On the public citation graph
YuccaschidigeraBark: Phenolic Constituents and Antioxidant Activity
0 signed · 116 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known work and none has been retracted — and get a dated CiteStamped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/10.1007/978-1-4613-0413-5_1openalex-snapshot
Application of Saponins in Foods and Cosmetics: Saponins of Mohave Yucca and Sapindus Mukurossi
inferredcites →https://doi.org/10.1016/0031-9422(93)85492-aopenalex-snapshot
Phenolic compounds in food and their effects on health
inferredcites →https://doi.org/10.1016/0378-8741(94)01206-fopenalex-snapshot
Effects of stilbenes isolated from medicinal plants on arachidonate metabolism and degranulation in human polymorphonuclear leukocytes
inferredcites →https://doi.org/10.1016/0891-5849(94)90202-xopenalex-snapshot
The correlation between active oxygens scavenging and antioxidative effects of flavonoids
inferredcites →https://doi.org/10.1016/s0027-5107(96)00191-1openalex-snapshot
Antimutagenic effect of resveratrol against Trp-P-1
inferredcites →https://doi.org/10.1016/s0040-4039(02)02244-xopenalex-snapshot
A novel phenolic spiro derivative, Yuccaone A, from Yucca schidigera bark
inferredcites →https://doi.org/10.1021/jf00047a015openalex-snapshot
Flavonoids from Vernonia amygdalina and their antioxidant activities
inferredcites →https://doi.org/10.1021/jf980310popenalex-snapshot
Antioxidant Activity of Selected Medicinal Plants
inferredcites →https://doi.org/10.1021/np50100a021openalex-snapshot
Kinase Inhibitors from Polygonum cuspidatum
inferredcites →https://doi.org/10.1021/np970069topenalex-snapshot
Isolation, Synthesis, and Antiplatelet Aggregation Activity of Resveratrol 3-O-β- d -Glucopyranoside and Related Compounds
inferredcites →https://doi.org/10.1021/np9904354openalex-snapshot
Antiyeast Steroidal Saponins fromYucca schidigera(Mohave Yucca), a New Anti-Food-Deteriorating Agent
inferredcites →https://doi.org/10.1111/j.1439-0434.1995.tb00246.xopenalex-snapshot
Production of the Phytoalexin Resveratrol by Grapes as a Response to Botrytis Attack Under Natural Conditions
inferredcites →https://doi.org/10.1111/j.1469-8137.1993.tb03836.xopenalex-snapshot
Resveratrol production as a part of the hypersensitive‐like response of grapevine cells to an elicitor from Trichoderma viride
inferredcites →https://doi.org/10.1126/science.275.5297.218openalex-snapshot
Cancer Chemopreventive Activity of Resveratrol, a Natural Product Derived from Grapes
inferredcites →https://doi.org/10.1126/science.275.5297.221openalex-snapshot
Synaptic Depression and Cortical Gain Control
inferredcites →https://doi.org/10.1128/aem.60.6.1762-1767.1994openalex-snapshot
Influence of Yucca shidigera extract on ruminal ammonia concentrations and ruminal microorganisms
inferredcites →https://doi.org/10.1161/01.atv.19.2.419openalex-snapshot
Resveratrol, a Polyphenolic Compound Found in Wine, Inhibits Tissue Factor Expression in Vascular Cells
inferredcites →https://doi.org/10.5344/ajev.1992.43.1.49openalex-snapshot
Concentration of the Phytoalexin Resveratrol in Wine
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113584zenodo-depositor-declared
Absolute configuration of spiro-flavostilbenoids from Yucca schidigera Roezl ex Ortgies: First indication of (2R)-naringenin as the key building block
inferred← citeshttps://doi.org/10.1002/adsc.201301038openalex-snapshot
Catalytic Asymmetric Synthesis of Chiral Benzofuranones
inferred← citeshttps://doi.org/10.1002/adsc.201801138openalex-snapshot
Direct Oxidative Disulfenylation/Cyclization of 2′‐Hydroxyacetophenones with Thiophenols for the Synthesis of 2,2‐Dithio‐Benzofuran‐3(2 H )‐Ones
inferred← citeshttps://doi.org/10.1002/ange.201601028openalex-snapshot
Asymmetric Conjugate Addition of Benzofuran‐2‐ones to Alkyl 2‐Phthalimidoacrylates: Modeling Structure–Stereoselectivity Relationships with Steric and Electronic Parameters
inferred← citeshttps://doi.org/10.1002/anie.201601028openalex-snapshot
