On the public citation graph
Mitogenomics and mitochondrial gene phylogeny decipher the evolution of Saccharomycotina yeasts
0 signed · 140 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known work and none has been retracted — and get a dated CiteStamped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/10.1002/0471250953.bi0604s00openalex-snapshot
Inferring Evolutionary Trees with PAUP *
inferredcites →https://doi.org/10.1002/biot.201800421openalex-snapshot
Yeast Systems Biology: Model Organism and Cell Factory
inferredcites →https://doi.org/10.1002/ece3.6640openalex-snapshot
Genetic hitchhiking, mitonuclear coadaptation, and the origins of mt DNA barcode gaps
inferredcites →https://doi.org/10.1002/iub.146openalex-snapshot
Origin and evolution of the genetic code: The universal enigma
inferredcites →https://doi.org/10.1002/j.1460-2075.1987.tb02767.xopenalex-snapshot
Preferential recombination between GC clusters in yeast mitochondrial DNA.
inferredcites →https://doi.org/10.1002/ps.1236openalex-snapshot
Cytochrome b gene structure and consequences for resistance to Qo inhibitor fungicides in plant pathogens
inferredcites →https://doi.org/10.1002/yea.1034openalex-snapshot
Analysis of the genetic variability in the species of theSaccharomyces sensu strictocomplex
inferredcites →https://doi.org/10.1002/yea.1350openalex-snapshot
Evolution of the genetic code in yeasts
inferredcites →https://doi.org/10.1007/978-1-4939-9173-0_1openalex-snapshot
tRNAscan-SE: Searching for tRNA Genes in Genomic Sequences
inferredcites →https://doi.org/10.1007/978-3-319-61575-2openalex-snapshot
Yeasts in Natural Ecosystems: Ecology
inferredcites →https://doi.org/10.1007/978-3-319-61575-2_1openalex-snapshot
Yeasts as Distinct Life Forms of Fungi
inferredcites →https://doi.org/10.1007/bf00311880openalex-snapshot
The complete mitochondrial DNA sequence of Hansenula wingei reveals new characteristics of yeast mitochondria
inferredcites →https://doi.org/10.1007/bf00329938openalex-snapshot
A yeast with linear molecules of mitochondrial DNA
inferredcites →https://doi.org/10.1007/s00239-006-0284-7openalex-snapshot
The Mechanisms of Codon Reassignments in Mitochondrial Genetic Codes
inferredcites →https://doi.org/10.1007/s00239-015-9686-8openalex-snapshot
Pathways of Genetic Code Evolution in Ancient and Modern Organisms
inferredcites →https://doi.org/10.1007/s00253-018-9350-5openalex-snapshot
Fungal mitochondrial genomes and genetic polymorphisms
inferredcites →https://doi.org/10.1007/s00294-003-0426-zopenalex-snapshot
Mitochondrial genome diversity: evolution of the molecular architecture and replication strategy
inferredcites →https://doi.org/10.1007/s10482-010-9505-6openalex-snapshot
Phylogeny of the ascomycetous yeasts and the renaming of Pichia anomala to Wickerhamomyces anomalus
inferredcites →https://doi.org/10.1016/0378-1119(85)90252-5openalex-snapshot
Sequence organization of the mitochondrial genome of yeast — a review
inferredcites →https://doi.org/10.1016/0378-1119(86)90262-3openalex-snapshot
The GC clusters of the mitochondrial genome of yeast and their evolutionary origin
inferredcites →https://doi.org/10.1016/j.cell.2018.10.023openalex-snapshot
Tempo and Mode of Genome Evolution in the Budding Yeast Subphylum
inferredcites →https://doi.org/10.1016/j.crvi.2011.05.007openalex-snapshot
Yeast cell morphology and sexual reproduction – A short overview and some considerations
inferredcites →https://doi.org/10.1016/j.cub.2004.05.015openalex-snapshot
Evolutionary Genomics: Yeasts Accelerate beyond BLAST
inferredcites →https://doi.org/10.1016/j.fgb.2004.07.003openalex-snapshot
The analysis of the complete mitochondrial genome of Lecanicillium muscarium (synonym Verticillium lecanii) suggests a minimum common gene organization in mtDNAs of Sordariomycetes: phylogenetic implications
