On the public citation graph
DrugPred: A Structure-Based Approach To Predict Protein Druggability Developed Using an Extensive Nonredundant Data Set
0 signed · 148 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/1097-0282(2001/2002)61:2<99::aid-bip10075>3.0.co;2-8openalex-snapshot
Use of Relibase for retrieving complex three-dimensional interaction patterns including crystallographic packing effects
inferredcites →https://doi.org/10.1002/pro.5560070411openalex-snapshot
Flexible ligand docking using conformational ensembles
inferredcites →https://doi.org/10.1006/jmbi.2001.4551openalex-snapshot
FlexE: efficient molecular docking considering protein structure variations
inferredcites →https://doi.org/10.1007/978-1-60761-762-4_8openalex-snapshot
Recent Progress in the Structure Determination of GPCRs, a Membrane Protein Family with High Potential as Pharmaceutical Targets
inferredcites →https://doi.org/10.1016/0022-2836(82)90515-0openalex-snapshot
A simple method for displaying the hydropathic character of a protein
inferredcites →https://doi.org/10.1016/j.cbpa.2008.01.045openalex-snapshot
Structural genomics and drug discovery: all in the family
inferredcites →https://doi.org/10.1016/j.drudis.2007.08.017openalex-snapshot
Topography-biased compound library design: the shape of things to come?
inferredcites →https://doi.org/10.1016/j.drudis.2010.05.015openalex-snapshot
Druggable pockets and binding site centric chemical space: a paradigm shift in drug discovery
inferredcites →https://doi.org/10.1016/s0167-9473(99)00069-9openalex-snapshot
Computing the cumulative distribution function of the Kolmogorov–Smirnov statistic
inferredcites →https://doi.org/10.1016/s0169-409x(96)00423-1openalex-snapshot
Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings
inferredcites →https://doi.org/10.1016/s0169-7439(01)00155-1openalex-snapshot
PLS-regression: a basic tool of chemometrics
inferredcites →https://doi.org/10.1016/s1359-6446(02)02595-3openalex-snapshot
Fulfilling the promise: drug discovery in the post-genomic era
inferredcites →https://doi.org/10.1016/s1359-6446(04)03069-7openalex-snapshot
Ligand efficiency: a useful metric for lead selection
inferredcites →https://doi.org/10.1016/s1359-6446(05)03624-xopenalex-snapshot
Predicting protein druggability
inferredcites →https://doi.org/10.1016/s1359-6446(05)03667-6openalex-snapshot
The potential impact of structural genomics on tuberculosis drug discovery
inferredcites →https://doi.org/10.1021/ci010366aopenalex-snapshot
Is There a Difference between Leads and Drugs? A Historical Perspective
inferredcites →https://doi.org/10.1021/ci1002558openalex-snapshot
Molecular Topology Analysis of the Differences between Drugs, Clinical Candidate Compounds, and Bioactive Molecules
inferredcites →https://doi.org/10.1021/ci100312topenalex-snapshot
Drug-like Density: A Method of Quantifying the “Bindability” of a Protein Target Based on a Very Large Set of Pockets and Drug-like Ligands from the Protein Data Bank
inferredcites →https://doi.org/10.1021/ci6002202openalex-snapshot
Use of Amino Acid Composition to Predict Ligand-Binding Sites
inferredcites →https://doi.org/10.1021/ci800324mopenalex-snapshot
Identifying and Characterizing Binding Sites and Assessing Druggability
inferredcites →https://doi.org/10.1021/jm020964wopenalex-snapshot
Potential Tumor-Selective Nitroimidazolylmethyluracil Prodrug Derivatives: Inhibitors of the Angiogenic Enzyme Thymidine Phosphorylase
inferredcites →https://doi.org/10.1021/jm021053popenalex-snapshot
A Comparison of Physiochemical Property Profiles of Development and Marketed Oral Drugs
inferredcites →https://doi.org/10.1021/jm030580lopenalex-snapshot
The PDBbind Database: Collection of Binding Affinities for Protein−Ligand Complexes with Known Three-Dimensional Structures
inferredcites →https://doi.org/10.1021/jm049131ropenalex-snapshot
Druggability Indices for Protein Targets Derived from NMR-Based Screening Data
inferredcites →https://doi.org/10.1021/jm060511hopenalex-snapshot
Fragment-Based Drug Design: How Big Is Too Big?
