On the public citation graph

The making of a branching annelid: an analysis of complete mitochondrial genome and ribosomal data of Ramisyllis multicaudata

https://doi.org/10.1038/srep12072
0 signed · 105 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/10.1007/978-94-017-2887-4_1openalex-snapshot
Reproductive and developmental phenomena in annelids: a source of exemplary research problems
inferredcites →https://doi.org/10.1007/978-94-017-2887-4_3openalex-snapshot
Reproduction of the Syllidae (Annelida: Polychaeta)
inferredcites →https://doi.org/10.1007/bf01215182openalex-snapshot
Patterns of nucleotide composition at fourfold degenerate sites of animal mitochondrial genomes
inferredcites →https://doi.org/10.1007/s13127-014-0183-5openalex-snapshot
Description of a new syllid species as a model for evolutionary research of reproduction and regeneration in annelids
inferredcites →https://doi.org/10.1016/j.mito.2014.05.009openalex-snapshot
GC skew and mitochondrial origins of replication
inferredcites →https://doi.org/10.1016/j.thbio.2005.11.002openalex-snapshot
The proper place of hopeful monsters in evolutionary biology
inferredcites →https://doi.org/10.1016/j.ympev.2010.04.024openalex-snapshot
FASconCAT: Convenient handling of data matrices
inferredcites →https://doi.org/10.1016/j.ympev.2012.03.013openalex-snapshot
Multiple rearrangements in mitochondrial genomes of Isopoda and phylogenetic implications
inferredcites →https://doi.org/10.1016/j.ympev.2012.08.023openalex-snapshot
MITOS: Improved de novo metazoan mitochondrial genome annotation
inferredcites →https://doi.org/10.1016/j.ympev.2013.03.026openalex-snapshot
Mitochondrial genomes to the rescue – Diurodrilidae in the myzostomid trap
inferredcites →https://doi.org/10.1016/j.ympev.2013.05.002openalex-snapshot
A comprehensive analysis of bilaterian mitochondrial genomes and phylogeny
inferredcites →https://doi.org/10.1016/j.ympev.2013.07.003openalex-snapshot
Next-generation sequencing and phylogenetic signal of complete mitochondrial genomes for resolving the evolutionary history of leaf-nosed bats (Phyllostomidae)
inferredcites →https://doi.org/10.1017/s0025315400010079openalex-snapshot
Stolonization in Myrianida
inferredcites →https://doi.org/10.1017/s0025315400038613openalex-snapshot
Variation in Genome Size in Benthic Polychaetes: Systematic and Ecological Relationships
inferredcites →https://doi.org/10.1017/s0025315407054355openalex-snapshot
A new species of Trypanosyllis (Polychaeta: Syllidae) from the Levantine coast of Turkey (eastern Mediterranean)
inferredcites →https://doi.org/10.1017/s0025315408001707openalex-snapshot
A new species ofTrypanosyllis(Polychaeta: Syllidae) from Brazil, with a redescription of Brazilian material ofTrypanosyllis zebra
inferredcites →https://doi.org/10.1023/a:1003719906378openalex-snapshot
Reproductive and developmental phenomena in annelids: a source of exemplary research problems
inferredcites →https://doi.org/10.1023/a:1003732307286openalex-snapshot
Reproduction of the Syllidae (Annelida: Polychaeta)
inferredcites →https://doi.org/10.1080/14772000.2014.992379openalex-snapshot
Indo-Pacific Syllidae (Annelida, Phyllodocida) share an evolutionary history
inferredcites →https://doi.org/10.1086/275581openalex-snapshot
Bifurcated Annelids
inferredcites →https://doi.org/10.1086/278120openalex-snapshot
Collateral Budding in Annelids of the Genus Trypanosyllis
inferredcites →https://doi.org/10.1093/bioinformatics/btm468openalex-snapshot
CREx: inferring genomic rearrangements based on common intervals
inferredcites →https://doi.org/10.1093/bioinformatics/bts174openalex-snapshot
IDBA-UD: a de novo assembler for single-cell and metagenomic sequencing data with highly uneven depth
inferredcites →https://doi.org/10.1093/bioinformatics/btt086openalex-snapshot
QUAST: quality assessment tool for genome assemblies
inferredcites →https://doi.org/10.1093/bioinformatics/btt117openalex-snapshot
freeIbis: an efficient basecaller with calibrated quality scores for Illumina sequencers
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/biosci/biu099openalex-snapshot
Macroevolution of Animal Body Plans: Is There Science after the Tree?