Asymmetric Conjugate Addition of Benzofuran‐2‐ones to Alkyl 2‐Phthalimidoacrylates: Modeling Structure–Stereoselectivity Relationships with Steric and Electronic Parameters
inferred← citeshttps://doi.org/10.1002/asia.201600873openalex-snapshot
A Convenient Palladium‐Catalyzed Carbonylative Synthesis of Benzofuran‐2(3 H)‐ones with Formic Acid as the CO Source
inferred← citeshttps://doi.org/10.1002/asia.202500001openalex-snapshot
Metal‐free Cross‐Dehydrogenative Coupling for α‐Arylation of 3‐Aryloxindoles
inferred← citeshttps://doi.org/10.1002/ejoc.201301686openalex-snapshot
Catalytic Friedel–Crafts/Lactonization Domino Reaction: Facile Access to 3‐Hydroxybenzofuran‐2‐one Scaffold
inferred← citeshttps://doi.org/10.1002/ejoc.201900439openalex-snapshot
Heterocycle Synthesis through Pd‐Catalyzed Carbonylative Coupling
inferred← citeshttps://doi.org/10.1002/hlca.200590232openalex-snapshot
Spiro‐biflavonoids from Larix olgensis Henry var. koreana Nakai
inferred← citeshttps://doi.org/10.1002/jms.688openalex-snapshot
Liquid chromatography/tandem mass spectrometry of unusual phenols from Yucca schidigera bark: comparison with other analytical techniques
inferred← citeshttps://doi.org/10.1007/978-81-322-2163-0_4openalex-snapshot
Natural Sources of Anti-inflammation
inferred← citeshttps://doi.org/10.1007/978-981-32-9147-8_4openalex-snapshot
Plants with Anticancer Potential
inferred← citeshttps://doi.org/10.1007/s11101-005-1234-5openalex-snapshot
Saponins and Phenolics of Yucca schidigera Roezl: Chemistry and Bioactivity
inferred← citeshttps://doi.org/10.1007/s11356-018-3546-1openalex-snapshot
Yucca schidigera can mitigate ammonia emissions from manure and promote poultry health and production
inferred← citeshttps://doi.org/10.1007/s11418-009-0338-4openalex-snapshot
The protective potential of Yucca schidigera (Sarsaponin 30®) against nitrite-induced oxidative stress in rats
inferred← citeshttps://doi.org/10.1016/b978-0-323-91097-2.00006-6openalex-snapshot
Bioactive stilbenes from plants
inferred← citeshttps://doi.org/10.1016/b978-0-7020-3422-0.00019-5openalex-snapshot
Specialized dietary supplements
inferred← citeshttps://doi.org/10.1016/j.anireprosci.2017.06.001openalex-snapshot
Yucca schidigera can promote rabbit growth, fecundity, affect the release of hormones in vivo and in vitro, induce pathological changes in liver, and reduce ovarian resistance to benzene
inferred← citeshttps://doi.org/10.1016/j.bcp.2006.01.021openalex-snapshot
Relative effects of phenolic constituents from Yucca schidigera Roezl. bark on Kaposi's sarcoma cell proliferation, migration, and PAF synthesis
inferred← citeshttps://doi.org/10.1016/j.bjp.2015.12.005openalex-snapshot
Determination of the regulatory properties of Yucca schidigera extracts on the biochemical parameters and plasma hormone levels associated with obesity
inferred← citeshttps://doi.org/10.1016/j.bmc.2012.03.072openalex-snapshot
Inverse Virtual Screening allows the discovery of the biological activity of natural compounds
inferred← citeshttps://doi.org/10.1016/j.bmcl.2019.126943openalex-snapshot
Spirobiflavonoid stereoisomers from the endangered conifer Glyptostrobus pensilis and their protein tyrosine phosphatase 1B inhibitory activity
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2018.03.010openalex-snapshot
Yucca schidigera extract modulates the lead-induced oxidative damage, nephropathy and altered inflammatory response and glucose homeostasis in Japanese quails
inferred← citeshttps://doi.org/10.1016/j.fitote.2011.10.003openalex-snapshot
Iridoid, phenylethanoid and flavonoid glycosides from Sideritis trojana
inferred← citeshttps://doi.org/10.1016/j.fitote.2016.04.009openalex-snapshot
Yuccalides A–C, three new phenolic compounds with spiro-structures from the roots of Yucca gloriosa
inferred← citeshttps://doi.org/10.1016/j.foodchem.2020.126365openalex-snapshot
Origin of the extremely high elasticity of bulk emulsions, stabilized by Yucca Schidigera saponins
inferred← citeshttps://doi.org/10.1016/j.foodchem.2022.132143openalex-snapshot
Why natural antioxidants are readily recognized by biological systems? 3D architecture plays a role!
