ศ.ทพ. พีรนิธ กันตะบุตร (Piranit Kantaputra)
ศ.ทพ. พีรนิธ กันตะบุตร
Piranit Kantaputra piranit.k@cmu.ac.th คณะทันตแพทยศาสตร์ มหาวิทยาลัยเชียงใหม่

ศ.ทพ. พีรนิธ กันตะบุตร

Piranit Kantaputra

ส่วนวิชาการ/ภาควิชาทันตกรรมจัดฟันและทันตกรรมสำหรับเด็ก/สาขาวิชาทันตกรรมสำหรับเด็ก
  • วิทยาศาสตรมหาบัณฑิต, ทันตกรรมสำหรับเด็ก
    University of Minnesota, 2534
  • ประกาศนียบัตรชั้นสูง, Pediatric Dentistry
    University of Minnesota, 2533
  • ทันตแพทยศาสตรบัณฑิต
    มหาวิทยาลัยเชียงใหม่, 2529
1. Kantaputra,P., Panichkul,W., Sillapasorn,P., Adisornkanj,P., Kitsadayurach,P., Kaewgaya,M., Intachai,W., Olsen,B., Ngamphiw,C., Leethanakul,C., Jatooratthawichot,P., Ketudat Cairns,J.R., Tongsima,S., LRP4 mutations, dental anomalies, and oral exostoses: International Journal of Paediatric Dentistry, 2024
2. Sangphukieo,A., Thongkumkoon,P., Noisagul,P., LoPiccolo,L., O’Brien,T.E., Chaowattanapanit,S., Choonhakarn,C., Amornpinyo,W., Chaiwarith,R., Kiratikanon,S., Rujiwetpongstorn,R., Tovanabutra,N., Chiewchanvit,S., Kantaputra,P., Intachai,W., Dissook,S., Chuamanochan,M., Human Leukocyte Antigen Markers for Distinguishing Pustular Psoriasis and Adult-Onset Immunodeficiency with Pustular Reaction: Genes, 2024
3. Ruangchan,C., Ngamphiw,C., Krasaesin,A., Intarak,N., Tongsima,S., Kaewgahya,M., Kawasaki,K., Mahawong,P., Paripurana,K., Sookawat,B., Jatooratthawichot,P., Cox,T.C., Ohazama,A., KetudatCairns,J.R., Porntaveetus,T., Kantaputra,P., Genetic Variants in KCTD1 Are Associated with Isolated Dental Anomalies: International Journal of Molecular Sciences, 2024
4. Kantaputra,P., Daroontum,T., Kitiyamas,K., Piyakhunakorn,P., Kawasaki,K., Sathienkijkanchai,A., Wasant,P., Vatanavicharn,N., Yasanga,T., Kaewgahya,M., Tongsima,S., Cox,T.C., Arold,S.T., Ohazama,A., Ngamphiw,C., Homozygosity for a Rare Plec Variant Suggests a Contributory Role in Congenital Insensitivity to Pain: International Journal of Molecular Sciences, 2024
5. LoPiccolo,L., Wongkummool,W., Jantaree,P., Daroontum,T., Chaowattanapanit,S., Choonhakarn,C., Amornpinyo,W., Chaiwarith,R., Kiratikanon,S., Rujiwetpongstorn,R., Tovanabutra,N., Chiewchanvit,S., Ngamphiw,C., Intachai,W., Kantaputra,P., Chuamanochan,M., Rare Filaggrin Variants Are Associated with Pustular Skin Diseases in Asians: International Journal of Molecular Sciences, 2024
6. Kantaputra,P., Daroontum,T., Kitiyamas,K., Piyakhunakorn,P., Kawasaki,K., Sathienkijkanchai,A., Wasant,P., Vatanavicharn,N., Yasanga,T., Kaewgahya,M., Tongsima,S., Cox,T.C., Arold,S.T., Ohazama,A., Ngamphiw,C., Homozygosity for a Rare Plec Variant Suggests a Contributory Role in Congenital Insensitivity to Pain: International Journal of Molecular Sciences, 2024
7. LoPiccolo,L., Wongkummool,W., Jantaree,P., Daroontum,T., Chaowattanapanit,S., Choonhakarn,C., Amornpinyo,W., Chaiwarith,R., Kiratikanon,S., Rujiwetpongstorn,R., Tovanabutra,N., Chiewchanvit,S., Ngamphiw,C., Intachai,W., Kantaputra,P., Chuamanochan,M., Rare Filaggrin Variants Are Associated with Pustular Skin Diseases in Asians: International Journal of Molecular Sciences, 2024
8. Kularbkaew,T., Thongmak,T., Sandeth,P., Durward,C.S., Vittayakittipong,P., Duke,P., Iamaroon,A., Kintarak,S., Intachai,W., Ngamphiw,C., Tongsima,S., Jatooratthawichot,P., Cox,T.C., KetudatCairns,J.R., Kantaputra,P., Genetic Variants in the TBC1D2B Gene Are Associated with Ramon Syndrome and Hereditary Gingival Fibromatosis: International Journal of Molecular Sciences, 2024
9. Kantaputra,P., Butali,A., Eliason,S., Chalkley,C., Nakornchai,S., Bongkochwilawan,C., Kawasaki,K., Kumchiang,A., Ngamphiw,C., Tongsima,S., Ketudat Cairns,J.R., Olsen,B., Intachai,W., Ohazama,A., Tucker,A.S., Amendt,B.A., CACNA1S mutation-associated dental anomalies: A calcium channelopathy: Oral Diseases, 2024
