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Rungnapa Ittiwut · SciRah

Researcher profile · Semantic Scholar

Rungnapa Ittiwut

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Rungnapa Ittiwut — researcher profile on SciRah

h-index: 12
Works: 37
Citations: 379

Most-cited papers

Mutations in Kinesin family member 6 reveal specific role in ependymal cell ciliogenesis and human neurological development
Mia J. Konjikusic, Patra Yeetong, C. Boswell, Chanjae Lee +8 more
2018PLoS Genetics49 citations Open access
Semantic Scholar
A germline STAT6 gain-of-function variant is associated with early-onset allergies.
Narissara Suratannon, C. Ittiwut, W. Dik, Rungnapa Ittiwut +19 more
2022Journal of Allergy and Clinical Immunology46 citations Open access
Semantic Scholar
Association between polymorphisms in catechol-O-methyltransferase (COMT) and cocaine-induced paranoia in European-American and African-American populations
Rungnapa Ittiwut, Jennifer B. Listman, C. Ittiwut, Joseph F. Cubells +6 more
2011American Journal of Medical Genetics Part B: Neuropsychiatric Genetics35 citations Open access
Semantic Scholar
Exome sequencing as first-tier genetic testing in infantile-onset pharmacoresistant epilepsy: diagnostic yield and treatment impact
Ponghatai Boonsimma, C. Ittiwut, Wuttichart Kamolvisit, Rungnapa Ittiwut +7 more
2022European Journal of Human Genetics30 citations
Semantic Scholar
Trinucleotide repeat expansion in the transcription factor 4 (TCF4) gene in Thai patients with Fuchs endothelial corneal dystrophy
Naoki Okumura, V. Puangsricharern, Raina Jindasak, N. Koizumi +11 more
2019Eye22 citations Open access
Semantic Scholar
Genetic basis of sudden death after COVID-19 vaccination in Thailand
C. Ittiwut, S. Mahasirimongkol, S. Srisont, Rungnapa Ittiwut +16 more
2022Heart Rhythm18 citations Open access
Semantic Scholar
The phenotypic and mutational spectrum of Thai female patients with ornithine transcarbamylase deficiency.
V. Chongsrisawat, Ponghatai Damrongphol, C. Ittiwut, Rungnapa Ittiwut +2 more
2018Gene17 citations
Semantic Scholar
Rapid exome sequencing as the first‐tier investigation for diagnosis of acutely and severely ill children and adults in Thailand
Wuttichart Kamolvisit, P. Phowthongkum, Ponghatai Boonsimma, C. Kuptanon +14 more
2021Clinical Genetics15 citations
Semantic Scholar
Pyridoxal 5ꞌ-phosphate-responsive epilepsy with novel mutations in the PNPO gene: a case report.
M. Veeravigrom, Ponghatai Damrongphol, Rungnapa Ittiwut, C. Ittiwut +2 more
2015Genetics and Molecular Research15 citations Open access
Semantic Scholar
Identification and Functional Analysis of Six DAX1 Mutations in Patients With X-Linked Adrenal Hypoplasia Congenita
Chanisara Suthiworachai, R. Tammachote, C. Srichomthong, Rungnapa Ittiwut +3 more
2018Journal of the Endocrine Society14 citations Open access
Semantic Scholar
Epidemiology of cleft lip with or without cleft palate in Thais
Rungnapa Ittiwut, P. Siriwan, K. Suphapeetiporn, Vorasuk Shotelersuk
201714 citations Open access
Semantic Scholar
Novel Mutations, Including a Large Deletion in the ARSB Gene, Causing Mucopolysaccharidosis Type VI
C. Ittiwut, Sukanya Boonbuamas, C. Srichomthong, Rungnapa Ittiwut +2 more
2017Genetic Testing and Molecular Biomarkers12 citations
Semantic Scholar
Whole exome sequencing for diagnosis of hereditary thrombocytopenia
Ponthip Mekchay, C. Ittiwut, Rungnapa Ittiwut, B. Akkawat +8 more
2020Medicine11 citations Open access
Semantic Scholar
Variants of the CDH1 (E-Cadherin) Gene Associated with Oral Clefts in the Thai Population
Rungnapa Ittiwut, C. Ittiwut, P. Siriwan, V. Chichareon +2 more
2016Genetic Testing and Molecular Biomarkers11 citations
Semantic Scholar
Phenotypic heterogeneity and genotypic spectrum of inborn errors of immunity identified through whole exome sequencing in a Thai patient cohort
M. Tengsujaritkul, Narissara Suratannon, C. Ittiwut, Rungnapa Ittiwut +3 more
2021Pediatric Allergy and Immunology7 citations
Semantic Scholar
Novel de novo mutation substantiates ATP6V0C as a gene causing epilepsy with intellectual disability.
C. Ittiwut, Sathida Poonmaksatit, Ponghatai Boonsimma, T. Desudchit +3 more
2020Brain & development (Tokyo. 1979)7 citations
Semantic Scholar
rs11567842 SNP in SLC13A2 gene associates with hypocitraturia in Thai patients with nephrolithiasis
Pattarin Udomsilp, Sarawut Saepoo, Rungnapa Ittiwut, Vorasuk Shotelersuk +3 more
2018Genes & Genomics7 citations
Semantic Scholar
FOXE1 mutations in Thai patients with oral clefts.
C. Srichomthong, Rungnapa Ittiwut, P. Siriwan, K. Suphapeetiporn +1 more
2013Genetics Research7 citations Open access
Semantic Scholar
Novel CD55 Mutation Associated With Severe Small Bowel Ulceration Mimicking Inflammatory Bowel Disease in a Pair of Siblings.
