64 citations as recorded by crossref.

1. The extended osteoderm shield in Paleosuchus sp.: a dwarf crocodylian adaptation to the equatorial forest ecosystem? F. CLARAC et al. https://doi.org/10.5852/cr-palevol2024v23a12
2. Osteoderm microstructure of “rauisuchian” archosaurs from South America I. Cerda et al. https://doi.org/10.1016/j.geobios.2013.01.004
3. Ontogenetic and interelemental study of appendicular bones of Caiman latirostris Daudin, 1802 sheds light on osteohistological variability in crocodylians M. Pereyra et al. https://doi.org/10.1002/jmor.21687
4. Osteohistological Evidence for Determinate Growth in the American Alligator H. Woodward et al. https://doi.org/10.1670/10-274.1
5. Microanatomical and Histological Features in the Long Bones of Mosasaurine Mosasaurs (Reptilia, Squamata) – Implications for Aquatic Adaptation and Growth Rates A. Houssaye et al. https://doi.org/10.1371/journal.pone.0076741
6. Bone microanatomy of Pepesuchus deiseae (Mesoeucrocodylia, Peirosauridae) reveals a mature individual from the Upper Cretaceous of Brazil M. Sena et al. https://doi.org/10.1016/j.cretres.2018.06.008
7. Bone Histology of Phytosaur, Aetosaur, and Other Archosauriform Osteoderms (Eureptilia, Archosauromorpha) T. Scheyer et al. https://doi.org/10.1002/ar.22849
8. Osteohistology and paleobiological inferences of proterochampsids (Eucrocopoda: Proterochampsia) from the Chañares Formation (late Ladinian–early Carnian), La Rioja, Argentina D. Ponce et al. https://doi.org/10.1080/02724634.2021.1926273
9. The pseudosuchian record in paleohistology: A small review T. Scheyer https://doi.org/10.1002/ar.25455
10. Morphology, microanatomy, and histology of titanosaur (Dinosauria, Sauropoda) osteoderms from the Upper Cretaceous of Patagonia I. Cerda et al. https://doi.org/10.1080/02724634.2014.905791
11. Morfología e Histología de Osteodermos de Un Peirosauridae De La Cuenca Neuquina L. Filippi et al. https://doi.org/10.5710/AMGH.8.6.2012.430
12. Dorsal rib histology of dinosaurs and a crocodylomorph from western Portugal: Skeletochronological implications on age determination and life history traits K. Waskow & O. Mateus https://doi.org/10.1016/j.crpv.2017.01.003
13. The development of cephalic armor in the tokay gecko (Squamata: Gekkonidae: Gekko gecko) R. Laver et al. https://doi.org/10.1002/jmor.21092
14. Palaeohistology and external microanatomy of rauisuchian osteoderms (Archosauria: Pseudosuchia) T. SCHEYER & J. DESOJO https://doi.org/10.1111/j.1475-4983.2011.01098.x
15. Developmental plasticity highlighted in Crocodylus niloticus through in vivo fluorochrome labelling M. Pereyra & A. Chinsamy https://doi.org/10.1098/rsos.260040
16. Sexual dimorphism in osteoderm expression and the role of male intrasexual aggression C. Broeckhoven et al. https://doi.org/10.1093/biolinnean/blx066
17. Osteohistology and sequence of suture fusion reveal complex environmentally influenced growth in the teiid lizard Aspidoscelis tigris — Implications for fossil squamates H. Petermann et al. https://doi.org/10.1016/j.palaeo.2017.02.034
18. Do the ornamented osteoderms influence the heat conduction through the skin? A finite element analysis in Crocodylomorpha F. Clarac et al. https://doi.org/10.1016/j.jtherbio.2017.06.003
19. Review of osteoderm function and future research directions R. Ebel et al. https://doi.org/10.1111/jzo.13224
20. Growth record and histological variation in the dorsal ribs ofCamarasaurussp. (Sauropoda) K. Waskow & P. Sander https://doi.org/10.1080/02724634.2014.840645
21. Quantification of intraskeletal histovariability inAlligator mississippiensisand implications for vertebrate osteohistology H. Woodward et al. https://doi.org/10.7717/peerj.422
22. Osteoderm microstructure indicates ontogenetic shifts in the growth pattern of some Cretaceous notosuchians (Crocodylomorpha) A. Cajado et al. https://doi.org/10.1111/joa.70012
