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John Baierl

Showing results (1-10 of 6) with videos related to

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Journal of the American Medical Informatics Association : JAMIA|January 13, 2026
Measuring the accuracy of electronic health record-based phenotyping in the All of Us Research Program to optimize statistical power for genetic association testingJohn Baierl, Yi-Wen Hsiao, Michelle R Jones, et al.
STAR Protocols|July 3, 2026
Protocol for constructing multi-ancestry polygenic models using S4-MultiPing-Hung Lai, Jonathan P Tyrer, John Baierl, et al.
HGG Advances|November 28, 2025
S4-multi: Enhancing polygenic score prediction in ancestrally diverse populationsJohn Baierl, Jonathan P Tyrer, Ping-Hung Lai, et al.
Medrxiv : the Preprint Server for Health Sciences|April 18, 2024
Exome sequencing identifies <i>HELB</i> as a novel susceptibility gene for non-mucinous, non-high-grade-serous epithelial ovarian cancerEd M Dicks, Jonthan P Tyrer, Suzana Ezquina, et al.
Biorxiv : the Preprint Server for Biology|June 22, 2026
Saturation Genome Editing reveals the functional impact of RAD51D <i>and</i> XRCC2 variantsSilvia Casadei, Matthew W Snyder, Ivan Woo, et al.
European Journal of Human Genetics : EJHG|February 12, 2025
Exome sequencing identifies HELB as a novel susceptibility gene for non-mucinous, non-high-grade-serous epithelial ovarian cancerEd M Dicks, Jonthan P Tyrer, Suzana Ezquina, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Journal of the American Medical Informatics Association : JAMIA|January 13, 2026
Measuring the accuracy of electronic health record-based phenotyping in the All of Us Research Program to optimize statistical power for genetic association testingJohn Baierl, Yi-Wen Hsiao, Michelle R Jones, et al.
STAR Protocols|July 3, 2026
Protocol for constructing multi-ancestry polygenic models using S4-MultiPing-Hung Lai, Jonathan P Tyrer, John Baierl, et al.
HGG Advances|November 28, 2025
S4-multi: Enhancing polygenic score prediction in ancestrally diverse populationsJohn Baierl, Jonathan P Tyrer, Ping-Hung Lai, et al.
Medrxiv : the Preprint Server for Health Sciences|April 18, 2024
Exome sequencing identifies <i>HELB</i> as a novel susceptibility gene for non-mucinous, non-high-grade-serous epithelial ovarian cancerEd M Dicks, Jonthan P Tyrer, Suzana Ezquina, et al.
Biorxiv : the Preprint Server for Biology|June 22, 2026
Saturation Genome Editing reveals the functional impact of RAD51D <i>and</i> XRCC2 variantsSilvia Casadei, Matthew W Snyder, Ivan Woo, et al.
European Journal of Human Genetics : EJHG|February 12, 2025
Exome sequencing identifies HELB as a novel susceptibility gene for non-mucinous, non-high-grade-serous epithelial ovarian cancerEd M Dicks, Jonthan P Tyrer, Suzana Ezquina, et al.
Pageof 1