Piranit Nik Kantaputra (Piranit N Kantaputra, P Kantaputra, Piranit Kantaputra, P N Kantaputra)

ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 69

Top Venues

Genes

International journal of molecular sciences

Clinical genetics

The Journal of dermatology

This page only lists publications with an associated author ORCID identifier.

Publications

Cholaporn Ruangchan, Chumpol Ngamphiw, Annop Krasaesin, Narin Intarak, Sissades Tongsima, Massupa Kaewgahya, Katsushige Kawasaki, Phitsanu Mahawong, Kullaya Paripurana, Bussaneeya Sookawat, Peeranat Jatooratthawichot, Timothy C Cox, Atsushi Ohazama, James R Ketudat Cairns, Thantrira Porntaveetus, Piranit Nik Kantaputra
Genetic Variants in KCTD1 Are Associated with Isolated Dental Anomalies. International journal of molecular sciences 25 (10) (2024)
Thatphicha Kularbkaew, Tipaporn Thongmak, Phan Sandeth, Callum S Durward, Pichai Vittayakittipong, Paul Duke, Anak Iamaroon, Sompid Kintarak, Worrachet Intachai, Chumpol Ngamphiw, Sissades Tongsima, Peeranat Jatooratthawichot, Timothy C Cox, James R Ketudat Cairns, Piranit Nik Kantaputra
Genetic Variants in the TBC1D2B Gene Are Associated with Ramon Syndrome and Hereditary Gingival Fibromatosis. International journal of molecular sciences 25 (16) (2024)
Piranit Nik Kantaputra, Teerada Klaisuwan, Kantapong Kitiyamas, Panat Piyakhunakorn, Katsushige Kawasaki, Achara Sathienkijkanchai, Pornswan Wasant, Nithiwat Vatanavicharn, Thippawan Yasanga, Massupa Kaewgahya, Sissades Tongsima, Timothy C Cox, Stefan T Arold, Atsushi Ohazama, Chumpol Ngamphiw
Homozygosity for a Rare Plec Variant Suggests a Contributory Role in Congenital Insensitivity to Pain. International journal of molecular sciences 25 (12) (2024)
Luca Lo Piccolo, Wasinee Wongkummool, Phatcharida Jantaree, Teerada Klaisuwan, Suteeraporn Chaowattanapanit, Chareon Choonhakarn, Warayuwadee Amornpinyo, Romanee Chaiwarith, Salin Kiratikanon, Rujira Rujiwetpongstorn, Napatra Tovanabutra, Siri Chiewchanvit, Chumpol Ngamphiw, Worrachet Intachai, Piranit Nik Kantaputra, Mati Chuamanochan
Rare Filaggrin Variants Are Associated with Pustular Skin Diseases in Asians. International journal of molecular sciences 25 (12) (2024)
Apiwat Sangphukieo, Patcharawadee Thongkumkoon, Pitiporn Noisagul, Luca Lo Piccolo, Timothy E O'Brien, Suteeraporn Chaowattanapanit, Charoen Choonhakarn, Warayuwadee Amornpinyo, Romanee Chaiwarith, Salin Kiratikanon, Rujira Rujiwetpongstorn, Napatra Tovanabutra, Siri Chiewchanvit, Piranit Nik Kantaputra, Worrachet Intachai, Sivamoke Dissook, Mati Chuamanochan
Human Leukocyte Antigen Markers for Distinguishing Pustular Psoriasis and Adult-Onset Immunodeficiency with Pustular Reaction. Genes 15 (3) (2024)
Apiwat Sangphukieo, Patcharawadee Thongkumkoon, Pitiporn Noisagul, Luca Lo Piccolo, Timothy E O'Brien, Suteeraporn Chaowattanapanit, Charoen Choonhakarn, Warayuwadee Amornpinyo, Romanee Chaiwarith, Salin Kiratikanon, Rujira Rujiwetpongstorn, Napatra Tovanabutra, Siri Chiewchanvit, Piranit Nik Kantaputra, Worrachet Intachai, Sivamoke Dissook, Mati Chuamanochan
