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Stephanie Portelli
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Genome-wide analysis of multi- and extensively drug-resistant Mycobacterium tuberculosis
F Coll, J Phelan, GA Hill-Cawthorne, MB Nair, K Mallard, S Ali, ...
Nature genetics 50 (2), 307-316, 2018
3302018
Understanding molecular consequences of putative drug resistant mutations in Mycobacterium tuberculosis
S Portelli, JE Phelan, DB Ascher, TG Clark, N Furnham
Scientific reports 8 (1), 15356, 2018
712018
ThermoMutDB: a thermodynamic database for missense mutations
JS Xavier, TB Nguyen, M Karmarkar, S Portelli, PM Rezende, JPL Velloso, ...
Nucleic acids research 49 (D1), D475-D479, 2021
602021
Exploring the structural distribution of genetic variation in SARS-CoV-2 with the COVID-3D online resource
S Portelli, M Olshansky, CHM Rodrigues, EN D’Souza, Y Myung, M Silk, ...
Nature genetics 52 (10), 999-1001, 2020
602020
Prediction of rifampicin resistance beyond the RRDR using structure-based machine learning approaches
S Portelli, Y Myung, N Furnham, SC Vedithi, DEV Pires, DB Ascher
Scientific reports 10 (1), 18120, 2020
372020
Computational saturation mutagenesis to predict structural consequences of systematic mutations in the beta subunit of RNA polymerase in Mycobacterium leprae
SC Vedithi, CHM Rodrigues, S Portelli, MJ Skwark, M Das, DB Ascher, ...
Computational and Structural Biotechnology Journal 18, 271-286, 2020
272020
Distinguishing between PTEN clinical phenotypes through mutation analysis
S Portelli, L Barr, AGC de Sá, DEV Pires, DB Ascher
Computational and Structural Biotechnology Journal 19, 3097-3109, 2021
202021
Combining structure and genomics to understand antimicrobial resistance
T Tunstall, S Portelli, J Phelan, TG Clark, DB Ascher, N Furnham
Computational and Structural Biotechnology Journal 18, 3377-3394, 2020
202020
Structure-guided machine learning prediction of drug resistance mutations in Abelson 1 kinase
Y Zhou, S Portelli, M Pat, CHM Rodrigues, TB Nguyen, DEV Pires, ...
Computational and Structural Biotechnology Journal 19, 5381-5391, 2021
122021
toxCSM: comprehensive prediction of small molecule toxicity profiles
AGC de Sá, Y Long, S Portelli, DEV Pires, DB Ascher
Briefings in Bioinformatics 23 (5), bbac337, 2022
102022
Definition of the immune evasion-replication interface of rabies virus P protein
J Zhan, AR Harrison, S Portelli, TB Nguyen, I Kojima, S Zheng, F Yan, ...
PLoS Pathogens 17 (7), e1009729, 2021
92021
COVID-3D: An online resource to explore the structural distribution of genetic variation in SARS-CoV-2 and its implication on therapeutic development
S Portelli, M Olshansky, CHM Rodrigues, EN D’Souza, Y Myung, M Silk, ...
bioRxiv, 2020.05. 29.124610, 2020
72020
Author Correction: Genome-wide analysis of multi- and extensively drug-resistant Mycobacterium tuberculosis
F Coll, J Phelan, GA Hill-Cawthorne, MB Nair, K Mallard, S Ali, ...
Nature genetics 50 (5), 764-764, 2018
72018
Identifying the molecular drivers of ALS-implicated missense mutations
S Portelli, A Albanaz, DEV Pires, DB Ascher
Journal of Medical Genetics 60 (5), 484-490, 2023
52023
Identifying Genotype–Phenotype Correlations via Integrative Mutation Analysis
E Airey, S Portelli, JS Xavier, YC Myung, M Silk, M Karmakar, JPL Velloso, ...
Artificial Neural Networks, 1-32, 2021
52021
A comprehensive computational platform to guide drug development using graph-based signature methods
DEV Pires, S Portelli, PM Rezende, WNP Veloso, JS Xavier, M Karmakar, ...
Structural Bioinformatics: Methods and Protocols, 91-106, 2020
52020
Exploring protein supersecondary structure through changes in protein folding, stability, and flexibility
DEV Pires, CHM Rodrigues, ATS Albanaz, M Karmakar, Y Myung, ...
Protein Supersecondary Structures: Methods and Protocols, 173-185, 2019
52019
AI-Driven Enhancements in Drug Screening and Optimization
A Serghini, S Portelli, DB Ascher
Computational Drug Discovery and Design, 269-294, 2023
32023
Author correction: exploring the structural distribution of genetic variation in SARS-CoV-2 with the COVID-3D online resource
S Portelli, M Olshansky, CHM Rodrigues, EN D’Souza, Y Myung, M Silk, ...
Nature Genetics 53 (2), 254-254, 2021
32021
Characterizing and predicting ccRCC-causing missense mutations in Von Hippel-Lindau disease
A Serghini, S Portelli, G Troadec, C Song, Q Pan, DEV Pires, DB Ascher
Human Molecular Genetics 33 (3), 224-232, 2024
12024
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