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Deborah I Ritter

Showing results (1-10 of 39) with videos related to

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Plos One|May 9, 2012
Transcriptional enhancers in protein-coding exons of vertebrate developmental genesDeborah I Ritter, Zhiqiang Dong, Su Guo, et al.
Biorxiv : the Preprint Server for Biology|May 13, 2026
Distinct mutational landscapes when comparing germline and somatic cancer variants in forty tumor suppressor genesSuhasini D Lulla, Deborah I Ritter, Chimene Kesserwan, et al.
Biorxiv : the Preprint Server for Biology|September 26, 2025
Specification of frequency criteria for secondary findings genes to improve variant classification concordanceJennifer J Johnston, Kristy Lee, Deborah I Ritter, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 17, 2026
Specification of frequency criteria for secondary findings genes to improve variant classification concordanceJennifer J Johnston, Kristy Lee, Deborah I Ritter, et al.
Cold Spring Harbor Molecular Case Studies|October 25, 2019
A case for expert curation: an overview of cancer curation in the Clinical Genome Resource (ClinGen)Deborah I Ritter, Shruti Rao, Shashikant Kulkarni, et al.
Molecular Biology and Evolution|May 25, 2010
The importance of being cis: evolution of orthologous fish and mammalian enhancer activityDeborah I Ritter, Qiang Li, Dennis Kostka, et al.
Bioinformatics (Oxford, England)|August 23, 2008
cneViewer: a database of conserved non-coding elements for studies of tissue-specific gene regulationJason Persampieri, Deborah I Ritter, Daniel Lees, et al.
Database : the Journal of Biological Databases and Curation|January 8, 2023
Developing a disease-specific annotation protocol for VHL gene curation using Hypothes.isDena Salehipour, Kirsten M Farncombe, Veronica Andric, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 9, 2015
Identifying gene disruptions in novel balanced de novo constitutional translocations in childhood cancer patients by whole-genome sequencingDeborah I Ritter, Katherine Haines, Hannah Cheung, et al.
Pharmacogenetics and Genomics|February 25, 2016
Pharmacogenetic characterization of naturally occurring germline NT5C1A variants to chemotherapeutic nucleoside analogsJason Saliba, Ryan Zabriskie, Rajarshi Ghosh, et al.
Pageof 4

Showing results (1-10 of 39) with videos related to

Sort By:
Pageof 4
Plos One|May 9, 2012
Transcriptional enhancers in protein-coding exons of vertebrate developmental genesDeborah I Ritter, Zhiqiang Dong, Su Guo, et al.
Biorxiv : the Preprint Server for Biology|May 13, 2026
Distinct mutational landscapes when comparing germline and somatic cancer variants in forty tumor suppressor genesSuhasini D Lulla, Deborah I Ritter, Chimene Kesserwan, et al.
Biorxiv : the Preprint Server for Biology|September 26, 2025
Specification of frequency criteria for secondary findings genes to improve variant classification concordanceJennifer J Johnston, Kristy Lee, Deborah I Ritter, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 17, 2026
Specification of frequency criteria for secondary findings genes to improve variant classification concordanceJennifer J Johnston, Kristy Lee, Deborah I Ritter, et al.
Cold Spring Harbor Molecular Case Studies|October 25, 2019
A case for expert curation: an overview of cancer curation in the Clinical Genome Resource (ClinGen)Deborah I Ritter, Shruti Rao, Shashikant Kulkarni, et al.
Molecular Biology and Evolution|May 25, 2010
The importance of being cis: evolution of orthologous fish and mammalian enhancer activityDeborah I Ritter, Qiang Li, Dennis Kostka, et al.
Bioinformatics (Oxford, England)|August 23, 2008
cneViewer: a database of conserved non-coding elements for studies of tissue-specific gene regulationJason Persampieri, Deborah I Ritter, Daniel Lees, et al.
Database : the Journal of Biological Databases and Curation|January 8, 2023
Developing a disease-specific annotation protocol for VHL gene curation using Hypothes.isDena Salehipour, Kirsten M Farncombe, Veronica Andric, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 9, 2015
Identifying gene disruptions in novel balanced de novo constitutional translocations in childhood cancer patients by whole-genome sequencingDeborah I Ritter, Katherine Haines, Hannah Cheung, et al.
Pharmacogenetics and Genomics|February 25, 2016
Pharmacogenetic characterization of naturally occurring germline NT5C1A variants to chemotherapeutic nucleoside analogsJason Saliba, Ryan Zabriskie, Rajarshi Ghosh, et al.
Pageof 4