Human Leukocyte Antigen Markers for Distinguishing Pustular Psoriasis and Adult-Onset Immunodeficiency with Pustular Reaction. Genes 15 (3) (2024)
Thatphicha Kularbkaew, Tipaporn Thongmak, Phan Sandeth, Callum S Durward, Pichai Vittayakittipong, Paul Duke, Anak Iamaroon, Sompid Kintarak, Worrachet Intachai, Chumpol Ngamphiw, Sissades Tongsima, Peeranat Jatooratthawichot, Timothy C Cox, James R Ketudat Cairns, Piranit Nik Kantaputra
Genetic Variants in the TBC1D2B Gene Are Associated with Ramon Syndrome and Hereditary Gingival Fibromatosis. International journal of molecular sciences 25 (16) (2024)
Cholaporn Ruangchan, Chumpol Ngamphiw, Annop Krasaesin, Narin Intarak, Sissades Tongsima, Massupa Kaewgahya, Katsushige Kawasaki, Phitsanu Mahawong, Kullaya Paripurana, Bussaneeya Sookawat, Peeranat Jatooratthawichot, Timothy C Cox, Atsushi Ohazama, James R Ketudat Cairns, Thantrira Porntaveetus, Piranit Nik Kantaputra
Genetic Variants in KCTD1 Are Associated with Isolated Dental Anomalies. International journal of molecular sciences 25 (10) (2024)
Luca Lo Piccolo, Wasinee Wongkummool, Phatcharida Jantaree, Teerada Klaisuwan, Suteeraporn Chaowattanapanit, Chareon Choonhakarn, Warayuwadee Amornpinyo, Romanee Chaiwarith, Salin Kiratikanon, Rujira Rujiwetpongstorn, Napatra Tovanabutra, Siri Chiewchanvit, Chumpol Ngamphiw, Worrachet Intachai, Piranit Nik Kantaputra, Mati Chuamanochan
Rare Filaggrin Variants Are Associated with Pustular Skin Diseases in Asians. International journal of molecular sciences 25 (12) (2024)
Piranit Nik Kantaputra, Teerada Klaisuwan, Kantapong Kitiyamas, Panat Piyakhunakorn, Katsushige Kawasaki, Achara Sathienkijkanchai, Pornswan Wasant, Nithiwat Vatanavicharn, Thippawan Yasanga, Massupa Kaewgahya, Sissades Tongsima, Timothy C Cox, Stefan T Arold, Atsushi Ohazama, Chumpol Ngamphiw
Homozygosity for a Rare Plec Variant Suggests a Contributory Role in Congenital Insensitivity to Pain. International journal of molecular sciences 25 (12) (2024)
Apiwat Sangphukieo, Patcharawadee Thongkumkoon, Pitiporn Noisagul, Luca Lo Piccolo, Timothy E O'Brien, Suteeraporn Chaowattanapanit, Charoen Choonhakarn, Warayuwadee Amornpinyo, Romanee Chaiwarith, Salin Kiratikanon, Rujira Rujiwetpongstorn, Napatra Tovanabutra, Siri Chiewchanvit, Piranit Nik Kantaputra, Worrachet Intachai, Sivamoke Dissook, Mati Chuamanochan
Human Leukocyte Antigen Markers for Distinguishing Pustular Psoriasis and Adult-Onset Immunodeficiency with Pustular Reaction. Genes 15 (3) (2024)
Cholaporn Ruangchan, Chumpol Ngamphiw, Annop Krasaesin, Narin Intarak, Sissades Tongsima, Massupa Kaewgahya, Katsushige Kawasaki, Phitsanu Mahawong, Kullaya Paripurana, Bussaneeya Sookawat, Peeranat Jatooratthawichot, Timothy C Cox, Atsushi Ohazama, James R Ketudat Cairns, Thantrira Porntaveetus, Piranit Nik Kantaputra
Genetic Variants in KCTD1 Are Associated with Isolated Dental Anomalies. International journal of molecular sciences 25 (10) (2024)
Apiwat Sangphukieo, Patcharawadee Thongkumkoon, Pitiporn Noisagul, Luca Lo Piccolo, Timothy E O'Brien, Suteeraporn Chaowattanapanit, Charoen Choonhakarn, Warayuwadee Amornpinyo, Romanee Chaiwarith, Salin Kiratikanon, Rujira Rujiwetpongstorn, Napatra Tovanabutra, Siri Chiewchanvit, Piranit Nik Kantaputra, Worrachet Intachai, Sivamoke Dissook, Mati Chuamanochan
