Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Andrew J Sharp

Showing results (51-60 of 85) with videos related to

Pageof 9
Sort By:
Brain : a Journal of Neurology|January 31, 2019
Fumarates target the metabolic-epigenetic interplay of brain-homing T cells in multiple sclerosisAchilles Ntranos, Vasilis Ntranos, Valentina Bonnefil, et al.
American Journal of Human Genetics|September 16, 2020
A Survey of Rare Epigenetic Variation in 23,116 Human Genomes Identifies Disease-Relevant Epivariations and CGG ExpansionsParas Garg, Bharati Jadhav, Oscar L Rodriguez, et al.
Human Mutation|January 4, 2020
Elucidation of de novo small insertion/deletion biology with parent-of-origin phasingAllison H Seiden, Felix Richter, Nihir Patel, et al.
Nature Genetics|May 17, 2005
Fine-scale structural variation of the human genomeEray Tuzun, Andrew J Sharp, Jeffrey A Bailey, et al.
American Journal of Human Genetics|July 11, 2006
Linkage disequilibrium and heritability of copy-number polymorphisms within duplicated regions of the human genomeDevin P Locke, Andrew J Sharp, Steven A McCarroll, et al.
Nature Communications|February 15, 2017
Foxa2 identifies a cardiac progenitor population with ventricular differentiation potentialEvan Bardot, Damelys Calderon, Francis Santoriello, et al.
Human Molecular Genetics|February 25, 2006
High-throughput genotyping of intermediate-size structural variationTera L Newman, Mark J Rieder, V Anne Morrison, et al.
American Journal of Human Genetics|October 10, 2007
Recurrent reciprocal genomic rearrangements of 17q12 are associated with renal disease, diabetes, and epilepsyHeather C Mefford, Severine Clauin, Andrew J Sharp, et al.
Plos Genetics|March 25, 2015
Opposite phenotypes of muscle strength and locomotor function in mouse models of partial trisomy and monosomy 21 for the proximal Hspa13-App regionVéronique Brault, Arnaud Duchon, Caroline Romestaing, et al.
Genome Research|July 16, 2010
Methylation profiling in individuals with uniparental disomy identifies novel differentially methylated regions on chromosome 15Andrew J Sharp, Eugenia Migliavacca, Yann Dupre, et al.
Pageof 9

Showing results (51-60 of 85) with videos related to

Sort By:
Pageof 9
Brain : a Journal of Neurology|January 31, 2019
Fumarates target the metabolic-epigenetic interplay of brain-homing T cells in multiple sclerosisAchilles Ntranos, Vasilis Ntranos, Valentina Bonnefil, et al.
American Journal of Human Genetics|September 16, 2020
A Survey of Rare Epigenetic Variation in 23,116 Human Genomes Identifies Disease-Relevant Epivariations and CGG ExpansionsParas Garg, Bharati Jadhav, Oscar L Rodriguez, et al.
Human Mutation|January 4, 2020
Elucidation of de novo small insertion/deletion biology with parent-of-origin phasingAllison H Seiden, Felix Richter, Nihir Patel, et al.
Nature Genetics|May 17, 2005
Fine-scale structural variation of the human genomeEray Tuzun, Andrew J Sharp, Jeffrey A Bailey, et al.
American Journal of Human Genetics|July 11, 2006
Linkage disequilibrium and heritability of copy-number polymorphisms within duplicated regions of the human genomeDevin P Locke, Andrew J Sharp, Steven A McCarroll, et al.
Nature Communications|February 15, 2017
Foxa2 identifies a cardiac progenitor population with ventricular differentiation potentialEvan Bardot, Damelys Calderon, Francis Santoriello, et al.
Human Molecular Genetics|February 25, 2006
High-throughput genotyping of intermediate-size structural variationTera L Newman, Mark J Rieder, V Anne Morrison, et al.
American Journal of Human Genetics|October 10, 2007
Recurrent reciprocal genomic rearrangements of 17q12 are associated with renal disease, diabetes, and epilepsyHeather C Mefford, Severine Clauin, Andrew J Sharp, et al.
Plos Genetics|March 25, 2015
Opposite phenotypes of muscle strength and locomotor function in mouse models of partial trisomy and monosomy 21 for the proximal Hspa13-App regionVéronique Brault, Arnaud Duchon, Caroline Romestaing, et al.
Genome Research|July 16, 2010
Methylation profiling in individuals with uniparental disomy identifies novel differentially methylated regions on chromosome 15Andrew J Sharp, Eugenia Migliavacca, Yann Dupre, et al.
Pageof 9