inferredcites →https://doi.org/10.1016/j.gene.2008.04.009openalex-snapshot
The complete mitochondrial genome of Fusarium oxysporum: Insights into fungal mitochondrial evolution
inferredcites →https://doi.org/10.1016/j.meegid.2012.12.012openalex-snapshot
Intraspecific comparative genomics of Candida albicans mitochondria reveals non-coding regions under neutral evolution
inferredcites →https://doi.org/10.1016/j.mycres.2008.01.016openalex-snapshot
Mitochondrial gene sequences alone or combined with ITS region sequences provide firm molecular criteria for the classification of Lecanicillium species
inferredcites →https://doi.org/10.1016/j.tig.2003.10.012openalex-snapshot
Mitochondrial genomes: anything goes
inferredcites →https://doi.org/10.1016/j.tig.2006.05.007openalex-snapshot
Yeasts illustrate the molecular mechanisms of eukaryotic genome evolution
inferredcites →https://doi.org/10.1016/j.tig.2007.01.006openalex-snapshot
Mitochondrial introns: a critical view
inferredcites →https://doi.org/10.1016/j.tig.2007.03.008openalex-snapshot
Positive and negative selection on the mitochondrial genome
inferredcites →https://doi.org/10.1016/j.tig.2018.09.008openalex-snapshot
Whole-Genome Duplication and Yeast’s Fruitful Way of Life
inferredcites →https://doi.org/10.1016/j.tim.2010.08.001openalex-snapshot
Mitochondrial inheritance in budding yeasts: towards an integrated understanding
inferredcites →https://doi.org/10.1016/j.ympev.2018.04.037openalex-snapshot
Mt-rps3 is an ancient gene which provides insight into the evolution of fungal mitochondrial genomes
inferredcites →https://doi.org/10.1016/s0005-2728(98)00161-3openalex-snapshot
The mitochondrial genome: structure, transcription, translation and replication
inferredcites →https://doi.org/10.1016/s0014-5793(98)01467-7openalex-snapshot
The complete sequence of the mitochondrial genome of Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1016/s0022-2836(05)80360-2openalex-snapshot
Basic Local Alignment Search Tool
inferredcites →https://doi.org/10.1016/s0168-9525(98)01443-7openalex-snapshot
Linear mitochondrial genomes: 30 years down the line
inferredcites →https://doi.org/10.1016/s0378-1119(99)00270-xopenalex-snapshot
Evolutionary genomics in Metazoa: the mitochondrial DNA as a model system
inferredcites →https://doi.org/10.1017/s0016672300014634openalex-snapshot
The hitch-hiking effect of a favourable gene
inferredcites →https://doi.org/10.1017/s0016672308009579openalex-snapshot
The hitch-hiking effect of a favourable gene
inferredcites →https://doi.org/10.1038/42711openalex-snapshot
Molecular evidence for an ancient duplication of the entire yeast genome
inferredcites →https://doi.org/10.1038/nature02424openalex-snapshot
Proof and evolutionary analysis of ancient genome duplication in the yeast Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1038/nrg814openalex-snapshot
The curious history of yeast mitochondrial DNA
inferredcites →https://doi.org/10.1038/nrm856openalex-snapshot
Mechanisms and functions of eph and ephrin signalling
inferredcites →https://doi.org/10.1038/s41467-018-04374-7openalex-snapshot
Evolutionary instability of CUG-Leu in the genetic code of budding yeasts
inferredcites →https://doi.org/10.1038/s41559-018-0588-1openalex-snapshot
Genomic signatures of mitonuclear coevolution across populations of Tigriopus californicus
inferredcites →https://doi.org/10.1038/s41586-018-0030-5openalex-snapshot
Genome evolution across 1,011 Saccharomyces cerevisiae isolates
inferredcites →https://doi.org/10.1046/j.1365-294x.2003.02063.xopenalex-snapshot
The incomplete natural history of mitochondria
inferredcites →https://doi.org/10.1046/j.1365-2958.1997.5891961.xopenalex-snapshot
The non‐standard genetic code of Candida spp.: an evolving genetic code or a novel mechanism for adaptation?