10. Kantaputra,P., Dejkhamron,P., Sittiwangkul,R., Katanyuwong,K., Ngamphiw,C., Sonsuwan,N., Intachai,W., Tongsima,S., Beales,P.L., Buranaphatthana,W., Dental Anomalies in Ciliopathies: Lessons from Patients with BBS2, BBS7, and EVC2 Mutations: Genes, 2023
11. Kantaputra,P., Leelaadisorn,N., Hatsadaloi,A., Quarto,N., Intachai,W., Tongsima,S., Kawasaki,K., Ohazama,A., Ngamphiw,C., Wiriyakijja,P., A Mutation in CACNA1S Is Associated with Multiple Supernumerary Cusps and Root Maldevelopment: Diagnostics, 2023
12. Kantaputra,P.N., Tripuwabhrut,K., Anthonappa,R.P., Chintakanon,K., Ngamphiw,C., Adisornkanj,P., Porntrakulseree,N., Olsen,B., Intachai,W., Hennekam,R.C., Vieira,A.R., Tongsima,S., Heterozygous Variants in FREM2 Are Associated with Mesiodens, Supernumerary Teeth, Oral Exostoses, and Odontomas: Diagnostics, 2023
13. Panyarat,C., Nakornchai,S., Chintakanon,K., Leelaadisorn,N., Intachai,W., Olsen,B., Tongsima,S., Adisornkanj,P., Ngamphiw,C., Cox,T.C., Kantaputra,P., Rare Genetic Variants in Human APC Are Implicated in Mesiodens and Isolated Supernumerary Teeth: International Journal of Molecular Sciences, 2023
14. Kantaputra,P., Jatooratthawichot,P., Kottege,N., Anthonappa,R.P., Kaewgahya,M., Tongsima,S., Ngamphiw,C., KetudatCairns,J.R., Predes,D., He,X., DKK1 is a strong candidate for mesiodens and taurodontism: Clinical Genetics, 2023
15. Kantaputra,P.N., Jatooratthawichot,P., Adisornkanj,P., Kitsadayurach,P., Kaewgahya,M., Olsen,B., Ohazama,A., Ngamphiw,C., Tongsima,S., Cox,T.C., KetudatCairns,J.R., Rare Variants in LRP4 Are Associated with Mesiodens, Root Maldevelopment, and Oral Exostoses in Humans: Biology, 2023
16. Huang,T., Li,J., Zhao,H., Ngamphiw,C., Tongsima,S., Kantaputra,P., Kittitharaphan,W., MingWang,S., Core promoter in TNBC is highly mutated with rich ethnic signature: Briefings in Functional Genomics, 2023
17. Kantaputra,P., Daroontum,T., Chuamanochan,M., Chaowattanapanit,S., Intachai,W., Olsen,B., Sastraruji,T., Tongsima,S., Ngamphiw,C., Kampuansai,J., Cox,T.C., Kiratikanon,S., Loss of Function TGFBR2 Variant as a Contributing Factor in Generalized Pustular Psoriasis and Adult-Onset Immunodeficiency: Genes, 2023
18. Adisornkanj,P., Chanprasit,R., Eliason,S., Fons,J.M., Intachai,W., Tongsima,S., Olsen,B., Arold,S.T., Ngamphiw,C., Amendt,B.A., Tucker,A.S., Kantaputra,P., Genetic Variants in Protein Tyrosine Phosphatase Non-Receptor Type 23 Are Responsible for Mesiodens Formation: Biology, 2023
19. Kantaputra,P., Jatooratthawichot,P., Tantachamroon,O., Nanekrungsan,K., Intachai,W., Olsen,B., Tongsima,S., Ngamphiw,C., Cairns,J.R.K., Novel Dental Anomaly–associated Mutations in WNT10A Protein Binding Sites: International Dental Journal, 2023
20. Kantaputra,P., Tripuwabhrut,K., Jatooratthawichot,P., Adisornkanj,P., Hatsadaloi,A., Porntrakoolsaree,N., Kaewgaya,M., Olsen,B., Tongsima,S., Ngamphiw,C., KetudatCairns,J.R., Mutations in the WLS are associated with dental anomalies, torus palatinus, and torus mandibularis: European Journal of Orthodontics, 2023
21. Wejaphikul,K., Dejkhamron,P., Khorana,J., Watcharachan,K., Intachai,W., Olsen,B., Tongsima,S., KetudatCairns,J.R., Ngamphiw,C., Kantaputra,P., Subtotal Parathyroidectomy Successfully Controls Calcium Levels of Patients with Neonatal Severe Hyperparathyroidism Carrying a Novel CASR Mutation: Hormone Research in Paediatrics, 2023
22. Kantaputra,P.N., Angkurawaranon,S., Intachai,W., Ngamphiw,C., Olsen,B., Tongsima,S., Cox,T.C., KetudatCairns,J.R., A Founder Intronic Variant in P3H1 Likely Results in Aberrant Splicing and Protein Truncation in Patients of Karen Descent with Osteogenesis Imperfecta Type VIII: Genes, 2023
23. Kantaputra,P., Daroontum,T., Chuamanochan,M., Chaowattanapanit,S., Kiratikanon,S., Choonhakarn,C., Intachai,W., Olsen,B., Tongsima,S., Ngamphiw,C., Pontisso,P., Cox,T.C., Ounjai,P., SERPINB3, Adult-Onset Immunodeficiency, and Generalized Pustular Psoriasis: Genes, 2023
