Research & Literature
Explore the leading researchers and institutions driving advances in this area, and dive into the full body of literature that informs this resource.
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Broad Institute
Cambridge, United States
Chulalongkorn University
Bangkok, Thailand
University of Michigan
Ann Arbor, United States
Texas A&M University
College Station, United States
Inserm
Paris, France
Karolinska Institutet
Stockholm, Sweden
Wuhan University
Wuhan, China
National Institutes of Health
Bethesda, United States
University of Oxford
Oxford, United Kingdom
University of Leeds
Leeds, United Kingdom
References
References (43)
- 1
The dentin phosphoprotein repeat region and inherited defects of dentin.
Yang J, Kawasaki K, Lee M, et al.
Molecular genetics & genomic medicine 2016; (4(1)):28-38 doi:10.1002/mgg3.176.
PMID: 26788535 - 2
Dental Management of a Child with Dentinogenesis Imperfecta: A Case Report.
Akhlaghi N, Eshghi AR, Mohamadpour M
Journal of dentistry (Tehran, Iran) 2016; (13(2)):133-138.
PMID: 27928242 - 3
Early Rehabilitation of Incisors with Dentinogenesis Imperfecta Type II - Case Report.
Beltrame AP, Rosa MM, Noschang RA, Almeida IC
The Journal of clinical pediatric dentistry 2017; (41(2)):112-115 doi:10.17796/1053-4628-41.2.112.
PMID: 28288297 - 4
Dentinogenesis imperfecta type II: A case report with 17 years of follow-up.
Gama FJR, Corrêa IS, Valerio CS, et al.
Imaging science in dentistry 2017; (47(2)):129-133 doi:10.5624/isd.2017.47.2.129.
PMID: 28680850 - 5
Dentinogenesis imperfecta type II- genotype and phenotype analyses in three Danish families.
Taleb K, Lauridsen E, Daugaard-Jensen J, et al.
Molecular genetics & genomic medicine 2018; (6(3)):339-349 doi:10.1002/mgg3.375.
PMID: 29512331 - 6
[Genetic variants analysis and histological observation of teeth in a patient with hereditary opalescent dentin].
Li F, Liu Y, Liu HC, Feng HL
Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences 2018; (50(4)):666-671.
PMID: 30122769 - 7
Dentinogenesis imperfecta type II in Swedish children and adolescents.
Andersson K, Malmgren B, Åström E, Dahllöf G
Orphanet journal of rare diseases 2018; (13(1)):145 doi:10.1186/s13023-018-0887-2.
PMID: 30134932 - 8
Endodontic management of type II dens invaginatus with open apex and large periradicular lesion using the XP-endo Finisher: A case report.
Rodrigues EA, Belladonna FG, De-Deus G, Silva EJ
Journal of clinical and experimental dentistry 2018; (10(10)):e1040-e1044 doi:10.4317/jced.55031.
PMID: 30386511 - 9
Indirect adhesive rehabilitation by cementation under pressure of a case of Dentinogenesis Imperfecta type II: follow-up after 13 years.
Campanella V, Di Taranto V, Libonati A, et al.
European journal of paediatric dentistry 2018; (19(4)):303-306 doi:10.23804/ejpd.2018.19.04.10.
PMID: 30567448 - 10
Dentinogenesis Imperfecta Type II in Children: A Scoping Review.
Garrocho-Rangel A, Dávila-Zapata I, Martínez-Rider R, et al.
The Journal of clinical pediatric dentistry 2019; (43(3)):147-154 doi:10.17796/1053-4625-43.3.1.
PMID: 30964718 - 11
A multidisciplinary approach to the functional and esthetic rehabilitation of dentinogenesis imperfecta type II: A clinical report.
Fan F, Li N, Huang S, Ma J
The Journal of prosthetic dentistry 2019; (122(2)):95-103 doi:10.1016/j.prosdent.2018.10.028.
PMID: 30979433 - 12
Mutant Dentin Sialophosphoprotein Causes Dentinogenesis Imperfecta.
Liang T, Zhang H, Xu Q, et al.
Journal of dental research 2019; (98(8)):912-919 doi:10.1177/0022034519854029.
PMID: 31173534 - 13
A novel hypothesis based on clinical, radiological, and histological data to explain the dentinogenesis imperfecta type II phenotype.
Turkkahraman H, Galindo F, Tulu US, Helms JA
Connective tissue research 2020; (61(6)):526-536 doi:10.1080/03008207.2019.1631296.
PMID: 31284784 - 14
Novel frameshift mutations in DSPP cause dentin dysplasia type II.
