, 2012
Hemizygous mutations in SNAP29 unmask autosomal recessive conditions and contribute to atypical findings in patients with 22q11.2DSDonna M McDonald-McGinn, Somayyeh Fahiminiya, Timothée Revil, et al.
Cell Reports|November 2, 2017
A Targetable EGFR-Dependent Tumor-Initiating Program in Breast CancerPaul Savage, Alexis Blanchet-Cohen, Timothée Revil, et al.
Frontiers in Oncology|March 27, 2023
Genetic analyses of DNA repair pathway associated genes implicate new candidate cancer predisposing genes in ancestrally defined ovarian cancer casesWejdan M Alenezi, Caitlin T Fierheller, Corinne Serruya, et al.
International Journal of Molecular Sciences|January 28, 2026
The Genetic and Molecular Analyses of Rare Candidate Germline <i>BRIP1/FANCJ</i> Variants Implicated in Hereditary Breast and Ovarian CancersWejdan M Alenezi, Larissa Milano, Caitlin T Fierheller, et al.
Pageof 3

Showing results (11-20 of 27) with videos related to

Sort By:
Pageof 3
Congenital Heart Disease|February 6, 2018
Analysis of DICER1 in familial and sporadic cases of transposition of the great arteriesNelly Sabbaghian, Maria C Digilio, Gillian M Blue, et al.
The Journal of Clinical Endocrinology and Metabolism|July 27, 2016
Deep Sequencing Reveals Spatially Distributed Distinct Hot Spot Mutations in DICER1-Related Multinodular GoiterLeanne de Kock, Ismaël Bah, Timothée Revil, et al.
NPJ Breast Cancer|May 5, 2026
Co-occurring rare germline DNA repair gene variants in BRCA1/BRCA2 implicated hereditary breast cancer familiesWejdan M Alenezi, Neil Recio, Caitlin T Fierheller, et al.
Genes|April 23, 2022
Case Review: Whole-Exome Sequencing Analyses Identify Carriers of a Known Likely Pathogenic Intronic <i>BRCA1</i> Variant in Ovarian Cancer Cases Clinically Negative for Pathogenic <i>BRCA1</i> and <i>BRCA2</i> VariantsWejdan M Alenezi, Caitlin T Fierheller, Timothée Revil, et al.
British Journal of Cancer|May 20, 2017
Sequencing of DICER1 in sarcomas identifies biallelic somatic DICER1 mutations in an adult-onset embryonal rhabdomyosarcomaLeanne de Kock, Barbara Rivera, Timothée Revil, et al.
Scientific Reports|August 21, 2019
Analysis of head and neck carcinoma progression reveals novel and relevant stage-specific changes associated with immortalisation and malignancyRatna Veeramachaneni, Thomas Walker, Timothée Revil, et al.
Journal of Medical Genetics|December 13, 2012
Hemizygous mutations in SNAP29 unmask autosomal recessive conditions and contribute to atypical findings in patients with 22q11.2DSDonna M McDonald-McGinn, Somayyeh Fahiminiya, Timothée Revil, et al.
Cell Reports|November 2, 2017
A Targetable EGFR-Dependent Tumor-Initiating Program in Breast CancerPaul Savage, Alexis Blanchet-Cohen, Timothée Revil, et al.
Frontiers in Oncology|March 27, 2023
Genetic analyses of DNA repair pathway associated genes implicate new candidate cancer predisposing genes in ancestrally defined ovarian cancer casesWejdan M Alenezi, Caitlin T Fierheller, Corinne Serruya, et al.
International Journal of Molecular Sciences|January 28, 2026
The Genetic and Molecular Analyses of Rare Candidate Germline <i>BRIP1/FANCJ</i> Variants Implicated in Hereditary Breast and Ovarian CancersWejdan M Alenezi, Larissa Milano, Caitlin T Fierheller, et al.
Pageof 3