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L Michaud

Showing results (441-450 of 509) with videos related to

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Journal of Medical Genetics|February 5, 2015
Disruption of CLPB is associated with congenital microcephaly, severe encephalopathy and 3-methylglutaconic aciduriaJosé-Mario Capo-Chichi, Sarah Boissel, Edna Brustein, et al.
Plos Genetics|April 13, 2018
Global characterization of copy number variants in epilepsy patients from whole genome sequencingJean Monlong, Simon L Girard, Caroline Meloche, et al.
Obesity (Silver Spring, Md.)|January 16, 2010
Analysis of the SIM1 contribution to polygenic obesity in the French populationMaya Ghoussaini, Fanny Stutzmann, Cyril Couturier, et al.
American Journal of Preventive Medicine|February 13, 2022
Effects of a Digital Diabetes Prevention Program: An RCTJeffrey A Katula, Emily V Dressler, Carol A Kittel, et al.
Annals of Neurology|June 27, 2009
De novo STXBP1 mutations in mental retardation and nonsyndromic epilepsyFadi F Hamdan, Amélie Piton, Julie Gauthier, et al.
Science (New York, N.Y.)|March 27, 2004
G protein-coupled receptor-dependent development of human frontal cortexXianhua Piao, R Sean Hill, Adria Bodell, et al.
Translational Behavioral Medicine|March 7, 2021
Using a population health management approach to enroll participants in a diabetes prevention trial: reach outcomes from the PREDICTS randomized clinical trialKathryn E Wilson, Tzeyu L Michaud, Fabio A Almeida, et al.
Human Genetics|November 6, 2019
Association of rare non-coding SNVs in the lung-specific FOXF1 enhancer with a mitigation of the lethal ACDMPV phenotypePrzemyslaw Szafranski, Qian Liu, Justyna A Karolak, et al.
Human Genetics|December 15, 2021
Variant-specific effects define the phenotypic spectrum of HNRNPH2-associated neurodevelopmental disorders in malesHans-Jürgen Kreienkamp, Matias Wagner, Heike Weigand, et al.
Human Molecular Genetics|September 20, 2008
Mutations in the calcium-related gene IL1RAPL1 are associated with autismAmélie Piton, Jacques L Michaud, Huashan Peng, et al.
Pageof 51

Showing results (441-450 of 509) with videos related to

Sort By:
Pageof 51
Journal of Medical Genetics|February 5, 2015
Disruption of CLPB is associated with congenital microcephaly, severe encephalopathy and 3-methylglutaconic aciduriaJosé-Mario Capo-Chichi, Sarah Boissel, Edna Brustein, et al.
Plos Genetics|April 13, 2018
Global characterization of copy number variants in epilepsy patients from whole genome sequencingJean Monlong, Simon L Girard, Caroline Meloche, et al.
Obesity (Silver Spring, Md.)|January 16, 2010
Analysis of the SIM1 contribution to polygenic obesity in the French populationMaya Ghoussaini, Fanny Stutzmann, Cyril Couturier, et al.
American Journal of Preventive Medicine|February 13, 2022
Effects of a Digital Diabetes Prevention Program: An RCTJeffrey A Katula, Emily V Dressler, Carol A Kittel, et al.
Annals of Neurology|June 27, 2009
De novo STXBP1 mutations in mental retardation and nonsyndromic epilepsyFadi F Hamdan, Amélie Piton, Julie Gauthier, et al.
Science (New York, N.Y.)|March 27, 2004
G protein-coupled receptor-dependent development of human frontal cortexXianhua Piao, R Sean Hill, Adria Bodell, et al.
Translational Behavioral Medicine|March 7, 2021
Using a population health management approach to enroll participants in a diabetes prevention trial: reach outcomes from the PREDICTS randomized clinical trialKathryn E Wilson, Tzeyu L Michaud, Fabio A Almeida, et al.
Human Genetics|November 6, 2019
Association of rare non-coding SNVs in the lung-specific FOXF1 enhancer with a mitigation of the lethal ACDMPV phenotypePrzemyslaw Szafranski, Qian Liu, Justyna A Karolak, et al.
Human Genetics|December 15, 2021
Variant-specific effects define the phenotypic spectrum of HNRNPH2-associated neurodevelopmental disorders in malesHans-Jürgen Kreienkamp, Matias Wagner, Heike Weigand, et al.
Human Molecular Genetics|September 20, 2008
Mutations in the calcium-related gene IL1RAPL1 are associated with autismAmélie Piton, Jacques L Michaud, Huashan Peng, et al.
Pageof 51