Human Leukocyte Antigen Markers for Distinguishing Pustular Psoriasis and Adult-Onset Immunodeficiency with Pustular Reaction. Genes 15 (3) (2024)
Luca Lo Piccolo, Wasinee Wongkummool, Phatcharida Jantaree, Teerada Klaisuwan, Suteeraporn Chaowattanapanit, Chareon Choonhakarn, Warayuwadee Amornpinyo, Romanee Chaiwarith, Salin Kiratikanon, Rujira Rujiwetpongstorn, Napatra Tovanabutra, Siri Chiewchanvit, Chumpol Ngamphiw, Worrachet Intachai, Piranit Nik Kantaputra, Mati Chuamanochan
Rare Filaggrin Variants Are Associated with Pustular Skin Diseases in Asians. International journal of molecular sciences 25 (12) (2024)
Piranit Nik Kantaputra, Kittikhoon Buaban, Napaphat Thongsee, Massupa Kaewgahya, Natalina Quarto, Bruce M Carlson, Chumpol Ngamphiw, Sissades Tongsima
Broad spectrum of anomalies including quadricuspid aortic valve associated with a novel frameshift SALL4 variant. Clinical genetics (2023)
Piranit Nik Kantaputra, Peeranat Jatooratthawichot, Naomi Kottege, Robert P Anthonappa, Massupa Kaewgahya, Sissades Tongsima, Chumpol Ngamphiw, James R Ketudat Cairns, Danilo Predes, Xi He
DKK1 is a strong candidate for mesiodens and taurodontism. Clinical genetics (2023)
Piranit Nik Kantaputra, Teerada Klaisuwan, Mati Chuamanochan, Suteeraporn Chaowattanapanit, Salin Kiratikanon, Charoen Choonhakarn, Worrachet Intachai, Bjorn Olsen, Sissades Tongsima, Chumpol Ngamphiw, Patrizia Pontisso, Timothy C Cox, Puey Ounjai
SERPINB3 , Adult-Onset Immunodeficiency, and Generalized Pustular Psoriasis. Genes 14 (2) (2023)
Piranit Nik Kantaputra, Teerada Klaisuwan, Mati Chuamanochan, Suteeraporn Chaowattanapanit, Salin Kiratikanon, Charoen Choonhakarn, Worrachet Intachai, Bjorn Olsen, Sissades Tongsima, Chumpol Ngamphiw, Patrizia Pontisso, Timothy C Cox, Puey Ounjai
SERPINB3 , Adult-Onset Immunodeficiency, and Generalized Pustular Psoriasis. Genes 14 (2) (2023)
Chomchanok Panyarat, Siriruk Nakornchai, Kanoknart Chintakanon, Niramol Leelaadisorn, Worrachet Intachai, Bjorn Olsen, Sissades Tongsima, Ploy Adisornkanj, Chumpol Ngamphiw, Timothy C Cox, Piranit Nik Kantaputra
Rare Genetic Variants in Human APC Are Implicated in Mesiodens and Isolated Supernumerary Teeth. International journal of molecular sciences 24 (5) (2023)
Piranit Nik Kantaputra, Peeranat Jatooratthawichot, Ploy Adisornkanj, Panita Kitsadayurach, Massupa Kaewgahya, Bjorn Olsen, Atsushi Ohazama, Chumpol Ngamphiw, Sissades Tongsima, Timothy C Cox, James R Ketudat Cairns
Rare Variants in LRP4 Are Associated with Mesiodens, Root Maldevelopment, and Oral Exostoses in Humans. Biology 12 (2) (2023)
Chomchanok Panyarat, Siriruk Nakornchai, Kanoknart Chintakanon, Niramol Leelaadisorn, Worrachet Intachai, Bjorn Olsen, Sissades Tongsima, Ploy Adisornkanj, Chumpol Ngamphiw, Timothy C Cox, Piranit Nik Kantaputra
Rare Genetic Variants in Human APC Are Implicated in Mesiodens and Isolated Supernumerary Teeth. International journal of molecular sciences 24 (5) (2023)
