Chiang Mai University (Thailand)

Professor in Medical Genetics
Director, Center of Excellence in Medical Genetics Research (CEMGR) , Chiang Mai University_;
Department of Orthodontic and Pediatric Dentistry, Faculty of Dentistry, Chiang Mai Univer- sity, Chiang Mai 50200, THAILAND Tel: +66-053-944460 Fax: +66-053-222844 Cell:
+66-81-9524529
DENTALAND
7 Nimmanhemin Lane 17 Chiang Mai 50200, THAILAND

Education:

Fellowship in Clinical Genetics and Dysmorphology, U. of Minnesota 1990-1991; Master of Science (M.S.) U. of Minnesota 1988-1990; Certificate in Pediatric Dentistry U. of Minnesota 1988-1990; Doctor of Dental Surgery (D.D.S.) Chiang Mai University (1981-1987) Administration Experience
Associate dean (Faculty of Dentistry, Chiang Mai University)1992-1993.
Academic positions Instructor 1991-2017 Professor 2017-present
Member of Academic Committee of The Thai Society of Pediatric Dentistry 2002-present Academic Advisor of the The Thai Society of Pediatric Dentistry 2005-present Member of Academic Committee of The Thai Dental Association 2002-present Member of Thailand Medical Genetic Association 2001-present
Editorial Board member of American Journal of Medical Genetics, Journal of Human Genet- ics, and Journal of Clinical Investigative Dentistry.
Reviewer of American Journal of Medical genetics, Clinical Genetics, Journal of Dental Re- search, European Journal of Medical Genetics, European Journal of Orthodontics,

International Experience (in short)

