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Elizabeth T Cirulli

Showing results (31-40 of 85) with videos related to

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The Journal of Infectious Diseases|February 1, 2011
Host genetic determinants of T cell responses to the MRKAd5 HIV-1 gag/pol/nef vaccine in the step trialJacques Fellay, Nicole Frahm, Kevin V Shianna, et al.
Circulation. Genomic and Precision Medicine|April 22, 2026
Scalable System-Wide CYP2C19 Pharmacogenomic Testing Reveals 38% Excess Incidence of Adverse Events in Metabolizers Receiving Inappropriate PrescriptionsNatalie Telis, Douglas Stoller, Christopher N Chapman, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 13, 2021
Positive predictive value highlights four novel candidates for actionable genetic screening from analysis of 220,000 clinicogenomic recordsKelly M Schiabor Barrett, Alexandre Bolze, Yunyun Ni, et al.
Communications Medicine|November 20, 2024
Underestimated risk of secondary complications in pathogenic and glucose-elevating GCK variant carriers with type 2 diabetesKelly M Schiabor Barrett, Natalie Telis, Lisa M McEwen, et al.
Cell Metabolism|October 16, 2018
Profound Perturbation of the Metabolome in Obesity Is Associated with Health RiskElizabeth T Cirulli, Lining Guo, Christine Leon Swisher, et al.
HGG Advances|April 24, 2025
Hypertension increases PPV for polycystic kidney disease in PKD1 and PKD2 variant carriersNatalie Telis, Lisa McEwen, Alexandre Bolze, et al.
JAMA Network Open|September 25, 2024
Screening Familial Risk for Hereditary Breast and Ovarian CancerDaniel Kiser, Gai Elhanan, Alexandre Bolze, et al.
Nature Communications|January 30, 2020
Genome-wide rare variant analysis for thousands of phenotypes in over 70,000 exomes from two cohortsElizabeth T Cirulli, Simon White, Robert W Read, et al.
Bioinformatics (Oxford, England)|June 1, 2011
SVA: software for annotating and visualizing sequenced human genomesDongliang Ge, Elizabeth K Ruzzo, Kevin V Shianna, et al.
Neurology|November 16, 2012
Novel mutation in VCP gene causes atypical amyotrophic lateral sclerosisPaloma González-Pérez, Elizabeth T Cirulli, Vivian E Drory, et al.
Pageof 9

Showing results (31-40 of 85) with videos related to

Sort By:
Pageof 9
The Journal of Infectious Diseases|February 1, 2011
Host genetic determinants of T cell responses to the MRKAd5 HIV-1 gag/pol/nef vaccine in the step trialJacques Fellay, Nicole Frahm, Kevin V Shianna, et al.
Circulation. Genomic and Precision Medicine|April 22, 2026
Scalable System-Wide CYP2C19 Pharmacogenomic Testing Reveals 38% Excess Incidence of Adverse Events in Metabolizers Receiving Inappropriate PrescriptionsNatalie Telis, Douglas Stoller, Christopher N Chapman, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 13, 2021
Positive predictive value highlights four novel candidates for actionable genetic screening from analysis of 220,000 clinicogenomic recordsKelly M Schiabor Barrett, Alexandre Bolze, Yunyun Ni, et al.
Communications Medicine|November 20, 2024
Underestimated risk of secondary complications in pathogenic and glucose-elevating GCK variant carriers with type 2 diabetesKelly M Schiabor Barrett, Natalie Telis, Lisa M McEwen, et al.
Cell Metabolism|October 16, 2018
Profound Perturbation of the Metabolome in Obesity Is Associated with Health RiskElizabeth T Cirulli, Lining Guo, Christine Leon Swisher, et al.
HGG Advances|April 24, 2025
Hypertension increases PPV for polycystic kidney disease in PKD1 and PKD2 variant carriersNatalie Telis, Lisa McEwen, Alexandre Bolze, et al.
JAMA Network Open|September 25, 2024
Screening Familial Risk for Hereditary Breast and Ovarian CancerDaniel Kiser, Gai Elhanan, Alexandre Bolze, et al.
Nature Communications|January 30, 2020
Genome-wide rare variant analysis for thousands of phenotypes in over 70,000 exomes from two cohortsElizabeth T Cirulli, Simon White, Robert W Read, et al.
Bioinformatics (Oxford, England)|June 1, 2011
SVA: software for annotating and visualizing sequenced human genomesDongliang Ge, Elizabeth K Ruzzo, Kevin V Shianna, et al.
Neurology|November 16, 2012
Novel mutation in VCP gene causes atypical amyotrophic lateral sclerosisPaloma González-Pérez, Elizabeth T Cirulli, Vivian E Drory, et al.
Pageof 9