inferredcites →https://doi.org/10.1080/15476286.2020.1763024openalex-snapshot
Discovery of new group I-D introns leads to creation of subtypes and link to an adaptive response of the mitochondrial genome in fungi
inferredcites →https://doi.org/10.1093/bioinformatics/btg180openalex-snapshot
MrBayes 3: Bayesian phylogenetic inference under mixed models
inferredcites →https://doi.org/10.1093/bioinformatics/bti263openalex-snapshot
ProtTest: selection of best-fit models of protein evolution
inferredcites →https://doi.org/10.1093/bioinformatics/btq003openalex-snapshot
CD-HIT Suite: a web server for clustering and comparing biological sequences
inferredcites →https://doi.org/10.1093/bioinformatics/bts091openalex-snapshot
Unipro UGENE: a unified bioinformatics toolkit
inferredcites →https://doi.org/10.1093/bioinformatics/btu033openalex-snapshot
RAxML version 8: a tool for phylogenetic analysis and post-analysis of large phylogenies
inferredcites →https://doi.org/10.1093/database/baaa062openalex-snapshot
NCBI Taxonomy: a comprehensive update on curation, resources and tools
inferredcites →https://doi.org/10.1093/femsyr/foab051openalex-snapshot
Comparative analysis ofMalassezia furfurmitogenomes and the development of a mitochondria-based typing approach
inferredcites →https://doi.org/10.1093/femsyr/fov023openalex-snapshot
Mitochondrial genome evolution in yeasts: an all-encompassing view
inferredcites →https://doi.org/10.1093/femsyr/foz077openalex-snapshot
The mitochondrial intergenic regions nad1-cob and cob-rps3 as molecular identification tools for pathogenic members of the genus Cryptococcus
inferredcites →https://doi.org/10.1093/gbe/evaa126openalex-snapshot
The Coevolution of Fungal Mitochondrial Introns and Their Homing Endonucleases (GIY-YIG and LAGLIDADG)
inferredcites →https://doi.org/10.1093/gbe/evaa202openalex-snapshot
Evolution of a Record-Setting AT-Rich Genome: Indel Mutation, Recombination, and Substitution Bias
inferredcites →https://doi.org/10.1093/gbe/evx232openalex-snapshot
Genetic Drift and Indel Mutation in the Evolution of Yeast Mitochondrial Genome Size
inferredcites →https://doi.org/10.1093/molbev/msh112openalex-snapshot
A Bayesian Mixture Model for Across-Site Heterogeneities in the Amino-Acid Replacement Process
inferredcites →https://doi.org/10.1093/molbev/msu300openalex-snapshot
IQ-TREE: A Fast and Effective Stochastic Algorithm for Estimating Maximum-Likelihood Phylogenies
inferredcites →https://doi.org/10.1093/molbev/msw054openalex-snapshot
MEGA7: Molecular Evolutionary Genetics Analysis Version 7.0 for Bigger Datasets
inferredcites →https://doi.org/10.1093/molbev/msx116openalex-snapshot
TimeTree: A Resource for Timelines, Timetrees, and Divergence Times
inferredcites →https://doi.org/10.1093/nar/14.13.5125openalex-snapshot
Codon usage in yeast: cluster analysis clearly differentiates highly and lowly expressed genes
inferredcites →https://doi.org/10.1093/nar/22.22.4673openalex-snapshot
CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice
inferredcites →https://doi.org/10.1093/nar/gkg134openalex-snapshot
A comparison of three fission yeast mitochondrial genomes
inferredcites →https://doi.org/10.1093/nar/gkz268openalex-snapshot
The EMBL-EBI search and sequence analysis tools APIs in 2019
inferredcites →https://doi.org/10.1093/sysbio/syv068openalex-snapshot
Fast Dating Using Least-Squares Criteria and Algorithms
inferredcites →https://doi.org/10.1099/mic.0.038646-0openalex-snapshot
The mitochondrial genome of the pathogenic yeast Candida subhashii: GC-rich linear DNA with a protein covalently attached to the 5′ termini
inferredcites →https://doi.org/10.1101/gr.849004openalex-snapshot
WebLogo: A Sequence Logo Generator: Figure 1