24. Kantaputra,P., Buaban,K., Thongsee,N., Kaewgahya,M., Quarto,N., Carlson,B.M., Ngamphiw,C., Tongsima,S., Broad spectrum of anomalies including quadricuspid aortic valve associated with a novel frameshift SALL4 variant: Clinical Genetics, 2023
25. Kantaputra,P.N., Angkurawaranon,S., Khwanngern,K., Ngamphiw,C., Intachai,W., Adisornkanj,P., Tongsima,S., Olsen,B., Sonsuwan,N., Katanyuwong,K., Clinical and Genetic Studies of the First Monozygotic Twins with Pfeiffer Syndrome: Genes, 2022
26. Kantaputra,P.N., Guven,Y., Tripuwabhrut,K., Adisornkanj,P., Hatsadaloi,A., Kaewgahya,M., Olsen,B., Ngamphiw,C., Jatooratthawichot,P., Tongsima,S., KetudatCairns,J.R., Mutations in LRP5 and BMP4 are associated with mesiodens, tooth agenesis, root malformation, and oral exostoses: Clinical Genetics, 2022
27. Kantaputra,P., Jatooratthawichot,P., Chintakanon,K., Intachai,W., Pradermdutsadeeporn,P., Adisornkanj,P., Tongsima,S., Ngamphiw,C., Olsen,B., Tucker,A.S., KetudatCairns,J.R., Mutations in LRP6 highlight the role of WNT signaling in oral exostoses and dental anomalies: Archives of Oral Biology, 2022
28. Cardoso,L.C.D.A., Parra,A., Gil,C.R., Arias,P., Gallego,N., Romanelli,V., Kantaputra,P.N., Lima,L., LlerenaJúnior,J.C., Arberas,C., Guillén-Navarro,E., Nevado,J., Tenorio-Castano,J., Lapunzina,P., Clinical Spectrum and Tumour Risk Analysis in Patients with Beckwith-Wiedemann Syndrome Due to CDKN1C Pathogenic Variants: Cancers, 2022
29. Kantaputra,P., Olsen,B., McGrath,J.A., WNT10A variant and severe scoliosis?: Journal of Dermatology, 2022
30. Kantaputra,P.N., Wangtiraumnuay,N., Ngamphiw,C., Olsen,B., Intachai,W., Tucker,A.S., Tongsima,S., Cryptophthalmos, dental anomalies, oral vestibule defect, and a novel FREM2 mutation: Journal of Human Genetics, 2022
31. Kantaputra,P., Guven,Y., Kalayci,T., Özer,P.K., Panyarak,W., Intachai,W., Olsen,B., Carlson,B.M., Praditsap,O., Tongsima,S., Ngamphiw,C., Jatooratthawichot,P., Tucker,A.S., KetudatCairns,J.R., Expanding genotypic and phenotypic spectrums of LTBP3 variants in dental anomalies and short stature syndrome: Clinical Genetics, 2022
32. Doolan,B.J., Onoufriadis,A., Kantaputra,P., McGrath,J.A., WNT10A, dermatology and dentistry: British Journal of Dermatology, 2021
33. Kantaputra,P.N., Dejkhamron,P., Intachai,W., Ngamphiw,C., KetudatCairns,J.R., Kawasaki,K., Ohazama,A., Olsen,B., Tongsima,S., Angkurawaranon,S., A novel P3H1 mutation is associated with osteogenesis imperfecta type VIII and dental anomalies: Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology, 2021
34. Kantaputra,P., Chaowattanapanit,S., Kiratikanon,S., Chaiwarith,R., Choonhakarn,C., Intachai,W., Quarto,N., Tongsima,S., KetudatCairns,J.R., Ngamphiw,C., McGrath,J.A., Chuamanochan,M., SERPINA1, generalized pustular psoriasis, and adult-onset immunodeficiency: Journal of Dermatology, 2021
35. Shotelersuk,V., Wichadakul,D., Ngamphiw,C., Srichomthong,C., Phokaew,C., Wilantho,A., Pakchuen,S., Nakhonsri,V., Shaw,P.J., Wasitthankasem,R., Piriyapongsa,J., Wangkumhang,P., Assawapitaksakul,A., Chetruengchai,W., Lapphra,K., Khuninthong,A., Makarawate,P., Suphapeetiporn,K., Mahasirimongkol,S., Satproedprai,N., Porntaveetus,T., Pisitkun,P., Praphanphoj,V., Kantaputra,P., Tassaneeyakul,W., Tongsima,S., The Thai reference exome (T-REx) variant database: Clinical Genetics, 2021
36. Kantaputra,P.N., Chuamanochan,M., Kiratikanon,S., Chiewchanvit,S., Chaiwarith,R., Intachai,W., Quarto,N., Tongsima,S., McGrath,J.A., Ngamphiw,C., A truncating variant in SERPINA3, skin pustules and adult-onset immunodeficiency: Journal of Dermatology, 2021
37. Tananuvat,N., Tananuvat,R., Chartapisak,W., Mahanupab,P., Hokierti,C., Srikummool,M., Kampuansai,J., Intachai,W., Olsen,B., KetudatCairns,J.R., Kantaputra,P., Harboyan syndrome: novel SLC4A11 mutation, clinical manifestations, and outcome of corneal transplantation: Journal of Human Genetics, 2021
