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The big potential of the small frog Eleutherodactylus coqui
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1097-010x(19981215)282:6<669::aid-jez3>3.0.co;2-dopenalex-snapshot
Apical ectodermal ridge in retrospect
inferredcites →https://doi.org/10.1002/dvdy.21153openalex-snapshot
Nutritional endoderm in a direct developing frog: A potential parallel to the evolution of the amniote egg
inferredcites →https://doi.org/10.1002/jez.1136openalex-snapshot
Limb development in a “nonmodel” vertebrate, the direct‐developing frog Eleutherodactylus coqui
inferredcites →https://doi.org/10.1002/jez.1401080304openalex-snapshot
The proximo‐distal sequence of origin of the parts of the chick wing and the role of the ectoderm
inferredcites →https://doi.org/10.1002/jez.1402700209openalex-snapshot
Leg development in a frog without a tadpole (Eleutherodactylus coqui)
inferredcites →https://doi.org/10.1002/jez.b.21218openalex-snapshot
Nutritional endoderm: a way to breach the holoblastic–meroblastic barrier in tetrapods
inferredcites →https://doi.org/10.1002/jmor.10246openalex-snapshot
Development of the nasal chemosensory organs in two terrestrial anurans: The directly developing frog, Eleutherodactylus coqui (Anura: Leptodactylidae), and the metamorphosing toad, Bufo americanus (Anura: Bufonidae)
inferredcites →https://doi.org/10.1002/jmor.1052110111openalex-snapshot
Cranial ontogeny in the direct‐developing frog, Eleutherodactylus coqui (anura: Leptodactylidae), analyzed using whole‐mount immunohistochemistry
inferredcites →https://doi.org/10.1002/jmor.20223openalex-snapshot
Cranial muscle development in frogs with different developmental modes: Direct development versus biphasic development
inferredcites →https://doi.org/10.1002/sce.20338openalex-snapshot
Rethinking trends in minority participation in the sciences
inferredcites →https://doi.org/10.1006/dbio.1998.9078openalex-snapshot
Evolutionary Alteration in Anterior Patterning:otx2Expression in the Direct Developing FrogEleutherodactylus coqui
inferredcites →https://doi.org/10.1006/dbio.1999.9404openalex-snapshot
Loss of Ectodermal Competence for Lateral Line Placode Formation in the Direct Developing Frog Eleutherodactylus coqui
inferredcites →https://doi.org/10.1006/dbio.2001.0310openalex-snapshot
Mesoderm Formation in Eleutherodactylus coqui: Body Patterning in a Frog with a Large Egg
inferredcites →https://doi.org/10.1007/978-1-4615-6983-1_7openalex-snapshot
Developmental Evidence for Amphibian Origins
inferredcites →https://doi.org/10.1007/bf00194575openalex-snapshot
Diversity of form in the amphibian papilla of Puerto Rican frogs
inferredcites →https://doi.org/10.1007/bf00300859openalex-snapshot
The costs of male parental care and its evolution in a neotropical frog
inferredcites →https://doi.org/10.1007/bf00611921openalex-snapshot
Communicative significance of the two-note call of the treefrogEleutherodactylus coqui
inferredcites →https://doi.org/10.1007/bf01131168openalex-snapshot
Hearing through the lungs: Lung-eardrum transmission of sound in the frogEleutherodactylus coqui
inferredcites →https://doi.org/10.1007/pl00008184openalex-snapshot
Ectopic expression of Xenopus noggin RNA induces complete secondary body axes in embryos of the direct developing frog Eleutherodactylus coqui
inferredcites →https://doi.org/10.1007/s004270050203openalex-snapshot
Secondary coverage of the yolk by the body wall in the direct developing frog, Eleutherodactylus coqui: an unusual process for amphibian embryos
inferredcites →https://doi.org/10.1007/s00429-002-0291-4openalex-snapshot
Mosaic evolution of neural development in anurans: acceleration of spinal cord development in the direct developing frog Eleutherodactylus coqui
