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Karim Labreche

Showing results (1-10 of 24) with videos related to

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International Journal of Molecular Sciences|December 30, 2020
Tracking the Genetic Susceptibility Background of B-Cell Non-Hodgkin's Lymphomas from Genome-Wide Association StudiesIsaias Hernández-Verdin, Karim Labreche, Marion Benazra, et al.
The Oncologist|July 13, 2016
Chromosome 17p Homodisomy Is Associated With Better Outcome in 1p19q Non-Codeleted and IDH-Mutated GliomasMarianne Labussière, Amithys Rahimian, Marine Giry, et al.
Acta Neuropathologica|June 23, 2017
Same-day genomic and epigenomic diagnosis of brain tumors using real-time nanopore sequencingPhilipp Euskirchen, Franck Bielle, Karim Labreche, et al.
NPJ Precision Oncology|December 1, 2022
Pan-cancer landscape of AID-related mutations, composite mutations, and their potential role in the ICI responseIsaias Hernández-Verdin, Kadir C Akdemir, Daniele Ramazzotti, et al.
Oncotarget|June 28, 2014
Mutational analysis of primary central nervous system lymphomaAurélie Bruno, Blandine Boisselier, Karim Labreche, et al.
Acta Neuropathologica|February 21, 2018
Diffuse gliomas classified by 1p/19q co-deletion, TERT promoter and IDH mutation status are associated with specific genetic risk lociKarim Labreche, Ben Kinnersley, Giulia Berzero, et al.
Nature Communications|January 23, 2015
Whole-exome sequencing reveals the mutational spectrum of testicular germ cell tumoursKevin Litchfield, Brenda Summersgill, Shawn Yost, et al.
The New England Journal of Medicine|September 8, 2021
Somatic <i>PIK3CA</i> Mutations in Sporadic Cerebral Cavernous MalformationsMatthieu Peyre, Danielle Miyagishima, Franck Bielle, et al.
Frontiers in Cell and Developmental Biology|October 28, 2021
Low-Coverage Whole Genome Sequencing of Cell-Free DNA From Immunosuppressed Cancer Patients Enables Tumor Fraction Determination and Reveals Relevant Copy Number AlterationsAmira Bouzidi, Karim Labreche, Marine Baron, et al.
European Journal of Human Genetics : EJHG|April 23, 2023
Lynch syndrome: influence of additional susceptibility variants on cancer riskRoseline Vibert, Jasmine Hasnaoui, Alexandre Perrier, et al.
Pageof 3

Showing results (1-10 of 24) with videos related to

Sort By:
Pageof 3
International Journal of Molecular Sciences|December 30, 2020
Tracking the Genetic Susceptibility Background of B-Cell Non-Hodgkin's Lymphomas from Genome-Wide Association StudiesIsaias Hernández-Verdin, Karim Labreche, Marion Benazra, et al.
The Oncologist|July 13, 2016
Chromosome 17p Homodisomy Is Associated With Better Outcome in 1p19q Non-Codeleted and IDH-Mutated GliomasMarianne Labussière, Amithys Rahimian, Marine Giry, et al.
Acta Neuropathologica|June 23, 2017
Same-day genomic and epigenomic diagnosis of brain tumors using real-time nanopore sequencingPhilipp Euskirchen, Franck Bielle, Karim Labreche, et al.
NPJ Precision Oncology|December 1, 2022
Pan-cancer landscape of AID-related mutations, composite mutations, and their potential role in the ICI responseIsaias Hernández-Verdin, Kadir C Akdemir, Daniele Ramazzotti, et al.
Oncotarget|June 28, 2014
Mutational analysis of primary central nervous system lymphomaAurélie Bruno, Blandine Boisselier, Karim Labreche, et al.
Acta Neuropathologica|February 21, 2018
Diffuse gliomas classified by 1p/19q co-deletion, TERT promoter and IDH mutation status are associated with specific genetic risk lociKarim Labreche, Ben Kinnersley, Giulia Berzero, et al.
Nature Communications|January 23, 2015
Whole-exome sequencing reveals the mutational spectrum of testicular germ cell tumoursKevin Litchfield, Brenda Summersgill, Shawn Yost, et al.
The New England Journal of Medicine|September 8, 2021
Somatic <i>PIK3CA</i> Mutations in Sporadic Cerebral Cavernous MalformationsMatthieu Peyre, Danielle Miyagishima, Franck Bielle, et al.
Frontiers in Cell and Developmental Biology|October 28, 2021
Low-Coverage Whole Genome Sequencing of Cell-Free DNA From Immunosuppressed Cancer Patients Enables Tumor Fraction Determination and Reveals Relevant Copy Number AlterationsAmira Bouzidi, Karim Labreche, Marine Baron, et al.
European Journal of Human Genetics : EJHG|April 23, 2023
Lynch syndrome: influence of additional susceptibility variants on cancer riskRoseline Vibert, Jasmine Hasnaoui, Alexandre Perrier, et al.
Pageof 3