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Yannick Marie

Showing results (81-90 of 96) with videos related to

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Tremor and Other Hyperkinetic Movements (New York, N.Y.)|December 12, 2019
Association of Rare Genetic Variants in Opioid Receptors with Tourette SyndromeChristel Depienne, Sorana Ciura, Oriane Trouillard, et al.
Neurobiology of Aging|November 21, 2020
Genetic screening of ANXA11 revealed novel mutations linked to amyotrophic lateral sclerosisElisa Teyssou, François Muratet, Maria-Del-Mar Amador, et al.
American Journal of Human Genetics|February 7, 2012
RAD51 haploinsufficiency causes congenital mirror movements in humansChristel Depienne, Delphine Bouteiller, Aurélie Méneret, et al.
Nature Communications|June 20, 2018
A recurrent point mutation in PRKCA is a hallmark of chordoid gliomasShai Rosenberg, Iva Simeonova, Franck Bielle, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|July 28, 2012
Recurrent mutations of MYD88 and TBL1XR1 in primary central nervous system lymphomasAlberto Gonzalez-Aguilar, Ahmed Idbaih, Blandine Boisselier, et al.
Clinical and Translational Medicine|July 9, 2022
Identification of growth hormone receptor as a relevant target for precision medicine in low-EGFR expressing glioblastomaMaïté Verreault, Irma Segoviano Vilchis, Shai Rosenberg, et al.
JCO Precision Oncology|June 1, 2023
Mismatch Repair Deficiency and Lynch Syndrome Among Adult Patients With GliomaPatrick R Benusiglio, Fikret Elder, Mehdi Touat, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|January 23, 2015
Detection, Characterization, and Inhibition of FGFR-TACC Fusions in IDH Wild-type GliomaAnna Luisa Di Stefano, Alessandra Fucci, Veronique Frattini, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 31, 2021
Impact of a frequent nearsplice <i>SOD1</i> variant in amyotrophic lateral sclerosis: optimising <i>SOD1</i> genetic screening for gene therapy opportunitiesFrançois Muratet, Elisa Teyssou, Aude Chiot, et al.
Journal of Thoracic Oncology : Official Publication of the International Association for the Study of Lung Cancer|February 9, 2025
Human Immunodeficiency Virus Impairs Immune Responses to Tumor Neoepitopes Without Altering Mutational Profiles in NSCLCBaptiste Abbar, Karim Labreche, Jacques Cadranel, et al.
Pageof 10

Showing results (81-90 of 96) with videos related to

Sort By:
Pageof 10
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|December 12, 2019
Association of Rare Genetic Variants in Opioid Receptors with Tourette SyndromeChristel Depienne, Sorana Ciura, Oriane Trouillard, et al.
Neurobiology of Aging|November 21, 2020
Genetic screening of ANXA11 revealed novel mutations linked to amyotrophic lateral sclerosisElisa Teyssou, François Muratet, Maria-Del-Mar Amador, et al.
American Journal of Human Genetics|February 7, 2012
RAD51 haploinsufficiency causes congenital mirror movements in humansChristel Depienne, Delphine Bouteiller, Aurélie Méneret, et al.
Nature Communications|June 20, 2018
A recurrent point mutation in PRKCA is a hallmark of chordoid gliomasShai Rosenberg, Iva Simeonova, Franck Bielle, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|July 28, 2012
Recurrent mutations of MYD88 and TBL1XR1 in primary central nervous system lymphomasAlberto Gonzalez-Aguilar, Ahmed Idbaih, Blandine Boisselier, et al.
Clinical and Translational Medicine|July 9, 2022
Identification of growth hormone receptor as a relevant target for precision medicine in low-EGFR expressing glioblastomaMaïté Verreault, Irma Segoviano Vilchis, Shai Rosenberg, et al.
JCO Precision Oncology|June 1, 2023
Mismatch Repair Deficiency and Lynch Syndrome Among Adult Patients With GliomaPatrick R Benusiglio, Fikret Elder, Mehdi Touat, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|January 23, 2015
Detection, Characterization, and Inhibition of FGFR-TACC Fusions in IDH Wild-type GliomaAnna Luisa Di Stefano, Alessandra Fucci, Veronique Frattini, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 31, 2021
Impact of a frequent nearsplice <i>SOD1</i> variant in amyotrophic lateral sclerosis: optimising <i>SOD1</i> genetic screening for gene therapy opportunitiesFrançois Muratet, Elisa Teyssou, Aude Chiot, et al.
Journal of Thoracic Oncology : Official Publication of the International Association for the Study of Lung Cancer|February 9, 2025
Human Immunodeficiency Virus Impairs Immune Responses to Tumor Neoepitopes Without Altering Mutational Profiles in NSCLCBaptiste Abbar, Karim Labreche, Jacques Cadranel, et al.
Pageof 10