Piranit Nik Kantaputra, Kittikhoon Buaban, Napaphat Thongsee, Massupa Kaewgahya, Natalina Quarto, Bruce M Carlson, Chumpol Ngamphiw, Sissades Tongsima
Broad spectrum of anomalies including quadricuspid aortic valve associated with a novel frameshift SALL4 variant. Clinical genetics (2023)
Piranit Nik Kantaputra, Niramol Leelaadisorn, Athiwat Hatsadaloi, Natalina Quarto, Worrachet Intachai, Sissades Tongsima, Katsushige Kawasaki, Atsushi Ohazama, Chumpol Ngamphiw, Paswach Wiriyakijja
A Mutation in CACNA1S Is Associated with Multiple Supernumerary Cusps and Root Maldevelopment. Diagnostics (Basel, Switzerland) 13 (5) (2023)
Piranit Nik Kantaputra, Niramol Leelaadisorn, Athiwat Hatsadaloi, Natalina Quarto, Worrachet Intachai, Sissades Tongsima, Katsushige Kawasaki, Atsushi Ohazama, Chumpol Ngamphiw, Paswach Wiriyakijja
A Mutation in CACNA1S Is Associated with Multiple Supernumerary Cusps and Root Maldevelopment. Diagnostics (Basel, Switzerland) 13 (5) (2023)
Piranit Nik Kantaputra, Salita Angkurawaranon, Worrachet Intachai, Chumpol Ngamphiw, Bjorn Olsen, Sissades Tongsima, Timothy C Cox, James R Ketudat Cairns
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 14 (2) (2023)
Piranit Nik Kantaputra, Weena Panichkul, Parisri Sillapasorn, Ploy Adisornkanj, Panita Kitsadayurach, Massupa Kaewgaya, Worrachet Intachai, Bjorn Olsen, Chumpol Ngamphiw, Chidchanok Leethanakul, Peeranat Jatooratthawichot, James R Ketudat Cairns, Sissades Tongsima
LRP4 mutations, dental anomalies, and oral exostoses. International journal of paediatric dentistry (2023)
Piranit Nik Kantaputra, Peeranat Jatooratthawichot, Naomi Kottege, Robert P Anthonappa, Massupa Kaewgahya, Sissades Tongsima, Chumpol Ngamphiw, James R Ketudat Cairns, Danilo Predes, Xi He
DKK1 is a strong candidate for mesiodens and taurodontism. Clinical genetics (2023)
Piranit Nik Kantaputra, Salita Angkurawaranon, Worrachet Intachai, Chumpol Ngamphiw, Bjorn Olsen, Sissades Tongsima, Timothy C Cox, James R Ketudat Cairns
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 14 (2) (2023)
Piranit Nik Kantaputra, Peeranat Jatooratthawichot, Naomi Kottege, Robert P Anthonappa, Massupa Kaewgahya, Sissades Tongsima, Chumpol Ngamphiw, James R Ketudat Cairns, Danilo Predes, Xi He
DKK1 is a strong candidate for mesiodens and taurodontism. Clinical genetics (2023)
Piranit Nik Kantaputra, Peeranat Jatooratthawichot, Ploy Adisornkanj, Panita Kitsadayurach, Massupa Kaewgahya, Bjorn Olsen, Atsushi Ohazama, Chumpol Ngamphiw, Sissades Tongsima, Timothy C Cox, James R Ketudat Cairns
Rare Variants in LRP4 Are Associated with Mesiodens, Root Maldevelopment, and Oral Exostoses in Humans. Biology 12 (2) (2023)
Piranit Nik Kantaputra, Salita Angkurawaranon, Worrachet Intachai, Chumpol Ngamphiw, Bjorn Olsen, Sissades Tongsima, Timothy C Cox, James R Ketudat Cairns
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 14 (2) (2023)
Ploy Adisornkanj, Rajit Chanprasit, Steven Eliason, Juan M Fons, Worrachet Intachai, Sissades Tongsima, Bjorn Olsen, Stefan T Arold, Chumpol Ngamphiw, Brad A Amendt, Abigail S Tucker, Piranit Nik Kantaputra