*Dental School, U. of Otago, New Zealand (Dental morphology of Down Syndrome Re- search).
*Nagasaki University School of Medicine, Department of Human Genetics (Linkage analysis of Mesomelic Dysplasia, Kantaputra type; Mutation analysis of a new syndrome with upper limb anomalies: Mutation analysis of a Thai family with Distal symphalangism and associat- ed anomalies) 1997-2001
*Lectures in the areas of Craniofacial Genetics at UCLA, U. of Michigan, U. of Minnesota,
U. of Melbourne. July 2002.
*Editorial board member and reviewer of Oral Bioscience and Medicine 2002-2004
*Advisor of WHO on Registry of Craniofacial Anomalies. Bauru, Brazil, December 2001.
th
*Guest speaker of The 4 Conference of Pediatric Dentistry Association of Asia. Shangri-La
Hotel, Bangkok, September 23-24, 2004.
*“What Face and Teeth Can tell you About Syndromes” Visiting Researcher at the University of Iowa Medical School. April 2-27, 2005.
*Lecture at the Department of Pediatric Dentistry, School of Dentistry. The University of Minnesota. “What face and Teeth can Tell you About syndromes” April 29, 2005.
*Invited lecturer at the School of Dentistry, The University of Michigan, Ann Arbor. “Cranio- facial and Limbs Syndromes. October 17, 2005.
*Genetics of Hypodontia. IAPD Meeting in Sydney, Australia. November 2005.
*Craniofacial and Teeth Syndrome. Medical School, University of Florence, Italy. June 2006.
*Craniofacial Anomalies for Pediatric Dentists. Meeting of Postgraduate students of India. Chennai, June 2006.
*Clinical Genetics and Syndromes in Pediatric Dentistry. First Annual Robert J. Feigal Sym- posium in Pediatric Dentistry. U of Minnesota, October 20, 2007.
*What Face and Teeth Can Tell you about syndromes. University of North Carolina, at Chapel Hill, October 30, 2007
*What Face and Teeth Can Tell you about syndromes. Department of Pediatric Dentistry, University of Iowa, November 5, 2007.
*Molecular Dysmorphology of Rare Syndromes. Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan January 8, 2008.
*What Face and Teeth Can Tell you about syndromes. Seminar for Graduate Studies. Tokyo Medical and Dental University. January 11, 2008.
*Craniofacial Manifestations of p63-Associated Ectodermal Dysplasia. EPISTEM Meeting in Ghent, Belgium, February 29, 2008.
*Craniofacial Genetics. U of Manitoba. June 2009
*Research Presentation at Gordon research conference in Epithelial proliferation and differ- entiation. Les Diablerets, Switzerland, June 2009.
*Research Presentation at Gordon research conference in Cartilage biology and pathology. Les Diablerets, Switzerland, June 2009.
*“Ectodermal Dysplasia”. Department of Pediatrics, Craniofacial genetics Lab, University of Iowa. July 2009.
*Craniofacial genetics for undergraduate students. School of Dentistry, U of Pittsburgh. July 2009.
*“Cleft Lip with Cleft Palate, Ankyloglossia and Hypodontia are Associated with TBX22 Mu- tations”. Gordon research Conference, Ill Ciacco, Italy. April 14-17, 2010.
*“What face and teeth can tell you about syndromes”. International Symposium on Genet- ics. Manipal, India. February 19, 2011.
*Molecular Pathogenesis of Craniofacial Anomalies. Center for DNA Fingerprint and Diag- nostics. Hyderabad, India. March 14, 2011.
*Oral Manifestations of Patients with Mucopolysaccharidosis type VI, BioMarin Pharmaceu- tical Company, CA, USA. June 20, 2011.
*The smallest teeth in the world are caused by mutations in PCNT gene. Invited short talk. Gordon Research Conference in Bones and Teeth. Les Diablerets, Switzerland. July 16, 2011.
*Oral manifestations of Patients with Mucopolysaccharidosis type VI. Annual Meeting of Polish Society of Mucopolysaccharidosis, Warsaw, Poland. March 5, 2012.
*Teeth and Gum and syndrome diagnosis. Indian Society of Human Genetics, Chandigarh, India.March 8, 2012.
*What face and teeth and tell you about syndromes. Department of Medical Genetics. Uni- versity of Lucknow, India. March 10, 2012.
*What face and teeth and tell you about syndromes. Department of Medical Genetics. AI- IMS, India. March, 2012
*What face and teeth and tell you about syndromes. University of Leuven, Belgium.March 2013.
*What face and teeth and tell you about syndromes. University of Nijmegen, March 2013.
*What face and teeth and tell you about syndromes. Department of Medical Genetics, Utrecht, The Netherlands. August 6, 2013.
*What face and teeth and tell you about syndromes. University of British Columbia, Canada.
*August 2013.
“Teeth and Human disease”. International Association of Dental Research-Asian Pacific Region. Bangkok. August 2013.
“Teeth, Gum, and Genetic diseases”. International congress of Dental Association of Thai- land. Bangkok. November 2013.
*”The Biggest Teeth in the World are Caused by Mutations in GFPT1 Gene”. Invited short talk. Gordon Research Conference in Bones and Teeth. Galveston, Texas, January 2014.
“Teeth and Genetic Diseases”. The 15th Anniversary of Genomic Center for Cancer Re- search and Diagnosis, University of Manitoba, Canada. June 13, 2014.
“Genetics for Pediatirc dentists”. Pediatric Dental Assoication of Asia. Tokyo, May 2016 Tooth and its genetic syndromes. Seminar in Genetics, University of Oxford, UK June 2016.
“What face and teeth and tell you about syndromes”. Pediatric Dental Group meeting, Bris- bane, Australia, February, 2017.
“What face and teeth and tell you about syndromes” University of Otago, New Zealand, February 2017.
“What face and teeth and tell you about syndromes”. Australasian Academy of Paediatric Dentistry, Auckland, New Zealand. February 2017.
Tooth and its genetic syndromes. Kyushu university . May 26, 2017.
“Strange teeth and Gum” Dental Association of Thailand annual meeting June 14, 2560.
“What face and teeth and tell you about syndromes” University of Dundee, Scotland June 21, 2017
“What face and teeth and tell you about syndromes” Harvard Medical School. August 23, 2017
ADAMTSL1 and Habsburg jaw. David Smith Dysmorphology conference, Vermont, Sep- tember 27, 2017
Writing case reports in order to understand human biology. Indian Society of Pediatric Dentistry, Chennai, India, September 15, 2017
Dental anomalies and syndromes. Asian Pacific Congress of Human Genetics, Bangkok. November 8-10, 2017
Tooth and Its syndromes. Faculty of Dentistry, October 6 University. June 26, 2018
“What face and teeth and tell you about syndromes” Alexandria Regional Centre, Alexan- dria, Egypt. June 27, 2018.
“What face and teeth and Gum can tell you about syndromes” Ramathibodi Hospital, Mahi- dol University November 15, 2018.
“Gene discovery for dental anomalies”. International Joint Conference on Genetics & Medi- cine, Seoul, Korea. November 29th– 30th, 2018.
Publications