23. Cranial bone histology ofMetoposaurus krasiejowensis(Amphibia, Temnospondyli) from the Late Triassic of Poland K. Gruntmejer et al. https://doi.org/10.7717/peerj.2685
24. Internal vascularity of the dermal plates of Stegosaurus (Ornithischia, Thyreophora) J. Farlow et al. https://doi.org/10.1007/s00015-010-0021-5
25. Ontogenetic and inter-elemental osteohistological variability in the leopard tortoise Stigmochelys pardalis A. Botha & J. Botha https://doi.org/10.7717/peerj.8030
26. Triassic nursery? Evidence of gregarious behavior in juvenile pseudosuchian archosaurs as inferred by humeral histology of Aetosaurus ferratus (Norian; southern Germany) E. Teschner et al. https://doi.org/10.1080/02724634.2023.2168196
27. Preliminary Analysis of Osteocyte Lacunar Density in Long Bones of Tetrapods: All Measures Are Bigger in Sauropod Dinosaurs K. Stein et al. https://doi.org/10.1371/journal.pone.0077109
28. The first ontogenetic model for non‐crocodylomorph loricatans, based on osteohistology of the ontogenetic series of Prestosuchus chiniquensis from the Middle Triassic of Brazil B. de Farias et al. https://doi.org/10.1002/ar.25598
29. Dog attacks on wild desert tortoises: A risk model A. Carlson et al. https://doi.org/10.1002/jwmg.70192
30. Analyzing the Life History of Caimans: The Growth Dynamics of Caiman latirostris From an Osteohistological Approach M. Pereyra et al. https://doi.org/10.1002/jmor.70010
31. Evolution of growth strategy in alligators and caimans informed by osteohistology of the late Eocene early‐diverging alligatoroid crocodylian Diplocynodon hantoniensis D. Hoffman et al. https://doi.org/10.1111/joa.14231
32. Vascularised endosteal bone tissue in armoured sauropod dinosaurs A. Chinsamy et al. https://doi.org/10.1038/srep24858
33. Long bone histology of a eusuchian crocodyliform from the Upper Cretaceous of Spain: Implications for growth strategy in extinct crocodiles J. Company & X. Pereda-Suberbiola https://doi.org/10.1016/j.cretres.2016.12.002
34. Determinate growth is predominant and likely ancestral in squamate reptiles P. Frýdlová et al. https://doi.org/10.1098/rspb.2020.2737
35. A review of the osteoderms of lizards (Reptilia: Squamata) C. Williams et al. https://doi.org/10.1111/brv.12788
36. Osteoderm microstructure indicates the presence of a crocodylian‐like trunk bracing system in a group of armoured basal tetrapods M. Buchwitz et al. https://doi.org/10.1111/j.1463-6395.2011.00502.x
37. Histology and growth pattern of the pachy-osteosclerotic premaxillae of the fossil beaked whale Aporotus recurvirostris (Mammalia, Cetacea, Odontoceti) V. de Buffrénil & O. Lambert https://doi.org/10.1016/j.geobios.2010.09.001
38. Fossildiagenesis and ontogenetic insights of crocodyliform bones from the Adamantina Formation, Bauru Basin, Brazil I. Marchetti et al. https://doi.org/10.1016/j.jsames.2019.102327
39. Osteohistology of the unusually fast‐growing theropod dinosaur Ceratosaurus R. Sombathy et al. https://doi.org/10.1111/joa.14186
40. Osteohistological study on both fossil and living Caimaninae (Crocodyliformes, Crocodylia) from South America and preliminary comments on growth physiology and ecology R. Andrade et al. https://doi.org/10.1080/08912963.2018.1493475
41. Osteohistology of Greererpeton provides insight into the life history of an early Carboniferous tetrapod M. Whitney & S. Pierce https://doi.org/10.1111/joa.13520
42. Bone histology of aquatic reptiles: what does it tell us about secondary adaptation to an aquatic life? A. Houssaye https://doi.org/10.1111/j.1095-8312.2012.02002.x
43. Patterns of growth in monitor lizards (Varanidae) as revealed by computed tomography of femoral growth plates P. Frýdlová et al. https://doi.org/10.1007/s00435-016-0338-3
