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Emmanuelle Genin

Showing results (21-30 of 34) with videos related to

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Annals of Neurology|July 3, 2003
Genetic interaction of CTLA-4 with HLA-DR15 in multiple sclerosis patientsMehdi Alizadeh, Marie-Claude Babron, Brigitte Birebent, et al.
Human Mutation|July 12, 2022
Burden of rare variants in arrhythmogenic cardiomyopathy with right dominant form-associated genes provides new insights for molecular diagnosis and clinical managementAdeline Goudal, Matilde Karakachoff, Pierre Lindenbaum, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|November 19, 2020
Phenotypic Differences Between Polygenic and Monogenic HypobetalipoproteinemiaAntoine Rimbert, Xavier Vanhoye, Dramane Coulibaly, et al.
Human Genetics|August 10, 2006
Clinical and molecular genetic features of ARC syndromePaul Gissen, Louise Tee, Colin A Johnson, et al.
Neurogenetics|November 5, 2003
Investigation of seven proposed regions of linkage in multiple sclerosis: an American and French collaborative studyMargaret A Pericak-Vance, Jackie B Rimmler, Jonathan L Haines, et al.
The New England Journal of Medicine|August 19, 2011
Interleukin-36-receptor antagonist deficiency and generalized pustular psoriasisSlaheddine Marrakchi, Philippe Guigue, Blair R Renshaw, et al.
Neurobiology of Aging|August 10, 2017
Contribution to Alzheimer's disease risk of rare variants in TREM2, SORL1, and ABCA7 in 1779 cases and 1273 controlsCéline Bellenguez, Camille Charbonnier, Benjamin Grenier-Boley, et al.
European Heart Journal|May 23, 2019
RRAD mutation causes electrical and cytoskeletal defects in cardiomyocytes derived from a familial case of Brugada syndromeNadjet Belbachir, Vincent Portero, Zeina R Al Sayed, et al.
The Lancet. Rheumatology|January 24, 2024
Contribution of rare and predicted pathogenic gene variants to childhood-onset lupus: a large, genetic panel analysis of British and French cohortsAlexandre Belot, Gillian I Rice, Sulliman Ommar Omarjee, et al.
Molecular Psychiatry|October 23, 2019
Correction: Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulationJoshua C Bis, Xueqiu Jian, Brian W Kunkle, et al.
Pageof 4

Showing results (21-30 of 34) with videos related to

Sort By:
Pageof 4
Annals of Neurology|July 3, 2003
Genetic interaction of CTLA-4 with HLA-DR15 in multiple sclerosis patientsMehdi Alizadeh, Marie-Claude Babron, Brigitte Birebent, et al.
Human Mutation|July 12, 2022
Burden of rare variants in arrhythmogenic cardiomyopathy with right dominant form-associated genes provides new insights for molecular diagnosis and clinical managementAdeline Goudal, Matilde Karakachoff, Pierre Lindenbaum, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|November 19, 2020
Phenotypic Differences Between Polygenic and Monogenic HypobetalipoproteinemiaAntoine Rimbert, Xavier Vanhoye, Dramane Coulibaly, et al.
Human Genetics|August 10, 2006
Clinical and molecular genetic features of ARC syndromePaul Gissen, Louise Tee, Colin A Johnson, et al.
Neurogenetics|November 5, 2003
Investigation of seven proposed regions of linkage in multiple sclerosis: an American and French collaborative studyMargaret A Pericak-Vance, Jackie B Rimmler, Jonathan L Haines, et al.
The New England Journal of Medicine|August 19, 2011
Interleukin-36-receptor antagonist deficiency and generalized pustular psoriasisSlaheddine Marrakchi, Philippe Guigue, Blair R Renshaw, et al.
Neurobiology of Aging|August 10, 2017
Contribution to Alzheimer's disease risk of rare variants in TREM2, SORL1, and ABCA7 in 1779 cases and 1273 controlsCéline Bellenguez, Camille Charbonnier, Benjamin Grenier-Boley, et al.
European Heart Journal|May 23, 2019
RRAD mutation causes electrical and cytoskeletal defects in cardiomyocytes derived from a familial case of Brugada syndromeNadjet Belbachir, Vincent Portero, Zeina R Al Sayed, et al.
The Lancet. Rheumatology|January 24, 2024
Contribution of rare and predicted pathogenic gene variants to childhood-onset lupus: a large, genetic panel analysis of British and French cohortsAlexandre Belot, Gillian I Rice, Sulliman Ommar Omarjee, et al.
Molecular Psychiatry|October 23, 2019
Correction: Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulationJoshua C Bis, Xueqiu Jian, Brian W Kunkle, et al.
Pageof 4