Skip to content

Home Search Authors Pakistan News Saved

SciRah

SciRah does not host or store research papers. Results come live from free, official scholarly APIs, and every paper links back to its original source.

Data sources

OpenAlex
Semantic Scholar
Crossref
CORE
arXiv
PubMed

Privacy policy Terms of service

C. Ittiwut · SciRah

Researcher profile · Semantic Scholar

C. Ittiwut

Share profile

C. Ittiwut — researcher profile on SciRah

h-index: 17
Works: 71
Citations: 931

Most-cited papers

Hypomethylation of Intragenic LINE-1 Represses Transcription in Cancer Cells through AGO2
C. Aporntewan, C. Phokaew, J. Piriyapongsa, C. Ngamphiw +3 more
2011PLoS ONE107 citations Open access
Semantic Scholar
NUDT15 c.415C>T increases risk of 6-mercaptopurine induced myelosuppression during maintenance therapy in children with acute lymphoblastic leukemia
Kanhatai Chiengthong, C. Ittiwut, Sasipa Muensri, J. Sophonphan +5 more
2016Haematologica90 citations Open access
Semantic Scholar
Maternal 677CT/1298AC genotype of the MTHFR gene as a risk factor for cleft lip
Vorasuk Shotelersuk, C. Ittiwut, P. Siriwan, A. Angspatt
2003Journal of Medical Genetics68 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
GABRG1 and GABRA2 Variation Associated with Alcohol Dependence in African Americans
C. Ittiwut, Bao-Zhu Yang, H. Kranzler, R. Anton +5 more
2011Alcoholism: Clinical and Experimental Research42 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
Targeted therapies for rare gynaecological cancers.
T. Manchana, C. Ittiwut, A. Mutirangura, J. Kavanagh
2010The Lancet Oncology32 citations
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
FGFR2 Mutations among Thai Children with Crouzon and Apert Syndromes
Vorasuk Shotelersuk, Charan Mahatumarat, C. Ittiwut, Nond Rojvachiranonda +3 more
2003The Journal of craniofacial surgery (Print)28 citations
Semantic Scholar
Distinct craniofacial-skeletal-dermatological dysplasia in a patient with W290C mutation in FGFR2.
Vorasuk Shotelersuk, C. Ittiwut, S. Srivuthana, Charan Mahatumarat +2 more
2002American journal of medical genetics27 citations
Semantic Scholar
A novel PITX2 mutation in non-syndromic orodental anomalies.
N. Intarak, T. Theerapanon, C. Ittiwut, K. Suphapeetiporn +2 more
2018Oral Diseases26 citations
Semantic Scholar
Novel mutations in SPTA1 and SPTB identified by whole exome sequencing in eight Thai families with hereditary pyropoikilocytosis presenting with severe fetal and neonatal anaemia
C. Ittiwut, R. Natesirinilkul, F. Tongprasert, L. Sathitsamitphong +5 more
2018British Journal of Haematology24 citations Open access
Semantic Scholar
ATP1A3-related epilepsy: Report of seven cases and literature-based analysis of treatment response.
Marius Gasser, Ponghatai Boonsimma, Wiracha Netbaramee, Thanin Wechapinan +15 more
2020Journal of clinical neuroscience20 citations
Semantic Scholar
Interpopulation linkage disequilibrium patterns of GABRA2 and GABRG1 genes at the GABA cluster locus on human chromosome 4.
C. Ittiwut, Jennifer B. Listman, A. Mutirangura, R. Malison +5 more
2008Genomics19 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
Expanding phenotypic and mutational spectra of mitochondrial HMG-CoA synthase deficiency.
K. Rojnueangnit, Parisa Maneechai, Patcharapa Thaweekul, Punnapatch Piriyanon +8 more
2020European Journal of Medical Genetics17 citations
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
Novel mutations of the SRD5A2 and AR genes in Thai patients with 46, XY disorders of sex development
C. Ittiwut, J. Pratuangdejkul, V. Supornsilchai, Sasipa Muensri +5 more
2017Journal of Pediatric Endocrinology & Metabolism (JPEM)17 citations
Semantic Scholar
Massive parallel sequencing as a new diagnostic approach for phenylketonuria and tetrahydrobiopterin-deficiency in Thailand
Pongsathorn Chaiyasap, C. Ittiwut, C. Srichomthong, Apiruk Sangsin +2 more
2017BMC Medical Genetics17 citations Open access
Semantic Scholar
Southeast Asian origins of five Hill Tribe populations and correlation of genetic to linguistic relationships inferred with genome-wide SNP data
Jennifer B. Listman, R. Malison, K. Sanichwankul, C. Ittiwut +2 more
2011American Journal of Physical Anthropology16 citations Open access
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
Nine patients with KCNQ2-related neonatal seizures and functional studies of two missense variants
Suphalak Chokvithaya, Natarin Caengprasath, Aayalida Buasong, Supavadee Jantasuwan +9 more
2023Scientific Reports13 citations Open access
Semantic Scholar
Whole exome sequencing revealed mutations in FBXL4, UNC80, and ADK in Thai patients with severe intellectual disabilities.
C. Kuptanon, C. Srichomthong, C. Ittiwut, Thanin Wechapinan +5 more
2019Gene13 citations
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