inferredcites →https://doi.org/10.1007/s10530-011-0127-3openalex-snapshot
Coqui frog invasions change invertebrate communities in Hawaii
inferredcites →https://doi.org/10.1007/s11218-019-09538-xopenalex-snapshot
Why are there so few ethnic minorities in ecology and evolutionary biology? Challenges to inclusion and the role of sense of belonging
inferredcites →https://doi.org/10.1016/0018-506x(87)90034-1openalex-snapshot
Plasma androgen levels during male parental care in a tropical frog (Eleutherodactylus)
inferredcites →https://doi.org/10.1016/b978-0-12-385979-2.00009-5openalex-snapshot
Metamorphosis in a Frog That Does Not Have a Tadpole
inferredcites →https://doi.org/10.1016/j.bbr.2008.05.001openalex-snapshot
Serotonin modulates vocalizations and territorial behavior in an amphibian
inferredcites →https://doi.org/10.1016/j.biocon.2005.07.004openalex-snapshot
Infection of an invasive frog Eleutherodactylus coqui by the chytrid fungus Batrachochytrium dendrobatidis in Hawaii
inferredcites →https://doi.org/10.1016/j.biocon.2014.09.044openalex-snapshot
A social–ecological systems approach to non-native species: Habituation and its effect on management of coqui frogs in Hawaii
inferredcites →https://doi.org/10.1016/j.ijppaw.2016.12.001openalex-snapshot
The things they carried: The pathogenic effects of old and new parasites following the intercontinental invasion of the Australian cane toad (Rhinella marina)
inferredcites →https://doi.org/10.1016/j.neulet.2012.07.058openalex-snapshot
Arginine vasotocin activates aggressive calls during paternal care in the Puerto Rican coquí frog, Eleutherodactylus coqui
inferredcites →https://doi.org/10.1016/j.neuron.2021.02.002openalex-snapshot
Expanding evolutionary neuroscience: insights from comparing variation in behavior
inferredcites →https://doi.org/10.1016/j.pbb.2020.173068openalex-snapshot
Serotonin and vasotocin function in territoriality
inferredcites →https://doi.org/10.1016/j.physbeh.2017.06.020openalex-snapshot
Mammalian nonapeptides activate territorial behavior in an amphibian
inferredcites →https://doi.org/10.1016/j.psyneuen.2012.12.005openalex-snapshot
Deconstructing sociality, social evolution and relevant nonapeptide functions
inferredcites →https://doi.org/10.1016/j.ygcen.2010.09.009openalex-snapshot
Corticotropin-releasing factor regulates the development in the direct developing frog, Eleutherodactylus coqui
inferredcites →https://doi.org/10.1016/j.ygcen.2015.01.029openalex-snapshot
Development of neuroendocrine components of the thyroid axis in the direct-developing frog Eleutherodactylus coqui: Formation of the median eminence and onset of pituitary TSH production
inferredcites →https://doi.org/10.1016/j.ympev.2005.03.006openalex-snapshot
Cenozoic biogeography and evolution in direct-developing frogs of Central America (Leptodactylidae: Eleutherodactylus) as inferred from a phylogenetic analysis of nuclear and mitochondrial genes
inferredcites →https://doi.org/10.1016/j.ympev.2007.06.025openalex-snapshot
Phylogenetic Study of Eleutherodactylus Coqui (Anura: Leptodactylidae) Reveals Deep Genetic Fragmentation in Puerto Rico and Origins in Hawaii
inferredcites →https://doi.org/10.1016/s0003-3472(84)80278-xopenalex-snapshot
Male parental care and its adaptive significance in a neotropical frog
inferredcites →https://doi.org/10.1016/s0079-6123(08)00401-9openalex-snapshot
Nonapeptides and the evolutionary patterning of sociality
inferredcites →https://doi.org/10.1016/s0304-3940(97)00174-2openalex-snapshot
Development of the retina is altered in the directly developing frog Eleutherodactylus coqui (Leptodactylidae)
inferredcites →https://doi.org/10.1016/s0925-4773(98)00226-3openalex-snapshot