inferredcites →https://doi.org/10.1111/1365-2435.12177openalex-snapshot
Mitochondrial DNA : more than an evolutionary bystander
inferredcites →https://doi.org/10.1111/j.1567-1364.2005.00018.xopenalex-snapshot
The mitochondrial genome of the wine yeastHanseniaspora uvarum: a unique genome organization among yeast/fungal counterparts
inferredcites →https://doi.org/10.1111/j.1567-1364.2009.00551.xopenalex-snapshot
Complete mitochondrial genome sequences of threeNakaseomycesspecies reveal invasion by palindromic GC clusters and considerable size expansion
inferredcites →https://doi.org/10.1128/aem.02548-10openalex-snapshot
Deleterious Effect of the Q o Inhibitor Compound Resistance-Conferring Mutation G143A in the Intron-Containing Cytochrome b Gene and Mechanisms for Bypassing It
inferredcites →https://doi.org/10.1128/mbio.01205-18openalex-snapshot
The Genome of the Human Pathogen Candida albicans Is Shaped by Mutation and Cryptic Sexual Recombination
inferredcites →https://doi.org/10.1128/mcb.1.5.387openalex-snapshot
Linear mitochondrial deoxyribonucleic acid from the yeast Hansenula mrakii.
inferredcites →https://doi.org/10.1128/mcb.1.5.387-393.1981openalex-snapshot
Linear Mitochondrial Deoxyribonucleic Acid from the Yeast Hansenula mrakii
inferredcites →https://doi.org/10.1134/s0006297916130046openalex-snapshot
Genomics and biochemistry of Saccharomyces cerevisiae wine yeast strains
inferredcites →https://doi.org/10.1146/annurev.bi.54.070185.005055openalex-snapshot
THE MITOCHONDRIAL ELECTRON TRANSPORT AND OXIDATIVE PHOSPHORYLATION SYSTEM
inferredcites →https://doi.org/10.1146/annurev.genet.33.1.351openalex-snapshot
Mitochondrial Genome Evolution and the Origin of Eukaryotes
inferredcites →https://doi.org/10.1146/annurev.publhealth.23.100901.140546openalex-snapshot
The Importance of the Normality Assumption in Large Public Health Data Sets
inferredcites →https://doi.org/10.1186/1471-2164-13-166openalex-snapshot
Mitochondrial genome evolution in species belonging to the Phialocephala fortinii s.l. - Acephala applanata species complex
inferredcites →https://doi.org/10.1186/s12864-015-1664-4openalex-snapshot
Population structure of mitochondrial genomes in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1186/s12864-017-4116-5openalex-snapshot
Mitochondrial genomes reveal recombination in the presumed asexual Fusarium oxysporum species complex
inferredcites →https://doi.org/10.1186/s12915-020-00786-4openalex-snapshot
Discordant evolution of mitochondrial and nuclear yeast genomes at population level
inferredcites →https://doi.org/10.1371/journal.pbio.1002220openalex-snapshot
Beyond the Whole-Genome Duplication: Phylogenetic Evidence for an Ancient Interspecies Hybridization in the Baker's Yeast Lineage
inferredcites →https://doi.org/10.1371/journal.pbio.1002221openalex-snapshot
Origin of the Yeast Whole-Genome Duplication
inferredcites →https://doi.org/10.1371/journal.pcbi.1008214openalex-snapshot
Galaxy and Apollo as a biologist-friendly interface for high-quality cooperative phage genome annotation
inferredcites →https://doi.org/10.1371/journal.pgen.1007396openalex-snapshot
Adaptive genome duplication affects patterns of molecular evolution in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1371/journal.pgen.1008304openalex-snapshot
Variation and selection on codon usage bias across an entire subphylum
inferredcites →https://doi.org/10.1385/1-59259-192-2:71openalex-snapshot
DNASTAR's Lasergene Sequence Analysis Software
inferredcites →https://doi.org/10.1534/g3.115.017822openalex-snapshot
A Dynamic Mobile DNA Family in the Yeast Mitochondrial Genome
inferredcites →https://doi.org/10.1534/genetics.104.037887openalex-snapshot