inferred← citeshttps://doi.org/10.1016/j.foodres.2010.05.013openalex-snapshot
Gelatin-based films containing hydrophobic plasticizers and saponin from Yucca schidigera as the surfactant
inferred← citeshttps://doi.org/10.1016/j.indcrop.2016.01.014openalex-snapshot
Effect of the natural surfactant Yucca schidigera extract on the properties of biodegradable emulsified films produced from soy protein isolate and coconut oil
inferred← citeshttps://doi.org/10.1016/j.indcrop.2022.115706openalex-snapshot
Blue to black: Hypotheses on plant use complexity in traditional dyeing processes in Southeast Asia and China
inferred← citeshttps://doi.org/10.1016/j.jfoodeng.2012.05.031openalex-snapshot
Functional properties of gelatin-based films containing Yucca schidigera extract produced via casting, extrusion and blown extrusion processes: A preliminary study
inferred← citeshttps://doi.org/10.1016/j.jpba.2006.02.018openalex-snapshot
Stability and antioxidant activity of polyphenols in extracts of Myrtus communis L. berries used for the preparation of myrtle liqueur
inferred← citeshttps://doi.org/10.1016/j.jpba.2008.04.011openalex-snapshot
Determination of phenolic compounds in Yucca gloriosa bark and root by LC–MS/MS
inferred← citeshttps://doi.org/10.1016/j.jpba.2011.05.019openalex-snapshot
Strong antioxidant phenolics from Acacia nilotica: Profiling by ESI-MS and qualitative–quantitative determination by LC–ESI-MS
inferred← citeshttps://doi.org/10.1016/j.jpba.2012.09.014openalex-snapshot
LC–ESI-MS quali-quantitative determination of phenolic constituents in different parts of wild and cultivated Astragalus gombiformis
inferred← citeshttps://doi.org/10.1016/j.prmcm.2024.100451openalex-snapshot
Computational investigation of Y. aloifolia variegate as anti-Human Immunodeficiency Virus (HIV) targeting HIV-1 protease: A multiscale in-silico exploration
inferred← citeshttps://doi.org/10.1016/j.tet.2006.10.034openalex-snapshot
Gloriosaols A and B, two novel phenolics from Yucca gloriosa: structural characterization and configurational assignment by a combined NMR-quantum mechanical strategy
inferred← citeshttps://doi.org/10.1016/j.tetasy.2015.10.010openalex-snapshot
Ruthenium–Me-BIPAM-catalyzed addition reaction of aryl-boronic acids to benzofuran-2,3-diones for the enantioselective synthesis of 3-aryl-3-hydroxybenzofuran-2-ones
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.04.111openalex-snapshot
Enantioselective synthesis of spirocyclic tetrahydrothiophene derivatives bearing a benzofuran-3(2H)-one scaffold. Unusual supramolecular crystal structure with high Z′
inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.151059openalex-snapshot
First total synthesis of rhuscholide A, glabralide B and denudalide
inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.151396openalex-snapshot
Cobalt-catalyzed C H activation/C O formation: Synthesis of benzofuranones
inferred← citeshttps://doi.org/10.1016/j.tvjl.2007.06.004openalex-snapshot
Some commonly fed herbs and other functional foods in equine nutrition: A review
inferred← citeshttps://doi.org/10.1021/acs.joc.8b01774openalex-snapshot
Organocatalytic Aza-Friedel–Crafts/Lactonization Domino Reaction of Naphthols and Phenols with 2-Acetamidoacrylate to Naphtho- and Benzofuranones Bearing a Quaternary Center at the C3 Position
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c03014openalex-snapshot