inferredcites →https://doi.org/10.1093/icb/icj051openalex-snapshot
Distribution of segment regeneration ability in the Annelida
inferredcites →https://doi.org/10.1093/molbev/msi008openalex-snapshot
Mitochondrial Genomes of Clymenella torquata (Maldanidae) and Riftia pachyptila (Siboglinidae): Evidence for Conserved Gene Order in Annelida
inferredcites →https://doi.org/10.1093/molbev/msm086openalex-snapshot
Mitochondrial Genome and Nuclear Sequence Data Support Myzostomida As Part of the Annelid Radiation
inferredcites →https://doi.org/10.1093/molbev/mst010openalex-snapshot
MAFFT Multiple Sequence Alignment Software Version 7: Improvements in Performance and Usability
inferredcites →https://doi.org/10.1093/molbev/mst064openalex-snapshot
DAMBE5: A Comprehensive Software Package for Data Analysis in Molecular Biology and Evolution
inferredcites →https://doi.org/10.1093/molbev/msu080openalex-snapshot
Illuminating the Base of the Annelid Tree Using Transcriptomics
inferredcites →https://doi.org/10.1093/nar/gku699openalex-snapshot
leeHom: adaptor trimming and merging for Illumina sequencing reads
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a026241openalex-snapshot
Mitochondrial Genomes of Galathealinum, Helobdella, and Platynereis: Sequence and Gene Arrangement Comparisons Indicate that Pogonophora Is Not a Phylum and Annelida and Arthropoda Are Not Sister Taxa
inferredcites →https://doi.org/10.1101/pdb.prot5448openalex-snapshot
Illumina Sequencing Library Preparation for Highly Multiplexed Target Capture and Sequencing
inferredcites →https://doi.org/10.1111/j.1096-0031.2007.00163.xopenalex-snapshot
Phylogeny of Syllidae (Polychaeta) based on combined molecular analysis of nuclear and mitochondrial genes
inferredcites →https://doi.org/10.1111/j.1096-0031.2011.00377.xopenalex-snapshot
Systematics and evolution of syllids (Annelida, Syllidae)
inferredcites →https://doi.org/10.1111/j.1096-3642.1879.tb02356.xopenalex-snapshot
On a Remarkably Branched Syllis, dredged by H.M.S. ‘Challenger.’
inferredcites →https://doi.org/10.1111/j.1096-3642.2011.00800.xopenalex-snapshot
Branching out: a remarkable new branching syllid (Annelida) living in a Petrosia sponge (Porifera: Demospongiae)
inferredcites →https://doi.org/10.1111/j.1463-6409.2008.00380.xopenalex-snapshot
Phylogeny of Syllidae (Polychaeta) based on morphological data
inferredcites →https://doi.org/10.1111/j.1469-185x.1952.tb01512.xopenalex-snapshot
REGENERATON AND BUDDING IN WORMS
inferredcites →https://doi.org/10.11646/zootaxa.3734.2.4openalex-snapshot
A new species and new record of the commensal genus Alcyonosyllis Glasby & Watson, 2001 and a new species of Parahaplosyllis Hartmann-Schröder, 1990, (Annelida: Syllidae: Syllinae) from Philippines Islands
inferredcites →https://doi.org/10.11646/zootaxa.4019.1.5openalex-snapshot
Syllidae (Annelida: Phyllodocida) from Lizard Island, Great Barrier Reef, Australia
inferredcites →https://doi.org/10.1186/1471-2164-10-27openalex-snapshot
Mitochondrial genome sequence and gene order of Sipunculus nudus give additional support for an inclusion of Sipuncula into Annelida
inferredcites →https://doi.org/10.1186/2041-9139-4-14openalex-snapshot
Expression of Hox genes during regeneration of nereid polychaete Alitta (Nereis) virens (Annelida, Lophotrochozoa)
inferredcites →https://doi.org/10.1186/gb-2014-15-2-r34openalex-snapshot
A multi-split mapping algorithm for circular RNA, splicing, trans-splicing and fusion detection