Genetic Variants in Protein Tyrosine Phosphatase Non-Receptor Type 23 Are Responsible for Mesiodens Formation. Biology 12 (3) (2023)
Piranit Nik Kantaputra, Kanich Tripuwabhrut, Robert P Anthonappa, Kanoknart Chintakanon, Chumpol Ngamphiw, Ploy Adisornkanj, Nop Porntrakulseree, Bjorn Olsen, Worrachet Intachai, Raoul C Hennekam, Alexandre Rezende Vieira, Sissades Tongsima
Heterozygous Variants in FREM2 Are Associated with Mesiodens, Supernumerary Teeth, Oral Exostoses, and Odontomas. Diagnostics (Basel, Switzerland) 13 (7) (2023)
Piranit Nik Kantaputra, Teerada Klaisuwan, Mati Chuamanochan, Suteeraporn Chaowattanapanit, Salin Kiratikanon, Charoen Choonhakarn, Worrachet Intachai, Bjorn Olsen, Sissades Tongsima, Chumpol Ngamphiw, Patrizia Pontisso, Timothy C Cox, Puey Ounjai
SERPINB3 , Adult-Onset Immunodeficiency, and Generalized Pustular Psoriasis. Genes 14 (2) (2023)
Piranit Nik Kantaputra, Salita Angkurawaranon, Worrachet Intachai, Chumpol Ngamphiw, Bjorn Olsen, Sissades Tongsima, Timothy C Cox, James R Ketudat Cairns
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 14 (2) (2023)
Chomchanok Panyarat, Siriruk Nakornchai, Kanoknart Chintakanon, Niramol Leelaadisorn, Worrachet Intachai, Bjorn Olsen, Sissades Tongsima, Ploy Adisornkanj, Chumpol Ngamphiw, Timothy C Cox, Piranit Nik Kantaputra
Rare Genetic Variants in Human APC Are Implicated in Mesiodens and Isolated Supernumerary Teeth. International journal of molecular sciences 24 (5) (2023)
Piranit Nik Kantaputra, Teerada Klaisuwan, Mati Chuamanochan, Suteeraporn Chaowattanapanit, Salin Kiratikanon, Charoen Choonhakarn, Worrachet Intachai, Bjorn Olsen, Sissades Tongsima, Chumpol Ngamphiw, Patrizia Pontisso, Timothy C Cox, Puey Ounjai
SERPINB3 , Adult-Onset Immunodeficiency, and Generalized Pustular Psoriasis. Genes 14 (2) (2023)
Ploy Adisornkanj, Rajit Chanprasit, Steven Eliason, Juan M Fons, Worrachet Intachai, Sissades Tongsima, Bjorn Olsen, Stefan T Arold, Chumpol Ngamphiw, Brad A Amendt, Abigail S Tucker, Piranit Nik Kantaputra
Genetic Variants in Protein Tyrosine Phosphatase Non-Receptor Type 23 Are Responsible for Mesiodens Formation. Biology 12 (3) (2023)
Chomchanok Panyarat, Siriruk Nakornchai, Kanoknart Chintakanon, Niramol Leelaadisorn, Worrachet Intachai, Bjorn Olsen, Sissades Tongsima, Ploy Adisornkanj, Chumpol Ngamphiw, Timothy C Cox, Piranit Nik Kantaputra
Rare Genetic Variants in Human APC Are Implicated in Mesiodens and Isolated Supernumerary Teeth. International journal of molecular sciences 24 (5) (2023)
Piranit Nik Kantaputra, Salita Angkurawaranon, Worrachet Intachai, Chumpol Ngamphiw, Bjorn Olsen, Sissades Tongsima, Timothy C Cox, James R Ketudat Cairns
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 14 (2) (2023)
Piranit Nik Kantaputra, Azeez Butali, S Eliason, C Chalkley, S Nakornchai, C Bongkochwilawan, K Kawasaki, A Kumchiang, C Ngamphiw, S Tongsima, J R Ketudat Cairns, Bjorn R Olsen, W Intachai, Atsushi Ohazama, A S Tucker, B A Amendt
CACNA1S mutation-associated dental anomalies: A calcium channelopathy. Oral diseases (2023)