Rearranging gastrulation in the name of yolk: evolution of gastrulation in yolk-rich amniote eggs
inferredcites →https://doi.org/10.1023/a:1020909205908openalex-snapshot
Human-mediated Escalation of a Formerly Eradicable Problem: The Invasion of Caribbean Frogs in the Hawaiian Islands
inferredcites →https://doi.org/10.1037/e558442013-001openalex-snapshot
Women, Minorities, and Persons with Disabilities in Science and Engineering: 2013
inferredcites →https://doi.org/10.1038/nature13307openalex-snapshot
Galanin neurons in the medial preoptic area govern parental behaviour
inferredcites →https://doi.org/10.1038/s41467-019-12608-5openalex-snapshot
The evolution of parental care diversity in amphibians
inferredcites →https://doi.org/10.1046/j.1469-7580.1998.19230379.xopenalex-snapshot
Limb development and evolution: a frog embryo with no apical ectodermal ridge (AER)
inferredcites →https://doi.org/10.1046/j.1525-142x.2003.03061.xopenalex-snapshot
Localization of RNAs in oocytes of Eleutherodactylus coqui, a direct developing frog, differs from Xenopus laevis
inferredcites →https://doi.org/10.1073/pnas.050501097openalex-snapshot
Thyroid hormone-dependent metamorphosis in a direct developing frog
inferredcites →https://doi.org/10.1073/pnas.0611051104openalex-snapshot
Major Caribbean and Central American frog faunas originated by ancient oceanic dispersal
inferredcites →https://doi.org/10.1073/pnas.2100765118openalex-snapshot
The evolution of targeted cannibalism and cannibal-induced defenses in invasive populations of cane toads
inferredcites →https://doi.org/10.1073/pnas.85.5.1508openalex-snapshot
Accessory pathway for sound transfer in a neotropical frog.
inferredcites →https://doi.org/10.1086/655116openalex-snapshot
The Ecological Impact of Invasive Cane Toads (Bufo Marinus) in Australia
inferredcites →https://doi.org/10.1093/beheco/9.1.1openalex-snapshot
Amphisexual parental behavior of a terrestrial breeding frog Eleutherodactylus johnstonei in Guyana
inferredcites →https://doi.org/10.1093/molbev/msv037openalex-snapshot
Tree of Life Reveals Clock-Like Speciation and Diversification
inferredcites →https://doi.org/10.1093/sysbio/syu042openalex-snapshot
Biogeographic Analysis Reveals Ancient Continental Vicariance and Recent Oceanic Dispersal in Amphibians
inferredcites →https://doi.org/10.1098/rsbl.2009.0763openalex-snapshot
Frequency matching of vocalizations to inner-ear sensitivity along an altitudinal gradient in the coqui frog
inferredcites →https://doi.org/10.1098/rsbl.2017.0317openalex-snapshot
Behavioural tuning in a tropical amphibian along an altitudinal gradient
inferredcites →https://doi.org/10.1098/rsbl.2019.0947openalex-snapshot
The earliest record of Caribbean frogs: a fossil coquí from Puerto Rico
inferredcites →https://doi.org/10.1098/rspb.1997.0187openalex-snapshot
Jaw muscle development as evidence for embryonic repatterning in direct–developing frogs
inferredcites →https://doi.org/10.1098/rspb.2018.2737openalex-snapshot
Parental care and the evolution of terrestriality in frogs
inferredcites →https://doi.org/10.1111/bij.12623openalex-snapshot
Stress and immunity at the invasion front: a comparison across cane toad (Rhinella marina) populations
inferredcites →https://doi.org/10.1111/j.1366-9516.2005.00178.xopenalex-snapshot
Potential consequences of the coqui frog invasion in Hawaii
inferredcites →https://doi.org/10.1111/j.1439-0469.1987.tb00913.xopenalex-snapshot
Evolution of parental care in dart poison frogs (Amphibia: Anura: Dendrobatidae)
inferredcites →https://doi.org/10.1111/j.1525-142x.2008.00255.xopenalex-snapshot
Gene expression reveals unique skeletal patterning in the limb of the direct‐developing frog, Eleutherodactylus coqui
inferredcites →https://doi.org/10.1111/j.1525-142x.2010.00424.xopenalex-snapshot