38. Kantaputra,P.N., Dejkhamron,P., Intachai,W., Ngamphiw,C., Kawasaki,K., Ohazama,A., Krisanaprakornkit,S., Olsen,B., Tongsima,S., KetudatCairns,J.R., Juberg-Hayward syndrome is a cohesinopathy, caused by mutation in ESCO2: European Journal of Orthodontics, 2021
39. Kantaputra,P.N., Coury,S.A., Tan,W.-H., Impaired dentin mineralization, supernumerary teeth, hypoplastic mandibular condyles with long condylar necks, and a TRPS1 mutation: Archives of Oral Biology, 2020
40. Kantaputra,P., Intachai,W., Kawasaki,K., Ohazama,A., Carlson,B., Quarto,N., Pruksachatkun,C., Chuamanochan,M., Clouston syndrome with pili canaliculi, pili torti, overgrown hyponychium, onycholysis, taurodontism and absence of palmoplantar keratoderma: Journal of Dermatology, 2020
41. Kantaputra,P.N., Intachai,W., Carlson,B.M., Pruksachatkunakorn,C., Clouston syndrome with dental anomalies, micropores of hair shafts and absence of palmoplantar keratoderma: Journal of Dermatology, 2020
42. Kantaputra,P.N., Dejkhamron,P., Tongsima,S., Ngamphiw,C., Intachai,W., Ngiwsara,L., Sawangareetrakul,P., Svasti,J., Olsen,B., Cairns,J.R.K., Bumroongkit,K., Juberg-Hayward syndrome and Roberts syndrome are allelic, caused by mutations in ESCO2: Archives of Oral Biology, 2020
43. NikKantaputra,P., Jotikasthira,D., Carlson,B., Wongmaneerung,T., Quarto,N., Khankasikum,T., Powcharoen,W., Intachai,W., Tripuwabhrut,K., TRPS1 mutation associated with trichorhinophalangeal syndrome type 1 with 15 supernumerary teeth, hypoplastic mandibular condyles with slender condylar necks and unique hair morphology: Journal of Dermatology, 2020
44. Kantaputra,P.N., Intachai,W., Carlson,B., Olsen,B., Ngaohirunphat,S., Sri-Oon,J., KetudatCairns,J.R., Choovuthayakorn,J., Are dental anomalies associated with Tietz syndrome?: European Journal of Dermatology, 2020
45. Kantaputra,P.N., Tripuwabhrut,K., Intachai,W., Carlson,B.M., Quarto,N., Ngamphiw,C., Tongsima,S., Sonsuwan,N., Treacher Collins syndrome: A novel TCOF1 mutation and monopodial stapes: Clinical Otolaryngology, 2020
46. Kantaputra,P.N., Pruksametanan,A., Phondee,N., Hutsadaloi,A., Intachai,W., Kawasaki,K., Ohazama,A., Ngamphiw,C., Tongsima,S., KetudatCairns,J.R., Tripuwabhrut,P., ADAMTSL1 and mandibular prognathism: Clinical Genetics, 2019
47. Kantaputra,P.N., Smith,L.J., Casal,M.L., Kuptanon,C., Chang,Y.-C., Nampoothiri,S., Paiyarom,A., Veerasakulwong,T., Trachoo,O., KetudatCairns,J.R., Chinadet,W., Tanpaiboon,P., Oral manifestations in patients and dogs with mucopolysaccharidosis Type VII: American Journal of Medical Genetics, Part A, 2019
48. Gowans,L.J.J., Cameron-Christie,S., Slayton,R.L., Busch,T., Romero-Bustillos,M., Eliason,S., Sweat,M., Sobreira,N., Yu,W., Kantaputra,P.N., Wohler,E., Adeyemo,W.L., Lachke,S.A., Anand,D., Campbell,C., Drummond,B.K., Markie,D.M., vanVuuren,W.J., vanVuuren,L.J., Casamassimo,P.S., Ettinger,R., Owais,A., vanStaden,I., Amendt,B.A., Adeyemo,A.A., Murray,J.C., Robertson,S.P., Butali,A., Missense Pathogenic variants in KIF4A Affect Dental Morphogenesis Resulting in X-linked Taurodontism, Microdontia and Dens-Invaginatus: Frontiers in Genetics, 2019
49. Kantaputra,P.N., Sirirungruangsarn,Y., Visrutaratna,P., Petcharunpaisan,S., Carlson,B.M., Intachai,W., Sudasna,J., Kampuansai,J., Dejkhamron,P., WNT1-associated osteogenesis imperfecta with atrophic frontal lobes and arachnoid cysts: Journal of Human Genetics, 2019
50. Kantaputra,P.N., Carlson,B.M., Genetic regulatory pathways of split-hand/foot malformation: Clinical Genetics, 2019
51. Kantaputra,P.N., Hutsadaloi,A., Kaewgahya,M., Intachai,W., German,R., Koparal,M., Leethanakul,C., Tolun,A., KetudatCairns,J.R., WNT10B mutations associated with isolated dental anomalies: Clinical Genetics, 2018