1. Kantaputra PN, Gorlin RJ. Double dens invaginatus of molarized maxillary central in- cisors, premolarization of maxillary lateral incisors, multituberculism of the mandibular in- cisors, canines and first premolar, and sensorineural hearing loss. Clin Dysmorphol 1992;1:128-136.
2. Kantaputra PN, Gorlin RJ, Langer LO Jr. Dominant mesomelic dysplasia, ankle, carpal and tarsal synostosis type: A new autosomal dominantbone disorder. Report of cases. Am J Med Genet Part A 1992;44A:730-737.
3. Gorlin RJ, Kantaputra PN, Aughton DJ, and Mulliken JB. Marked female predilection in some syndromes associated with facial hemangiomas. Am J Med Genet Pat A 1994;52A: 130-135.
4. Fujimoto M, Kantaputra PN, Ikegawa S, Fukushima Y, Sonta S, Matsuo M, Ishida T, Matsumoto T, Kondo S, Tomita H, Deng H, D'urso M, Rinaldi MM, Ventruto V, Takagi T,

Nakamura Y, Niikawa N. The gene for mesomelic dysplasia, Kantaputra type is mapped to chromosome 2q24-q32. J Hum Genet 1998;43:32-36.

1. Kantaputra PN, Pruksachatkunakorn C, Vanittanakom P. Rapp-Hodgkin syndrome with palmoplantar keratoderma, glossy tongue, and congenital absence of lingual frenum and sublingual caruncles: Newly recognized findings. Am J Med Genet Part A 1998;79A:

343-346.

1. Kantaputra PN, Gorlin RJ, Ukarapol N, Unachak K, Sudasna J. Robinow (fetal face) syndrome: Report of a patient with the dominant type and another with recessive type. Am J Med Genet Part A 1999;84A:1-7.
2. Kantaputra PN, Mongkolchaisup S. Juberg-Hayward syndrome: a new case report and clinical delineation of the syndrome. Clin Dysmorphol 1999;8:123-127.
3. Kantaputra PN, Chalidapong P. 2000. Are Triphalangeal thumb-Polysyndactyly Syn- drome and Tibia Hemimelia-Polysyndactyly-Triphalangeal Thumb Syndrome identical? Am J Med Genet Oart A 2001;93A:126-131.
4. Kantaputra PN. Laurin-Sandrow syndrome with mental retardation, underdeveloped nasal bone, scar-like seams under the nose, large heads of mandibular condyles, and brachymesophalangy of toes: The newly recognized findings and clinical delineation of the syndrome. Am J Med Genet Part A 2001;98A:210-215.
5. Kantaputra PN, Eiumtrakul P, Matin T, Opastirakul S, Visrutaratna P, Mevatee U. Cryptophthalmos associated with delayed dental development, hypodontia, microdontia,and brachymesophalangy. Am J Med Genet Part A 2001;98A:263-268.
6. Kantaputra PN. A newly recognized syndrome of skeletal dysplasia with opalescent and rootless teeth. Oral Surg Oral Pathol Oral Med Oral Radiol Endodont

2001;92:303-307.