Early cranial patterning in the direct‐developing frog Eleutherodactylus coqui revealed through gene expression
inferredcites →https://doi.org/10.1111/j.1525-142x.2011.00500.xopenalex-snapshot
Molecular anatomy of the developing limb in the coquí frog, E leutherodactylus coqui
inferredcites →https://doi.org/10.1111/j.1558-5646.2012.01715.xopenalex-snapshot
PHYLOGENETIC ANALYSES REVEAL UNEXPECTED PATTERNS IN THE EVOLUTION OF REPRODUCTIVE MODES IN FROGS
inferredcites →https://doi.org/10.1111/jbi.12146openalex-snapshot
Human‐facilitated jump dispersal of a non‐native frog species on Hawai'i Island
inferredcites →https://doi.org/10.1111/mec.13184openalex-snapshot
A genetic perspective on rapid evolution in cane toads (Rhinella marina)
inferredcites →https://doi.org/10.1126/science.1257772openalex-snapshot
Sexual Differences in the Auditory System of the Tree Frog Eleutherodactylus coqui
inferredcites →https://doi.org/10.1126/science.221.4610.570openalex-snapshot
Population Density of Tropical Forest Frogs: Relation to Retreat Sites
inferredcites →https://doi.org/10.1126/science.6894203openalex-snapshot
Internal Fertilization in an Oviparous Frog
inferredcites →https://doi.org/10.1146/annurev.ecolsys.30.1.133openalex-snapshot
Global Amphibian Declines: A Problem in Applied Ecology
inferredcites →https://doi.org/10.1159/000147725openalex-snapshot
Early Cranial Neural Crest Migration in the Direct-Developing Frog, Eleutherodactylus coqui
inferredcites →https://doi.org/10.11606/issn.2316-9079.v18i1p101-107openalex-snapshot
Distribution and invasion progress of Eleutherodactylus coqui (Anura: Eleutherodactylidae) introduced in Costa Rica
inferredcites →https://doi.org/10.11646/zootaxa.1737.1.1openalex-snapshot
New World direct-developing frogs (Anura: Terrarana): Molecular phylogeny, classification, biogeography, and conservation
inferredcites →https://doi.org/10.11646/zootaxa.2211.1.1openalex-snapshot
A new frog family (Anura: Terrarana) from South America and an expanded direct-developing clade revealed by molecular phylogeny
inferredcites →https://doi.org/10.1177/1538192720968276openalex-snapshot
Latinx Students Charting Their Own STEM Pathways: How Community Cultural Wealth Informs Their STEM Identities
inferredcites →https://doi.org/10.1186/2041-9139-2-20openalex-snapshot
Germ plasm in Eleutherodactylus coqui, a direct developing frog with large eggs
inferredcites →https://doi.org/10.1201/9781482280074openalex-snapshot
Reproductive Biology and Phylogeny of Anura
inferredcites →https://doi.org/10.1206/0003-0082(2002)357<0001:fotebg>2.0.co;2openalex-snapshot
Frogs of the Eleutherodactylus biporcatus Group (Leptodactylidae) of Central America and Northern South America, Including Rediscovered, Resurrected, and New Taxa
inferredcites →https://doi.org/10.1242/dev.26.2.169openalex-snapshot
Early limb development of Xenopus laevis
inferredcites →https://doi.org/10.1242/jeb.143859openalex-snapshot
Modification of feeding circuits in the evolution of social behavior
inferredcites →https://doi.org/10.1371/journal.pbio.2002079openalex-snapshot
Less fear, more diversity
inferredcites →https://doi.org/10.1504/ier.2006.053951openalex-snapshot
Economic impacts of E. Coqui frogs in Hawaii
inferredcites →https://doi.org/10.1525/9780520948433openalex-snapshot
Encyclopedia of Biological Invasions
inferredcites →https://doi.org/10.1643/0045-8511(2007)7[281:dotife]2.0.co;2openalex-snapshot
Diet of the Invasive Frog, Eleutherodactylus Coqui, in Hawaii
inferredcites →https://doi.org/10.1643/cg-06-092openalex-snapshot
Spatial and Temporal Variation in Color Pattern Morphology in the Tropical Frog, Eleutherodactylus coqui
inferredcites →https://doi.org/10.1643/ch-10-012openalex-snapshot