52. Kantaputra,P.N., Kapoor,S., Verma,P., Intachai,W., KetudatCairns,J.R., Split hand-foot malformation and a novel WNT10B mutation: European Journal of Medical Genetics, 2018
53. Kantaputra,P.N., Sirirungruangsarn,Y., Intachai,W., Ngamphiw,C., Tongsima,S., Dejkhamron,P., Osteogenesis imperfecta with ectopic mineralizations in dentin and cementum and a COL1A2 mutation: Journal of Human Genetics, 2018
54. Kantaputra,P.N., Chinadet,W., Intachai,W., Ngamphiw,C., KetudatCairns,J.R., Tongsima,S., Isolated dentinogenesis imperfecta with glass-like enamel caused by COL1A2 mutation: American Journal of Medical Genetics, Part A, 2018
55. Kunotai,W., Ananpornruedee,P., Lubinsky,M., Pruksametanan,A., Kantaputra,P.N., Making extra teeth: Lessons from a TRPS1 mutation: American Journal of Medical Genetics, Part A, 2017
56. Tanasubsinn,N., Sittiwangkul,R., Pongprot,Y., Kawasaki,K., Ohazama,A., Sastraruji,T., Kaewgahya,M., Kantaputra,P.N., TFAP2B mutation and dental anomalies: Journal of Human Genetics, 2017
57. Kantaputra,P.N., Kapoor,S., Verma,P., Kaewgahya,M., Kawasaki,K., Ohazama,A., KetudatCairns,J.R., Al-Awadi-Raas-Rothschild syndrome with dental anomalies and a novel WNT7A mutation: European Journal of Medical Genetics, 2017
58. Kantaputra,P.N., Bongkochwilawan,C., Lubinsky,M., Pata,S., Kaewgahya,M., Tong,H.J., KetudatCairns,J.R., Guven,Y., Chaisrisookumporn,N., Periodontal disease and FAM20A mutations: Journal of Human Genetics, 2017
59. Kantaputra,P.N., Intachai,W., Auychai,P., All enamel is not created equal: Supports from a novel FAM83H mutation: American Journal of Medical Genetics, Part A, 2016
60. Vogel,P., Read,R.W., Hansen,G.M., Powell,D.R., Kantaputra,P.N., Zambrowicz,B., Brommage,R., Dentin Dysplasia in Notum Knockout Mice: Veterinary Pathology, 2016
61. Wattanarat,O., Kantaputra,P.N., Preaxial polydactyly associated with a MSX1 mutation and report of two novel mutations: American Journal of Medical Genetics, Part A, 2016
62. Lubinsky,M., Kantaputra,P.N., Syndromes with supernumerary teeth: American Journal of Medical Genetics, Part A, 2016
63. Kantaputra,P.N., Response to the Letter to the Editor by Idil Kurtulus-Waschulewski; Gerhard Wahl, Prof. Dr.; Katalyn Dittrich; Volker Schuster: European Journal of Medical Genetics, 2015
64. Kantaputra,P.N., Kaewgahya,M., Hatsadaloi,A., Vogel,P., Kawasaki,K., Ohazama,A., KetudatCairns,J.R., GREMLIN 2 mutations and dental anomalies: Journal of Dental Research, 2015
65. Kantaputra,P.N., Kayserili,H., Güven,Y., Kantaputra,W., Balci,M.C., Tanpaiboon,P., Uttarilli,A., Dalal,A., Oral manifestations of 17 patients affected with mucopolysaccharidosis type VI: Journal of Inherited Metabolic Disease, 2014
66. Guven,Y., Altunoglu,U., Aktoren,O., Uyguner,Z.O., Kayserili,H., Kaewkahya,M., Kantaputra,P.N., Twins with hereditary sensory and autonomic neuropathy type IV with preserved periodontal sensation: European Journal of Medical Genetics, 2014
67. Kantaputra,P., Kaewgahya,M., Kantaputra,W., WNT10A mutations also associated with agenesis of the maxillary permanent canines, a separate entity: American Journal of Medical Genetics, Part A, 2014
68. Kantaputra,P.N., Kaewgahya,M., Wiwatwongwana,A., Wiwatwongwana,D., Sittiwangkul,R., Iamaroon,A., Dejkhamron,P., Cutis laxa with pulmonary emphysema, conjunctivochalasis, nasolacrimal duct obstruction, abnormal hair, and a novel FBLN5 mutation: American Journal of Medical Genetics, Part A, 2014
69. Kantaputra,P., Kaewgahya,M., Jotikasthira,D., Kantaputra,W., Tricho-odonto-onycho-dermal dysplasia and WNT10A mutations: American Journal of Medical Genetics, Part A, 2014
70. Kantaputra,P.N., Kayserili,H., Guven,Y., Kantaputra,W., Balci,M.C., Tanpaiboon,P., Tananuvat,N., Uttarilli,A., Dalal,A., Clinical manifestations of 17 patients affected with mucopolysaccharidosis type VI and eight novel ARSB mutations: American Journal of Medical Genetics, Part A, 2014