Asymmetric Synthesis of Benzofuranones with a C3 Quaternary Center via an Addition/Cyclization Cascade Using Noncovalent N-Heterocyclic Carbene Catalysis
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c04342openalex-snapshot
Catalytic Asymmetric Desymmetrizing [4+2] Cycloaddition/Base-Mediated Oxidative Aromatization Sequence: De Novo Synthesis of Isobenzofuranone-Embedded Chiral Arenes
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b02440openalex-snapshot
Catalytic Asymmetric Synthesis of 3-Hydroxy-3-trifluoromethyl Benzofuranones via Tandem Friedel–Crafts/Lactonization Reaction
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b00163openalex-snapshot
Amination of 3-Substituted Benzofuran-2(3H)-ones Triggered by Single-Electron Transfer
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b01482openalex-snapshot
Phosphine-Catalyzed Domino β/γ-Additions of Benzofuranones with Allenoates: A Method for Unsymmetrical 3,3-Disubstituted Benzofuranones
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b01755openalex-snapshot
Cu-Catalyzed Cross-Dehydrogenative Coupling of Heteroaryl C(sp2)–H and Tertiary C(sp3)–H Bonds for the Construction of All-Carbon Triaryl Quaternary Centers
inferred← citeshttps://doi.org/10.1021/acscatal.9b00091openalex-snapshot
Palladium-Catalyzed Chemoselective Activation of sp 3 vs sp 2 C–H Bonds: Oxidative Coupling To Form Quaternary Centers
inferred← citeshttps://doi.org/10.1021/jf0479867openalex-snapshot
Phenylpropanoid Glycosides from Tynanthus panurensis: Characterization and LC-MS Quantitative Analysis
inferred← citeshttps://doi.org/10.1021/jf071131nopenalex-snapshot
Yucca gloriosa: A Source of Phenolic Derivatives with Strong Antioxidant Activity
inferred← citeshttps://doi.org/10.1021/jf801289mopenalex-snapshot
Influence of Phenolic Constituents from Yucca schidigera Bark on Arachidonate Metabolism in Vitro
inferred← citeshttps://doi.org/10.1021/jo300395xopenalex-snapshot
Metal-Free Tandem Friedel–Crafts/Lactonization Reaction to Benzofuranones Bearing a Quaternary Center at C3 Position
inferred← citeshttps://doi.org/10.1021/np200604kopenalex-snapshot
HPLC-ESIMSn Profiling, Isolation, Structural Elucidation, and Evaluation of the Antioxidant Potential of Phenolics from Paepalanthus geniculatus
inferred← citeshttps://doi.org/10.1021/ol303569bopenalex-snapshot
Direct Lactonization of 2-Arylacetic Acids through Pd(II)-Catalyzed C–H Activation/C–O Formation
inferred← citeshttps://doi.org/10.1021/ol401087aopenalex-snapshot
Asymmetric Construction of Spirocyclopentenebenzofuranone Core Structures via Highly Selective Phosphine-Catalyzed [3 + 2] Cycloaddition Reactions
inferred← citeshttps://doi.org/10.1039/c2np20049jopenalex-snapshot
Natural stilbenoids: distribution in the plant kingdom and chemotaxonomic interest in Vitaceae
inferred← citeshttps://doi.org/10.1039/c6ob02782bopenalex-snapshot
Palladium-catalyzed carbonylative synthesis of benzofuran-2(3H)-ones from 2-hydroxybenzyl alcohols using formic acid as the CO source
inferred← citeshttps://doi.org/10.1039/d1ra01170gopenalex-snapshot
Spirocyclic derivatives as antioxidants: a review
inferred← citeshttps://doi.org/10.1039/d2ra06231copenalex-snapshot
DTBP-mediated cross-dehydrogenative coupling of 3-aryl benzofuran-2(3 H )-ones with toluenes/phenols for all-carbon quaternary centers
