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W. Thongnoppakhun · SciRah

Researcher profile · Semantic Scholar

W. Thongnoppakhun

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W. Thongnoppakhun — researcher profile on SciRah

h-index: 20
Works: 76
Citations: 1,708

Most-cited papers

Adult-onset immunodeficiency in Thailand and Taiwan
S. Browne, P. Burbelo, P. Chetchotisakd, Y. Suputtamongkol +30 more
2012New England Journal of Medicine530 citations Open access
Semantic Scholar
Molecular alterations of isocitrate dehydrogenase 1 and 2 (IDH1 and IDH2) metabolic genes and additional genetic mutations in newly diagnosed acute myeloid leukemia patients
S. Chotirat, W. Thongnoppakhun, Orathai Promsuwicha, Chetsada Boonthimat +1 more
2012Journal of Hematology & Oncology117 citations Open access
Semantic Scholar
High prevalence of V37I genetic variant in the connexin‐26 (GJB2) gene among non‐syndromic hearing‐impaired and control Thai individuals
D. Wattanasirichaigoon, C. Limwongse, C. Jariengprasert, P. Yenchitsomanus +7 more
2004Clinical Genetics86 citations
Semantic Scholar
Orientia tsutsugamushi Stimulates an Original Gene Expression Program in Monocytes: Relationship with Gene Expression in Patients with Scrub Typhus
W. Tantibhedhyangkul, T. Prachason, D. Waywa, Adil El Filali +7 more
2011PLoS Neglected Tropical Diseases73 citations Open access
Semantic Scholar
HLA-DRB1 and HLA-DQB1 Are Associated with Adult-Onset Immunodeficiency with Acquired Anti-Interferon-Gamma Autoantibodies
Manop Pithukpakorn, E. Roothumnong, Nasikarn Angkasekwinai, B. Suktitipat +6 more
2015PLoS ONE59 citations Open access
Semantic Scholar
Whole exome sequencing in Thai patients with retinitis pigmentosa reveals novel mutations in six genes.
Worapoj Jinda, T. Taylor, Yutaka Suzuki, W. Thongnoppakhun +5 more
2014Investigative Ophthalmology and Visual Science58 citations
Semantic Scholar
Mutation analysis of the GNE gene in distal myopathy with rimmed vacuoles (DMRV) patients in Thailand
T. Liewluck, T. Pho-iam, C. Limwongse, W. Thongnoppakhun +6 more
2006Muscle and Nerve49 citations
Semantic Scholar
Nucleophosmin mutation in Southeast Asian acute myeloid leukemia: eight novel variants, FLT3 coexistence and prognostic impact of NPM1/FLT3 mutations
Chetsada Boonthimat, W. Thongnoppakhun, C. Auewarakul
2008Haematologica42 citations Open access
Semantic Scholar
Hematological abnormalities in patients with distal renal tubular acidosis and hemoglobinopathies
S. Khositseth, Apiwan Sirikanaerat, Siri Khoprasert, Sauwalak Opastirakul +3 more
2008American journal of hematology/oncology41 citations Open access
Semantic Scholar
Mutations of the FLT3 gene in adult acute myeloid leukemia: determination of incidence and identification of a novel mutation in a Thai population.
C. Auewarakul, Narongrit Sritana, C. Limwongse, W. Thongnoppakhun +1 more
2005Cancer Genetics and Cytogenetics35 citations
Semantic Scholar
Distal renal tubular acidosis associated with anion exchanger 1 mutations in children in Thailand.
S. Khositseth, Apiwan Sirikanerat, Kulruedee Wongbenjarat, Sauwalak Opastirakul +6 more
2007American Journal of Kidney Diseases32 citations
Semantic Scholar
Association between ADAM33 polymorphisms and asthma in a Thai population.
T. Thongngarm, Aree Jameekornrak, C. Limwongse, A. Sangasapaviliya +5 more
2008Asian Pacific Journal of Allergy and Immunology28 citations
Semantic Scholar
Tumor mutational profile of triple negative breast cancer patients in Thailand revealed distinctive genetic alteration in chromatin remodeling gene
S. Niyomnaitham, N. Parinyanitikul, E. Roothumnong, Worapoj Jinda +6 more
2019PeerJ25 citations Open access
Semantic Scholar