71. Tananuvat,N., Charoenkwan,P., Ohazama,A., KetudaCairns,J.R., Kaewgahya,M., Kantaputra,P.N., Root dentin anomaly and a PLG mutation: European Journal of Medical Genetics, 2014
72. Kantaputra,P.N., BCOR mutations and unstoppable root growth: A commentary on oculofaciocardiodental syndrome: Novel BCOR mutations and expression in dental cells: Journal of Human Genetics, 2014
73. Kantaputra,P.N., Bongkochwilawan,C., Kaewgahya,M., Ohazama,A., Kayserili,H., Erdem,A.P., Aktoren,O., Guven,Y., Enamel-Renal-Gingival syndrome, hypodontia, and a novel FAM20A mutation: American Journal of Medical Genetics, Part A, 2014
74. Kantaputra,P.N., Kaewgahya,M., Khemaleelakul,U., Dejkhamron,P., Sutthimethakorn,S., Thongboonkerd,V., Iamaroon,A., Enamel-renal-gingival syndrome and FAM20A mutations: American Journal of Medical Genetics, Part A, 2014
75. Kantaputra,P.N., Clinical Correlate: CLCN7-Associated Autosomal Recessive Osteopetrosis: Mineralized Tissues in Oral and Craniofacial Science: Biological Principles and Clinical Correlates, 2013
76. Kantaputra,P.N., Sittiwangkul,R., Sonsuwan,N., Romanelli,V., Tenorio,J., Lapunzina,P., A novel mutation in CDKN1C in sibs with Beckwith-Wiedemann syndrome and cleft palate, sensorineural hearing loss, and supernumerary flexion creases: American Journal of Medical Genetics, Part A, 2013
77. Kantaputra,P.N., Chinadet,W., Ohazama,A., Kono,M., Dyschromatosis symmetrica hereditaria with long hair on the forearms, hypo/hyperpigmented hair, and dental anomalies: Report of a novel ADAR1 mutation: American Journal of Medical Genetics, Part A, 2012
78. Kantaputra,P.N., Thawanaphong,S., Issarangporn,W., Klangsinsirikul,P., Ohazama,A., Sharpe,P., Supanchart,C., Long-term survival in infantile malignant autosomal recessive osteopetrosis secondary to homozygous p.Arg526Gln mutation in CLCN7: American Journal of Medical Genetics, Part A, 2012
79. Kayserili,H., Kantaputra,P.N., Multiple supernumerary molars, anterior openbite, and large ear lobules in mucopolysaccharidosis type VI patient: American Journal of Medical Genetics, Part A, 2012
80. Kantaputra,P.N., Matangkasombut,O., Sripathomsawat,W., Split hand-split foot-ectodermal dysplasia and amelogenesis imperfecta with a TP63 mutation: American Journal of Medical Genetics, Part A, 2012
81. Kaewkhampa,A., Jotikasthira,D., Malaivijitnond,S., Kantaputra,P., TBX22 mutation associated with cleft lip/palate, hypodontia, and limb anomaly: Cleft Palate-Craniofacial Journal, 2012
82. Kantaputra,P.N., vandenOuweland,A., Sangruchi,T., Limwongse,C., Severe plexiform facial neurofibromatosis, type 1 with underdeveloped eyes and a novel NF1 mutation: American Journal of Medical Genetics, Part A, 2012
83. Kantaputra,P.N., Paramee,M., Kaewkhampa,A., Hoshino,A., Lees,M., McEntagart,M., Masrour,N., Moore,G.E., Pauws,E., Stanier,P., Cleft lip with cleft palate, ankyloglossia, and hypodontia are associated with TBX22 mutations: Journal of Dental Research, 2011
84. Kantaputra,P., Tanpaiboon,P., Porntaveetus,T., Ohazama,A., Sharpe,P., Rauch,A., Hussadaloy,A., Thiel,C.T., The smallest teeth in the world are caused by mutations in the PCNT gene: American Journal of Medical Genetics, Part A, 2011
85. Kantaputra,P.N., Malaivijitnond,S., Vieira,A.R., Heering,J., Dötsch,V., Khankasikum,T., Sripathomsawat,W., Mutation in SAM domain of TP63 is associated with nonsyndromic cleft lip and palate and cleft palate: American Journal of Medical Genetics, Part A, 2011
86. Kantaputra,P., Sripathomsawat,W., WNT10A and isolated hypodontia: American Journal of Medical Genetics, Part A, 2011
87. Sripathomsawat,W., Tanpaiboon,P., Heering,J., Dötsch,V., Hennekam,R.C., Kantaputra,P., Phenotypic analysis of Arg227 mutations of TP63 with emphasis on dental phenotype and micturition difficulties in EEC syndrome: American Journal of Medical Genetics, Part A, 2011