Lee JW, Hong J, Seymen F, et al.
Oral diseases 2019; (25(8)):2044-2046 doi:10.1111/odi.13182.
PMID: 31454439 - 15
A family with homozygous and heterozygous p.Gly337Ser mutations in COL1A2.
Udomchaiprasertkul W, Kuptanon C, Porntaveetus T, Shotelersuk V
European journal of medical genetics 2020; (63(6)):103896 doi:10.1016/j.ejmg.2020.103896.
PMID: 32081708 - 16
Tooth ultrastructure of a novel COL1A2 mutation expanding its genotypic and phenotypic spectra.
Intarak N, Budsamongkol T, Theerapanon T, et al.
Oral diseases 2021; (27(5)):1257-1267 doi:10.1111/odi.13657.
PMID: 32989910 - 17
Full Mouth Rehabilitation of Two Siblings with Dentinogenesis Imperfecta Type II Using Different Treatment Modalities.
Alrashdi M, Schoener J, Contreras CI, Chen S
International journal of environmental research and public health 2020; (17(19)) doi:10.3390/ijerph17197029.
PMID: 32992978 - 18
Dentinogenesis Imperfecta and Caries in Osteogenesis Imperfecta among Vietnamese Children.
Nguyen HTT, Vu DC, Nguyen DM, et al.
Dentistry journal 2021; (9(5)) doi:10.3390/dj9050049.
PMID: 33925433 - 19
Nanoscopic wear behavior of dentinogenesis imperfecta type II tooth dentin.
Mao J, Wang L, Jiang Y, et al.
Journal of the mechanical behavior of biomedical materials 2021; (120()):104585 doi:10.1016/j.jmbbm.2021.104585.
PMID: 34010797 - 20
Dentinogenesis imperfecta type II: Diagnosis, functional and esthetic rehabilitation in mixed dentition.
Kaur R, Karadwal A, Sharma D, Sandhu MK
Journal of oral and maxillofacial pathology : JOMFP 2021; (25(Suppl 1)):S76-S80 doi:10.4103/jomfp.JOMFP_172_20.
PMID: 34083977 - 21
Non-Syndromic Dentinogenesis Imperfecta Caused by Mild Mutations in COL1A2.
Lee Y, Kim YJ, Hyun HK, et al.
Journal of personalized medicine 2021; (11(6)) doi:10.3390/jpm11060526.
PMID: 34201399 - 22
Case Report: A Novel COL1A1 Missense Mutation Associated With Dentineogenesis Imperfecta Type I.
Zeng Y, Pan Y, Mo J, et al.
Frontiers in genetics 2021; (12()):699278 doi:10.3389/fgene.2021.699278.
PMID: 34249109 - 23
Dentinogenesis imperfecta type 2: a case report.
Mohan KR, Narayanan M, Ravikumar PT
General dentistry 2021; (69(6)):74-76.
PMID: 34678748 - 24
Phenotype and molecular characterizations of a family with dentinogenesis imperfecta shields type II with a novel DSPP mutation.
Du Q, Cao L, Liu Y, et al.
Annals of translational medicine 2021; (9(22)):1672 doi:10.21037/atm-21-5369.
PMID: 34988181 - 25
The Modified Shields Classification and 12 Families with Defined DSPP Mutations.
Simmer JP, Zhang H, Moon SJH, et al.
Genes 2022; (13(5)) doi:10.3390/genes13050858.
PMID: 35627243 - 26
Interdisciplinary Management of a Patient with Dentinogenesis Imperfecta Type II Using a Combination of CAD-CAM and Analog Techniques: A Clinical Report.
Azpiazu-Flores FX, Knobloch LA, Larsen PE
Journal of prosthodontics : official journal of the American College of Prosthodontists 2022; (31(8)):647-654 doi:10.1111/jopr.13556.
PMID: 35675448 - 27
Dentin defects caused by a Dspp-1 frameshift mutation are associated with the activation of autophagy.
Liang T, Smith CE, Hu Y, et al.
Scientific reports 2023; (13(1)):6393 doi:10.1038/s41598-023-33362-1.
PMID: 37076504 - 28
Regenerative Endodontic Treatment in Dentinogenesis Imperfecta-Induced Apical Periodontitis.
Liao Y, Pan T, Xing X
Case reports in dentistry 2024; (2024()):5128588 doi:10.1155/2024/5128588.
PMID: 38223911 - 29
A novel approach to full-mouth rehabilitation of dentinogenesis imperfecta type II: Case series with review of literature.
Zhang Y, Jin X, Zhang Z, et al.