inferredcites →https://doi.org/10.1021/jm061277yopenalex-snapshot
Diverse, High-Quality Test Set for the Validation of Protein−Ligand Docking Performance
inferredcites →https://doi.org/10.1021/jm070644iopenalex-snapshot
Discovery of 5-Substituted-6-chlorouracils as Efficient Inhibitors of Human Thymidine Phosphorylase
inferredcites →https://doi.org/10.1021/jm100118xopenalex-snapshot
An Analysis of the Binding Efficiencies of Drugs and Their Leads in Successful Drug Discovery Programs
inferredcites →https://doi.org/10.1021/jm100574mopenalex-snapshot
Understanding and Predicting Druggability. A High-Throughput Method for Detection of Drug Binding Sites
inferredcites →https://doi.org/10.1021/jm701255bopenalex-snapshot
Ligand Binding Efficiency: Trends, Physical Basis, and Implications
inferredcites →https://doi.org/10.1021/jm8008597openalex-snapshot
Covalent Modifiers: An Orthogonal Approach to Drug Design
inferredcites →https://doi.org/10.1021/jm901371vopenalex-snapshot
Physicochemical Space for Optimum Oral Bioavailability: Contribution of Human Intestinal Absorption and First-Pass Elimination
inferredcites →https://doi.org/10.1038/nbt1273openalex-snapshot
Structure-based maximal affinity model predicts small-molecule druggability
inferredcites →https://doi.org/10.1038/nrd2132openalex-snapshot
Drugs, their targets and the nature and number of drug targets
inferredcites →https://doi.org/10.1038/nrd2201openalex-snapshot
Drugs for bad bugs: confronting the challenges of antibacterial discovery
inferredcites →https://doi.org/10.1038/nrd2684openalex-snapshot
Genomic-scale prioritization of drug targets: the TDR Targets database
inferredcites →https://doi.org/10.1038/nrd3185openalex-snapshot
The discovery and development of rivaroxaban, an oral, direct factor Xa inhibitor
inferredcites →https://doi.org/10.1093/jac/32.suppl_a.121openalex-snapshot
Antivirals for the treatment of herpesvirus infections
inferredcites →https://doi.org/10.1093/nar/gkj067openalex-snapshot
DrugBank: a comprehensive resource for in silico drug discovery and exploration
inferredcites →https://doi.org/10.1113/jphysiol.2009.183160openalex-snapshot
Atomic structure and dynamics of pentameric ligand-gated ion channels: new insight from bacterial homologues
inferredcites →https://doi.org/10.1124/pr.58.2.4openalex-snapshot
Therapeutic Targets: Progress of Their Exploration and Investigation of Their Characteristics
inferredcites →https://doi.org/10.1146/annurev-physiol-021909-135917openalex-snapshot
Structural Overview of the Nuclear Receptor Superfamily: Insights into Physiology and Therapeutics
inferredcites →https://doi.org/10.1186/1471-2105-10-168openalex-snapshot
Fpocket: An open source platform for ligand pocket detection
inferredcites →https://doi.org/10.1371/journal.pcbi.1000530openalex-snapshot
The Role of Medical Structural Genomics in Discovering New Drugs for Infectious Diseases
inferredcites →https://doi.org/10.1592/phco.30.5.463openalex-snapshot
Dipeptidyl Peptidase‐4 Inhibitors for the Treatment of Type 2 Diabetes Mellitus
inferredcites →https://doi.org/10.2165/11318430-000000000-00000openalex-snapshot
Current Challenges in Antimicrobial Chemotherapy
inferredcites →https://doi.org/10.2174/1381612023394809openalex-snapshot
The Promise of Structural Genomics in the Discovery of New Antimicrobial Agents
inferredcites →https://doi.org/10.2174/138161209788682523openalex-snapshot
Current Prodrug Design for Drug Discovery
inferredcites →https://doi.org/10.2174/156802611795429185openalex-snapshot
Target Validation: Linking Target and Chemical Properties to Desired Product Profile
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/0471266949.bmc301openalex-snapshot
Docking, Scoring, and Virtual Screening in Drug Discovery
inferred← citeshttps://doi.org/10.1002/9781118681121.ch2openalex-snapshot
A Structural View on Druggability
inferred← citeshttps://doi.org/10.1002/9781394182862.ch8openalex-snapshot
