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PubMed This is a summary of 43 peer-reviewed journal articles Updated

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.

Explore the Literature Visualize citation networks across 43 referenced papers

Top Authors

Vorasuk Shotelersuk
Thai Red Cross Society
Joan C. Marini
National Institutes of Health
Tian Liang
University of Michigan–Ann Arbor
Yongbo Lu
Texas A&M University
James P. Simmer
University of Michigan
Antonella Forlino
University of Pavia
Mariano Sanz
Universidad Complutense de Madrid
Agnès Bloch‐Zupan
Centre National de la Recherche Scientifique
Heidi L. Rehm
Broad Institute
Sue Richards
Oregon Health & Science University

Top Institutions

Ranked by publications Top 10 institutions
04

Texas A&M University

College Station, United States

16 papers

References

References (43)
  1. 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. 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. 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. 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. 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. 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. 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. 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. 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. 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. 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. 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. 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. 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. 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. 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. 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. 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. 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. 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. 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. 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. 23

    Dentinogenesis imperfecta type 2: a case report.

    Mohan KR, Narayanan M, Ravikumar PT

    General dentistry 2021; (69(6)):74-76.

    PMID: 34678748
  24. 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. 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. 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. 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. 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. 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. 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. 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. 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. 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. 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. 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. 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. 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. 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. 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. 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. 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. 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. 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