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 (61-70 of 85) with videos related to

Pageof 9
Sort By:
Frontiers in Immunology|October 19, 2020
A Novel Framework for Characterizing Genomic Haplotype Diversity in the Human Immunoglobulin Heavy Chain LocusOscar L Rodriguez, William S Gibson, Tom Parks, et al.
American Journal of Human Genetics|May 27, 2005
Segmental duplications and copy-number variation in the human genomeAndrew J Sharp, Devin P Locke, Sean D McGrath, et al.
BMC Biology|June 26, 2019
RNA-Seq in 296 phased trios provides a high-resolution map of genomic imprintingBharati Jadhav, Ramin Monajemi, Kristina K Gagalova, et al.
Journal of Medical Genetics|April 14, 2012
Genome-wide linkage and copy number variation analysis reveals 710 kb duplication on chromosome 1p31.3 responsible for autosomal dominant omphaloceleUppala Radhakrishna, Swapan K Nath, Ken McElreavey, et al.
The Journal of Allergy and Clinical Immunology|December 16, 2019
Dual transcriptomic and epigenomic study of reaction severity in peanut-allergic childrenAnh N Do, Corey T Watson, Ariella T Cohain, et al.
Human Mutation|March 13, 2018
Robust identification of deletions in exome and genome sequence data based on clustering of Mendelian errorsKathryn B Manheimer, Nihir Patel, Felix Richter, et al.
Circulation. Cardiovascular Genetics|September 12, 2013
Effect of copy number variants on outcomes for infants with single ventricle heart defectsAbigail S Carey, Li Liang, Jonathan Edwards, et al.
Medrxiv : the Preprint Server for Health Sciences|May 19, 2023
A phenome-wide association study of methylated GC-rich repeats identifies a GCC repeat expansion in <i>AFF3</i> as a significant cause of intellectual disabilityBharati Jadhav, Paras Garg, Joke J F A van Vugt, et al.
Human Molecular Genetics|March 16, 2007
Characterization of a recurrent 15q24 microdeletion syndromeAndrew J Sharp, Rebecca R Selzer, Joris A Veltman, et al.
Nature Communications|September 28, 2016
Loss of RNA expression and allele-specific expression associated with congenital heart diseaseDavid M McKean, Jason Homsy, Hiroko Wakimoto, et al.
Pageof 9

Showing results (61-70 of 85) with videos related to

Sort By:
Pageof 9
Frontiers in Immunology|October 19, 2020
A Novel Framework for Characterizing Genomic Haplotype Diversity in the Human Immunoglobulin Heavy Chain LocusOscar L Rodriguez, William S Gibson, Tom Parks, et al.
American Journal of Human Genetics|May 27, 2005
Segmental duplications and copy-number variation in the human genomeAndrew J Sharp, Devin P Locke, Sean D McGrath, et al.
BMC Biology|June 26, 2019
RNA-Seq in 296 phased trios provides a high-resolution map of genomic imprintingBharati Jadhav, Ramin Monajemi, Kristina K Gagalova, et al.
Journal of Medical Genetics|April 14, 2012
Genome-wide linkage and copy number variation analysis reveals 710 kb duplication on chromosome 1p31.3 responsible for autosomal dominant omphaloceleUppala Radhakrishna, Swapan K Nath, Ken McElreavey, et al.
The Journal of Allergy and Clinical Immunology|December 16, 2019
Dual transcriptomic and epigenomic study of reaction severity in peanut-allergic childrenAnh N Do, Corey T Watson, Ariella T Cohain, et al.
Human Mutation|March 13, 2018
Robust identification of deletions in exome and genome sequence data based on clustering of Mendelian errorsKathryn B Manheimer, Nihir Patel, Felix Richter, et al.
Circulation. Cardiovascular Genetics|September 12, 2013
Effect of copy number variants on outcomes for infants with single ventricle heart defectsAbigail S Carey, Li Liang, Jonathan Edwards, et al.
Medrxiv : the Preprint Server for Health Sciences|May 19, 2023
A phenome-wide association study of methylated GC-rich repeats identifies a GCC repeat expansion in <i>AFF3</i> as a significant cause of intellectual disabilityBharati Jadhav, Paras Garg, Joke J F A van Vugt, et al.
Human Molecular Genetics|March 16, 2007
Characterization of a recurrent 15q24 microdeletion syndromeAndrew J Sharp, Rebecca R Selzer, Joris A Veltman, et al.
Nature Communications|September 28, 2016
Loss of RNA expression and allele-specific expression associated with congenital heart diseaseDavid M McKean, Jason Homsy, Hiroko Wakimoto, et al.
Pageof 9