On the public citation graph

Cluster-based selection

https://doi.org/10.1007/bf03380181
0 signed · 32 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.
Claim with ORCID
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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1007/bf00123998openalex-snapshot
Enhancing the diversity of a corporate database using chemical database clustering and analysis
inferredcites →https://doi.org/10.1007/s11030-006-2894-9openalex-snapshot
Molecular Diversity and Combinatorial Chemistry
inferredcites →https://doi.org/10.1016/0223-5234(87)90020-1openalex-snapshot
Similarity and clustering in chemical information systems
inferredcites →https://doi.org/10.1021/ci9501047openalex-snapshot
Use of Structure−Activity Data To Compare Structure-Based Clustering Methods and Descriptors for Use in Compound Selection
inferredcites →https://doi.org/10.1021/ci960373copenalex-snapshot
The Information Content of 2D and 3D Structural Descriptors Relevant to Ligand-Receptor Binding
inferredcites →https://doi.org/10.1021/ci960463hopenalex-snapshot
Rapid Quantification of Molecular Diversity for Selective Database Acquisition
inferredcites →https://doi.org/10.1021/jm960290nopenalex-snapshot
Neighborhood Behavior: A Useful Concept for Validation of “Molecular Diversity” Descriptors
inferredcites →https://doi.org/10.1021/jm960291fopenalex-snapshot
Bioisosterism as a Molecular Diversity Descriptor: Steric Fields of Single “Topomeric” Conformers
inferredcites →https://doi.org/10.1109/t-c.1973.223640openalex-snapshot
Clustering Using a Similarity Measure Based on Shared Near Neighbors

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.bmc005openalex-snapshot
Combinatorial Library Design, Molecular Similarity, and Diversity Applications
inferred← citeshttps://doi.org/10.1002/0471433519.ch1openalex-snapshot
Clustering Methods and Their Uses in Computational Chemistry
inferred← citeshttps://doi.org/10.1002/9780470125939.ch1openalex-snapshot
Computer‐Aided Molecular Diversity Analysis and Combinatorial Library Design
inferred← citeshttps://doi.org/10.1002/9783527613106.biblioopenalex-snapshot
Bibliography
inferred← citeshttps://doi.org/10.1002/9783527614141.ch07openalex-snapshot
Computer‐Assisted Library Design
inferred← citeshttps://doi.org/10.1002/minf.201400024openalex-snapshot
The Calculation of Molecular Structural Similarity: Principles and Practice
inferred← citeshttps://doi.org/10.1007/0-306-46873-5openalex-snapshot
Molecular Diversity in Drug Design
inferred← citeshttps://doi.org/10.1007/0-306-46873-5_6openalex-snapshot
Subset-Selection Methods For Chemical Databases
inferred← citeshttps://doi.org/10.1007/978-1-60761-931-4_2openalex-snapshot
Chemoinformatics and Library Design
inferred← citeshttps://doi.org/10.1007/978-3-540-36213-5_1openalex-snapshot
Application of Evolutionary Algorithms to Combinatorial Library Design
inferred← citeshttps://doi.org/10.1016/b0-08-045044-x/00257-1openalex-snapshot
Library Design: Reactant and Product-Based Approaches
inferred← citeshttps://doi.org/10.1016/j.bmc.2012.03.010openalex-snapshot
Combining multiple classifications of chemical structures using consensus clustering
inferred← citeshttps://doi.org/10.1016/s0003-2670(02)00651-7openalex-snapshot
Representative subset selection
inferred← citeshttps://doi.org/10.1016/s0169-7439(99)00010-6openalex-snapshot
Approaches to the design of combinatorial libraries
inferred← citeshttps://doi.org/10.1016/s0958-1669(99)00059-2openalex-snapshot
Chemoinformatics – similarity and diversity in chemical libraries
inferred← citeshttps://doi.org/10.1021/ci020270wopenalex-snapshot
On the Optimal Partitioning of Data with K-Means, Growing K-Means, Neural Gas, and Growing Neural Gas
inferred← citeshttps://doi.org/10.1089/106652799318382openalex-snapshot
Dissimilarity-Based Algorithms for Selecting Structurally Diverse Sets of Compounds
inferred← citeshttps://doi.org/10.1109/cibcb.2006.330958openalex-snapshot
A Fuzzy Kohonen SOM Implementation and Clustering of Bio-active Compound Structures for Drug Discovery
inferred← citeshttps://doi.org/10.1109/mcg.2011.91openalex-snapshot
Real-Time Visualization of Streaming Text with a Force-Based Dynamic System
inferred← citeshttps://doi.org/10.1145/299432.299510openalex-snapshot
Computational analysis of molecular diversity for drug discovery
inferred← citeshttps://doi.org/10.1177/1087057104269570openalex-snapshot
Practical Approaches to Efficient Screening: Information-Rich Screening Protocol
inferred← citeshttps://doi.org/10.3390/ph15091159openalex-snapshot
Deconstructing Markush: Improving the R&D Efficiency Using Library Selection in Early Drug Discovery
inferred← citeshttps://doi.org/10.3929/ethz-a-004447026openalex-snapshot
Development and application of new methods for the virtual screening of chemical databases
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.