Acquired somatic mutations of isocitrate dehydrogenases 1 and 2 (IDH1 and IDH2) in preleukemic disorders.
S. Chotirat, W. Thongnoppakhun, W. Wanachiwanawin, C. Auewarakul
2015Blood Cells, Molecules & Diseases25 citations
Semantic Scholar
Six novel ATP7B mutations in Thai patients with Wilson disease.
B. Panichareon, K. Taweechue, W. Thongnoppakhun, Monthikan Aksornworanart +4 more
2011European Journal of Medical Genetics24 citations
Semantic Scholar
BCR-ABL kinase domain mutations in tyrosine kinase inhibitors-naïve and -exposed Southeast Asian chronic myeloid leukemia patients.
Wanwisa Wongboonma, W. Thongnoppakhun, C. Auewarakul
2012Experimental and molecular pathology (Print)22 citations
Semantic Scholar
A single-tube allele specific-polymerase chain reaction to detect T315I resistant mutation in chronic myeloid leukemia patients
Wanwisa Wongboonma, W. Thongnoppakhun, C. Auewarakul
2011Journal of Hematology & Oncology21 citations Open access
Semantic Scholar
Combination of multiplex PCR and DHPLC-based strategy for CYP2D6 genotyping scheme in Thais.
Payiarat Suwannasri, W. Thongnoppakhun, Pornpen Pramyothin, A. Assawamakin +1 more
2011Clinical Biochemistry21 citations
Semantic Scholar
Analysis of published PKD1 gene sequence variants
A. Gout, D. Ravine, Peter C. Harris, Sandro Rossetti +31 more
2007Nature Genetics21 citations
Semantic Scholar
A Thai family with hereditary pancreatitis and increased cancer risk due to a mutation in PRSS1 gene.
T. Pho-iam, W. Thongnoppakhun, P. Yenchitsomanus, C. Limwongse
2005World Journal of Gastroenterology20 citations Open access
Semantic Scholar
Molecular investigation by whole exome sequencing revealed a high proportion of pathogenic variants among Thai victims of sudden unexpected death syndrome
B. Suktitipat, S. Sathirareuangchai, E. Roothumnong, W. Thongnoppakhun +5 more
2017PLoS ONE19 citations Open access
Semantic Scholar
The Study on Telomere Length for Age Estimation in a Thai Population
Supawon Srettabunjong, Saravut Satitsri, W. Thongnoppakhun, N. Tirawanchai
2014American Journal of Forensic Medicine and Pathology19 citations
Semantic Scholar
Two-round allele specific-polymerase chain reaction: a simple and highly sensitive method for JAK2V617F mutation detection.
Supattra Kannim, W. Thongnoppakhun, C. Auewarakul
2009Clinica chimica acta; international journal of clinical chemistry19 citations
Semantic Scholar
Classification of haemoglobin typing chromatograms by neural networks and decision trees for thalassaemia screening
Theera Piroonratana, W. Wongseree, A. Assawamakin, Nuttawut Paulkhaolarn +5 more
200919 citations
Semantic Scholar
A novel start codon mutation of the MERTK gene in a patient with retinitis pigmentosa
Worapoj Jinda, N. Poungvarin, T. Taylor, Yutaka Suzuki +5 more
2016Molecular Vision18 citations
Semantic Scholar
Long RT-PCR Amplification of the entire coding sequence of the polycystic kidney disease 1 (PKD1) gene.
W. Thongnoppakhun, P. Wilairat, K. Vareesangthip, P. Yenchitsomanus
1999BioTechniques18 citations Open access
Semantic Scholar
High Frequency of KRAS Codon 146 and FBXW7 Mutations in Thai Patients with Stage II-III Colon Cancer
K. Korphaisarn, A. Pongpaibul, E. Roothumnong, Khontawan Pongsuktavorn +5 more
2019Asian Pacific Journal of Cancer Prevention16 citations Open access
Semantic Scholar
Simple, efficient, and cost-effective multiplex genotyping with matrix assisted laser desorption/ionization time-of-flight mass spectrometry of hemoglobin beta gene mutations.
W. Thongnoppakhun, Surasak Jiemsup, S. Yongkiettrakul, Chompunut Kanjanakorn +5 more
2009Journal of Molecular Diagnostics16 citations Open access
Semantic Scholar
Hemoglobin Pakse: Presence on Red Blood Cell Membrane and Detection by Polymerase Chain Reaction-Single-Strand Conformational Polymorphism