Toward Mechanism‐based Therapies and Network Pharmacology
inferred← citeshttps://doi.org/10.1002/9783527677016.ch6openalex-snapshot
Hit and Lead Identification from Fragments
inferred← citeshttps://doi.org/10.1002/9783527683604.ch09openalex-snapshot
Computational Methods to Support Fragment‐based Drug Discovery
inferred← citeshttps://doi.org/10.1002/9783527806539.ch6gopenalex-snapshot
Prediction, Analysis, and Comparison of Active Sites
inferred← citeshttps://doi.org/10.1002/minf.201700040openalex-snapshot
Statistical Profiling of One Promiscuous Protein Binding Site: Illustrated by Urokinase Catalytic Domain
inferred← citeshttps://doi.org/10.1002/pro.4406openalex-snapshot
A structural database of chain–chain and domain–domain interfaces of proteins
inferred← citeshttps://doi.org/10.1002/wcms.1134openalex-snapshot
Druggability predictions: methods, limitations, and applications
inferred← citeshttps://doi.org/10.1002/wcms.1676openalex-snapshot
Ligandability and druggability assessment via machine learning
inferred← citeshttps://doi.org/10.1007/7653_2015_45openalex-snapshot
CAVITY: Mapping the Druggable Binding Site
inferred← citeshttps://doi.org/10.1007/978-1-4939-2486-8_12openalex-snapshot
Protein Binding Site Analysis for Drug Discovery Using a Computational Fragment-Based Method
inferred← citeshttps://doi.org/10.1007/978-3-030-95895-4_5openalex-snapshot
Structure-Based Binding Pocket Detection and Druggability Assessment
inferred← citeshttps://doi.org/10.1007/978-3-031-81728-1_31openalex-snapshot
Validation Aspects in Structure-Based Drug Design
inferred← citeshttps://doi.org/10.1007/978-981-15-6815-2_8openalex-snapshot
Computational Approaches for Drug Target Identification
inferred← citeshttps://doi.org/10.1007/978-981-95-2525-6_29openalex-snapshot
Drug Targetability Identification Based on Structure and Network
inferred← citeshttps://doi.org/10.1007/s00894-020-04385-6openalex-snapshot
Druggability and drug-likeness concepts in drug design: are biomodelling and predictive tools having their say?
inferred← citeshttps://doi.org/10.1007/s10822-019-00197-wopenalex-snapshot
Elucidating the druggability of the human proteome with eFindSite
inferred← citeshttps://doi.org/10.1007/s10822-021-00390-wopenalex-snapshot
CAVIAR: a method for automatic cavity detection, description and decomposition into subcavities
inferred← citeshttps://doi.org/10.1007/s10822-026-00949-5openalex-snapshot
Uncovering hidden druggable sites: computational approaches to allosteric and cryptic pocket discovery—from molecular dynamics to AI
inferred← citeshttps://doi.org/10.1007/s12013-016-0769-yopenalex-snapshot
Can We Rely on Computational Predictions To Correctly Identify Ligand Binding Sites on Novel Protein Drug Targets? Assessment of Binding Site Prediction Methods and a Protocol for Validation of Predicted Binding Sites
inferred← citeshttps://doi.org/10.1016/b978-0-12-801238-3.11531-4openalex-snapshot
Computational Drug Target Tractability Analysis
inferred← citeshttps://doi.org/10.1016/bs.armc.2017.08.001openalex-snapshot
Kinase-Centric Computational Drug Development
inferred← citeshttps://doi.org/10.1016/j.abb.2025.110715openalex-snapshot
Staphylococcus aureus sensor histidine kinase VraS mutations linked to antibiotic resistance affect enzymatic catalysis, stability, and substrate interactions
inferred← citeshttps://doi.org/10.1016/j.aca.2015.02.032openalex-snapshot
Large-scale identification of potential drug targets based on the topological features of human protein–protein interaction network
inferred← citeshttps://doi.org/10.1016/j.drudis.2016.11.021openalex-snapshot
Global vision of druggability issues: applications and perspectives
inferred← citeshttps://doi.org/10.1016/j.drudis.2018.02.015openalex-snapshot
Quantitative metrics for drug–target ligandability
inferred← citeshttps://doi.org/10.1016/j.drudis.2024.104197openalex-snapshot
Which cryptic sites are feasible drug targets?