1. Kantaputra PN, Chalidapong P, Visrutaratna P. Digitotalar dysmorphism with cranio- facial manifestations: The newly recognized findings in a Thai family. Clin Dysmorphol 2001;10:171-175.
2. Kantaputra PN. Dentinogenesis Imperfecta-Associated Syndromes. Am J Med Genet Part A 2001;104A:75-78.
3. Kantaputra PN, Kunachaichote J, Patikulsila P. Mental Retardation, Obesity, Mandibular prognathism with eye and skin anomalies (MOMES syndrome): A Newly Rec- ognized Autosomal Recessive Syndrome. Am J Med Genet Part A 2002;103A:283-288.
4. Kantaputra PK, Kinoshita A, Chanin Limwongse, Oranud Praditsup, Niikawa N. Distal symphalangism with hypoplastic carpal bones, microdontia, dental pulp stone, narrowing of zygomatic arch: A newly recognized syndrome. Am J Med Genet Part A 2002;109A: 56-60.
5. Kantaputra PN, Sumitsawan Y, Schutte B, Tochareontanaphol C. Van der Woude syndrome with sensorineural hearing loss, large craniofacial sinuses, dental pulp stones, and limb anomalies: Report of a four-generation Thai family. Am J Med Genet Part A 2002;108A:275-280.
6. Kantaputra PN, Yamasaki K, Ishida T, Kishino T, Niikawa N: A dominantly inherited malformation syndrome with short stature, upper limb anomaly, minor craniofacial anom- alies, and absence of TBX5 mutations: report of a Thai family. AM J Med Genet Part A 2002;111A:301-306.
7. Kantaputra PN. 2002. Apparently new osteodysplastic and primordial short stature with severe microdontia, opalescent teeth, and rootless molars in two siblings. Am J Med Genet111:420-428.
8. S. Kondoh, H. Sugawara, N. Harada, N. Matsumoto, H. Ohashi, M. Sato, P. N. Kanta- putra, T. Ogino, H. Tomita, T. Ohta, T. Kishino, Y. Fukushima, N. Niikawa, K. Yoshiura. 2002. A novel gene is disrupted at a 14q13 breakpoint of t(2;14) in a patient with mirror- image polydactyly of hands and feet. J Hum Genet 47:136-139.
9. Kantaputra PN, 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. Am J Med Genet Part A 2003;120A:

381-385.

