ศ.ทพ. พีรนิธ กันตะบุตร
Piranit Kantaputra piranit.k@cmu.ac.th คณะทันตแพทยศาสตร์ มหาวิทยาลัยเชียงใหม่ศ.ทพ. พีรนิธ กันตะบุตร
Piranit Kantaputra
ส่วนวิชาการ/ภาควิชาทันตกรรมจัดฟันและทันตกรรมสำหรับเด็ก/สาขาวิชาทันตกรรมสำหรับเด็ก
| 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 |