Piranit Nik Kantaputra, Azeez Butali, S Eliason, C Chalkley, S Nakornchai, C Bongkochwilawan, K Kawasaki, A Kumchiang, C Ngamphiw, S Tongsima, J R Ketudat Cairns, Bjorn R Olsen, W Intachai, Atsushi Ohazama, A S Tucker, B A Amendt
CACNA1S mutation-associated dental anomalies: A calcium channelopathy. Oral diseases (2023)
Piranit Nik Kantaputra, Teerada Klaisuwan, Mati Chuamanochan, Suteeraporn Chaowattanapanit, Worrachet Intachai, Bjorn Olsen, Thanapat Sastraruji, Sissades Tongsima, Chumpol Ngamphiw, Jatupol Kampuansai, Timothy C Cox, Salin Kiratikanon
Loss of Function TGFBR2 Variant as a Contributing Factor in Generalized Pustular Psoriasis and Adult-Onset Immunodeficiency. Genes 14 (1) (2022)
Piranit Nik Kantaputra, Prapai Dejkhamron, Rekwan Sittiwangkul, Kamornwan Katanyuwong, Chumpol Ngamphiw, Nuntigar Sonsuwan, Worrachet Intachai, Sissades Tongsima, Philip L Beales, Worakanya Buranaphatthana
Dental Anomalies in Ciliopathies: Lessons from Patients with BBS2 , BBS7, and EVC2 Mutations. Genes 14 (1) (2022)
Piranit Nik Kantaputra, Yeliz Guven, Tugba Kalayci, Pelin Karaca Özer, Wannakamon Panyarak, Worrachet Intachai, Bjorn Olsen, Bruce M Carlson, Oranud Praditsap, Sissades Tongsima, Chumpol Ngamphiw, Peeranat Jatooratthawichot, Abigail S Tucker, James R Ketudat Cairns
Expanding genotypic and phenotypic spectrums of LTBP3 variants in dental anomalies and short stature syndrome. Clinical genetics 102 (1) (2022)
Piranit Nik Kantaputra, Prapai Dejkhamron, Rekwan Sittiwangkul, Kamornwan Katanyuwong, Chumpol Ngamphiw, Nuntigar Sonsuwan, Worrachet Intachai, Sissades Tongsima, Philip L Beales, Worakanya Buranaphatthana
Dental Anomalies in Ciliopathies: Lessons from Patients with BBS2 , BBS7, and EVC2 Mutations. Genes 14 (1) (2022)
Piranit Nik Kantaputra, Teerada Klaisuwan, Mati Chuamanochan, Suteeraporn Chaowattanapanit, Worrachet Intachai, Bjorn Olsen, Thanapat Sastraruji, Sissades Tongsima, Chumpol Ngamphiw, Jatupol Kampuansai, Timothy C Cox, Salin Kiratikanon
Loss of Function TGFBR2 Variant as a Contributing Factor in Generalized Pustular Psoriasis and Adult-Onset Immunodeficiency. Genes 14 (1) (2022)
Piranit Nik Kantaputra, Salita Angkurawaranon, Krit Khwanngern, Chumpol Ngamphiw, Worrachet Intachai, Ploy Adisornkanj, Sissades Tongsima, Bjorn Olsen, Nuntigar Sonsuwan, Kamornwan Katanyuwong
Clinical and Genetic Studies of the First Monozygotic Twins with Pfeiffer Syndrome. Genes 13 (10) (2022)
Piranit Nik Kantaputra, Prapai Dejkhamron, Rekwan Sittiwangkul, Kamornwan Katanyuwong, Chumpol Ngamphiw, Nuntigar Sonsuwan, Worrachet Intachai, Sissades Tongsima, Philip L Beales, Worakanya Buranaphatthana
Dental Anomalies in Ciliopathies: Lessons from Patients with BBS2 , BBS7, and EVC2 Mutations. Genes 14 (1) (2022)
Piranit Nik Kantaputra, Yeliz Guven, Kanich Tripuwabhrut, Ploy Adisornkanj, Athiwat Hatsadaloi, Massupa Kaewgahya, Bjorn Olsen, Chumpol Ngamphiw, Peeranat Jatooratthawichot, Sissades Tongsima, James R Ketudat Cairns
Mutations in LRP5 and BMP4 are associated with mesiodens, tooth agenesis, root malformation, and oral exostoses. Clinical genetics 102 (4) (2022)
Piranit Nik Kantaputra, Prapai Dejkhamron, Rekwan Sittiwangkul, Kamornwan Katanyuwong, Chumpol Ngamphiw, Nuntigar Sonsuwan, Worrachet Intachai, Sissades Tongsima, Philip L Beales, Worakanya Buranaphatthana