Congenital myasthenic syndromes in the Thai population: Clinical findings and novel mutations.
Nalinee Pattrakornkul, C. Ittiwut, Ponghatai Boonsimma, K. Boonyapisit +4 more
2020Neuromuscular Disorders11 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
Severe neonatal haemolytic anaemia caused by compound heterozygous KLF1 mutations: report of four families and literature review
Tanu Tangsricharoen, R. Natesirinilkul, Arunee Phusua, K. Fanhchaksai +7 more
2021British Journal of Haematology10 citations
Semantic Scholar
Mutational and phenotypic expansion of ATP1A3-related disorders: Report of nine cases.
Ponghatai Boonsimma, Marius Michael Gasser, Wiracha Netbaramee, Thanin Wechapinan +11 more
2020Gene10 citations
Semantic Scholar
Compound Heterozygous PGM3 Mutations in a Thai Patient with a Specific Antibody Deficiency Requiring Monthly IVIG Infusions
C. Ittiwut, Wiparat Manuyakorn, S. Tongkobpetch, Suwat Benjaponpitak +5 more
2019Journal of Clinical Immunology10 citations
Semantic Scholar
Female‐restricted syndromic intellectual disability in a patient from Thailand
Thivaratana Sinthuwiwat, C. Ittiwut, T. Porntaveetus, Vorasuk Shotelersuk
2019American Journal of Medical Genetics. Part A8 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
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
Nagashima-Type Palmoplantar Keratosis with Compound Heterozygous Mutations in SERPINB7
Chankiat Songsantiphap, Jirat Suwanwatana, C. Ittiwut, P. Asawanonda +2 more
2020Case Reports in Dermatology6 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
A case of Pfeiffer syndrome type 1 with an A344P mutation in the FGFR2 gene.
Vorasuk Shotelersuk, S. Srivuthana, C. Ittiwut, A. Theamboonlers +2 more
2001Southeast Asian Journal of Tropical Medicine and Public Health6 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
A case of GABRA5-related developmental and epileptic encephalopathy with response to a combination of antiepileptic drugs and a GABAering agent.
Ponghatai Boonsimma, S. Suwannachote, C. Phokaew, C. Ittiwut +2 more
2020Brain & development (Tokyo. 1979)5 citations
Semantic Scholar
Severe Hyperammonemic Encephalopathy Requiring Dialysis Aggravated by Prolonged Fasting and Intermittent High Fat Load in a Ramadan Fasting Month in a Patient with CPTII Homozygous Mutation.
P. Phowthongkum, C. Ittiwut, V. Shotelersuk
2017JIMD 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
Utilisation of exome sequencing for muscular disorders in Thai paediatric patients: diagnostic yield and mutational spectrum
Sarinya Summa, C. Ittiwut, P. Kulsirichawaroj, Tanitnun Paprad +5 more
2023Scientific Reports4 citations Open access
Semantic Scholar
Genetic diagnosis for adult patients at a genetic clinic
K. Rojnueangnit, Pimjai Anthanont, Thanitchet Khetkham, Sukita Puttamanee +1 more
2022Cold Spring Harbor molecular case studies4 citations Open access
Semantic Scholar
Whole-Exome Sequencing Solved over 2-Decade Kidney Disease Enigma
Suramath Isaranuwatchai, Ankanee Chanakul, C. Ittiwut, C. Srichomthong +3 more
2021Nephron4 citations
Semantic Scholar
Diagnosis of Hyper IgM syndrome in a Previously Healthy Adolescent Boy Presented with Cutaneous and Cerebral Cryptococcosis.
Athipat Athipongarporn, C. Ittiwut, Wiparat Manuyakorn, Surapat Assawawiroonhakarn +2 more
2020The Pediatric Infectious Disease Journal4 citations
Semantic Scholar
Bilateral Femoral Neck Fractures in Cerebrotendinous Xanthomatosis Treated by Hip Arthroplasties: The First Case Report and Literature Review
Witchuree Wejjakul, Swist Chatmaitri, Thongek Wattanarojanaporn, A. Pongkunakorn +2 more
2017Journal of Orthopaedic Case Reports4 citations
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
A Novel GNAS Mutation Causing Isolated Infantile Cushing’s Syndrome
Prapai Dejkhamron, C. Ittiwut, Hataitip Tangngam, K. Sunkonkit +3 more
2019Hormone Research in Paediatrics3 citations
Semantic Scholar

Frequent co-authors

Invite them to SciRah by sharing their profile.

Vorasuk Shotelersuk×38
Invite
Vorasuk Shotelersuk — researcher profile on SciRah
K. Suphapeetiporn×31
Invite
K. Suphapeetiporn — researcher profile on SciRah
Rungnapa Ittiwut×18
Invite
Rungnapa Ittiwut — researcher profile on SciRah
Ponghatai Boonsimma×9
Invite
Ponghatai Boonsimma — researcher profile on SciRah

C. Srichomthong×7

Invite

C. Srichomthong — researcher profile on SciRah

Invite

C. Phokaew — researcher profile on SciRah

Wuttichart Kamolvisit×5

Invite

Wuttichart Kamolvisit — researcher profile on SciRah

A. Mutirangura×4

Invite

A. Mutirangura — researcher profile on SciRah

T. Porntaveetus×4

Invite

T. Porntaveetus — researcher profile on SciRah

W. Chetruengchai×4

Invite

W. Chetruengchai — researcher profile on SciRah

D. Sosothikul×3

Invite

D. Sosothikul — researcher profile on SciRah

Narissara Suratannon×3

Invite

Narissara Suratannon — researcher profile on SciRah