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Plos One
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May 9, 2012
Transcriptional enhancers in protein-coding exons of vertebrate developmental genes
Deborah 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 genes
Suhasini 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 concordance
Jennifer 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 concordance
Jennifer 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 activity
Deborah 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 regulation
Jason 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.is
Dena 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 sequencing
Deborah 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 analogs
Jason Saliba, Ryan Zabriskie, Rajarshi Ghosh, et al.
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Search research articles
Search
Showing results (1-10 of 39) with videos related to
Sort By:
Page
of 4
Plos One
|
May 9, 2012
Transcriptional enhancers in protein-coding exons of vertebrate developmental genes
Deborah 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 genes
Suhasini 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 concordance
Jennifer 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 concordance
Jennifer 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 activity
Deborah 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 regulation
Jason 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.is
Dena 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 sequencing
Deborah 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 analogs
Jason Saliba, Ryan Zabriskie, Rajarshi Ghosh, et al.
Page
of 4