Dental Anomalies in Ciliopathies: Lessons from Patients with BBS2 , BBS7, and EVC2 Mutations. Genes 14 (1) (2022)
Piranit Nik Kantaputra, Teerada Klaisuwan, Mati Chuamanochan, Suteeraporn Chaowattanapanit, Worrachet Intachai, Bjorn Olsen, Thanapat Sastraruji, Sissades Tongsima, Chumpol Ngamphiw, Jatupol Kampuansai, Timothy C Cox, Salin Kiratikanon
Loss of Function TGFBR2 Variant as a Contributing Factor in Generalized Pustular Psoriasis and Adult-Onset Immunodeficiency. Genes 14 (1) (2022)
Piranit Nik Kantaputra, Bjorn Olsen, John A McGrath
WNT10A variant and severe scoliosis? The Journal of dermatology 49 (5) (2022)
Piranit Nik Kantaputra, Prapai Dejkhamron, Rekwan Sittiwangkul, Kamornwan Katanyuwong, Chumpol Ngamphiw, Nuntigar Sonsuwan, Worrachet Intachai, Sissades Tongsima, Philip L Beales, Worakanya Buranaphatthana
Dental Anomalies in Ciliopathies: Lessons from Patients with BBS2 , BBS7, and EVC2 Mutations. Genes 14 (1) (2022)
Piranit Nik Kantaputra, Teerada Klaisuwan, Mati Chuamanochan, Suteeraporn Chaowattanapanit, Worrachet Intachai, Bjorn Olsen, Thanapat Sastraruji, Sissades Tongsima, Chumpol Ngamphiw, Jatupol Kampuansai, Timothy C Cox, Salin Kiratikanon
Loss of Function TGFBR2 Variant as a Contributing Factor in Generalized Pustular Psoriasis and Adult-Onset Immunodeficiency. Genes 14 (1) (2022)
Piranit Nik Kantaputra, Teerada Klaisuwan, Mati Chuamanochan, Suteeraporn Chaowattanapanit, Worrachet Intachai, Bjorn Olsen, Thanapat Sastraruji, Sissades Tongsima, Chumpol Ngamphiw, Jatupol Kampuansai, Timothy C Cox, Salin Kiratikanon
Loss of Function TGFBR2 Variant as a Contributing Factor in Generalized Pustular Psoriasis and Adult-Onset Immunodeficiency. Genes 14 (1) (2022)
Vorasuk Shotelersuk, Duangdao Wichadakul, Chumpol Ngamphiw, Chalurmpon Srichomthong, Chureerat Phokaew, Alisa Wilantho, Sujiraporn Pakchuen, Vorthunju Nakhonsri, Philip James Shaw, Rujipat Wasitthankasem, Jittima Piriyapongsa, Pongsakorn Wangkumhang, Adjima Assawapitaksakul, Wanna Chetruengchai, Keswadee Lapphra, Athiphat Khuninthong, Pattarapong Makarawate, Kanya Suphapeetiporn, Surakameth Mahasirimongkol, Nusara Satproedprai, Thantrira Porntaveetus, Prapaporn Pisitkun, Verayuth Praphanphoj, Piranit Nik Kantaputra, Wichittra Tassaneeyakul, Sissades Tongsima
The Thai reference exome (T-REx) variant database. Clinical genetics 100 (6) (2021)
Brent J Doolan, Alexandros Onoufriadis, Piranit Nik Kantaputra, John A McGrath
WNT10A, dermatology and dentistry. The British journal of dermatology (2021)
Piranit Nik Kantaputra, Mati Chuamanochan, Salin Kiratikanon, Siri Chiewchanvit, Romanee Chaiwarith, Worrachet Intachai, Natalina Quarto, Sissades Tongsima, John A McGrath, Chumpol Ngamphiw
A truncating variant in SERPINA3, skin pustules and adult-onset immunodeficiency. The Journal of dermatology 48 (8) (2021)
Piranit Nik Kantaputra, Suteeraporn Chaowattanapanit, Salin Kiratikanon, Romanee Chaiwarith, Chareon Choonhakarn, Worrachet Intachai, Natalina Quarto, Sissades Tongsima, James R Ketudat Cairns, Chumpol Ngamphiw, John A McGrath, Mati Chuamanochan
