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

Xander Nuttle

Showing results (1-10 of 19) with videos related to

Pageof 2
Sort By:
Nature Protocols|May 31, 2014
Resolving genomic disorder-associated breakpoints within segmental DNA duplications using massively parallel sequencingXander Nuttle, Andy Itsara, Jay Shendure, et al.
American Journal of Human Genetics|January 11, 2016
Maternal Modifiers and Parent-of-Origin Bias of the Autism-Associated 16p11.2 CNVMichael H Duyzend, Xander Nuttle, Bradley P Coe, et al.
Nature Methods|July 30, 2013
Rapid and accurate large-scale genotyping of duplicated genes and discovery of interlocus gene conversionsXander Nuttle, John Huddleston, Brian J O'Roak, et al.
Clinical Case Reports|January 30, 2018
Longitudinal report of child with de novo 16p11.2 triplicationArianne S Wallace, Caitlin M Hudac, Kyle J Steinman, et al.
Cell Reports Methods|December 13, 2023
Parallelized engineering of mutational models using piggyBac transposon delivery of CRISPR librariesXander Nuttle, Nicholas D Burt, Benjamin Currall, et al.
Genome Biology|March 11, 2017
The birth of a human-specific neural gene by incomplete duplication and gene fusionMax L Dougherty, Xander Nuttle, Osnat Penn, et al.
Biorxiv : the Preprint Server for Biology|March 18, 2024
Activation of the imprinted Prader-Willi Syndrome locus by CRISPR-based epigenome editingDahlia Rohm, Joshua B Black, Sean R McCutcheon, et al.
Cell Genomics|February 13, 2025
Activation of the imprinted Prader-Willi syndrome locus by CRISPR-based epigenome editingDahlia Rohm, Joshua B Black, Sean R McCutcheon, et al.
NPJ Genomic Medicine|June 17, 2022
Possible association of 16p11.2 copy number variation with altered lymphocyte and neutrophil countsGiuliana Giannuzzi, Nicolas Chatron, Katrin Mannik, et al.
Cell|May 8, 2012
Evolution of human-specific neural SRGAP2 genes by incomplete segmental duplicationMegan Y Dennis, Xander Nuttle, Peter H Sudmant, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Nature Protocols|May 31, 2014
Resolving genomic disorder-associated breakpoints within segmental DNA duplications using massively parallel sequencingXander Nuttle, Andy Itsara, Jay Shendure, et al.
American Journal of Human Genetics|January 11, 2016
Maternal Modifiers and Parent-of-Origin Bias of the Autism-Associated 16p11.2 CNVMichael H Duyzend, Xander Nuttle, Bradley P Coe, et al.
Nature Methods|July 30, 2013
Rapid and accurate large-scale genotyping of duplicated genes and discovery of interlocus gene conversionsXander Nuttle, John Huddleston, Brian J O'Roak, et al.
Clinical Case Reports|January 30, 2018
Longitudinal report of child with de novo 16p11.2 triplicationArianne S Wallace, Caitlin M Hudac, Kyle J Steinman, et al.
Cell Reports Methods|December 13, 2023
Parallelized engineering of mutational models using piggyBac transposon delivery of CRISPR librariesXander Nuttle, Nicholas D Burt, Benjamin Currall, et al.
Genome Biology|March 11, 2017
The birth of a human-specific neural gene by incomplete duplication and gene fusionMax L Dougherty, Xander Nuttle, Osnat Penn, et al.
Biorxiv : the Preprint Server for Biology|March 18, 2024
Activation of the imprinted Prader-Willi Syndrome locus by CRISPR-based epigenome editingDahlia Rohm, Joshua B Black, Sean R McCutcheon, et al.
Cell Genomics|February 13, 2025
Activation of the imprinted Prader-Willi syndrome locus by CRISPR-based epigenome editingDahlia Rohm, Joshua B Black, Sean R McCutcheon, et al.
NPJ Genomic Medicine|June 17, 2022
Possible association of 16p11.2 copy number variation with altered lymphocyte and neutrophil countsGiuliana Giannuzzi, Nicolas Chatron, Katrin Mannik, et al.
Cell|May 8, 2012
Evolution of human-specific neural SRGAP2 genes by incomplete segmental duplicationMegan Y Dennis, Xander Nuttle, Peter H Sudmant, et al.
Pageof 2