inferredcites →https://doi.org/10.1242/jcs.s2-58.231.411openalex-snapshot
Stolon Formation in Certain Species of Trypanosyllis
inferredcites →https://doi.org/10.1387/ijdb.140142abopenalex-snapshot
Regeneration in spiralians: evolutionary patterns and developmental processes
inferredcites →https://doi.org/10.1387/ijdb.140148gbopenalex-snapshot
Segment formation in Annelids: patterns, processes and evolution
inferredcites →https://doi.org/10.4159/9780674417922openalex-snapshot
The Structure of Evolutionary Theory
inferredcites →https://doi.org/10.5860/choice.39-6411openalex-snapshot
The structure of evolutionary theory
inferredcites →https://doi.org/10.5860/choice.45-0862openalex-snapshot
The origins of genome architecture

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1007/s13127-021-00538-4zenodo-depositor-declared
Ramisyllis kingghidorahi n. sp., a new branching annelid from Japan
inferred← citeshttps://doi.org/10.11646/zootaxa.4019.1.5zenodo-depositor-declared
Syllidae (Annelida: Phyllodocida) from Lizard Island, Great Barrier Reef, Australia
inferred← citeshttps://doi.org/10.11646/zootaxa.4178.1.5zenodo-depositor-declared
Two new species and new records of the genus Paraopisthosyllis Hartmann-Schröder, 1991 (Annelida: Syllidae) from northeastern Brazil and Philippine Islands
inferred← citeshttps://doi.org/10.11646/zootaxa.5244.4.2zenodo-depositor-declared
Another piece for the syllid puzzle: A new species from Japan and its mitochondrial genome reveal the enigmatic Clavisyllis (Phyllodocida: Syllidae) as a member of Eusyllinae
inferred← citeshttps://doi.org/10.11646/zootaxa.5632.1.3zenodo-depositor-declared
Two new species of Syllidae (Annelida) from Misaki Bay and Sugashima Island, Japan
inferred← citeshttps://doi.org/10.3897/zookeys.1270.177446zenodo-depositor-declared
Partial mitochondrial genome of the enigmatic Bermuda fireworm Odontosyllis enopla Verrill, 1900 (Annelida, Syllidae, Eusyllinae) and its phylogenetic implications
inferred← citeshttps://doi.org/10.1002/jmor.21356openalex-snapshot
Integrative anatomical study of the branched annelid Ramisyllis multicaudata (Annelida, Syllidae)
inferred← citeshttps://doi.org/10.1002/reg2.98openalex-snapshot
Regeneration mechanisms in Syllidae (Annelida)
inferred← citeshttps://doi.org/10.1007/978-3-319-54064-1_10openalex-snapshot
Rare Genomic Changes
inferred← citeshttps://doi.org/10.1007/s12526-020-01046-yopenalex-snapshot
A new species of Syllis Grube, 1850 including transcriptomic data and an updated phylogeny of Syllinae (Annelida: Syllidae)
inferred← citeshttps://doi.org/10.1007/s12526-025-01501-8openalex-snapshot
Mitochondrial genome of Amphiglena cf. mediterranea IV, a small and cryptic polychaete (Annelida: Sabellidae)
inferred← citeshttps://doi.org/10.1007/s13127-016-0265-7openalex-snapshot
Current status of annelid phylogeny
inferred← citeshttps://doi.org/10.1016/j.gene.2016.08.050openalex-snapshot
Syllidae mitochondrial gene order is unusually variable for Annelida
inferred← citeshttps://doi.org/10.1016/j.gene.2016.12.024openalex-snapshot
Mitochondrial genome of the Christmas tree worm Spirobranchus giganteus (Annelida: Serpulidae) reveals a high substitution rate among annelids
inferred← citeshttps://doi.org/10.1016/j.gene.2021.146159openalex-snapshot
First mitochondrial genomes of Chrysopetalidae (Annelida) from shallow-water and deep-sea chemosynthetic environments
inferred← citeshttps://doi.org/10.1016/j.gene.2025.149763openalex-snapshot
Evolution of highly diverse gene orders in mitochondrial genomes of Syllidae (Annelida)