1. Kantaputra PN, Tanpaiboon P. Thyroid dysfunction in a patient with aglossia. Am J Med Genet Part A 2003;122A:274-277.
2. Kantaputra PN, Hamada T, Kumchai T, John A. McGrath JA. 2003. Heterozygous Mu- tation in the SAM domain of p63 Underlies Rapp-Hodgkin Ectodermal Dysplasia. J Dent Res 82(6):433-437.
3. Kantaputra PN. 2004. Thirteen-year-follow up report on Mesomelic dysplasia, Kanta- putra Type (MDK) and comments on the paper of the second reported family of MDK by Shears et al. Am J Med Genet Part A 128A(1):1-5.
4. Kantaputra PN, Tanpaiboon P, Unachak, Praphanphoj V. 2004. Microcephalic os- teodysplastic primordial dwarfism with severe microdontia and skin anomalies: Confirma- tion of a new syndrome. Am J Med Genet Part A 130A:181-190.
5. Kantaputra PN, Limwongse C, Assawamakin A, Praditsap O, Kemaleelakul U, Miedzybrodzka ZH, Kondo S, Schutte B. A novel mutaion in IRF6 underlies sensorineural hearing loss, dental pulp stones, large craniofacial sinuses, and limb anomalies in Van der Woude syndrome patients. Oral Biosci Med 2004;1:277-283.
6. Kantaputra PN, Tanpaiboon P. A Newly Recognized Syndrome Involving Limbs, Pelvis, and Genital Organs or a Variant of Al-Awadi/Raas-Rothschild Syndrome? Am J Med Genet Part A 2005;132A:63-67.
7. Kantaputra PN, Tanpaiboon P. Response to: Microcephalic osteodysplastic primordial dwarfism with severe microdontia and skin anomalies by Dr. Judith Hall. Am J Med Genet Part A 2004;130A:181-90.
8. Kantaputra P, Limwongse, Tochareontanaphol C, Mutirangura A, Mevatee U, Praphanphoj V. “New Ectodermal Dysplasia-Holoprosencephaly Syndrome Associated With 45,XY,der(15;18)t(15;18)(q10;q10)” Am J Med Genet Part A 2006;140A:2598-2602.
9. Kantaputra PN, Limwongse C, Koolvisoot A, Ausawamongkolkul A, TayavititS. A newly recognized polyosteolysis/hyperostosis syndrome. Am J Med Genet 2006;140A:2640-2645.
10. Kantaputra P, Chiewcharnvalijkit K, Wairatpanich, K, Aramrattana A, Malikaew P. Chil- drenʼs Attitudes Towards Behavior Management Techniques Used by Dentists. J Dent Child 2007;74:4-9.
11. Kantaputra P, Miletich I, Lüdecke HJ, Suzuki EY, Praphanphoj V, Shivdasani R, Wuelling M, Vortkamp A, Napierala D, Sharpe PT. Tricho-rhino-phalangeal syndrome with supernumerary teeth. J Dent Res 2008;87:1027-1031.
12. Koster MI, Marinari B, Payne AS, Kantaputra PN, Costanzo A, Roop DR. ΔNp63 Knockdown mice: A Mouse Model for AEC Syndrome. Am J Med Genet A. 2009 Sep; 149A(9): 1942-1947.
13. Tanpaiboon P, Sripathomsawat WJ, Srikummool M, Kantaputra P. Expanding the phe- notypic Spectrum of Acro-Cardio-Facial Syndrome. Am J Med Genet A. 2009 Aug;149A(8): 1749-1753.
14. van Haelst MM, Wang R, Kantaputra PN, Palmer R, Beales P. Obesity Syndrome, MOMES caused by deletion-duplication (4q35.2 del and 5p15 duplication). Am J Med Genet A. 2009;149A(4):833-834.
15. Tanpaiboon P, Sittiwangkul R, Dejkhamron P, Srikummool M, Sripathomsawat W, Kan- taputra P. Expanding the phenotypic spectrum of acro-cardio-facial syndrome (ACFS): Ex- clusion of P63 mutation. Am J Med Genet A. 2009;149A:1749-1753.
16. 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. Am J Med Genet A. 2010;152A(3):737-740.
17. Kantaputra P, Klopocki E, Hennig BP, Praphanphoj V, Le Caignec C, Isidor B, Kwee ML, Shears DJ, Mundlos S. 2010. Kantaputra type mesomelic dysplasia is associated with duplications of the HOXD locus on chromosome 2q. Eur J Hum Genet 18(12):1310-1314.
18. Kantaputra PN , Mundlos S, Sripathomsawat W. A Novel Homozygous Arg222Trp Mis- sense Mutation in WNT7A in two Sisters with Severe Al-Awadi/Raas-Rothschild/ Schinzel Phocomelia Syndrome. Am J Med Genet 2010 Part A 152A:2832–2837.
19. Sripathomsawat W, Tanpaiboon P, Heering J, Dötsch V, Hennekam RC, Kantaputra

P. 2011. Phenotypic analysis of Arg227 mutations of TP63 with emphasis on dental phenotype and micturition difficulties in EEC syndrome. Am J Med Genet Part A Jan; 155A(1):228-232.
39. Kantaputra PN, Paramee M, Kaewkhampa A, Hoshino A, Lees M, McEntagart M, Mas- rour N, Moore GE, Pauws E, Stanier P. Cleft Lip with Cleft Palate, Ankyloglossia and Hy- podontia are Associated with TBX22 Mutations. J Dent Res 2011 90:450-455.
40 Kantaputra P, Sripathomsawat S. 2011. Wnt10A and Isolated hypodontia. Am J Med Genet 2011 155:1119-1122.