Medicine 2024; (103(4)):e36882 doi:10.1097/MD.0000000000036882.
PMID: 38277536 - 30
An Aesthetic and Economic Approach of Smile Designing for a Patient With Dentinogenesis Imperfecta: A Rare Case Entity.
Kumar A, Chirom B, Nongthombam R, et al.
Cureus 2024; (16(2)):e53978 doi:10.7759/cureus.53978.
PMID: 38469028 - 31
Dentinogenesis imperfecta: case report with nanoceramic resin crowns restorative treatment.
Casaña-Ruiz MD, Frechina N, Estrela F, Catalá-Pizarro M
The Journal of clinical pediatric dentistry 2024; (48(2)):189-195 doi:10.22514/jocpd.2024.047.
PMID: 38548649 - 32
Regenerative Endodontic Procedures in Immature Teeth Affected by Regional Odontodysplasia.
Chebath-Taub D, Slutzky-Goldberg I
Journal of endodontics 2024; (50(7)):1017-1021 doi:10.1016/j.joen.2024.04.006.
PMID: 38626857 - 33
Isolated dentinogenesis imperfecta: Novel DSPP variants and insights on genetic counselling.
Hassib NF, Mehrez M, Mostafa MI, Abdel-Hamid MS
Clinical oral investigations 2024; (28(5)):254 doi:10.1007/s00784-024-05636-z.
PMID: 38630328 - 34
Dental Management of Genetic Dental Disorders: A Critical Review.
Dujic H, Bücher K, Schüler IM, et al.
Journal of dental research 2025; (104(4)):369-379 doi:10.1177/00220345241305330.
PMID: 39905279 - 35
A Novel Variant in Dentin Sialophosphoprotein (DSPP) Gene Causes Dentinogenesis Imperfecta Type III: Case Report.
Wang Y, Xu X, Ding Y, Yuan G
Molecular genetics & genomic medicine 2025; (13(3)):e70087 doi:10.1002/mgg3.70087.
PMID: 40040554 - 36
Prosthetic Rehabilitation of Three Dentinogenesis Imperfecta Patients using Hobo Twin Stage Technique and Implant Supported Overdenture - A Case Report.
Amina , Abirami S, Rajput G, et al.
Indian journal of dental research : official publication of Indian Society for Dental Research 2025; (36(1)):116-119 doi:10.4103/ijdr.ijdr_790_23.
PMID: 40208219 - 37
Dentinogenesis imperfecta type II dentin: nanostructural mechanics analysis.
Jia G, Tianle J, Haofu J, et al.
BMC oral health 2025; (25(1)):906 doi:10.1186/s12903-025-06315-5.
PMID: 40468273 - 38
Personalized Bonding Approach for Full-Mouth Adhesive Rehabilitation in Dentinogenesis Imperfecta.
Clark C, Kérourédan O, Massé L
Clinical case reports 2025; (13(6)):e70552 doi:10.1002/ccr3.70552.
PMID: 40469120 - 39
A Novel DSPP Mutation in Dentinogenesis Imperfecta Shields Type II: Clinical, Genetic and Stem Cell Perspectives.
Gao Q, Deng Z, Yang L, et al.
International dental journal 2025; (75(5)):100937 doi:10.1016/j.identj.2025.100937.
PMID: 40763686 - 40
Guided Endodontics in Managing Root Canal Treatment for Anomalous Teeth-A Narrative Review.
Sabanik P, Samiei M, Avval ST, Cavalcanti B
Australian endodontic journal : the journal of the Australian Society of Endodontology Inc 2025; (51(3)):836-848 doi:10.1111/aej.70007.
PMID: 40792425 - 41
Cone-Beam Computed Tomography (CBCT)-Guided Non-surgical Management of Type II Dens Invaginatus in Maxillary Lateral Incisors Using Calcium Silicate-Based Materials: A Case Series.
Priya P
Cureus 2026; (18(1)):e101205 doi:10.7759/cureus.101205.
PMID: 41669597 - 42
A radiological case series of three siblings with osteogenesis imperfecta and shared paternal inheritance.
Nelwan DA, Ilyas M, Rauf R, et al.
Radiology case reports 2026; (21(5)):1777-1782 doi:10.1016/j.radcr.2025.06.117.
PMID: 41717638 - 43
Diagnosis complexity of dentinogenesis imperfecta involving DSPP genetic variants.
Caravello G, Jiménez-Armijo A, Kawczynski M, et al.
Journal of medical genetics 2026; doi:10.1136/jmg-2025-111345.
PMID: 41819808