inferred← citeshttps://doi.org/10.1039/d3ob00126aopenalex-snapshot
Asymmetric synthesis of spirocyclic isobenzofuranones via a squaramide-catalysed sulfa-Michael desymmetrisation reaction
inferred← citeshttps://doi.org/10.1039/d4qo01641fopenalex-snapshot
Modular dehydrogenative cross-nucleophile coupling for direct construction of tetrasubstituted carbons
inferred← citeshttps://doi.org/10.1080/00397911.2016.1226341openalex-snapshot
SbCl3-catalyzed solvent-free Friedel–Crafts reaction of phenols with mandelic acids to 3-aryl benzofuran-2(3H)-ones: Synthesis of spirocyclic 2,3-dihydrobenzofuran-2-ones
inferred← citeshttps://doi.org/10.1080/10826076.2016.1234393openalex-snapshot
TLC fingerprint of phenolics and saponins in commercial extracts of Yucca schidigera Roezl.
inferred← citeshttps://doi.org/10.1080/14786419.2025.2592901openalex-snapshot
Yucca schidigera Roezl ex ortgies (Mojave yucca): an updated review of its phytochemistry, ethnopharmacological, and pharmacological properties
inferred← citeshttps://doi.org/10.1080/1828051x.2017.1302826openalex-snapshot
Dietary Yucca schidigera extract improved growth performance and liver antioxidative function in broilers
inferred← citeshttps://doi.org/10.1093/aob/mci123openalex-snapshot
Proposed Criteria for Assessing the Efficacy of Cancer Reduction by Plant Foods Enriched in Carotenoids, Glucosinolates, Polyphenols and Selenocompounds
inferred← citeshttps://doi.org/10.1111/j.1365-3059.2011.02517.xopenalex-snapshot
Yucca schidigera extract: a potential biofungicide against seedborne pathogens of sorghum
inferred← citeshttps://doi.org/10.1111/jpn.13067openalex-snapshot
Effects of Yucca schidigera extract on growth performance and antioxidative function of small intestine in broilers
inferred← citeshttps://doi.org/10.1177/0748233712446730openalex-snapshot
Dietary Yucca schidigera supplementation reduces arsenic-induced oxidative stress in Swiss albino mice
inferred← citeshttps://doi.org/10.1186/1476-9255-3-6openalex-snapshot
Anti-inflammatory and anti-arthritic effects of yucca schidigera: A review
inferred← citeshttps://doi.org/10.1201/9781420026474.ch19openalex-snapshot
Resveratrol as an Antifungal Agent
inferred← citeshttps://doi.org/10.1501/vetfak_0000000319openalex-snapshot
Effect of Yucca schidigera extract on blood pressure, antioxidant activity and some blood parameters in the L-name-induced hypertensive rats
inferred← citeshttps://doi.org/10.1515/jvetres-2016-0015openalex-snapshot
Effect of sodium butyrate and Yucca schidigera extract on bone characteristics in growing pigs
inferred← citeshttps://doi.org/10.1590/1678-4324-2016150035openalex-snapshot
Effects of Yucca Extract on Feed Efficiency, Immune and Antioxidative Functions in Broilers
inferred← citeshttps://doi.org/10.17094/avbd.17163openalex-snapshot
Saponinlerin Hayvan Beslemede Yem Katkı Maddesi Olarak Kullanımı
inferred← citeshttps://doi.org/10.20517/cs.2022.38openalex-snapshot
Recent advances in organocatalytic cascade reactions for enantioselective synthesis of chiral spirolactone skeletons
inferred← citeshttps://doi.org/10.2478/fv-2018-0038openalex-snapshot
Mojave Yucca ( Yucca Schidigera Roezl) Effects on Female Reproduction a Review
inferred← citeshttps://doi.org/10.3168/jds.2020-18980openalex-snapshot
Supplementation with Yucca schidigera improves antioxidant capability and immune function and decreases fecal score of dairy calves before weaning