88. Kantaputra,P.N., Klopocki,E., Hennig,B.P., Praphanphoj,V., LeCaignec,C., Isidor,B., Kwee,M.L., Shears,D.J., Mundlos,S., Mesomelic dysplasia Kantaputra type is associated with duplications of the HOXD locus on chromosome 2q: European Journal of Human Genetics, 2010
89. Tanpaiboon,P., Kantaputra,P., Wejathikul,K., Piyamongkol,W., c. 595-596 insC of FOXC2 underlies lymphedema, distichiasis, ptosis, ankyloglossia, and robin sequence in a Thai patient: American Journal of Medical Genetics, Part A, 2010
90. Kantaputra,P.N., Mundlos,S., Sripathomsawat,W., A novel homozygous Arg222Trp missense mutation in WNT7A in two sisters with severe Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome: American Journal of Medical Genetics, Part A, 2010
91. VanHaelst,M.M., Wang,R., Kantaputra,P.N., Palmer,R., Beales,P., Corrigendum to obesity syndrome, MOMES caused by deletion-duplication (4q35.1 del and 5p14.3 duplication) (American Journal of Medical Genetics Part A (2009) 149, 4, (833-834)): American Journal of Medical Genetics, Part A, 2010
92. Koster,M.I., Marinari,B., Payne,A.S., Kantaputra,P.N., Costanzo,A., Roop,D.R., ΔNp63 knockdown mice: A mouse model for AEC syndrome: American Journal of Medical Genetics, Part A, 2009
93. Tanpaiboon,P., Sittiwangkul,R., Dejkhamron,P., Srikummool,M., Sripathomsawat,W., Kantaputra,P., Expanding the phenotypic spectrum of acro-cardio-facial syndrome (ACFS): Exclusion of P63 mutation: American Journal of Medical Genetics, Part A, 2009
94. VanHaelst,M.M., Wang,R., Kantaputra,P.N., Palmer,R., Beales,P., Obesity Syndrome, MOMES caused by deletion-duplication (4q35.1 del and 5p14.3 dup): American Journal of Medical Genetics, Part A, 2009
95. Kantaputra,P., Miletich,I., Lüdecke,H.-J., Suzuki,E.Y., Praphanphoj,V., Shivdasani,H., Wuelling,M., Vortkamp,A., Napierala,D., Sharpe,P.T., Tricho-rhino-phalanqeal syndrome with supernumerary teeth: Journal of Dental Research, 2008
96. Kantaputra,P.N., Chiewcharnvalijkit,M.S.K., Wairatpanich,K., Malikaew,P., Aramrattana,A., Children's attitudes toward behavior management techniques used by dentists: Journal of Dentistry for Children, 2007
97. Kantaputra,P.N., Limwongse,C., Koolvisoot,A., Ausawamongkolkul,A., Tayavitit,S., A newly recognized polyosteolysis/hyperostosis syndrome: American Journal of Medical Genetics, Part A, 2006
98. Kantaputra,P.N., Limwongse,C., Tochareontanaphol,C., Mutirangura,A., Mevatee,U., Praphanphoj,V., Contiguous gene syndrome of holoprosencephaly and hypotrichosis simplex: Association with an 18p11.3 deletion: American Journal of Medical Genetics, Part A, 2006
99. Hall,J.G., Kantaputra,P.N., Tanpaiboon,P., Re: Microcephalic osteodysplastic primordial dwarfism with severe microdontia and skin anomalies [Kantaputra et al. 2004. Am J Med Genet 130A:181-190] [4] (multiple letters): American Journal of Medical Genetics, 2005
100. Kantaputra,P.N., Tanpaiboon,P., A newly recognized syndrome involving limbs, pelvis, and genital organs or a variant of Al-Awadi/Raas-Rothschild syndrome?: American Journal of Medical Genetics, 2005
101. Kantaputra,P.N., Thirteen-year-follow up report on mesomelic dysplasia, Kantaputra type (MDK), and comments on the paper of the second reported family of MDK by Shears et al.: American Journal of Medical Genetics, 2004
102. Kantaputra,P.N., Tanpaiboon,P., Unachak,K., Praphanphoj,V., Microcephalic osteodysplastic primordial dwarfism with severe microdontia and skin anomalies: Confirmation of a new syndrome: American Journal of Medical Genetics, 2004
103. Kantaputra,P., Tanpaiboon,P., Thyroid dysfunction in a patient with aglossia: American Journal of Medical Genetics, 2003
104. Kantaputra,P.N., Pongprot,Y., Praditsap,O., Pho-iam,T., Limwongse,C., A new syndrome of symphalangism, multiple frenula, postaxial polydactyly, dysplastic ears, dental anomalies, and exclusion of NOG and GDF5: American Journal of Medical Genetics, 2003
