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

J Karczewski

Showing results (91-100 of 144) with videos related to

Pageof 15
Sort By:
BMC Genomics|July 4, 2013
Pathway analysis of genome-wide data improves warfarin dose predictionRoxana Daneshjou, Nicholas P Tatonetti, Konrad J Karczewski, et al.
Science (New York, N.Y.)|February 12, 2026
Mechanisms linking cytoplasmic decay of translation-defective mRNA to transcriptional adaptationMohamed A El-Brolosy, Atharv Oak, An T Hoang, et al.
American Journal of Human Genetics|May 2, 2026
Meta-analysis across six global biobanks identifies recessive coding associations with complex traits and diseasesFrederik H Lassen, Georgios Kalantzis, Andrea Eoli, et al.
Nature|May 29, 2020
Transcript expression-aware annotation improves rare variant interpretationBeryl B Cummings, Konrad J Karczewski, Jack A Kosmicki, et al.
Nature Genetics|February 14, 2017
Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samplesJack A Kosmicki, Kaitlin E Samocha, Daniel P Howrigan, et al.
Journal of Lipid Research|July 23, 2015
Genetic meta-analysis of 15,901 African Americans identifies variation in EXOC3L1 is associated with HDL concentrationMatthew B Lanktree, Clara C Elbers, Yun Li, et al.
Bioorganic & Medicinal Chemistry Letters|October 10, 2001
Discovery and initial structure-activity relationships of trisubstituted ureas as thrombin receptor (PAR-1) antagonistsJ C Barrow, P G Nantermet, H G Selnick, et al.
The Lancet. Neurology|April 20, 2026
Identification of genetic risk loci associated with aquaporin 4-positive neuromyelitis optica spectrum disorder: a genome-wide association studyKathrine E Attfield, Angelos P Armen, Subita Balaram Kuttikkatte, et al.
Nature Communications|May 29, 2020
Characterising the loss-of-function impact of 5' untranslated region variants in 15,708 individualsNicola Whiffin, Konrad J Karczewski, Xiaolei Zhang, et al.
Nature|October 13, 2017
Landscape of X chromosome inactivation across human tissuesTaru Tukiainen, Alexandra-Chloé Villani, Angela Yen, et al.
Pageof 15

Showing results (91-100 of 144) with videos related to

Sort By:
Pageof 15
BMC Genomics|July 4, 2013
Pathway analysis of genome-wide data improves warfarin dose predictionRoxana Daneshjou, Nicholas P Tatonetti, Konrad J Karczewski, et al.
Science (New York, N.Y.)|February 12, 2026
Mechanisms linking cytoplasmic decay of translation-defective mRNA to transcriptional adaptationMohamed A El-Brolosy, Atharv Oak, An T Hoang, et al.
American Journal of Human Genetics|May 2, 2026
Meta-analysis across six global biobanks identifies recessive coding associations with complex traits and diseasesFrederik H Lassen, Georgios Kalantzis, Andrea Eoli, et al.
Nature|May 29, 2020
Transcript expression-aware annotation improves rare variant interpretationBeryl B Cummings, Konrad J Karczewski, Jack A Kosmicki, et al.
Nature Genetics|February 14, 2017
Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samplesJack A Kosmicki, Kaitlin E Samocha, Daniel P Howrigan, et al.
Journal of Lipid Research|July 23, 2015
Genetic meta-analysis of 15,901 African Americans identifies variation in EXOC3L1 is associated with HDL concentrationMatthew B Lanktree, Clara C Elbers, Yun Li, et al.
Bioorganic & Medicinal Chemistry Letters|October 10, 2001
Discovery and initial structure-activity relationships of trisubstituted ureas as thrombin receptor (PAR-1) antagonistsJ C Barrow, P G Nantermet, H G Selnick, et al.
The Lancet. Neurology|April 20, 2026
Identification of genetic risk loci associated with aquaporin 4-positive neuromyelitis optica spectrum disorder: a genome-wide association studyKathrine E Attfield, Angelos P Armen, Subita Balaram Kuttikkatte, et al.
Nature Communications|May 29, 2020
Characterising the loss-of-function impact of 5' untranslated region variants in 15,708 individualsNicola Whiffin, Konrad J Karczewski, Xiaolei Zhang, et al.
Nature|October 13, 2017
Landscape of X chromosome inactivation across human tissuesTaru Tukiainen, Alexandra-Chloé Villani, Angela Yen, et al.
Pageof 15