V. Chongsrisawat, Narissara Suratannon, P. Chatchatee, Rungnapa Ittiwut +7 more
2022Inflammatory Bowel Diseases6 citations Open access
Semantic Scholar
Clinical and molecular characteristics of Thai patients with ELANE-related neutropaenia
Rungnapa Ittiwut, Kunlapat Sengpanich, Supanun Lauhasurayotin, C. Ittiwut +3 more
2020Journal of Clinical Pathology6 citations
Semantic Scholar
Polymorphism of COMT Val158Met is associated with inhalant use and dependence: a Thai substance dependence treatment cohort
Wichaporn Intharachuti, Rungnapa Ittiwut, Jenifer Listman, V. Verachai +3 more
20126 citations
Semantic Scholar
Pathogenic variant detection rate by whole exome sequencing in Thai patients with biopsy-proven focal segmental glomerulosclerosis
Suramath Isaranuwatchai, Ankanee Chanakul, C. Ittiwut, Rungnapa Ittiwut +4 more
2023Scientific Reports5 citations Open access
Semantic Scholar
Molecular profiles and long-term outcomes of Thai children with hepatic glycogen storage disease in Thailand
Jaravee Vanduangden, Rungnapa Ittiwut, C. Ittiwut, Teerasak Phewplung +3 more
2024World Journal of Clinical Pediatrics4 citations Open access
Semantic Scholar
Novel PLEC variants associated with infantile cholestasis
Phawin Kor-anantakul, Huey-Ling Chen, Ya-Hui Chen, C. Ittiwut +4 more
2024Clinical Genetics3 citations
Semantic Scholar
Genetic, metabolic and clinical delineation of an MRPS23-associated mitochondrial disorder
C. Ittiwut, Rungnapa Ittiwut, C. Kuptanon, Tetsuro Matsuhashi +12 more
2023Scientific Reports3 citations Open access
Semantic Scholar
Novel mutations in Thai patients with glanzmann thrombasthenia
Rungnapa Ittiwut, Pintip Suchartlikitwong, Y. Kittikalayawong, C. Ittiwut +4 more
2017European Journal of Haematology3 citations
Semantic Scholar
TIGIT Monoallelic Nonsense Variant in Patient with Severe COVID-19 Infection, Thailand
P. Sodsai, C. Ittiwut, V. Ruenjaiman, Rungnapa Ittiwut +4 more
2022Emerging Infectious Diseases2 citations Open access
Semantic Scholar
F8 variants and their genotype-phenotype correlations in Thai patients with haemophilia A: a nationwide multicentre study
Chayanit Trirut, D. Sosothikul, Rungnapa Ittiwut, C. Ittiwut +8 more
2024Journal of Clinical Pathology1 citations
Semantic Scholar
Genetic variations of type 2 and type 3 von Willebrand diseases in Thailand
Supanun Lauhasurayotin, Chatphatai Moonla, Rungnapa Ittiwut, C. Ittiwut +7 more
2023Journal of Clinical Pathology1 citations
Semantic Scholar
A Novel NR5A1 Mutation in a Thai Boy with 46, XY DSD
S. Wacharasindhu, C. Ittiwut, Rungnapa Ittiwut, S. Aroonparkmongkol +1 more
2022Journal of Pediatric Genetics1 citations Open access
Semantic Scholar
A novel deletion in the fibrinogen beta chain (FGB) gene causing hypofibrinogenemia.
Arunothai Rakmanotham, Rungnapa Ittiwut, P. Komwilaisak, Vorasuk Shotelersuk +2 more
2019Thrombosis Research1 citations
Semantic Scholar
Two distinct phenotypes and a novel mutation in limb-girdle muscular dystrophy R7 telethonin-related patients from Thai neuromuscular center
Tanitnun Paprad, J. Amornvit, Thippamas Pobsuk, Manasawan Santananukarn +7 more
2025Neurological Sciences0 citations
Semantic Scholar
P359: Genetic characteristic of Thai patients with primary craniosynostosis
Rungroj Thangpong, Wuttichart Kamolvisit, Phawin Kor-anantakul, C. Ittiwut +9 more
2025Genetics in Medicine Open0 citations Open access
Semantic Scholar
Whole exome sequencing in relapsed or refractory childhood cancer: case series
Rungroj Thangpong, Pattarin Nuwongsri, C. Ittiwut, Rungnapa Ittiwut +3 more
2024Asian Biomedicine0 citations Open access
Semantic Scholar
Journal Pre-proof The Genetic Basis of Sudden Death after Covid-19 Vaccination in Thailand
S. Mahasirimongkol, S. Srisont, Rungnapa Ittiwut, Manoch Chockjamsai +16 more
20220 citations
Semantic Scholar
Phenotypic Heterogeneity and Genotypic Spectrum of Primary Immunodeficiencies with Whole Exome Sequencing in a Thai Patient Cohort
M. Tengsujaritkul, Narissara Suratannon, C. Ittiwut, Rungnapa Ittiwut +3 more
20210 citations Open access
Semantic Scholar
Mutations in Kinesin Family Member 6 Reveal Specific Role in Ependymal Cell Function and Human Neuro-Cranial Development
Mia J. Konjikusic, Patra Yeetong, Rungnapa Ittiwut, K. Suphapeetiporn +4 more
2018bioRxiv0 citations Open access
Semantic Scholar

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Vorasuk Shotelersuk×26
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Narissara Suratannon×4

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Wuttichart Kamolvisit×4

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Ponghatai Boonsimma×3

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