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

Laura E Covill

Showing results (1-10 of 20) with videos related to

Pageof 2
Sort By:
Annual Review of Genomics and Human Genetics|May 21, 2026
Experimental and Computational Approaches to Identify Noncoding Pathogenic Variation in Rare DiseaseLaura E Covill, Lindsay Romo, Anne O'Donnell-Luria
Journal of Clinical Immunology|March 11, 2025
No Association Between HLH-associated Gene Variants and Life-Threatening COVID-19Laura E Covill, Aurélie Cobat, , et al.
Current Behavioral Neuroscience Reports|November 21, 2014
Genome-Wide Studies of Specific Language ImpairmentRose H Reader, Laura E Covill, Ron Nudel, et al.
Neuroscience and Biobehavioral Reviews|November 26, 2020
Rodent and fly models in behavioral neuroscience: An evaluation of methodological advances, comparative research, and future perspectivesThiago C Moulin, Laura E Covill, Pavel M Itskov, et al.
Scientific Reports|February 4, 2016
Multidisciplinary investigation links backward-speech trait and working memory through genetic mutationStefan Prekovic, Dušica Filipović Đurđević, Gábor Csifcsák, et al.
European Journal of Human Genetics : EJHG|January 15, 2015
Genome-wide analysis identifies a role for common copy number variants in specific language impairmentNuala H Simpson, Fabiola Ceroni, Rose H Reader, et al.
Science Immunology|August 21, 2021
Hobit identifies tissue-resident memory T cell precursors that are regulated by EomesLoreto Parga-Vidal, Felix M Behr, Natasja A M Kragten, et al.
Medrxiv : the Preprint Server for Health Sciences|May 25, 2026
A genome-wide deletion map in 125,730 individuals for novel rare disease gene and variant discoveryAnthony McGuigan, Alistair T Pagnamenta, Laura E Covill, et al.
Biorxiv : the Preprint Server for Biology|April 25, 2024
Antibody-mediated cellular responses are dysregulated in Multisystem Inflammatory Syndrome in Children (MIS-C)Jenna K Dick, Jules A Sangala, Venkatramana D Krishna, et al.
Journal of Immunology (Baltimore, Md. : 1950)|October 11, 2024
NK Cell and Monocyte Dysfunction in Multisystem Inflammatory Syndrome in ChildrenJenna K Dick, Jules A Sangala, Venkatramana D Krishna, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
Annual Review of Genomics and Human Genetics|May 21, 2026
Experimental and Computational Approaches to Identify Noncoding Pathogenic Variation in Rare DiseaseLaura E Covill, Lindsay Romo, Anne O'Donnell-Luria
Journal of Clinical Immunology|March 11, 2025
No Association Between HLH-associated Gene Variants and Life-Threatening COVID-19Laura E Covill, Aurélie Cobat, , et al.
Current Behavioral Neuroscience Reports|November 21, 2014
Genome-Wide Studies of Specific Language ImpairmentRose H Reader, Laura E Covill, Ron Nudel, et al.
Neuroscience and Biobehavioral Reviews|November 26, 2020
Rodent and fly models in behavioral neuroscience: An evaluation of methodological advances, comparative research, and future perspectivesThiago C Moulin, Laura E Covill, Pavel M Itskov, et al.
Scientific Reports|February 4, 2016
Multidisciplinary investigation links backward-speech trait and working memory through genetic mutationStefan Prekovic, Dušica Filipović Đurđević, Gábor Csifcsák, et al.
European Journal of Human Genetics : EJHG|January 15, 2015
Genome-wide analysis identifies a role for common copy number variants in specific language impairmentNuala H Simpson, Fabiola Ceroni, Rose H Reader, et al.
Science Immunology|August 21, 2021
Hobit identifies tissue-resident memory T cell precursors that are regulated by EomesLoreto Parga-Vidal, Felix M Behr, Natasja A M Kragten, et al.
Medrxiv : the Preprint Server for Health Sciences|May 25, 2026
A genome-wide deletion map in 125,730 individuals for novel rare disease gene and variant discoveryAnthony McGuigan, Alistair T Pagnamenta, Laura E Covill, et al.
Biorxiv : the Preprint Server for Biology|April 25, 2024
Antibody-mediated cellular responses are dysregulated in Multisystem Inflammatory Syndrome in Children (MIS-C)Jenna K Dick, Jules A Sangala, Venkatramana D Krishna, et al.
Journal of Immunology (Baltimore, Md. : 1950)|October 11, 2024
NK Cell and Monocyte Dysfunction in Multisystem Inflammatory Syndrome in ChildrenJenna K Dick, Jules A Sangala, Venkatramana D Krishna, et al.
Pageof 2