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

Robin Andersson

Showing results (61-70 of 72) with videos related to

Pageof 8
Sort By:
European Journal of Human Genetics : EJHG|January 7, 2010
Frequent genetic differences between matched primary and metastatic breast cancer provide an approach to identification of biomarkers for disease progressionAndrzej B Popławski, Michał Jankowski, Stephen W Erickson, et al.
Genome Research|December 5, 2013
Genome-wide nucleosome map and cytosine methylation levels of an ancient human genomeJakob Skou Pedersen, Eivind Valen, Amhed M Vargas Velazquez, et al.
Nucleic Acids Research|October 30, 2016
Update of the FANTOM web resource: high resolution transcriptome of diverse cell types in mammalsMarina Lizio, Jayson Harshbarger, Imad Abugessaisa, et al.
Genome Research|July 29, 2020
Comparative transcriptomics of primary cells in vertebratesTanvir Alam, Saumya Agrawal, Jessica Severin, et al.
American Journal of Human Genetics|February 29, 2008
Phenotypically concordant and discordant monozygotic twins display different DNA copy-number-variation profilesCarl E G Bruder, Arkadiusz Piotrowski, Antoinet A C J Gijsbers, et al.
Nature Communications|April 27, 2018
Characterization of the enhancer and promoter landscape of inflammatory bowel disease from human colon biopsiesMette Boyd, Malte Thodberg, Morana Vitezic, et al.
Plos Computational Biology|March 2, 2018
Shared activity patterns arising at genetic susceptibility loci reveal underlying genomic and cellular architecture of human diseaseJ Kenneth Baillie, Andrew Bretherick, Christopher S Haley, et al.
Medrxiv : the Preprint Server for Health Sciences|November 28, 2024
Molecular convergence of risk variants for congenital heart defects leveraging a regulatory map of the human fetal heartX Rosa Ma, Stephanie D Conley, Michael Kosicki, et al.
Medrxiv : the Preprint Server for Health Sciences|November 28, 2024
Single cell variant to enhancer to gene map for coronary artery diseaseJunedh M Amrute, Paul C Lee, Ittai Eres, et al.
Nature|March 28, 2014
An atlas of active enhancers across human cell types and tissuesRobin Andersson, Claudia Gebhard, Irene Miguel-Escalada, et al.
Pageof 8

Showing results (61-70 of 72) with videos related to

Sort By:
Pageof 8
European Journal of Human Genetics : EJHG|January 7, 2010
Frequent genetic differences between matched primary and metastatic breast cancer provide an approach to identification of biomarkers for disease progressionAndrzej B Popławski, Michał Jankowski, Stephen W Erickson, et al.
Genome Research|December 5, 2013
Genome-wide nucleosome map and cytosine methylation levels of an ancient human genomeJakob Skou Pedersen, Eivind Valen, Amhed M Vargas Velazquez, et al.
Nucleic Acids Research|October 30, 2016
Update of the FANTOM web resource: high resolution transcriptome of diverse cell types in mammalsMarina Lizio, Jayson Harshbarger, Imad Abugessaisa, et al.
Genome Research|July 29, 2020
Comparative transcriptomics of primary cells in vertebratesTanvir Alam, Saumya Agrawal, Jessica Severin, et al.
American Journal of Human Genetics|February 29, 2008
Phenotypically concordant and discordant monozygotic twins display different DNA copy-number-variation profilesCarl E G Bruder, Arkadiusz Piotrowski, Antoinet A C J Gijsbers, et al.
Nature Communications|April 27, 2018
Characterization of the enhancer and promoter landscape of inflammatory bowel disease from human colon biopsiesMette Boyd, Malte Thodberg, Morana Vitezic, et al.
Plos Computational Biology|March 2, 2018
Shared activity patterns arising at genetic susceptibility loci reveal underlying genomic and cellular architecture of human diseaseJ Kenneth Baillie, Andrew Bretherick, Christopher S Haley, et al.
Medrxiv : the Preprint Server for Health Sciences|November 28, 2024
Molecular convergence of risk variants for congenital heart defects leveraging a regulatory map of the human fetal heartX Rosa Ma, Stephanie D Conley, Michael Kosicki, et al.
Medrxiv : the Preprint Server for Health Sciences|November 28, 2024
Single cell variant to enhancer to gene map for coronary artery diseaseJunedh M Amrute, Paul C Lee, Ittai Eres, et al.
Nature|March 28, 2014
An atlas of active enhancers across human cell types and tissuesRobin Andersson, Claudia Gebhard, Irene Miguel-Escalada, et al.
Pageof 8