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Julia di Iulio

VIR Biotechnology (United States) · US
Area of research
Infectious Diseases · Molecular Biology
Research interest
Research interests include SARS-CoV-2 and COVID-19 Research, COVID-19 Clinical Research Studies, Genomics and Phylogenetic Studies, and RNA and protein synthesis mechanisms.
h-index
37
citations
10,428
works
79
NIH funding
primary concept
Biology
email

Recent publications

A potent pan-sarbecovirus neutralizing antibody resilient to epitope diversification
Cell 2024cited by 63position: middledoi
Recommendations for Uniform Variant Calling of SARS-CoV-2 Genome Sequence across Bioinformatic Workflows.
2024cited by 3position: contributordoi
Resistance analysis in the phase III COMET-TAIL study: treatment of COVID-19 with intramuscular or intravenous sotrovimab
Future Virology 2024cited by 1position: contributordoi
A pan-influenza antibody inhibiting neuraminidase via receptor mimicry
Nature 2023cited by 92position: middledoi
A pan-influenza antibody inhibiting neuraminidase via receptor mimicry.
2023cited by 76position: contributordoi
Resistance analysis following sotrovimab treatment in participants with COVID-19 during the phase III COMET-ICE study.
2023cited by 6position: contributordoi
Author Correction: A pan-influenza antibody inhibiting neuraminidase via receptor mimicry.
2023cited by 0position: contributordoi
Imprinted antibody responses against SARS-CoV-2 Omicron sublineages
Science 2022cited by 255position: middledoi
Imprinted antibody responses against SARS-CoV-2 Omicron sublineages.
2022cited by 228position: contributordoi
Predicting the mutational drivers of future SARS-CoV-2 variants of concern
Science Translational Medicine 2022cited by 188position: middledoi
Predicting the mutational drivers of future SARS-CoV-2 variants of concern.
2022cited by 147position: contributordoi
Towards increased accuracy and reproducibility in SARS-CoV-2 next generation sequence analysis for public health surveillance
2022cited by 4position: contributordoi
Broadly neutralizing antibodies overcome SARS-CoV-2 Omicron antigenic shift
Nature 2021cited by 1,200position: middledoi
N-terminal domain antigenic mapping reveals a site of vulnerability for SARS-CoV-2
Cell 2021cited by 1,013position: middledoi
Circulating SARS-CoV-2 spike N439K variants maintain fitness while evading antibody-mediated immunity
Cell 2021cited by 655position: middledoi
SARS-CoV-2 RBD antibodies that maximize breadth and resistance to escape
Nature 2021cited by 582position: middledoi
Broad betacoronavirus neutralization by a stem helix–specific human antibody
Science 2021cited by 429position: middledoi
SARS-CoV-2 immune evasion by the B.1.427/B.1.429 variant of concern.
2021cited by 408position: contributordoi
Broad betacoronavirus neutralization by a stem helix-specific human antibody.
2021cited by 403position: contributordoi
Broad sarbecovirus neutralization by a human monoclonal antibody
Nature 2021cited by 315position: middledoi
Broadly neutralizing antibodies overcome SARS-CoV-2 Omicron antigenic shift
Nature 2021cited by 213position: middledoi
Broadly neutralizing antibodies overcome SARS-CoV-2 Omicron antigenic shift
2021cited by 34position: contributordoi
Predicting the mutational drivers of future SARS-CoV-2 variants of concern
2021cited by 21position: contributordoi
Structural basis for broad sarbecovirus neutralization by a human monoclonal antibody
2021cited by 17position: contributordoi
Antibodies to the SARS-CoV-2 receptor-binding domain that maximize breadth and resistance to viral escape
2021cited by 16position: contributordoi
Transfer transcriptomic signatures for infectious diseases.
2021cited by 12position: contributordoi
Antibody therapy reverses biological signatures of COVID-19 progression
2021cited by 0position: contributordoi
Ranking of non-coding pathogenic variants and putative essential regions of the human genome
Nature Communications 2019cited by 89position: lastdoi
Ranking of non-coding pathogenic variants and putative essential regions of the human genome.
2019cited by 69position: contributordoi
BET Bromodomain Proteins Function as Master Transcription Elongation Factors Independent of CDK9 Recruitment
Molecular Cell 2017cited by 485position: middledoi

Grants

No grants ingested yet.

Frequent collaborators

· 11 papers (2019–2024)Amalio Telenti · Scripps Institution of Oceanography8 papers (2019–2023) · 6 papers (2021–2023)Davide Corti · University of Trento5 papers (2021–2023)Herbert W. Virgin · Southwestern Medical Center5 papers (2021–2022) · 4 papers (2021–2022)Lisa A. Purcell · The University of Texas Southwestern Medical Center4 papers (2021–2024)Leah Soriaga · Vir Biotechnology (Switzerland)3 papers (2021–2022)Roberto Spreafico · Institute for Quantitative and Computational Biosciences3 papers (2021–2023) · 3 papers (2021–2024) · 3 papers (2021–2024)Cyrus Maher · Vir Biotechnology (Switzerland)3 papers (2021–2022)Gyorgy Snell · 3 papers (2022–2023) · 3 papers (2021–2022)Bonnie Berger · Broad Institute3 papers (2021–2022)Matteo Samuele Pizzuto · 2 papers (2023–2023)Florian A. Lempp · Heidelberg University2 papers (2021–2022)David L. Robertson · Imperial College London2 papers (2021–2022)David M. Belnap · University of Utah2 papers (2023–2023)Michael A. Schmid · Hegau-Bodensee-Klinikum Singen2 papers (2023–2023)