SERPINA1, generalized pustular psoriasis, and adult-onset immunodeficiency. The Journal of dermatology 48 (10) (2021)
Piranit Nik Kantaputra, Apitchaya Pruksametanan, Nattapol Phondee, Athiwat Hutsadaloi, Worrachet Intachai, Katsushig Kawasaki, Atsushi Ohazama, Chumpol Ngamphiw, Sissades Tongsima, James R Ketudat Cairns, Polbhat Tripuwabhrut
ADAMTSL1 and mandibular prognathism. Clinical genetics 95 (4) (2020)
Piranit Nik Kantaputra, Worrachet Intachai, Bruce M Carlson, Chulabhorn Pruksachatkunakorn
Clouston syndrome with dental anomalies, micropores of hair shafts and absence of palmoplantar keratoderma. The Journal of dermatology 47 (3) (2020)
Piranit Nik Kantaputra, Dhirawat Jotikasthira, Bruce Carlson, Teerapat Wongmaneerung, Natalina Quarto, Theerapong Khankasikum, Warit Powcharoen, Worrachet Intachai, Kanich Tripuwabhrut
TRPS1 mutation associated with trichorhinophalangeal syndrome type 1 with 15 supernumerary teeth, hypoplastic mandibular condyles with slender condylar necks and unique hair morphology. The Journal of dermatology 47 (7) (2020)
Piranit Nik Kantaputra, Kanich Tripuwabhrut, Worrachet Intachai, Bruce M Carlson, Natalina Quarto, Chumpol Ngamphiw, Sissades Tongsima, Nuntigar Sonsuwan
Treacher Collins syndrome: A novel TCOF1 mutation and monopodial stapes. Clinical otolaryngology : official journal of ENT-UK ; official journal of Netherlands Society for Oto-Rhino-Laryngology & Cervico-Facial Surgery 45 (5) (2020)
Piranit Nik Kantaputra, Worrachet Intachai, Katsushige Kawasaki, Atsushi Ohazama, Bruce Carlson, Natalina Quarto, Chulabhorn Pruksachatkun, Mati Chuamanochan
Clouston syndrome with pili canaliculi, pili torti, overgrown hyponychium, onycholysis, taurodontism and absence of palmoplantar keratoderma. The Journal of dermatology 47 (6) (2020)
Piranit Nik Kantaputra, Lachlan J Smith, Margret L Casal, Chulaluck Kuptanon, Yu-Cheng Chang, Sheela Nampoothiri, Apichai Paiyarom, Thanat Veerasakulwong, Objoon Trachoo, James R Ketudat Cairns, Wannapa Chinadet, Pranoot Tanpaiboon
Oral manifestations in patients and dogs with mucopolysaccharidosis Type VII. American journal of medical genetics. Part A 179 (3) (2019)
Piranit Nik Kantaputra, Bruce M Carlson
Genetic regulatory pathways of split-hand/foot malformation. Clinical genetics 95 (1) (2018)
Piranit Nik Kantaputra, Wannapa Chinadet, Worrachet Intachai, Chumpol Ngamphiw, James R Ketudat Cairns, Sissades Tongsima
Isolated dentinogenesis imperfecta with glass-like enamel caused by COL1A2 mutation. American journal of medical genetics. Part A 176 (12) (2018)
Piranit Nik Kantaputra, A Hutsadaloi, M Kaewgahya, W Intachai, R German, M Koparal, C Leethanakul, A Tolun, J R Ketudat Cairns
WNT10B mutations associated with isolated dental anomalies. Clinical genetics 93 (5) (2018)

Piranit Nik Kantaputra.css-eqlu8i{font-size:small;padding-left:4px;} (Piranit N Kantaputra, P Kantaputra, Piranit Kantaputra, P N Kantaputra)

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Piranit Nik Kantaputra (Piranit N Kantaputra, P Kantaputra, Piranit Kantaputra, P N Kantaputra)