1. Kantaputra PN , Malaivijitnond S, Vieira AR, Heering J, Dötsch V, Khankasikum T, Sripathomsawat W. Mutation in SAM domain of P63 is associated with isolated cleft lip and Palate. Am J Med Genet 2011 155:1432-1436.
2. Kantaputra P, Tanpaiboon P, Porntaveetus T, Ohazama A, Sharpe P, Rauch A, Hus- sadaloy A, Thiel CT. The smallest teeth in the world are caused by mutations in the PCNT gene. Am J Med Genet 2011 155:1398-1403.
3. Kaewkhampa A, Jotikasthirautti D, Malaivijitnond S, Kantaputra P. TBX22 Mutation Associated with Cleft Lip/Palate, Hypodontia, and Limb Anomaly. Cleft Palate and Craniofacial Journal March 2012 Mar;49(2):240-244.
4. Kantaputra PN , Matangkasombut O, Sripathomsawat W. TP63 mutation and Ec- trodactyly, Ectodermal Dysplasia, and Amelogenesis Imperfecta. Am J Med Genet Part A 2012;158A:188–192.
5. Kantaputra PN, Thawanaphong S, Issarangporn W, Klangsinsirikul P, Ohazama O, Sharpe P, Chayarop Supanchart C. 2012 Long Term Survival in Infantile Malignant Autosomal Recessive Osteopetrosis Secondary to Homozygous p.Arg526Gln Muta- tion in CLC7. Am J Med Genet Part A 158A(4):909-916.
6. Kayserili H, Kantaputra PN. 2012. Multiple supernumerary molars, anterior open-

bite, and large ear lobules in mucopolysaccharidosis Type VI patient. Am J Med Genet Part A 158A:1798-1800.

1. Kantaputra PN, Ouweland AVD, Sangruchi T, Limwongse C. 2012. Severe facial manifestation of neurofibromatosis type I with underdeveloped eyeballs and a novel NF1 mutation. Am J Med Genet Part A 158A:1750-1753.
2. Kantaputra PN, Chinadet W, Ohazama A, Kono M. 2012. Dyschromatosis Symmet- rica Hereditaria with long hair of the forearms, Hypo/Hyperpigmented Hair, and Den- tal Anomalies: Report of a novel ADAR1 mutation. Am J Med Genet A. Part A. 158A: 2258-2265.
3. Kantaputra PN*, Sittiwangkul R, Romanelli V, Tenorio J, Lapunzina P. 2013. Novel Mutation in CDKN1C in Three sibs with Beckwith-Wiedemann Syndrome with Sen- sorineural hearing loss and cleft Palate. Am J Med Genet Part A 161A:192-197. Q2
4. Kantaputra PN*, Kaewgahya M, Khemaleelakul U, Dejkhamron P, Sutthimethakorn S, Thongboonkerd V, Iamaroon A. 2014. Enamel-Renal-Gingival Syndrome and FAM20A Mutations. Am J Med Genet Part A 164A(1):1-9. Q2
5. Kantaputra PN*, Kayserili H, Güven Y, Kantaputra W, Balci MC, Tanpaiboon P,

Uttarilli A, Dalal A. 2014. Oral Manifestations of 17 Patients Affected With Mucopolysaccharidosis Type VI. J Inherit Metab Dis 2014;37:263–268.
Impact factor = 4.07

1. Kantaputra PN*, Kaewgahya M, Kantaputra W. 2014. WNT10A mutations also as- sociated with agenesis of the maxillary permanent canines, a separate entity. Amer- ican Journal of Medical Genetics Part A 164A(2):360-363. Q2
2. Kantaputra PN*, Kaewgahya M, Jotikasthira D, Kantaputra W. 2014. Tricho-Odon- to-Onycho-Dermal Dysplasia and WNT10A Mutations. American Journal of Medical Genetics Part A 164(4):1041-1048. Q2
3. Guven Y, Altunoglu U, Aktoren O, Uyguner ZO, Kayserili H, Kaewkahya M, Kanta- putra PN*. 2014. Twins with hereditary sensory and autonomic neuropathy type IV with preserved periodontal sensation. Eur J Med Genet 57:240-246.
4. Kantaputra PN*, Bongkochwilawan C, Kaewgahya M, Ohazama A, Kayserili H, Er- dem AP, Aktoren O, Guven Y. 2014. Enamel-Renal-Gingival Syndrome, Hypodontia, and a Novel FAM20A mutation. Am J Med Genet Part A. 164A:2124-2128.
5. Kantaputra PN*. 2014. BCOR mutations and Unstoppable Root Growth. Invited commentary on "Oculofaciocardiodental syndrome: Novel BCOR mutations and Expression in Dental Cells". J Hum Genet 9:297-299.
6. Kantaputra PN*, Kaewgahya M, Wiwatwongwana A, Wiwatwongwana D, Rekwan Sittiwangkul R, Iamaroon A, Dejkhamron P. 2014. Cutis Laxa with Pulmonary Em- physema, Conjunctivochalasis, Obstruction of Nasolacrimal Ducts, Abnormal Hair, and a Novel FBLN5 Mutation. Am J Med Genet Part A 164:2370-2377.
7. Tananuvat N, Charoenkwan P, Ohazama A, Ketudat Cairns JR, Kaewgahya M, Kan- taputra PN*. Root dentin Anomaly and a PLG mutation. Eur J Med Genet. 2014; 57(11-12):630-635.
8. Kantaputra PN, Kayserili H, Guven Y, Kantaputra W, Balci MC, Tanpaiboon P, Tananuvat N, Uttarilli A, Dalal A. 2014. Clinical manifestations of 17 patients affected