inferred← citeshttps://doi.org/10.1016/j.ejps.2019.105166openalex-snapshot
Enabling design of screening libraries for antibiotic discovery by modeling ChEMBL data
inferred← citeshttps://doi.org/10.1016/j.jbiotec.2011.12.005openalex-snapshot
Structure-based computational analysis of protein binding sites for function and druggability prediction
inferred← citeshttps://doi.org/10.1016/j.pharmthera.2017.02.034openalex-snapshot
The impact of in silico screening in the discovery of novel and safer drug candidates
inferred← citeshttps://doi.org/10.1016/j.ymeth.2014.08.001openalex-snapshot
Virtual screening: An in silico tool for interlacing the chemical universe with the proteome
inferred← citeshttps://doi.org/10.1017/s0031182013001017openalex-snapshot
Target-based drug discovery for human African trypanosomiasis: selection of molecular target and chemical matter
inferred← citeshttps://doi.org/10.1021/acs.jcim.1c00155openalex-snapshot
DrugPred_RNA—A Tool for Structure-Based Druggability Predictions for RNA Binding Sites
inferred← citeshttps://doi.org/10.1021/acs.jcim.5c00821openalex-snapshot
NanoShaperWeb: Molecular Surface and Pocket Detection Made Visual
inferred← citeshttps://doi.org/10.1021/acs.jcim.5c01576openalex-snapshot
Impact of Protein Conformational Diversity on Structure-Based Prediction of Druggability
inferred← citeshttps://doi.org/10.1021/acs.jcim.9b00332openalex-snapshot
D3Pockets: A Method and Web Server for Systematic Analysis of Protein Pocket Dynamics
inferred← citeshttps://doi.org/10.1021/acs.jcim.9b01185openalex-snapshot
Druggability Assessment in TRAPP Using Machine Learning Approaches
inferred← citeshttps://doi.org/10.1021/acs.jctc.2c01306openalex-snapshot
SiteFerret: Beyond Simple Pocket Identification in Proteins
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.5b00586openalex-snapshot
New Frontiers in Druggability
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.5b01286openalex-snapshot
How Beyond Rule of 5 Drugs and Clinical Candidates Bind to Their Targets
inferred← citeshttps://doi.org/10.1021/acs.jpcb.0c04963openalex-snapshot
Structural Fluctuations of Aromatic Residues in an Apo-Form Reveal Cryptic Binding Sites: Implications for Fragment-Based Drug Design
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b02319openalex-snapshot
Concise Synthesis of Tetrazole Macrocycle
inferred← citeshttps://doi.org/10.1021/acsabm.2c01079openalex-snapshot
Identifying Potential Ligand Binding Sites on Glycogen Synthase Kinase 3 Using Atomistic Cosolvent Simulations
inferred← citeshttps://doi.org/10.1021/ci200613bopenalex-snapshot
Development of a Rule-Based Method for the Assessment of Protein Druggability
inferred← citeshttps://doi.org/10.1021/ci300177popenalex-snapshot
Identification of Non-Macrocyclic Small Molecule Inhibitors against the NS3/4A Serine Protease of Hepatitis C Virus through in Silico Screening
inferred← citeshttps://doi.org/10.1021/ci300184xopenalex-snapshot
Comparison and Druggability Prediction of Protein–Ligand Binding Sites from Pharmacophore-Annotated Cavity Shapes
inferred← citeshttps://doi.org/10.1021/ci5006004openalex-snapshot
PockDrug: A Model for Predicting Pocket Druggability That Overcomes Pocket Estimation Uncertainties
inferred← citeshttps://doi.org/10.1021/ci500624sopenalex-snapshot
Pocketome of Human Kinases: Prioritizing the ATP Binding Sites of (Yet) Untapped Protein Kinases for Drug Discovery
inferred← citeshttps://doi.org/10.1021/ct501072topenalex-snapshot
A Collective Variable for the Rapid Exploration of Protein Druggability