inferred← citeshttps://doi.org/10.1016/j.jcz.2017.07.004openalex-snapshot
Nervous system regeneration in Typosyllis antoni (Annelida: Syllidae)
inferred← citeshttps://doi.org/10.1016/j.margen.2020.100772openalex-snapshot
Sex-specific gene expression differences in reproducing Syllis prolifera and Nudisyllis pulligera (Annelida, Syllidae)
inferred← citeshttps://doi.org/10.1016/j.ympev.2015.08.008openalex-snapshot
Evolution of mitochondrial gene order in Annelida
inferred← citeshttps://doi.org/10.1016/j.ympev.2018.04.002openalex-snapshot
Phylogeny, evolution and mitochondrial gene order rearrangement in scale worms (Aphroditiformia, Annelida)
inferred← citeshttps://doi.org/10.1016/j.ympev.2021.107124openalex-snapshot
Another blow to the conserved gene order in Annelida: Evidence from mitochondrial genomes of the calcareous tubeworm genus Hydroides
inferred← citeshttps://doi.org/10.1017/s002531541700039xopenalex-snapshot
New observations on reproduction in the branching polychaetes Ramisyllis multicaudata and Syllis ramosa (Annelida: Syllidae: Syllinae)
inferred← citeshttps://doi.org/10.1017/s0025315420000119openalex-snapshot
Atypical reproduction in a syllid worm: the stolon ofSyllis rosea(Annelida, Syllidae) takes care of its offspring
inferred← citeshttps://doi.org/10.1038/s41598-017-04094-wopenalex-snapshot
Multiple introns in a deep-sea Annelid (Decemunciger: Ampharetidae) mitochondrial genome
inferred← citeshttps://doi.org/10.1038/s41598-021-89459-yopenalex-snapshot
Morphological convergence and adaptation in cave and pelagic scale worms (Polynoidae, Annelida)
inferred← citeshttps://doi.org/10.1038/s41598-022-08103-5openalex-snapshot
Mitogenome of a stink worm (Annelida: Travisiidae) includes degenerate group II intron that is also found in five congeneric species
inferred← citeshttps://doi.org/10.1038/s41598-023-46358-8openalex-snapshot
Morphological, histological and gene-expression analyses on stolonization in the Japanese Green Syllid, Megasyllis nipponica (Annelida, Syllidae)
inferred← citeshttps://doi.org/10.1071/is17011openalex-snapshot
Phylogenetic relationships and evolution of reproductive modes within flattened syllids (Annelida : Syllidae) with the description of a new genus and six new species
inferred← citeshttps://doi.org/10.1080/23802359.2023.2167480openalex-snapshot
Mitochondrial genome of Leocrates chinensis Kinberg, 1866 (Annelida: Hesionidae)
inferred← citeshttps://doi.org/10.1093/gbe/evad219openalex-snapshot
ORFans in Mitochondrial Genomes of Marine Polychaete Polydora
inferred← citeshttps://doi.org/10.1093/gbe/evv224openalex-snapshot
The Utility of Genome Skimming for Phylogenomic Analyses as Demonstrated for Glycerid Relationships (Annelida, Glyceridae)
inferred← citeshttps://doi.org/10.1093/zoolinnean/zlag120openalex-snapshot
Many branches, one lineage: museomic insights into the diversity and evolution of branching syllid worms
inferred← citeshttps://doi.org/10.1111/brv.12826openalex-snapshot
Monsters reveal patterns: bifurcated annelids and their implications for the study of development and evolution
inferred← citeshttps://doi.org/10.1111/ede.12263openalex-snapshot
Expression of vasa, piwi, and nanos during gametogenesis in Typosyllis antoni (Annelida, Syllidae)
inferred← citeshttps://doi.org/10.1111/zoj.12443openalex-snapshot
Straightening the striped chaos: systematics and evolution of Trypanosyllis and the case of its pseudocryptic type species Trypanosyllis krohnii (Annelida, Syllidae)
