W. Intachai

发表

WNT1-associated osteogenesis imperfecta with atrophic frontal lobes and arachnoid cysts

P. Visrutaratna, Jatupol Kampuansai, P. Kantaputra, 2019, Journal of Human Genetics.

Expanding genotypic and phenotypic spectrums of LTBP3 variants in dental anomalies and short stature syndrome

Chumpol Ngamphiw, S. Tongsima, A. Tucker, 2022, Clinical genetics.

ADAMTSL1 and mandibular prognathism

Chumpol Ngamphiw, S. Tongsima, A. Ohazama, 2019, Clinical genetics.

Mutations in LRP6 highlight the role of WNT signaling in oral exostoses and dental anomalies.

Chumpol Ngamphiw, S. Tongsima, A. Tucker, 2022, Archives of oral biology.

Novel Dental Anomaly–associated Mutations in WNT10A Protein Binding Sites

Chumpol Ngamphiw, S. Tongsima, P. Kantaputra, 2022, International dental journal.

Clinical and Genetic Studies of the First Monozygotic Twins with Pfeiffer Syndrome

K. Katanyuwong, Chumpol Ngamphiw, S. Tongsima, 2022, Genes.

WNT1-associated osteogenesis imperfecta with atrophic frontal lobes and arachnoid cysts

P. Visrutaratna, Jatupol Kampuansai, P. Kantaputra, 2019, Journal of Human Genetics.

Harboyan syndrome: novel SLC4A11 mutation, clinical manifestations, and outcome of corneal transplantation

B. Olsen, Jatupol Kampuansai, P. Kantaputra, 2020, Journal of human genetics.

Harboyan syndrome: novel SLC4A11 mutation, clinical manifestations, and outcome of corneal transplantation

Jatupol Kampuansai, P. Kantaputra, M. Srikummool, 2020, Journal of Human Genetics.

All enamel is not created equal:Supports from a novel FAM83H mutation

P. Kantaputra, P. Auychai, W. Intachai, 2016, American journal of medical genetics. Part A.

Are dental anomalies associated with Tietz syndrome?

B. Olsen, P. Kantaputra, J. R. Ketudat Cairns, 2020, European Journal of Dermatology.

Genetic Variants in Protein Tyrosine Phosphatase Non-Receptor Type 23 Are Responsible for Mesiodens Formation

S. Eliason, S. Arold, S. Tongsima, 2023, Biology.

Dental Anomalies in Ciliopathies: Lessons from Patients with BBS2, BBS7, and EVC2 Mutations

K. Katanyuwong, P. Beales, S. Tongsima, 2022, Genes.

Cryptophthalmos, dental anomalies, oral vestibule defect, and a novel FREM2 mutation

S. Tongsima, A. Tucker, P. Kantaputra, 2021, Journal of Human Genetics.

Cryptophthalmos, dental anomalies, oral vestibule defect, and a novel FREM2 mutation

S. Tongsima, A. Tucker, P. Kantaputra, 2021, Journal of human genetics.

A Mutation in CACNA1S Is Associated with Multiple Supernumerary Cusps and Root Maldevelopment

S. Tongsima, A. Ohazama, N. Quarto, 2023, Diagnostics.

Osteogenesis imperfecta with ectopic mineralizations in dentin and cementum and aCOL1A2mutation

S. Tongsima, P. Kantaputra, Y. Sirirungruangsarn, 2018, Journal of Human Genetics.

WNT10B mutations associated with isolated dental anomalies

C. Leethanakul, A. Tolun, P. Kantaputra, 2018, Clinical genetics.

Split hand-foot malformation and a novel WNT10B mutation.

S. Kapoor, P. Kantaputra, J. R. Ketudat Cairns, 2018, European journal of medical genetics.

Clouston syndrome with pili canaliculi, pili torti, overgrown hyponychium, onycholysis, taurodontism and absence of palmoplantar keratoderma

A. Ohazama, N. Quarto, K. Kawasaki, 2020, The Journal of dermatology.

Clouston syndrome with dental anomalies, micropores of hair shafts and absence of palmoplantar keratoderma

P. Kantaputra, Bruce M. Carlson, C. Pruksachatkunakorn, 2020, The Journal of dermatology.

Distal renal tubular acidosis, autoimmune thyroiditis, enamel hypomaturation, and tooth agenesis caused by homozygosity of a novel double-nucleotide substitution in SLC4A4.

S. Tongsima, P. Kantaputra, Cezmi Doğan, 2022, Journal of the American Dental Association.

SERPINA1, generalized pustular psoriasis, and adult‐onset immunodeficiency

J. McGrath, S. Tongsima, N. Quarto, 2021, The Journal of dermatology.

Subtotal Parathyroidectomy Successfully Controls Calcium Levels of Patients with Neonatal Severe Hyperparathyroidism Carrying a Novel CASR Mutation

S. Tongsima, P. Kantaputra, J. R. Ketudat Cairns, 2023, Hormone Research in Paediatrics.

Isolated dentinogenesis imperfecta with glass‐like enamel caused by COL1A2 mutation

S. Tongsima, P. Kantaputra, J. R. Ketudat Cairns, 2018, American journal of medical genetics. Part A.

Rare Genetic Variants in Human APC Are Implicated in Mesiodens and Isolated Supernumerary Teeth

S. Tongsima, T. Cox, P. Kantaputra, 2023, International journal of molecular sciences.

Treacher Collins syndrome: A novel TCOF1 mutation and monopodial stapes

S. Tongsima, N. Quarto, P. Kantaputra, 2020, Clinical otolaryngology : official journal of ENT-UK ; official journal of Netherlands Society for Oto-Rhino-Laryngology & Cervico-Facial Surgery.

TRPS1 mutation associated with trichorhinophalangeal syndrome type 1 with 15 supernumerary teeth, hypoplastic mandibular condyles with slender condylar necks and unique hair morphology

N. Quarto, W. Powcharoen, Bruce M. Carlson, 2020, The Journal of dermatology.

Dental Anomalies in Ciliopathies: Lessons from Patients with BBS2, BBS7, and EVC2 Mutations

P. Kitcher, K. Katanyuwong, S. Tongsima, 2022, Genes.

Loss of Function TGFBR2 Variant as a Contributing Factor in Generalized Pustular Psoriasis and Adult-Onset Immunodeficiency

S. Tongsima, T. Cox, Jatupol Kampuansai, 2022, Genes.

Juberg-Hayward syndrome and Roberts syndrome are allelic, caused by mutations in ESCO2.

B. Olsen, S. Tongsima, L. Ngiwsara, 2020, Archives of oral biology.

SERPINB3, Adult-Onset Immunodeficiency, and Generalized Pustular Psoriasis

P. Pontisso, S. Tongsima, T. Cox, 2023, Genes.