inferred← citeshttps://doi.org/10.1021/jm300346wopenalex-snapshot
Druggability Analysis and Structural Classification of Bromodomain Acetyl-lysine Binding Sites
inferred← citeshttps://doi.org/10.1021/jm3011977openalex-snapshot
Scaling the Druggability Landscape of Human Bromodomains, a New Class of Drug Targets
inferred← citeshttps://doi.org/10.1038/psp.2013.66openalex-snapshot
Identifying Druggable Targets by Protein Microenvironments Matching: Application to Transcription Factors
inferred← citeshttps://doi.org/10.1039/9781849735377-00302openalex-snapshot
Expanding the Target Space: Druggability Assessments
inferred← citeshttps://doi.org/10.1088/0953-8984/28/34/344007openalex-snapshot
Exploring the role of water in molecular recognition: predicting protein ligandability using a combinatorial search of surface hydration sites
inferred← citeshttps://doi.org/10.1093/bib/bbac269openalex-snapshot
Mitigating cold-start problems in drug-target affinity prediction with interaction knowledge transferring
inferred← citeshttps://doi.org/10.1093/database/bau035openalex-snapshot
TuberQ: a Mycobacterium tuberculosis protein druggability database
inferred← citeshttps://doi.org/10.1093/nar/gkaf239openalex-snapshot
DRLiPS: a novel method for prediction of druggable RNA-small molecule binding pockets using machine learning
inferred← citeshttps://doi.org/10.1093/nar/gku928openalex-snapshot
sc-PDB: a 3D-database of ligandable binding sites—10 years on
inferred← citeshttps://doi.org/10.1093/nar/gkv462openalex-snapshot
PockDrug-Server: a new web server for predicting pocket druggability on holo and apo proteins
inferred← citeshttps://doi.org/10.1093/nar/gkx374openalex-snapshot
PharmMapper 2017 update: a web server for potential drug target identification with a comprehensive target pharmacophore database
inferred← citeshttps://doi.org/10.1107/s1744309112044739openalex-snapshot
The AEROPATH project targetingPseudomonas aeruginosa: crystallographic studies for assessment of potential targets in early-stage drug discovery
inferred← citeshttps://doi.org/10.1109/tcbb.2022.3150280openalex-snapshot
Deep Multi-Label Joint Learning for RNA and DNA-Binding Proteins Prediction
inferred← citeshttps://doi.org/10.1142/s0219720019500264openalex-snapshot
Glycine-induced formation and druggability score prediction of protein surface pockets
inferred← citeshttps://doi.org/10.1177/2472555218818786openalex-snapshot
Perspective on Antibacterial Lead Identification Challenges and the Role of Hypothesis-Driven Strategies
inferred← citeshttps://doi.org/10.1186/1471-2105-13-s17-s6openalex-snapshot
Large-scale reverse docking profiles and their applications
inferred← citeshttps://doi.org/10.1186/s13321-015-0059-5openalex-snapshot
Improving protein-ligand binding site prediction accuracy by classification of inner pocket points using local features
inferred← citeshttps://doi.org/10.1208/s12248-012-9426-6openalex-snapshot
Pocket-Based Drug Design: Exploring Pocket Space
inferred← citeshttps://doi.org/10.1248/cpb.c23-00790openalex-snapshot
Development of Drug Discovery Platforms Using Artificial Intelligence and Cheminformatics
inferred← citeshttps://doi.org/10.1371/journal.pone.0137279openalex-snapshot
To Hit or Not to Hit, That Is the Question – Genome-wide Structure-Based Druggability Predictions for Pseudomonas aeruginosa Proteins
inferred← citeshttps://doi.org/10.1371/journal.pone.0186801openalex-snapshot
Novel drug targets in cell wall biosynthesis exploited by gene disruption in Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.15406/mojpb.2017.05.00157openalex-snapshot