44. Paleobiological inferences for the Antarctic dinosaur Antarctopelta oliveroi (Ornithischia: Ankylosauria) based on bone histology of the holotype I. Cerda et al. https://doi.org/10.1016/j.cretres.2019.07.001
45. First report of desmatosuchine aetosaur (Pseudosuchia, Aetosauriformes) osteoderms from the Upper Triassic Tiki Formation of India: Their complex internal vascular system, functional significance and biostratigraphy A. Haldar & S. Ray https://doi.org/10.1111/joa.14255
46. Osteoderm histology of Proterochampsia and Doswelliidae (Reptilia: Archosauriformes) and their evolutionary and paleobiological implications I. Cerda et al. https://doi.org/10.1002/jmor.20348
47. A baurusuchid yearling (Mesoeucrocodylia, Crocodyliformes), from the Adamantina Formation, Bauru Group, Upper Cretaceous of Brazil D. Martins dos Santos et al. https://doi.org/10.1080/08912963.2021.2001807
48. A new juvenile Yamaceratops (Dinosauria, Ceratopsia) from the Javkhlant Formation (Upper Cretaceous) of Mongolia M. Son et al. https://doi.org/10.7717/peerj.13176
49. Ontogenetic changes in the long bone microstructure in the nine-banded armadillo (Dasypus novemcinctus) C. Heck et al. https://doi.org/10.1371/journal.pone.0215655
50. Dermal armour histology of aetosaurs (Archosauria: Pseudosuchia), from the Upper Triassic of Argentina and Brazil I. Cerda & J. Desojo https://doi.org/10.1111/j.1502-3931.2010.00252.x
51. Intraskeletal histovariability, allometric growth patterns, and their functional implications in bird-like dinosaurs E. Prondvai et al. https://doi.org/10.1038/s41598-017-18218-9
52. Microstructural characterization and growth dynamics in Notosuchus terrestris, a Mesoeucrocodylia crocodyliform from the Upper Cretaceous of Northern Patagonia, Argentina T. Navarro et al. https://doi.org/10.1016/j.cretres.2023.105607
53. Diverse Aquatic Adaptations in Nothosaurus spp. (Sauropterygia)—Inferences from Humeral Histology and Microanatomy N. Klein et al. https://doi.org/10.1371/journal.pone.0158448
54. New data on the palaeosteohistology and growth dynamic of the notosuchian Araripesuchus Price, 1959 M. Fernández Dumont et al. https://doi.org/10.1111/let.12423
55. Adaptive Patterns in Aquatic Amniote Bone Microanatomy—More Complex than Previously Thought A. Houssaye et al. https://doi.org/10.1093/icb/icw120
56. Histological variability in fossil and recent alligatoroid osteoderms: Systematic and functional implications M. Burns et al. https://doi.org/10.1002/jmor.20125
57. More diverse than expected: osteohistology of non‐crocodylomorph Pseudosuchia from the Triassic of South America D. Ponce et al. https://doi.org/10.1111/pala.70056
58. Maiasaura, a model organism for extinct vertebrate population biology: a large sample statistical assessment of growth dynamics and survivorship H. Woodward et al. https://doi.org/10.1017/pab.2015.19
59. Skeletochronology and Paleohistology of Hyposaurus rogersii (Crocodyliformes, Dyrosauridae) from the Early Paleogene of New Jersey, USA R. Pellegrini et al. https://doi.org/10.3390/ani11113067
60. Patterns of aquatic decay and disarticulation in juvenile Indo-Pacific crocodiles (Crocodylus porosus), and implications for the taphonomic interpretation of fossil crocodyliform material C. Syme & S. Salisbury https://doi.org/10.1016/j.palaeo.2014.07.031
61. Novel data on aetosaur (Archosauria, Pseudosuchia) osteoderm microanatomy and histology: palaeobiological implications I. Cerda et al. https://doi.org/10.1111/pala.12363
62. Lizards in chain mail: reconstructing the enigmatic past of dermal armour in squamate reptiles R. Ebel et al. https://doi.org/10.1093/biolinnean/blaf129
63. Evidence of determinate growth in an American alligator (Alligator mississippiensis) based on long‐term recapture and osteohistological confirmation T. Rainwater et al. https://doi.org/10.1002/ar.24688
64. Sex-specific growth arrest in a lizard L. Kubička et al. https://doi.org/10.1016/j.isci.2022.104041