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Matthew W Snyder

Showing results (11-20 of 16) with videos related to

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American Journal of Medical Genetics. Part A|August 14, 2012
Non-invasive fetal genome sequencing: opportunities and challengesHolly K Tabor, Jeffrey C Murray, Hilary S Gammill, et al.
Medrxiv : the Preprint Server for Health Sciences|November 24, 2025
Saturation genome editing of <i>BARD1</i> resolves VUS and provides insight into BRCA1-BARD1 tumor suppressionIvan Woo, Silvia Casadei, Matthew W Snyder, et al.
Biorxiv : the Preprint Server for Biology|January 16, 2026
High-throughput mapping of 6,888 <i>RAD51D</i> variants identifies distinct biochemical functions needed for homologous recombination and olaparib responseKristie E Darrah, Shelby L Hemker, Yashpal Rawal, 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.
Medrxiv : the Preprint Server for Health Sciences|June 4, 2026
Phenotype-Specific Recalibration of MAVE Data Enables Repurposing of <i>BAP1</i> Functional Assays for Küry-Isidor SyndromePankhuri Gupta, Elsa V Balton, Mavika Tejura, et al.
Biorxiv : the Preprint Server for Biology|February 23, 2026
A scalable approach to resolving variants of uncertain significanceMalvika Tejura, Yile Chen, Abbye E McEwen, et al.
Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
American Journal of Medical Genetics. Part A|August 14, 2012
Non-invasive fetal genome sequencing: opportunities and challengesHolly K Tabor, Jeffrey C Murray, Hilary S Gammill, et al.
Medrxiv : the Preprint Server for Health Sciences|November 24, 2025
Saturation genome editing of <i>BARD1</i> resolves VUS and provides insight into BRCA1-BARD1 tumor suppressionIvan Woo, Silvia Casadei, Matthew W Snyder, et al.
Biorxiv : the Preprint Server for Biology|January 16, 2026
High-throughput mapping of 6,888 <i>RAD51D</i> variants identifies distinct biochemical functions needed for homologous recombination and olaparib responseKristie E Darrah, Shelby L Hemker, Yashpal Rawal, 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.
Medrxiv : the Preprint Server for Health Sciences|June 4, 2026
Phenotype-Specific Recalibration of MAVE Data Enables Repurposing of <i>BAP1</i> Functional Assays for Küry-Isidor SyndromePankhuri Gupta, Elsa V Balton, Mavika Tejura, et al.
Biorxiv : the Preprint Server for Biology|February 23, 2026
A scalable approach to resolving variants of uncertain significanceMalvika Tejura, Yile Chen, Abbye E McEwen, et al.
Pageof 2