105. Kantaputra,P.N., Kinoshita,A., Limwonges,C., Praditsup,O., Niikawa,N., A Thai mother and son with distal symphalangism, hypoplastic carpal bones, microdontia, dental pulp stones, and narrowing of the zygomatic arch: A new distal symphalangism syndrome?: American Journal of Medical Genetics, 2002
106. Kantaputra,P.N., Sumitsawan,Y., Schutte,B.C., Tochareontanaphol,C., Van der Woude syndrome with sensorineural hearing loss, large craniofacial sinuses, dental pulp stones, and minor limb anomalies: Report of a four-generation Thai family: American Journal of Medical Genetics, 2002
107. Kondoh,S., Sugawara,H., Harada,N., Matsumoto,N., Ohashi,H., Sato,M., Kantaputra,P.N., Ogino,T., Tomita,H., Ohta,T., Kishino,T., Fukushima,Y., Niikawa,N., Yoshiura,K.-I., A novel gene is disrupted at a 14q13 breakpoint of t(2;14) in a patient with mirror-image polydactyly of hands and feet: Journal of Human Genetics, 2002
108. Kantaputra,P.N., Apparently new osteodysplastic and primordial short stature with severe microdontia, opalescent teeth, and rootless molars in two siblings: American Journal of Medical Genetics, 2002
109. Kantaputra,P.N., Yamasaki,K., Ishida,T., Kishino,T., Niikawa,N., A dominantly inherited malformation syndrome with short stature, upper limb anomaly, minor craniofacial anomalies, and absence of TBX5 mutations: Report of a Thai family: American Journal of Medical Genetics, 2002
110. Kantaputra,P.N., Kunachaichote,J., Patikulsila,P., Mental retardation, obesity, mandibular prognathism with eye and skin anomalies (MOMES Syndrome): A newly recognized autosomal recessive syndrome: American Journal of Medical Genetics, 2001
111. Kantaputra,P.N., Eiumtrakul,P., Matin,T., Opastirakul,S., Visrutaratna,P., Mevate,U., Cryptophthalmos, dental and oral abnormalities, and brachymesophalangy of second toes: New syndrome or Fraser syndrome?: American Journal of Medical Genetics, 2001
112. Kantaputra,P.N., Mai,C., A newly recognized syndrome of skeletal dysplasia with opalescent and rootless teeth: Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontics, 2001
113. Kantaputra,P.N., Laurin-Sandrow syndrome with additional associated manifestations: American Journal of Medical Genetics, 2001
114. Kantaputra,P.N., Chalidapong,P., Visrutaratna,P., Digitotalar dysmorphism with craniofacial and other new associated abnormalities: Clinical Dysmorphology, 2001
115. Kantaputra,P.N., Dentinogenesis imperfecta-associated syndromes: American Journal of Medical Genetics, 2001
116. Kantaputra,P.N., Chalidapong,P., Are triphalangeal thumb-polysyndactyly syndrome (TPTPS) and tibial hemimelia-polysyndactyly-triphalangeal thumb syndrome (THPTTS) identical? A father with TPTPS and his daughter with THPTTS in a Thai family: American Journal of Medical Genetics, 2000
117. Kantaputra,P.N., Gorlin,R.J., Ukarapol,N., Unachak,K., Sudasna,J., Robinow (fetal face) syndrome: Report of a boy with dominant type and an infant with recessive type: American Journal of Medical Genetics, 1999
118. Kantaputra,P.N., Mongkolchaisup,S., Juberg-Hayward syndrome: A new case report and clinical delineation of the syndrome: Clinical Dysmorphology, 1999
119. Fujimoto,M., Kantaputra,P.N., Ikegawa,S., Fukushima,Y., Sonta,S.-I., Matsuo,M., Ishida,T., Matsumoto,T., Kondo,S., Tomita,H., Deng,H.-X., D'urso,M., Rinaldi,M.M., Ventruto,V., Takagi,T., Nakamura,Y., Niikawa,N., The gen for mesomelic dysplasia Kantaputra type is mapped to chromosome 2q24-q32: Journal of Human Genetics, 1998
120. Kantaputra,P.N., Pruksachatkunakorn,C., Vanittanakom,P., Rapp-Hodgkin syndrome with palmoplantar keratoderma, glossy tongue, congenital absence of lingual frenum and of sublingual caruncles: Newly recognized findings: American Journal of Medical Genetics, 1998