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Piranit Nik Kantaputra

Department of Pediatric Dentistry

Faculty of Dentistry

Chiang Mai University



Name/email consistency: low



  • Department of Pediatric Dentistry, Faculty of Dentistry, Chiang Mai University, Thailand. 1999 - 2007


  1. Children's attitudes toward behavior management techniques used by dentists. Kantaputra, P.N., Chiewcharnvalijkit, K., Wairatpanich, K., Malikaew, P., Aramrattana, A. J. Dent. Child. (Chic) (2007) [Pubmed]
  2. Contiguous gene syndrome of holoprosencephaly and hypotrichosis simplex: association with an 18p11.3 deletion. Kantaputra, P.N., Limwongse, C., Tochareontanaphol, C., Mutirangura, A., Mevatee, U., Praphanphoj, V. Am. J. Med. Genet. A (2006) [Pubmed]
  3. A newly recognized polyosteolysis/hyperostosis syndrome. Kantaputra, P.N., Limwongse, C., Koolvisoot, A., Ausawamongkolkul, A., Tayavitit, S. Am. J. Med. Genet. A (2006) [Pubmed]
  4. 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. Kantaputra, P.N. Am. J. Med. Genet. A (2004) [Pubmed]
  5. Microcephalic osteodysplastic primordial dwarfism with severe microdontia and skin anomalies: confirmation of a new syndrome. Kantaputra, P.N., Tanpaiboon, P., Unachak, K., Praphanphoj, V. Am. J. Med. Genet. A (2004) [Pubmed]
  6. Heterozygous mutation in the SAM domain of p63 underlies Rapp-Hodgkin ectodermal dysplasia. Kantaputra, P.N., Hamada, T., Kumchai, T., McGrath, J.A. J. Dent. Res. (2003) [Pubmed]
  7. A new syndrome of symphalangism, multiple frenula, postaxial polydactyly, dysplastic ears, dental anomalies, and exclusion of NOG and GDF5. Kantaputra, P.N., Pongprot, Y., Praditsap, O., Pho-iam, T., Limwongse, C. Am. J. Med. Genet. A (2003) [Pubmed]
  8. Thyroid dysfunction in a patient with aglossia. Kantaputra, P., Tanpaiboon, P. Am. J. Med. Genet. A (2003) [Pubmed]
  9. 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. Kantaputra, P.N., Sumitsawan, Y., Schutte, B.C., Tochareontanaphol, C. Am. J. Med. Genet. (2002) [Pubmed]
  10. 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?. Kantaputra, P.N., Kinoshita, A., Limwonges, C., Praditsup, O., Niikawa, N. Am. J. Med. Genet. (2002) [Pubmed]
  11. Apparently new osteodysplastic and primordial short stature with severe microdontia, opalescent teeth, and rootless molars in two siblings. Kantaputra, P.N. Am. J. Med. Genet. (2002) [Pubmed]
  12. A dominantly inherited malformation syndrome with short stature, upper limb anomaly, minor craniofacial anomalies, and absence of TBX5 mutations: report of a Thai family. Kantaputra, P.N., Yamasaki, K., Ishida, T., Kishino, T., Niikawa, N. Am. J. Med. Genet. (2002) [Pubmed]
  13. Cryptophthalmos, dental and oral abnormalities, and brachymesophalangy of second toes: new syndrome or Fraser syndrome?. Kantaputra, P., Eiumtrakul, P., Matin, T., Opastirakul, S., Visrutaratna, P., Mevate, U. Am. J. Med. Genet. (2001) [Pubmed]
  14. Digitotalar dysmorphism with craniofacial and other new associated abnormalities. Kantaputra, P.N., Chalidapong, P., Visrutaratna, P. Clin. Dysmorphol. (2001) [Pubmed]
  15. A newly recognized syndrome of skeletal dysplasia with opalescent and rootless teeth. Kantaputra, P.N. Oral. Surg. Oral. Med. Oral. Pathol. Oral. Radiol. Endod (2001) [Pubmed]
  16. Mental retardation, obesity, mandibular prognathism with eye and skin anomalies (MOMES syndrome): a newly recognized autosomal recessive syndrome. Kantaputra, P.N., Kunachaichote, J., Patikulsila, P. Am. J. Med. Genet. (2001) [Pubmed]
  17. Robinow (fetal face) syndrome: report of a boy with dominant type and an infant with recessive type. Kantaputra, P.N., Gorlin, R.J., Ukarapol, N., Unachak, K., Sudasna, J. Am. J. Med. Genet. (1999) [Pubmed]
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