with mucopolysaccharidosis type VI and 8 novel ARSB mutations. Am J Med Genet Part A 164A:1443-1453.

1. Kantaputra PN*. 2015. Response to the letter to the editor by idil kurtulus-

waschulewski; gerhard wahl, prof. Dr.; katalyn dittrich; volker schuster. Eur J Med Genet. 58(3):201.

1. Kantaputra PN*, Kaewgahya M, Hatsadaloi A, Vogel P, Kawasaki K, Ohaza- ma A, Ketudat Cairns JR. 2015. GREMLIN 2 Mutations and Dental Anom- alies. J Dent Res 94(12):1646-1652.
2. Wattanarat O, Kantaputra PN*. 2015. Preaxial polydactyly associated with a MSX1 mutation and report of two novel mutations. Am J Med Genet Part A 170(1):254-259. Q2
3. Kantaputra PN*, Intachai W, and Auychai P. 2016. All Enamel Is not Created

Equal: Supports From a Novel FAM83H Mutation. Am J Med Genet Part A 170(1): 273-276.

1. Vogel P, Read RW, Hansen GM, Powell DR, Kantaputra PN, Zambrowicz B, Brommage R. 2016. Dentin Dysplasia in Notum Knockout Mice. Veterinary Patholo- gy 53(4):853-862.
2. Lubinsky M, Kantaputra PN*. 2016. Syndromes with supernumerary teeth. Am J Med Genet A. 170(10):2611-6.
3. Kunothai W, Ananpornruedee P, Lubinsky M, Pruksametanan A, Kantaputra PN. 2016. Making extra teeth: lessons from TRPS1 mutation. Am J Med Genet Part A 173(1):99-107.
4. Tanasubsinn N, Sittiwangkul R, Pongprot Y, Kawasaki K , Ohazama A, Sas- traruji T, Kaewgahya M, Kantaputra PN. 2017. TFAP2B mutation and dental anomalies. J Hum Genet. 2017 62(8):769-775. Impact factor = 2.942
5. Kantaputra PN, Bongkochwilawan C, Lubinsky M, Pata S, Kaewgahya M, Tong HJ, Ketudat Cairns JR, Guven Y, Chaisrisookumporn N. Periodontal disease and FAM20A mutations. J Hum Genet. 2017 Jul;62(7):679-686. Im- pact factor = 2.942
6. Kantaputra PN, Kapoor S, Verma P, Kaewgahya M, Kawasaki K, Ohazama A, Ketudat Cairns JR. Al-Awadi-Raas-Rothschild syndrome with dental anomalies and a novel WNT7A mutation. Eur J Med Genet. 201760(12):695- 700. Impact factor = 2.004
7. Kantaputra PN, Kapoor S, Verma P, Intachai W, Ketudat Cairns JR. Split hand-foot malformation and a novel WNT10B mutation. European Journal of Medical Genetics 2018: 61(7):372-375. Impact factor = 2.004
8. Kantaputra PN, Hutsadaloi A, Kaewkgayah M, Intachai W, German R, Koparal M, Leethanakul C, Tolun A, Ketudat Cairns JC. WNT10B mutations associated with isolated dental anomalies. Clinical Genetics 2018; 93(5):992- 999. Impact factor = 3.512
9. Kantaputra PN, Sirirungruangsarn Y, Intachai W, Ngamphiw C, Tongsima S, Dejkhamron P. Osteogenesis imperfecta with ectopic mineralizations in dentin and cementum and a COL1A2 mutation. J Hum Genet. 2018 ;63(7):811-820. Impact factor = 2.942
10. Kantaputra PN, Chinadet W, Intachai W, Ngamphiw C, Ketudat Cairns JR , Tongsima S. Isolated dentinogenesis imperfecta with glass-like enamel caused by COL1A2 mutation. AmericanJournal of MedicalGenetics Part A 176(12):2919-2923. doi: 10.1002/ajmg.a.40501. Impact factor = 2.264