A Unified Model of Codon Reassignment in Alternative Genetic Codes
inferredcites →https://doi.org/10.1534/genetics.111.130765openalex-snapshot
Yeast: An Experimental Organism for 21st Century Biology
inferredcites →https://doi.org/10.1534/genetics.114.166637openalex-snapshot
A Genome-Wide Map of Mitochondrial DNA Recombination in Yeast
inferredcites →https://doi.org/10.2144/00286ir01openalex-snapshot
The Sequence Manipulation Suite: JavaScript Programs for Analyzing and Formatting Protein and DNA Sequences
inferredcites →https://doi.org/10.2147/idr.s238002openalex-snapshot
Distribution of Pathogenic Yeasts in Different Clinical Samples: Their Identification, Antifungal Susceptibility Pattern, and Cell Invasion Assays
inferredcites →https://doi.org/10.2741/4525openalex-snapshot
Mitochondrial DNA repair and damage tolerance
inferredcites →https://doi.org/10.3389/fmicb.2018.02079openalex-snapshot
Comparison of the Mitochondrial Genome Sequences of Six Annulohypoxylon stygium Isolates Suggests Short Fragment Insertions as a Potential Factor Leading to Larger Genomic Size
inferredcites →https://doi.org/10.3389/fmicb.2022.806575openalex-snapshot
From Genome Variation to Molecular Mechanisms: What we Have Learned From Yeast Mitochondrial Genomes?
inferredcites →https://doi.org/10.3390/cells10082001openalex-snapshot
Organellar Introns in Fungi, Algae, and Plants
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.3897/imafungus.16.138363zenodo-depositor-declared
Characterisation and comparative analysis of mitochondrial genomes of false, yellow, black and blushing morels provide insights on their structure and evolution
inferred← citeshttps://doi.org/10.3897/imafungus.16.138572zenodo-depositor-declared
Mitochondrial genome and transcription of Shiraia-like species reveal evolutionary aspects in protein-coding genes
inferred← citeshttps://doi.org/10.3897/imafungus.16.141848zenodo-depositor-declared
Comparative mitogenomic analysis reveals variations and evolution of ectomycorrhizal fungal Strobilomyces
inferred← citeshttps://doi.org/10.1007/978-3-031-29199-9_3openalex-snapshot
The Evolution of Mitochondrial Genomes in Fungi
inferred← citeshttps://doi.org/10.1016/j.funbio.2025.101715openalex-snapshot
Comparative analysis of mitochondrial genomes and evolutionary characteristics of five Alternaria species causing potato leaf spot diseases
inferred← citeshttps://doi.org/10.1038/s41467-024-50991-wopenalex-snapshot
Extreme mitochondrial reduction in a novel group of free-living metamonads
inferred← citeshttps://doi.org/10.1038/s41586-025-09205-6openalex-snapshot
The role of metabolism in shaping enzyme structures over 400 million years
inferred← citeshttps://doi.org/10.1038/s41598-023-33486-4openalex-snapshot
Co-evolution of large inverted repeats and G-quadruplex DNA in fungal mitochondria may facilitate mitogenome stability: the case of Malassezia
inferred← citeshttps://doi.org/10.1093/evolut/qpad200openalex-snapshot
The pace of mitochondrial molecular evolution varies with seasonal migration distance
inferred← citeshttps://doi.org/10.1093/g3journal/jkaf162openalex-snapshot
The genome of Chenopodium ficifolium : developing genetic resources and a diploid model system for allotetraploid quinoa
inferred← citeshttps://doi.org/10.1093/gbe/evae281openalex-snapshot
Inferring the Demographic History of Aye-Ayes ( Daubentonia madagascariensis ) from High-Quality, Whole-Genome, Population-Level Data
inferred← citeshttps://doi.org/10.1093/genetics/iyae070openalex-snapshot
UV damage induces production of mitochondrial DNA fragments with specific length profiles
inferred← citeshttps://doi.org/10.1101/2024.04.26.591058openalex-snapshot