Intrinsically Disordered Proteins as Drug Targets
inferred← citeshttps://doi.org/10.2174/1389203720666190417120758openalex-snapshot
Structure-based Druggability Assessment of Anti-virulence Targets from Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.26434/chemrxiv-2022-jjm0jopenalex-snapshot
Uni-Mol: A Universal 3D Molecular Representation Learning Framework
inferred← citeshttps://doi.org/10.26434/chemrxiv-2022-jjm0j-v2openalex-snapshot
Uni-Mol: A Universal 3D Molecular Representation Learning Framework
inferred← citeshttps://doi.org/10.26434/chemrxiv-2022-jjm0j-v3openalex-snapshot
Uni-Mol: A Universal 3D Molecular Representation Learning Framework
inferred← citeshttps://doi.org/10.26434/chemrxiv-2022-jjm0j-v4openalex-snapshot
Uni-Mol: A Universal 3D Molecular Representation Learning Framework
inferred← citeshttps://doi.org/10.26434/chemrxiv.12806819.v1openalex-snapshot
Automatic Cavity Identification and Decomposition into Subpockets with CAVIAR
inferred← citeshttps://doi.org/10.26434/chemrxiv.12806819.v2openalex-snapshot
Automatic Cavity Identification and Decomposition into Subpockets with CAVIAR
inferred← citeshttps://doi.org/10.26434/chemrxiv.13303187openalex-snapshot
DrugPred_RNA – Structure-Based Druggability Predictions for RNA Binding Sites
inferred← citeshttps://doi.org/10.3389/fbinf.2022.958378openalex-snapshot
The druggable genome: Twenty years later
inferred← citeshttps://doi.org/10.3389/fmolb.2022.857000openalex-snapshot
Using Structure-guided Fragment-Based Drug Discovery to Target Pseudomonas aeruginosa Infections in Cystic Fibrosis
inferred← citeshttps://doi.org/10.3389/fphar.2022.870479openalex-snapshot
Probabilistic Pocket Druggability Prediction via One-Class Learning
inferred← citeshttps://doi.org/10.3390/biom12070967openalex-snapshot
CavitySpace: A Database of Potential Ligand Binding Sites in the Human Proteome
inferred← citeshttps://doi.org/10.3390/ijms232012462openalex-snapshot
Estimating the Similarity between Protein Pockets
inferred← citeshttps://doi.org/10.3390/ijms24065819openalex-snapshot
Pharmacological Chaperones and Protein Conformational Diseases: Approaches of Computational Structural Biology
inferred← citeshttps://doi.org/10.3390/ijms26146807openalex-snapshot
Digital Alchemy: The Rise of Machine and Deep Learning in Small-Molecule Drug Discovery
inferred← citeshttps://doi.org/10.3390/pathogens10091172openalex-snapshot
Challenges in Drug Discovery for Intracellular Bacteria
inferred← citeshttps://doi.org/10.3390/ph16020317openalex-snapshot
Computational Chemistry for the Identification of Lead Compounds for Radiotracer Development
inferred← citeshttps://doi.org/10.3390/pharmaceutics15010049openalex-snapshot
A Guide to In Silico Drug Design
inferred← citeshttps://doi.org/10.35537/10915/137336openalex-snapshot
BÚSQUEDA DE NUEVOS FÁRMACOS ANTICHAGÁSICOS INHIBIDORES DE LA TRIPANOTIÓN SINTETASA
inferred← citeshttps://doi.org/10.4155/ebo.13.193openalex-snapshot
Druggability of protein–protein interactions
inferred← citeshttps://doi.org/10.4155/fmc.12.147openalex-snapshot
Chemogenomics In Drug Discovery: Computational Methods Based On The Comparison Of Binding Sites
inferred← citeshttps://doi.org/10.4155/fmc.13.207openalex-snapshot
Reverse Docking: A Powerful Tool for Drug Repositioning and Drug Rescue
inferred← citeshttps://doi.org/10.4155/fmc.14.3openalex-snapshot
Exploiting Structural Information for Drug-Target Assessment
inferred← citeshttps://doi.org/10.5204/thesis.eprints.248736openalex-snapshot
Identification of multi-cancer risk genes
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.