Kanya Suphapeetiporn (K Suphapeetiporn)

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 17

Top Topics

Transforming Growth Factor

Intellectual Disability

Top Venues

Journal of clinical pathology

Clinical genetics

BMC medical genetics

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

Publications

Chayanit Trirut, Darintr Sosothikul, Rungnapa Ittiwut, Chupong Ittiwut, Sureeporn Pongsewalak, Natsaruth Songthawee, Rungrote Natesirinilkul, Pallapa Banjerdlak, Pokpong Na Songkhla, Patcharee Komwilaisak, Chatphatai Moonla, Kanya Suphapeetiporn
F8 variants and their genotype-phenotype correlations in Thai patients with haemophilia A: a nationwide multicentre study. Journal of clinical pathology (2024)
Phawin Kor-Anantakul, Huey-Ling Chen, Ya-Hui Chen, Chupong Ittiwut, Rungnapa Ittiwut, Nataruks Chaijitraruch, Kanya Suphapeetiporn, Voranush Chongsrisawat
Novel PLEC variants associated with infantile cholestasis. Clinical genetics (2024)
Supanun Lauhasurayotin, Chatphatai Moonla, Rungnapa Ittiwut, Chupong Ittiwut, Natsaruth Songthawee, Patcharee Komwilaisak, Rungrote Natesirinilkul, Nongnuch Sirachainan, Ponlapat Rojnuckarin, Darintr Sosothikul, Kanya Suphapeetiporn
Genetic variations of type 2 and type 3 von Willebrand diseases in Thailand. Journal of clinical pathology (2023)
Voranush Chongsrisawat, Narissara Suratannon, Pantipa Chatchatee, Rungnapa Ittiwut, Chupong Ittiwut, Wanlapa Weerapakorn, Apiradee Theamboonlers, Meino Rohlfs, Christoph Klein, Daniel Kotlarz, Kanya Suphapeetiporn
Novel CD55 Mutation Associated With Severe Small Bowel Ulceration Mimicking Inflammatory Bowel Disease in a Pair of Siblings. Inflammatory bowel diseases 28 (9) (2022)
Chulaluck Kuptanon, Verasak Thamkunanon, Chalurmpon Srichomthong, Thanakorn Theerapanon, Kanya Suphapeetiporn, Thantrira Porntaveetus, Vorasuk Shotelersuk
Novel BMP1, CRTAP, and SERPINF1 variants causing autosomal recessive osteogenesis imperfecta. Clinical genetics 102 (3) (2022)
Ponghatai Boonsimma, Chupong Ittiwut, Wuttichart Kamolvisit, Rungnapa Ittiwut, Wanna Chetruengchai, Chureerat Phokaew, Chalurmpon Srichonthong, Sathida Poonmaksatit, Tayard Desudchit, Kanya Suphapeetiporn, Vorasuk Shotelersuk
Exome sequencing as first-tier genetic testing in infantile-onset pharmacoresistant epilepsy: diagnostic yield and treatment impact. European journal of human genetics : EJHG (2022)
Maliwan Tengsujaritkul, Narissara Suratannon, Chupong Ittiwut, Rungnapa Ittiwut, Pantipa Chatchatee, Kanya Suphapeetiporn, Vorasuk Shotelersuk
Phenotypic heterogeneity and genotypic spectrum of inborn errors of immunity identified through whole exome sequencing in a Thai patient cohort. Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology (2021)
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)
Rungnapa Ittiwut, Kunlapat Sengpanich, Supanun Lauhasurayotin, Chupong Ittiwut, Vorasuk Shotelersuk, Darintr Sosothikul, Kanya Suphapeetiporn
Clinical and molecular characteristics of Thai patients with ELANE-related neutropaenia. Journal of clinical pathology (2020)
Narin Intarak, Thanakorn Theerapanon, Sermporn Thaweesapphithak, Kanya Suphapeetiporn, Thantrira Porntaveetus, Vorasuk Shotelersuk
Genotype-phenotype correlation and expansion of orodental anomalies in LTBP3-related disorders. Molecular genetics and genomics : MGG 294 (3) (2019)
Chulaluck Kuptanon, Chalurmpon Srichomthong, Apiruk Sangsin, Dool Kovitvanitcha, Kanya Suphapeetiporn, Vorasuk Shotelersuk
The most 5' truncating homozygous mutation of WNT1 in siblings with osteogenesis imperfecta with a variable degree of brain anomalies: a case report. BMC medical genetics 19 (1) (2018)
Thantrira Porntaveetus, T Osathanon, N Nowwarote, Prasit Pavasant, C Srichomthong, Kanya Suphapeetiporn, V Shotelersuk
Dental properties, ultrastructure, and pulp cells associated with a novel DSPP mutation. Oral diseases 24 (4) (2018)
Jaraspong Uaariyapanichkul, Sirinuch Chomtho, Kanya Suphapeetiporn, Vorasuk Shotelersuk, Santi Punnahitananda, Pannee Chinjarernpan, Orapa Suteerojntrakool
Age-Related Reference Intervals for Blood Amino Acids in Thai Pediatric Population Measured by Liquid Chromatography Tandem Mass Spectrometry. Journal of nutrition and metabolism 2018 (2018)
N Intarak, T Theerapanon, C Ittiwut, Kanya Suphapeetiporn, Thantrira Porntaveetus, V Shotelersuk
A novel PITX2 mutation in non-syndromic orodental anomalies. Oral diseases 24 (4) (2018)
Thantrira Porntaveetus, Chalurmpon Srichomthong, Kanya Suphapeetiporn, Vorasuk Shotelersuk
Monoallelic FGFR3 and Biallelic ALPL mutations in a Thai girl with hypochondroplasia and hypophosphatasia. American journal of medical genetics. Part A 173 (10) (2017)
T Porntaveetus, C Srichomthong, A Ohazama, Kanya Suphapeetiporn, V Shotelersuk
A novel GJA1 mutation in oculodentodigital dysplasia with extensive loss of enamel. Oral diseases 23 (6) (2017)
Pongsathorn Chaiyasap, Chupong Ittiwut, Chalurmpon Srichomthong, Apiruk Sangsin, Kanya Suphapeetiporn, Vorasuk Shotelersuk
Massive parallel sequencing as a new diagnostic approach for phenylketonuria and tetrahydrobiopterin-deficiency in Thailand. BMC medical genetics 18 (1) (2017)