Clinal Variation in Calls of Native and Introduced Populations of Eleutherodactylus coqui
inferredcites →https://doi.org/10.1670/0022-1511(2003)037[0010:qaohpf]2.0.co;2openalex-snapshot
Quantitative Assessment of Habitat Preferences for the Puerto Rican Terrestrial Frog, Eleutherodactylus coqui
inferredcites →https://doi.org/10.1670/07-314r1.1openalex-snapshot
Population Density Estimates and Growth Rates of Eleutherodactylus coqui in Hawaii
inferredcites →https://doi.org/10.1670/79-05w.1openalex-snapshot
Population Densities of the Coquí, Eleutherodactylus coqui (Anura: Leptodactylidae) in Newly Invaded Hawaii and in Native Puerto Rico
inferredcites →https://doi.org/10.18257/raccefyn.25(95).2001.2826openalex-snapshot
THREE NEW RAINFROGS OF THE ELEUTHERODACTYLUS DIASTEMA GROUP FROM COLOMBIA AND PANAMA
inferredcites →https://doi.org/10.2307/1442429openalex-snapshot
Another Exotic Amphibian in Florida, Eleutherodactylus coqui
inferredcites →https://doi.org/10.2307/1444854openalex-snapshot
Direct Development in Eleutherodactylus coqui (Anura: Leptodactylidae): A Staging Table
inferredcites →https://doi.org/10.2307/1446039openalex-snapshot
Foraging Success of the Tropical Frog, Eleutherodactylus coqui: The Cost of Calling
inferredcites →https://doi.org/10.2307/1446096openalex-snapshot
Vocalizations and the Defense of Retreat Sites by Male and Female Frogs, Eleutherodactylus coqui
inferredcites →https://doi.org/10.2307/1446898openalex-snapshot
Cave Breeding and Froglet Transport: A Novel Pattern of Anuran Brood Care in the Jamaican Frog, Eleutherodactylus cundalli
inferredcites →https://doi.org/10.2307/1447737openalex-snapshot
Contributions to West Indian Herpetology: A Tribute to Albert Schwartz
inferredcites →https://doi.org/10.2307/1467048openalex-snapshot
Taxonomic Reconsideration of Middle American Frogs of the Eleutherodactylus rugulosus Group (Anura: Leptodactylidae): A Reconnaissance of Subtle Nuances among Frogs
inferredcites →https://doi.org/10.2307/1541765openalex-snapshot
A Practical Guide to the Developmental Biology of Terrestrial-Breeding Frogs
inferredcites →https://doi.org/10.2307/1562976openalex-snapshot
A New Ovoviviparous Frog, Eleutherodactylus jasperi (Amphibia, Anura, Leptodactylidae), from Puerto Rico
inferredcites →https://doi.org/10.2307/1564679openalex-snapshot
Effects of Increased Sound Level of Advertisement Calls on Calling Male Frogs, Eleutherodactylus coqui
inferredcites →https://doi.org/10.2984/049.063.0301openalex-snapshot
Biology and Impacts of Pacific Island Invasive Species. 5.Eleutherodactylus coqui, the Coqui Frog (Anura: Leptodactylidae)
inferredcites →https://doi.org/10.3354/dao02823openalex-snapshot
Coqui frogs persist with the deadly chytrid fungus despite a lack of defensive antimicrobial peptides
inferredcites →https://doi.org/10.3389/fendo.2019.00307openalex-snapshot
Evolutionary Conservation of Thyroid Hormone Receptor and Deiodinase Expression Dynamics in ovo in a Direct-Developing Frog, Eleutherodactylus coqui
inferredcites →https://doi.org/10.3390/ijms21165593openalex-snapshot
The Specific Molecular Composition and Structural Arrangement of Eleutherodactylus Coqui Gular Skin Tissue Provide Its High Mechanical Compliance
inferredcites →https://doi.org/10.4324/9780203127230openalex-snapshot
A Handbook of Global Freshwater Invasive Species
inferredcites →https://doi.org/10.5860/choice.34-2744openalex-snapshot
The Food web of a tropical rain forest
inferredcites →https://doi.org/10.5860/choice.49-6872openalex-snapshot
IUCN Red List of Threatened Species
inferredcites →https://doi.org/10.5962/bhl.title.16169openalex-snapshot
Frogs of the genus Eleutherodactylus (Anura: Leptodactylidae) in the Andes of northern Peru / by William E. Duellman and Jennifer B. Pramuk.