11. Kantaputra PN, Carlson BM. Genetic regulatory pathways of split hand-foot

malformation. Clin Genet 2019 Jan;95(1):132-139. doi: 10.1111/cge.13434. Impact factor = 3.512

1. Kantaputra PN, Smith LJ, Casal ML, Kuptanon C, Chang YC, Nampoothiri S, Paiyarom A, Veerasakulwong T, Trachoo O, Ketudat Cairns JR, Chinadet W, Tanpaiboon P. Oral Manifestations in patients and dogs with mucopolysaccha- ridosis type VII. American Journal of Medical Genetics Part A (in press)

Book Chapters

1 Book Chapter in “Mineralized Tissues in Oral and Craniofacial Science: Biologi- cal Principles and Clinical Correlates” Edited by Laurie K. McCauley and Martha Somerman. Wiley Publisher. 2012. CHAPTER FIVE: CLINICAL CORRELATION: CLCN7-ASSOCIATED AUTOSOMAL RECESSIVE OSTEOPETROSIS.
2 Book Chapter in “Human Embryology and Developmental Biology” 5th edition. Edited by Bruce M. Carlson. Clinical Correlates: Dental Anomalies”. Mosby Elsevier 2014
3.  Book Chapter in “Human Embryology and Developmental Biology” 6th edition. Edited by Bruce M. Carlson. Clinical Correlates: Dental Anomalies”. Mosby Elsevier 2018
4.  Book Chapter in “Pediatric Dentistry: Infancy through Adolescence”. 6th edition. Elsevier. Congenital Genetic Disorders and Syndromes. 2018.
Awards
Graduate Student Research Award. American Academy of Pediatric Dentistry. 1992. Golden Elephant Best Research Award. Health Science Division. Chiang Mai University 2006.
Outstanding Research Presentation. Gordon Research Conference on Bone and Teeth. University of New England, Maine, USA. July 14-19, 2007.
Best Research Award in Oral-maxillofacial Surgery, Oral Pathology & Oral Medicine. IADR Southeast Asian Division 2007, Bali, Indonesia.

Brief biography of Nik Kantaputra

Professor Piranit Nik Kantaputra is the director of Center of Excellence in Medical Ge- netics Research, Chiang Mai University and a faculty of the Division of Pediatric Den- tistry, Department of Orthodontics and Pediatric Dentistry, Faculty of Dentistry, Chiang Mai University, Chiang Mai, Thailand. He graduated with Doctor of Dental Surgery from Chiang Mai University in 1986 and obtained Certificate and Master of Science in Pedi-
atric Dentistry from the University of Minnesota, USA in 1990. He had a fellowship train- ing in Clinical Dysmorphology with Prof. Robert J. Gorlin at the University of Minnesota during 1990-1991. His major research interest is finding the causes of rare craniofacial malformation syndromes, especially when teeth are involved. Recently his research team has identified the genes responsible for the smallest teeth and the biggest teeth in the world. Prof. Kantaputra has identified more than 13 new genetic syndromes, pub- lished more than 74 international publications, and 3 book chapters. Dr. Kantaputra is an editorial board members of American Journal of Medical Genetics and Journal of Human Genetics.