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Author Details
Full Name
Minji Byun
Affiliation
Icahn School of Medicine at Mount Sinai
ORCID
Career Start Year
2003
Papers
24
H Index
16
Expertise
CM4AI Collaborator
Nevan J Krogan (CM4AI)
PMID
Paper Title
Journal Title
Published Year
37995687
Nuclear RNA catabolism controls endogenous retroviruses, gene expression asymmetry, and dedifferentiation.
Mol Cell
2023
34146579
Convergence of cytokine dysregulation and antibody deficiency in common variable immunodeficiency with inflammatory complications.
J Allergy Clin Immunol
2022
35945277
Author Correction: Clonally expanded CD8 T cells characterize amyotrophic lateral sclerosis-4.
Nature
2022
33970190
DNMT3A haploinsufficiency causes dichotomous DNA methylation defects at enhancers in mature human immune cells.
J Exp Med
2021
33836156
TOP1 inhibition therapy protects against SARS-CoV-2-induced lethal inflammation.
Cell
2021
33299999
Topoisomerase 1 inhibition therapy protects against SARS-CoV-2-induced inflammation and death in animal models.
bioRxiv
2020
29730845
Disseminated Cutaneous Warts in X-Linked Hyper IgM Syndrome.
J Clin Immunol
2018
30177761
Influenza virus infection causes global RNAPII termination defects.
Nat Struct Mol Biol
2018
30404775
A novel <i>FAS</i> mutation with variable expressivity in a family with unicentric and idiopathic multicentric Castleman disease.
Blood Adv
2018
28475896
The RNA Exosome Syncs IAV-RNAPII Transcription to Promote Viral Ribogenesis and Infectivity.
Cell
2017
28359509
Autosomal Recessive Cardiomyopathy Presenting as Acute Myocarditis.
J Am Coll Cardiol
2017
25492914
Whole-Genome Sequencing Identifies STAT4 as a Putative Susceptibility Gene in Classic Kaposi Sarcoma.
J Infect Dis
2015
25339207
TLR3 deficiency in herpes simplex encephalitis: high allelic heterogeneity and recurrence risk.
Neurology
2014
23579497
Ribosomal protein SA haploinsufficiency in humans with isolated congenital asplenia.
Science
2013
23897980
Inherited human OX40 deficiency underlying classic Kaposi sarcoma of childhood.
J Exp Med
2013
22157133
Multicentric Castleman disease in an HHV8-infected child born to consanguineous parents with systematic review.
Pediatrics
2012
22859821
Mycobacterial disease and impaired IFN-γ immunity in humans with inherited ISG15 deficiency.
Science
2012
22238637
A mild form of SLC29A3 disorder: a frameshift deletion leads to the paradoxical translation of an otherwise noncoding mRNA splice variant.
PLoS One
2012
22258534
A major locus on chromosome 3p22 conferring predisposition to human herpesvirus 8 infection.
Eur J Hum Genet
2012
20876309
Whole-exome sequencing-based discovery of STIM1 deficiency in a child with fatal classic Kaposi sarcoma.
J Exp Med
2010
21109225
Whole-exome-sequencing-based discovery of human FADD deficiency.
Am J Hum Genet
2010
19917497
Two mechanistically distinct immune evasion proteins of cowpox virus combine to avoid antiviral CD8 T cells.
Cell Host Microbe
2009
18005752
Cowpox virus exploits the endoplasmic reticulum retention pathway to inhibit MHC class I transport to the cell surface.
Cell Host Microbe
2007
12845326
Crystal structure of peptidoglycan recognition protein LB from Drosophila melanogaster.
Nat Immunol
2003
1 - 24 of 24
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University of Toronto, Lunenfeld Tanenbaum Research Institute, Mount Sinai Hospital
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row(s) 1 - 30 of 30
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Co-authored papers
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Simin Zheng
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3
Sumit K Chanda
The Scripps Research Institute
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3
Ernesto Guccione
Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai
Co-authored papers
3
Christopher Benner
Michigan State University College of Human Medicine
Co-authored papers
3
Matthew T Weirauch
University of Cincinnati College of Medicine
Co-authored papers
3
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Department of Computer Science and Informatics Institute, University of Missouri
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The Rockefeller University
Co-authored papers
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Vittorio Sebastiano
Stanford University
Co-authored papers
2
Benjamin R tenOever
NYU Grossman School of Medicine
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Raveen Rathnasinghe
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