Robin Yong
Overview
Explore the profile of Robin Yong including associated specialties, affiliations and a list of published articles.
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Articles
9
Citations
36
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Recent Articles
1.
Bereza S, Yong R, Gronthos S, Arthur A, Ranjitkar S, Anderson P
Arch Oral Biol
. 2022 Mar;
137:105389.
PMID: 35299000
Objective: EFNB1 mutation causes craniofrontonasal dysplasia (CFND), a congenital syndrome associated with craniomaxillofacial anomalies characterised by coronal craniosynostosis, orbital hypertelorism, and midface dysplasia. The aim of this murine study was...
2.
Mian M, Tan J, Yong R, Williams R, Labrinidis A, Anderson P, et al.
Methods Mol Biol
. 2021 Dec;
2403:107-127.
PMID: 34913120
Craniofacial phenomics has opened up numerous opportunities to correlate genetic and epigenetic factors to craniofacial phenotypes in order to improve our understanding of growth and development in health and disease....
3.
Lee J, Fung S, Yong R, Ranjitkar S, Kaidonis J, Evans A, et al.
PLoS One
. 2021 Jul;
16(7):e0254151.
PMID: 34242291
The analysis of dental wear, at both the microscopic and macroscopic scale, is one of the most widely used tools in archeology and anthropology to reconstruct the diet and lifestyle...
4.
Fung S, Lee J, Yong R, Ranjitkar S, Kaidonis J, Pilbrow V, et al.
Am J Phys Anthropol
. 2020 Aug;
174(2):375-383.
PMID: 32779189
Objectives: Carabelli is a nonmetric dental trait variably expressed as a small pit to a prominent cusp in the maxillary molars of modern humans. Investigations on the occurrence and expression...
5.
Ranjitkar S, Yong R, Wu I, Gully G, Farmer D, Watson I, et al.
Aust Endod J
. 2019 Jul;
45(3):298-304.
PMID: 31310441
Dentine dysplasia type 1 is a rare and complex dental anomaly. Our aim was to conduct a morphometric assessment of a dentinal dysplasia type 1c (DD1c) caries-free mandibular second molar,...
6.
Lonsdale S, Yong R, Khominsky A, Mihailidis S, Townsend G, Ranjitkar S, et al.
Ann Anat
. 2019 Jun;
225:33-41.
PMID: 31199981
Background: Saethre-Chotzen Syndrome (SCS) is an autosomal dominant syndrome that occurs due to a mutation or deletion of the Twist1 gene at chromosome 7p21. Our aim was to conduct a...
7.
Fiorenza L, Yong R, Ranjitkar S, Hughes T, Quayle M, McMenamin P, et al.
Am J Phys Anthropol
. 2018 Aug;
167(2):400-406.
PMID: 30129183
Objectives: Rapid prototyping (RP) technology is becoming more affordable, faster, and is now capable of building models with a high resolution and accuracy. Due to technological limitations, 3D printing in...
8.
Yong R, Ranjitkar S, Lekkas D, Halazonetis D, Evans A, Brook A, et al.
Am J Phys Anthropol
. 2018 Feb;
166(2):373-385.
PMID: 29446438
Objectives: This study aimed to investigate size and shape variation of human premolars between Indigenous Australians and Australians of European ancestry, and to assess whether sex and ancestry could be...
9.
Khominsky A, Yong R, Ranjitkar S, Townsend G, Anderson P
Arch Oral Biol
. 2017 Dec;
86:123-130.
PMID: 29223639
Objectives: Fibroblast growth factor receptor 2 (FGFR2) mutation is a known cause of Crouzon syndrome that is characterised by craniosynostosis and midfacial hypoplasia. Our aim was to conduct extensive phenotyping...