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Full Name
Gloria M Sheynkman (CM4AI)
Affiliation
University of Virginia
ORCID
Career Start Year
2007
Papers
45
H Index
21
Expertise
Standards
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36597873
Genetic Regulation of SMC Gene Expression and Splicing Predict Causal CAD Genes.
Circ Res
2023
37546854
Systematic assessment of long-read RNA-seq methods for transcript identification and quantification.
bioRxiv
2023
37191809
Gain-of-Function Variomics and Multi-omics Network Biology for Precision Medicine.
Methods Mol Biol
2023
37197981
Connexin 37 sequestering of activated-ERK in the cytoplasm promotes p27-mediated endothelial cell cycle arrest.
Life Sci Alliance
2023
37095564
Transformation of alignment files improves performance of variant callers for long-read RNA sequencing data.
Genome Biol
2023
37066387
Single-cell long-read mRNA isoform regulation is pervasive across mammalian brain regions, cell types, and development.
bioRxiv
2023
37398049
Alternative splicing is coupled to gene expression in a subset of variably expressed genes.
bioRxiv
2023
36993769
Long-read proteogenomics to connect disease-associated sQTLs to the protein isoform effectors of disease.
bioRxiv
2023
36752347
AD-Syn-Net: systematic identification of Alzheimer's disease-associated mutation and co-mutation vulnerabilities via deep learning.
Brief Bioinform
2023
34628220
Interpretable artificial intelligence and exascale molecular dynamics simulations to reveal kinetics: Applications to Alzheimer's disease.
Curr Opin Struct Biol
2022
36457147
Characterization of protein isoform diversity in human umbilical vein endothelial cells via long-read proteogenomics.
RNA Biol
2022
36202789
Endothelial cell cycle state determines propensity for arterial-venous fate.
Nat Commun
2022
35961013
A roadmap for the functional annotation of protein families: a community perspective.
Database (Oxford)
2022
35960994
Bridging the splicing gap in human genetics with long-read RNA sequencing: finding the protein isoform drivers of disease.
Hum Mol Genet
2022
35241129
Enhanced protein isoform characterization through long-read proteogenomics.
Genome Biol
2022
34788620
Full-length transcript sequencing of human and mouse cerebral cortex identifies widespread isoform diversity and alternative splicing.
Cell Rep
2021
32393825
ORF Capture-Seq as a versatile method for targeted identification of full-length isoforms.
Nat Commun
2020
33173926
Characterization of a COPD-Associated <i>NPNT</i> Functional Splicing Genetic Variant in Human Lung Tissue via Long-Read Sequencing.
medRxiv
2020
32296183
A reference map of the human binary protein interactome.
Nature
2020
31116991
The lncRNA SLNCR Recruits the Androgen Receptor to EGR1-Bound Genes in Melanoma and Inhibits Expression of Tumor Suppressor p21.
Cell Rep
2019
31378069
Improved Protein Inference from Multiple Protease Bottom-Up Mass Spectrometry Data.
J Proteome Res
2019
29598823
Full-length mRNA sequencing uncovers a widespread coupling between transcription initiation and mRNA processing.
Genome Biol
2018
28284537
Proteome-Scale Human Interactomics.
Trends Biochem Sci
2017
27049631
Proteogenomics: Integrating Next-Generation Sequencing and Mass Spectrometry to Characterize Human Proteomic Variation.
Annu Rev Anal Chem (Palo Alto Calif)
2016
27935966
The Transcription Factor Nfatc2 Regulates β-Cell Proliferation and Genes Associated with Type 2 Diabetes in Mouse and Human Islets.
PLoS Genet
2016
26704769
Human Proteomic Variation Revealed by Combining RNA-Seq Proteogenomics and Global Post-Translational Modification (G-PTM) Search Strategy.
J Proteome Res
2016
26871637
Widespread Expansion of Protein Interaction Capabilities by Alternative Splicing.
Cell
2016
26418581
Global Identification of Protein Post-translational Modifications in a Single-Pass Database Search.
J Proteome Res
2015
24175627
Large-scale mass spectrometric detection of variant peptides resulting from nonsynonymous nucleotide differences.
J Proteome Res
2014
25053745
sapFinder: an R/Bioconductor package for detection of variant peptides in shotgun proteomics experiments.
Bioinformatics
2014
25149441
Using Galaxy-P to leverage RNA-Seq for the discovery of novel protein variations.
BMC Genomics
2014
23629695
Discovery and mass spectrometric analysis of novel splice-junction peptides using RNA-Seq.
Mol Cell Proteomics
2013
22714949
Absolute quantification of prion protein (90-231) using stable isotope-labeled chymotryptic peptide standards in a LC-MRM AQUA workflow.
J Am Soc Mass Spectrom
2012
1 - 33 of 33
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