Chairat Turbpaiboon, A. Siritantikorn, W. Thongnoppakhun, Duangkamon Bunditworapoom +4 more
2004International journal of hematology16 citations
Semantic Scholar
Thai patients who fulfilled NCCN criteria for breast/ovarian cancer genetic assessment demonstrated high prevalence of germline mutations in cancer susceptibility genes: implication to Asian population testing
P. Lertwilaiwittaya, E. Roothumnong, Panee Nakthong, Peerawat Dungort +9 more
2021Breast Cancer Research and Treatment15 citations Open access
Semantic Scholar
Novel DYSF mutations in Thai patients with distal myopathy.
T. Liewluck, S. Pongpakdee, R. Witoonpanich, T. Sangruchi +11 more
2009Clinical neurology and neurosurgery (Dutch-Flemish ed. Print)15 citations
Semantic Scholar
Novel and de novo PKD1 mutations identified by multiple restriction fragment-single strand conformation polymorphism (MRF-SSCP)
W. Thongnoppakhun, C. Limwongse, K. Vareesangthip, C. Sirinavin +3 more
2004BMC Medical Genetics15 citations Open access
Semantic Scholar
Germline mutations of 4567 patients with hereditary breast-ovarian cancer spectrum in Thailand
Chalermkiat Kansuttiviwat, P. Lertwilaiwittaya, E. Roothumnong, Panee Nakthong +16 more
2024npj Genomic Medicine14 citations Open access
Semantic Scholar
Whole Exome Sequencing in Eight Thai Patients With Leber Congenital Amaurosis Reveals Mutations in the CTNNA1 and CYP4V2 Genes.
Worapoj Jinda, T. Taylor, Yutaka Suzuki, W. Thongnoppakhun +4 more
2017Investigative Ophthalmology and Visual Science14 citations Open access
Semantic Scholar
Prothrombin haplotype associated with kidney stone disease in Northeastern Thai patients.
N. Rungroj, S. Sritippayawan, W. Thongnoppakhun, Atchara Paemanee +12 more
2011Urology14 citations
Semantic Scholar
AML1 mutation and its coexistence with different transcription factor gene families in de novo acute myeloid leukemia (AML): redundancy or synergism.
C. Auewarakul, Amporn Leecharendkeat, C. Tocharoentanaphol, Orathai Promsuwicha +2 more
2007Haematologica14 citations Open access
Semantic Scholar
Novel and De-novo Truncating PAX6 Mutations and Ocular Phenotypes in Thai Aniridia Patients
L. Atchaneeyasakul, A. Trinavarat, D. Dulayajinda, Kornphet Kumpornsin +3 more
2006Ophthalmic Genetics14 citations
Semantic Scholar
Identification of copy number variation of CAPN10 in Thais with type 2 diabetes by multiplex PCR and denaturing high performance liquid chromatography (DHPLC).
N. Plengvidhya, Kanjana Chanprasert, Watip Tangjittipokin, W. Thongnoppakhun +1 more
2012Gene11 citations
Semantic Scholar
Detection of CAPN10 copy number variation in Thai patients with type 2 diabetes by denaturing high performance liquid chromatography and real-time quantitative polymerase chain reaction
N. Plengvidhya, Kanjana Chanprasert, Watip Tangjittipokin, W. Thongnoppakhun +1 more
2015Journal of Diabetes Investigation10 citations Open access
Semantic Scholar
Novel Mutation of the TINF2 Gene in a Patient with Dyskeratosis Congenita
B. Panichareon, Thanawat Seedapan, W. Thongnoppakhun, C. Limwongse +2 more
2015Case Reports in Dermatology10 citations Open access
Semantic Scholar
Mutations of AML1 in non-M0 acute myeloid leukemia: six novel mutations and a high incidence of cooperative events in a South-east Asian population.
C. Auewarakul, Amporn Leecharendkeat, W. Thongnoppakhun, C. Limwongse +1 more
2006Haematologica9 citations
Semantic Scholar
No association between CYP17 ‐34T/C polymorphism and insulin resistance in Thai polycystic ovary syndrome
K. Techatraisak, Chenchit Chayachinda, T. Wongwananuruk, Chongdee Dangrat +3 more
2015The journal of obstetrics and gynaecology research8 citations
