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

Cecelia Laurie

Showing results (11-20 of 21) with videos related to

Pageof 3
Sort By:
Nature Communications|April 30, 2026
Admixture-informed polygenic risk reporting using the ePRS frameworkYu-Jyun Huang, Nuzulul Kurniansyah, Matthew O Goodman, et al.
Medrxiv : the Preprint Server for Health Sciences|January 7, 2025
The expected polygenic risk score (ePRS) framework: an equitable metric for quantifying polygenetic risk via modeling of ancestral makeupYu-Jyun Huang, Nuzulul Kurniansyah, Matthew O Goodman, et al.
Human Genetics|June 6, 2016
Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21Craig C Teerlink, Daniel Leongamornlert, Tokhir Dadaev, et al.
American Journal of Human Genetics|December 30, 2019
Allelic Heterogeneity at the CRP Locus Identified by Whole-Genome Sequencing in Multi-ancestry CohortsLaura M Raffield, Apoorva K Iyengar, Biqi Wang, et al.
JAMA|December 12, 2018
Association Between Titin Loss-of-Function Variants and Early-Onset Atrial FibrillationSeung Hoan Choi, Lu-Chen Weng, Carolina Roselli, et al.
Medrxiv : the Preprint Server for Health Sciences|September 4, 2024
The Genetic Determinants and Genomic Consequences of Non-Leukemogenic Somatic Point MutationsJoshua S Weinstock, Sharjeel A Chaudhry, Maria Ioannou, et al.
Nature Communications|October 16, 2025
Genetic determinants and genomic consequences of non-leukemogenic somatic point mutationsJoshua S Weinstock, Sharjeel A Chaudhry, Maria Ioannou, et al.
Nature Communications|October 9, 2024
Rare variant contribution to the heritability of coronary artery diseaseGhislain Rocheleau, Shoa L Clarke, Gaëlle Auguste, et al.
Journal of the American Heart Association|February 14, 2025
Unveiling the Genetic Landscape of Coronary Artery Disease Through Common and Rare Structural VariantsKruthika R Iyer, Shoa L Clarke, Rodrigo Guarischi-Sousa, et al.
Nature|October 15, 2020
Inherited causes of clonal haematopoiesis in 97,691 whole genomesAlexander G Bick, Joshua S Weinstock, Satish K Nandakumar, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Nature Communications|April 30, 2026
Admixture-informed polygenic risk reporting using the ePRS frameworkYu-Jyun Huang, Nuzulul Kurniansyah, Matthew O Goodman, et al.
Medrxiv : the Preprint Server for Health Sciences|January 7, 2025
The expected polygenic risk score (ePRS) framework: an equitable metric for quantifying polygenetic risk via modeling of ancestral makeupYu-Jyun Huang, Nuzulul Kurniansyah, Matthew O Goodman, et al.
Human Genetics|June 6, 2016
Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21Craig C Teerlink, Daniel Leongamornlert, Tokhir Dadaev, et al.
American Journal of Human Genetics|December 30, 2019
Allelic Heterogeneity at the CRP Locus Identified by Whole-Genome Sequencing in Multi-ancestry CohortsLaura M Raffield, Apoorva K Iyengar, Biqi Wang, et al.
JAMA|December 12, 2018
Association Between Titin Loss-of-Function Variants and Early-Onset Atrial FibrillationSeung Hoan Choi, Lu-Chen Weng, Carolina Roselli, et al.
Medrxiv : the Preprint Server for Health Sciences|September 4, 2024
The Genetic Determinants and Genomic Consequences of Non-Leukemogenic Somatic Point MutationsJoshua S Weinstock, Sharjeel A Chaudhry, Maria Ioannou, et al.
Nature Communications|October 16, 2025
Genetic determinants and genomic consequences of non-leukemogenic somatic point mutationsJoshua S Weinstock, Sharjeel A Chaudhry, Maria Ioannou, et al.
Nature Communications|October 9, 2024
Rare variant contribution to the heritability of coronary artery diseaseGhislain Rocheleau, Shoa L Clarke, Gaëlle Auguste, et al.
Journal of the American Heart Association|February 14, 2025
Unveiling the Genetic Landscape of Coronary Artery Disease Through Common and Rare Structural VariantsKruthika R Iyer, Shoa L Clarke, Rodrigo Guarischi-Sousa, et al.
Nature|October 15, 2020
Inherited causes of clonal haematopoiesis in 97,691 whole genomesAlexander G Bick, Joshua S Weinstock, Satish K Nandakumar, et al.
Pageof 3