inferred← citeshttps://doi.org/10.3389/fvets.2022.1077555openalex-snapshot
Effects of Yucca schidigera extract on serum biochemical parameters, humoral immune response, and intestinal health in young pigeons
inferred← citeshttps://doi.org/10.3390/ani11010093openalex-snapshot
Yucca schidigera Usage for Healthy Aquatic Animals: Potential Roles for Sustainability
inferred← citeshttps://doi.org/10.3390/ani13040755openalex-snapshot
Effects of Different Levels of Yucca Supplementation on Growth Rates, Metabolic Profiles, Fecal Odor Emissions, and Carcass Traits of Growing Lambs
inferred← citeshttps://doi.org/10.3390/ani14233356openalex-snapshot
Effects of Yucca Extract on Nutrient Digestibility, Antioxidant Status, Estrus and Faecal Microorganism in Gilts
inferred← citeshttps://doi.org/10.3390/ani16193020openalex-snapshot
Rumen Microbiota and Metabolome Reveal the Effects of Yucca schidigera Extract on Growth Performance and Serum Immune Parameters in Fattening Goats
inferred← citeshttps://doi.org/10.3390/antiox12030574openalex-snapshot
Antioxidant and Anti-Inflammatory Properties of Phytochemicals Found in the Yucca Genus
inferred← citeshttps://doi.org/10.3390/molecules23040710openalex-snapshot
Synthesis of Benzofuran-2-One Derivatives and Evaluation of Their Antioxidant Capacity by Comparing DPPH Assay and Cyclic Voltammetry
inferred← citeshttps://doi.org/10.3390/molecules24224162openalex-snapshot
Yuccalechins A–C from the Yucca schidigera Roezl ex Ortgies Bark: Elucidation of the Relative and Absolute Configurations of Three New Spirobiflavonoids and Their Cholinesterase Inhibitory Activities
inferred← citeshttps://doi.org/10.3390/molecules27123692openalex-snapshot
Neuroprotective Effect of Yucca schidigera Roezl ex Ortgies Bark Phenolic Fractions, Yuccaol B and Gloriosaol A on Scopolamine-Induced Memory Deficits in Zebrafish
inferred← citeshttps://doi.org/10.3390/molecules28145420openalex-snapshot
Spiro-Flavonoids in Nature: A Critical Review of Structural Diversity and Bioactivity
inferred← citeshttps://doi.org/10.3390/nu9091044openalex-snapshot
Polyphenols from Root, Tubercles and Grains Cropped in Brazil: Chemical and Nutritional Characterization and Their Effects on Human Health and Diseases
inferred← citeshttps://doi.org/10.3390/plants12020274openalex-snapshot
Use of Yucca (Yucca schidigera) Extracts as Biostimulants to Promote Germination and Early Vigor and as Natural Fungicides
inferred← citeshttps://doi.org/10.3906/vet-1504-92openalex-snapshot
The effect of Yucca schidigera powder added to lamb feed on fatteningperformance, some blood parameters, the immune system, and theantioxidative metabolism of the hepatic tissue
inferred← citeshttps://doi.org/10.4322/polimeros.2013.005openalex-snapshot
Effect of the addition of soy lecithin and Yucca schidigera extract on the properties of gelatin and glycerol based biodegradable films.
inferred← citeshttps://doi.org/10.52976/vansaglik.1028378openalex-snapshot
Saponin Bileşeninin Biyolojik Aktiviteleri, Kullanım Alanları ve Etkileri
inferred← citeshttps://doi.org/10.70675/8655bd8ez8b02z489fzbcc0zecc43a4428e9openalex-snapshot
Development and characterisation of starch and polyphenols for functional enhancement in high value food products from lontan vegetables
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.