Semantic Scholar
Mutation Analysis of the VMD2 Gene in Thai Families with Best Macular Dystrophy
L. Atchaneeyasakul, Worapoj Jinda, Natta Sakolsatayadorn, A. Trinavarat +4 more
2008Ophthalmic Genetics8 citations
Semantic Scholar
Meta-analysis of the plasminogen activator inhibitor-1 (PAI-1) gene with insertion/deletion 4G/5G polymorphism and its susceptibility to ischemic stroke in Thai population
A. Assawamakin, N. Sriratanaviriyakul, Yupaporn Lalerd, W. Thongnoppakhun +3 more
20127 citations
Semantic Scholar
Mutations in the XLRS1 gene in Thai families with X-linked juvenile retinoschisis
L. Atchaneeyasakul, A. Trinavarat, Auengporn Pituksung, Worapoj Jinda +2 more
2010Japanese Journal of Ophthalmology7 citations
Semantic Scholar
Effect of gene polymorphisms in ADAM33, TGFβ1, VEGFA, and PLAUR on asthma in Thai population.
T. Thongngarm, Aree Jameekornrak, N. Chaiyaratana, W. Thongnoppakhun +3 more
2019Asian Pacific Journal of Allergy and Immunology6 citations Open access
Semantic Scholar
A novel maternally‐derived insertional translocation resulting in partial trisomy 4q13.2–q22.1 with complex translocation t(8;20) in a family with intellectual disability
A. Assawamakin, D. Wattanasirichaigoon, C. Tocharoentanaphol, S. Waeteekul +3 more
2012American Journal of Medical Genetics. Part A6 citations
Semantic Scholar
Circulating thyrotropin receptor messenger ribonucleic acid is not an effective marker in the follow-up of differentiated thyroid carcinoma
Surasawadee Ausavarat, J. Sriprapaporn, B. Satayaban, W. Thongnoppakhun +4 more
2015Thyroid Research5 citations Open access
Semantic Scholar
Comprehensive germline and somatic profiling of high-risk Thai breast cancer via next-generation sequencing
Kornyok Kamdee, E. Roothumnong, W. Thongnoppakhun, K. Korphaisarn +14 more
2025Scientific Reports4 citations Open access
Semantic Scholar
The efficacy of low-dose warfarin initiation (3 mg versus 5 mg) in newly diagnosed venous thromboembolism patients among a population with a high prevalence of warfarin-sensitive haplotype of the VKORC1 gene: a randomized controlled trial
Bundarika Suwanawiboon, Wannaphorn Rotchanapanya, Komkrit Mahaprom, W. Thongnoppakhun +4 more
2022Hematology3 citations Open access
Semantic Scholar

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C. Limwongse×27
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C. Limwongse — researcher profile on SciRah
P. Yenchitsomanus×15
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P. Yenchitsomanus — researcher profile on SciRah
Manop Pithukpakorn×10
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Manop Pithukpakorn — researcher profile on SciRah
C. Auewarakul×9
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C. Auewarakul — researcher profile on SciRah

×7

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E. Roothumnong — researcher profile on SciRah

A. Assawamakin×6

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A. Assawamakin — researcher profile on SciRah

Worapoj Jinda×6

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Worapoj Jinda — researcher profile on SciRah

L. Atchaneeyasakul×6

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L. Atchaneeyasakul — researcher profile on SciRah

A. Trinavarat×5

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A. Trinavarat — researcher profile on SciRah

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T. Pho-iam — researcher profile on SciRah

B. Suktitipat×4

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B. Suktitipat — researcher profile on SciRah

Khontawan Pongsuktavorn×4

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Khontawan Pongsuktavorn — researcher profile on SciRah