Population genomic analysis reveals cryptic population structure in the commercially important Lake Malawi cichlid Copadichromis mloto
inferred← citeshttps://doi.org/10.1101/2024.10.30.616484openalex-snapshot
Contrasting dissemination patterns of diploid cultivated cotton species Gossypium herbaceum L. and G. arboreum L. in Antiquity
inferred← citeshttps://doi.org/10.1101/2025.08.29.673123openalex-snapshot
Mitochondrial genome rearrangements and virulence-associated features in a clinical isolate of the emerging pathogen Wickerhamomyces anomalus
inferred← citeshttps://doi.org/10.1101/2025.10.30.685479openalex-snapshot
Elevated methionine induces DNA hypermethylation of transposable elements in Arabidopsis
inferred← citeshttps://doi.org/10.1101/cshperspect.a041849openalex-snapshot
Hidden Treasures of the Genetic Systems in Yeast Mitochondria
inferred← citeshttps://doi.org/10.1128/mbio.02758-24openalex-snapshot
Frequent genetic exchanges revealed by a pan-mitogenome graph of a fungal plant pathogen
inferred← citeshttps://doi.org/10.1186/s12864-025-11911-4openalex-snapshot
Comparative analysis of mitochondrial genomes in lycoperdaceae fungi reveals intron dynamics and phylogenetic relationships
inferred← citeshttps://doi.org/10.1261/rna.080254.124openalex-snapshot
Mitochondrial mRNA and the small subunit rRNA in budding yeasts undergo 3′-end processing at conserved species-specific elements
inferred← citeshttps://doi.org/10.13057/biodiv/d250213openalex-snapshot
Diversity of fungi and dynamics of ethanol concentration during fermentation of porang (Amorphophallus oncophyllus)
inferred← citeshttps://doi.org/10.3389/fcimb.2025.1576485openalex-snapshot
Uncovering the role of mitochondrial genome in pathogenicity and drug resistance in pathogenic fungi
inferred← citeshttps://doi.org/10.3389/fmicb.2022.821638openalex-snapshot
Mitochondrial Transcription of Entomopathogenic Fungi Reveals Evolutionary Aspects of Mitogenomes
inferred← citeshttps://doi.org/10.3389/fmicb.2023.1268944openalex-snapshot
Mitochondrial genome diversity across the subphylum Saccharomycotina
inferred← citeshttps://doi.org/10.3390/jof12020117openalex-snapshot
Cladobotryum rhodochroum sp. nov. (Hypocreales, Ascomycota): A New Fungicolous Species Revealed by Morphology, Phylogeny, and Comparative Genomics
inferred← citeshttps://doi.org/10.3390/jof12030206openalex-snapshot
Insights into the Phylogeny of Ustilago maydis Strains via Comparative Analysis of Their Respective Mitogenomes
inferred← citeshttps://doi.org/10.3390/jof12030207openalex-snapshot
Phylogenetic Relationships of Five Phallales Species Based on Mitochondrial Genome Analysis
inferred← citeshttps://doi.org/10.3390/jof12100753openalex-snapshot
Nuclear and Mitochondrial Genome Characterization of a Clinical Isolate of the Emerging Pathogen Wickerhamomyces anomalus
inferred← citeshttps://doi.org/10.3390/microorganisms12061052openalex-snapshot
The Identification of the Mitochondrial DNA Polymerase γ (Mip1) of the Entomopathogenic Fungus Metarhizium brunneum
inferred← citeshttps://doi.org/10.64898/2026.01.14.699536openalex-snapshot
Contrasted dissemination patterns of Old-World cottons Gossypium herbaceum L. and G. arboreum L. highlight how wet climate phases determined Levant Cotton domestication and spread
inferred← citeshttps://doi.org/10.64898/2026.02.09.704906openalex-snapshot
The genomic basis of heat stress adaptation in indigenous Ethiopian cattle from arid and hot-humid climates
inferred← citeshttps://doi.org/10.64898/2026.06.15.732456openalex-snapshot
Prediction of Lignocellulose Degradation Potential of Wood Decay Fungi using Comparative Genomic Analysis
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.