inferred← citeshttps://doi.org/10.1134/s0031030123110060openalex-snapshot
An Unusual Body Plan in Bilateria: a Fractal Branching Body
inferred← citeshttps://doi.org/10.1155/2024/9886076openalex-snapshot
Morphology, Phylogeny, and Evolution of the Rarely Known Genus Admetella McIntosh, 1885 (Annelida, Polynoidae) with Recognition of Four New Species from Western Pacific Seamounts
inferred← citeshttps://doi.org/10.1163/18759866-bja10077openalex-snapshot
Insights into the second-known polychaete-asteroid symbiosis, involving a new species of Inermosyllis associated with Luidia maculata
inferred← citeshttps://doi.org/10.1186/s12862-016-0770-5openalex-snapshot
On the role of the proventricle region in reproduction and regeneration in Typosyllis antoni (Annelida: Syllidae)
inferred← citeshttps://doi.org/10.1186/s12862-016-0829-3openalex-snapshot
Monoplacophoran mitochondrial genomes: convergent gene arrangements and little phylogenetic signal
inferred← citeshttps://doi.org/10.1186/s12864-025-11587-wopenalex-snapshot
Sex-specific differential gene expression during stolonization in the branching syllid Ramisyllis kingghidorahi (Annelida, Syllidae)
inferred← citeshttps://doi.org/10.1371/journal.pone.0155441openalex-snapshot
Comparative Mitogenomics of Leeches (Annelida: Clitellata): Genome Conservation and Placobdella-Specific trnD Gene Duplication
inferred← citeshttps://doi.org/10.1371/journal.pone.0214211openalex-snapshot
Species delimitation in Amblyosyllis (Annelida, Syllidae)
inferred← citeshttps://doi.org/10.2108/zs190058openalex-snapshot
Life Cycle of the Japanese Green Syllid, Megasyllis nipponica (Annelida: Syllidae): Field Collection and Establishment of Rearing System
inferred← citeshttps://doi.org/10.3389/fmars.2024.1382212openalex-snapshot
Unraveling the phylogeny of Chaetopteridae (Annelida) through mitochondrial genome analysis
inferred← citeshttps://doi.org/10.3390/biology13120979openalex-snapshot
Phylogenetics of Lepidonotopodini (Macellicephalinae, Polynoidae, Annelida) and Comparative Mitogenomics of Shallow-Water vs. Deep-Sea Scaleworms (Aphroditiformia)
inferred← citeshttps://doi.org/10.3390/cimb47110897openalex-snapshot
A New Species of Macellicephaloides Uschakov, 1955 (Annelida, Polynoidae) from Cold Seeps in the South China Sea: Insights into the Taxonomy and Phylogeny of Macellicephaloides and Related Genera
inferred← citeshttps://doi.org/10.3390/d13030131openalex-snapshot
On the Diversity of Phyllodocida (Annelida: Errantia), with a Focus on Glyceridae, Goniadidae, Nephtyidae, Polynoidae, Sphaerodoridae, Syllidae, and the Holoplanktonic Families
inferred← citeshttps://doi.org/10.7287/peerj.11993v0.1/reviews/1openalex-snapshot
Peer Review #1 of "Who’s who in Magelona: phylogenetic hypotheses under Magelonidae Cunningham & Ramage, 1888 (Annelida: Polychaeta) (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.11993v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Who’s who in Magelona: phylogenetic hypotheses under Magelonidae Cunningham & Ramage, 1888 (Annelida: Polychaeta) (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.11993v0.1/reviews/3openalex-snapshot
Peer Review #3 of "Who’s who in Magelona: phylogenetic hypotheses under Magelonidae Cunningham & Ramage, 1888 (Annelida: Polychaeta) (v0.1)"
inferred← citeshttps://doi.org/10.7717/peerj.11993openalex-snapshot
Who’s who in Magelona: phylogenetic hypotheses under Magelonidae Cunningham & Ramage, 1888 (Annelida: Polychaeta)
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.