inferredcites →https://doi.org/10.5962/bhl.title.16179openalex-snapshot
Amphibian species of the world : Additions and corrections
inferredcites →https://doi.org/10.5962/bhl.title.8435openalex-snapshot
The ecological impact of man on the south Florida herpetofauna
inferredcites →https://doi.org/10.7208/chicago/9780226893334.001.0001openalex-snapshot
The Ecology and Behavior of Amphibians
inferredcites →https://doi.org/10.7554/elife.06813openalex-snapshot
Peromyscus mice as a model for studying natural variation
inferredcites →https://doi.org/10.7554/elife.46994openalex-snapshot
The untapped potential of medaka and its wild relatives
inferredcites →https://doi.org/10.7554/elife.52803openalex-snapshot
The house sparrow in the service of basic and applied biology
inferredcites →https://doi.org/10.7589/2013-10-268openalex-snapshot
SUSCEPTIBILITY TO THE AMPHIBIAN CHYTRID FUNGUS VARIES WITH ONTOGENY IN THE DIRECT-DEVELOPING FROG,ELEUTHERODACTYLUS COQUI
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4809405openalex-extracted
The Jumping Performance of Two Eleutherodactylus Frogs: The Effect of Temperature
inferred← citeshttps://doi.org/10.1002/jmor.21582openalex-snapshot
Direct development or endotrophic tadpole? Morphological aspects of the early ontogeny of the plump toad Osornophryne occidentalis (Anura: Bufonidae)
inferred← citeshttps://doi.org/10.1007/978-3-031-35159-4_5openalex-snapshot
Chemical Communication and Semiochemical Recognition in Frogs: From Eggs to Adults
inferred← citeshttps://doi.org/10.1016/j.anbehav.2022.10.005openalex-snapshot
Who cares? An integrative approach to understanding the evolution of behavioural plasticity in parental care
inferred← citeshttps://doi.org/10.1016/j.conb.2023.102753openalex-snapshot
From tadpole to adult frog locomotion
inferred← citeshttps://doi.org/10.1016/j.ecocom.2024.101080openalex-snapshot
Who notices Gymnophiona? Google Trends data reveal interesting trends for recent amphibian species
inferred← citeshttps://doi.org/10.1016/j.jtherbio.2025.104113openalex-snapshot
The jumping performance of two Eleutherodactylus frog species: the effect of temperature
inferred← citeshttps://doi.org/10.1093/conphys/coag075openalex-snapshot
Characterizing metabolic responses of Eleutherodactylus frogs in Puerto Rico to different thermal treatments: implications for conservation
inferred← citeshttps://doi.org/10.1093/cz/zoae055openalex-snapshot
Fortune may favor the flexible: environment-dependent behavioral shifts in invasive coquí frogs
inferred← citeshttps://doi.org/10.1098/rstb.2022.0141openalex-snapshot
Form, function, foam: evolutionary ecology of anuran nests and nesting behaviour
inferred← citeshttps://doi.org/10.1101/2025.03.31.646409openalex-snapshot
Developmental stages of Arthroleptella villiersi (Pyxicephalidae)
inferred← citeshttps://doi.org/10.1111/ede.70035openalex-snapshot
The Development of de Villiers' Moss Frog ( Arthroleptella villiersi , Pyxicephalidae) Reveals Heterochronic Patterns Underlying the Evolution of Endotrophic Development in Anura
inferred← citeshttps://doi.org/10.1371/journal.pone.0328623openalex-snapshot
Skin transcriptomics of invasive Coqui frogs: stress responses, parasite signatures, and antimicrobial peptides
inferred← citeshttps://doi.org/10.3389/fnmol.2023.1131093openalex-snapshot
Evolution of visual guanylyl cyclases and their activating proteins with respect to clade and species-specific visual system adaptation
inferred← citeshttps://doi.org/10.64898/2026.06.08.730926openalex-snapshot
Disparate introduction histories but similar climatic distribution patterns among congeneric invasive anurans
inferred← citeshttps://doi.org/10.7717/peerj.18694openalex-snapshot
Demography and homing behavior in the poorly-known Philippine flat-headed frog Barbourula busuangensis (Anura: Bombinatoridae)
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