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Wasun Chantratita

Explore the profile of Wasun Chantratita including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 138
Citations 1453
Followers 0
Related Specialties
Infectious Diseases
Microbiology
Public Health
Top 10 Co-Authors
Chonlaphat Sukasem
Somnuek Sungkanuparph
Ekawat Pasomsub
Surakameth Mahasirimongkol
Sasisopin Kiertiburanakul
Angkana Charoenyingwattana
Insee Sensorn
Taisei Mushiroda
Nareenart Iemwimangsa
George P Patrinos
Published In
Southeast Asian J Trop Med Public Health
J Virol Methods
Jpn J Infect Dis
Mol Cell Probes
J Med Assoc Thai
Affiliations
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Recent Articles
1.
Dynamic changes in immune repertoire profiles in patients with stage III unresectable non-small cell lung cancer during consolidation treatment with immunotherapy
Iemwimangsa N, Anantaya D, Oranratnachai S, Thamrongjirapat T, Lumjiaktase P, Teoh V, et al.
BMC Cancer . 2025 Feb; 25(1):333. PMID: 39994571
Background: One-year of immune checkpoint inhibitor (ICI) treatment after concurrent chemoradiation (CCRT) in unresectable stage III non-small cell lung cancer (NSCLC) is a standard of care. The precise predictive biomarkers...
2.
Nationwide carrier screening for congenital adrenal hyperplasia: integrated approach of CYP21A2 pathogenic variant genotyping and comprehensive large gene deletion analysis
Suwanlikit Y, Panthan B, Chitayanan P, Klumsathian S, Charoenyingwattana A, Chantratita W, et al.
BMC Med Genomics . 2025 Jan; 18(1):18. PMID: 39856693
Background: Congenital Adrenal Hyperplasia (CAH) due to 21-hydroxylase deficiency (21-OHD CAH) is an autosomal recessive disorder resulting from pathogenic variants in the CYP21A2 gene. The disorder exhibits variable clinical severity,...
3.
A common form of dominant human IFNAR1 deficiency impairs IFN-α and -ω but not IFN-β-dependent immunity
Al Qureshah F, Le Pen J, de Weerd N, Moncada-Velez M, Materna M, Lin D, et al.
J Exp Med . 2024 Dec; 222(2). PMID: 39680367
Autosomal recessive deficiency of the IFNAR1 or IFNAR2 chain of the human type I IFN receptor abolishes cellular responses to IFN-α, -β, and -ω, underlies severe viral diseases, and is...
4.
Severe acute respiratory syndrome coronavirus 2 variants in patients with coronavirus disease 2019 and environmental sampling from the hospital and market during the coronavirus disease 2019 pandemic in Thailand
Phumisantiphong U, Rupprom K, Wongsuk T, Manomaipiboon A, Maneerit J, Vimonvattana A, et al.
Diagn Microbiol Infect Dis . 2024 Nov; 111(2):116604. PMID: 39550978
Limited genomic surveillance data is available for SARS-CoV-2 in Thailand during the second and third wave outbreaks, including both patient and environmental samples. This study investigated the presence of SARS-CoV-2...
5.
Thai pharmacogenomics database -2 (TPGxD-2) sequel to TPGxD-1, analyzing genetic variants in 26 non-VIPGx genes within the Thai population
John S, Klumsathian S, Own-Eium P, Charoenyingwattana A, Eu-Ahsunthornwattana J, Sura T, et al.
Clin Transl Sci . 2024 Oct; 17(10):e70019. PMID: 39449569
Next-generation sequencing (NGS) has transformed pharmacogenomics (PGx), enabling thorough profiling of pharmacogenes using computational methods and advancing personalized medicine. The Thai Pharmacogenomic Database-2 (TPGxD-2) analyzed 948 whole genome sequences, primarily...
6.
Associations between clinical data, vaccination status, antibody responses, and post-COVID-19 symptoms in Thais infected with SARS-CoV-2 Delta and Omicron variants: a 1-year follow-up study
Khongsiri W, Poolchanuan P, Dulsuk A, Thippornchai N, Phunpang R, Runcharoen C, et al.
BMC Infect Dis . 2024 Oct; 24(1):1116. PMID: 39375604
Background: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), which causes coronavirus disease 2019 (COVID-19), led to a global pandemic from 2020. In Thailand, five waves of outbreaks were recorded, with...
7.
Genetic diversity, determinants, and dissemination of Burkholderia pseudomallei lineages implicated in melioidosis in Northeast Thailand
Seng R, Chomkatekaew C, Tandhavanant S, Saiprom N, Phunpang R, Thaipadungpanit J, et al.
Nat Commun . 2024 Jul; 15(1):5699. PMID: 38972886
Melioidosis is an often-fatal neglected tropical disease caused by an environmental bacterium Burkholderia pseudomallei. However, our understanding of the disease-causing bacterial lineages, their dissemination, and adaptive mechanisms remains limited. To...
8.
A comprehensive Thai pharmacogenomics database (TPGxD-1): Phenotype prediction and variants identification in 942 whole-genome sequencing data
John S, Klumsathian S, Own-Eium P, Eu-Ahsunthornwattana J, Sura T, Dejsuphong D, et al.
Clin Transl Sci . 2024 Jun; 17(6):e13830. PMID: 38853370
Computational methods analyze genomic data to identify genetic variants linked to drug responses, thereby guiding personalized medicine. This study analyzed 942 whole-genome sequences from the Electricity Generating Authority of Thailand...
9.
Coinfection with respiratory syncytial virus and rhinovirus increases IFN-λ1 and CXCL10 expression in human primary bronchial epithelial cells
Sankuntaw N, Punyadee N, Chantratita W, Lulitanond V
New Microbiol . 2024 May; 47(1):60-67. PMID: 38700885
Acute respiratory tract infection (ARTI) is common in all age groups, especially in children and the elderly. About 85% of children who present with bronchiolitis are infected with respiratory syncytial...
10.
Novel genetic variants of HLA gene associated with Thai Behcet's disease (BD) patients using next generation sequencing technology
Sornsamdang G, Shobana J, Chanprapaph K, Chantratita W, Chotewutmontri S, Limtong P, et al.
Sci Rep . 2024 Apr; 14(1):7967. PMID: 38575661
Behçet's disease (BD) manifests as an autoimmune disorder featuring recurrent ulcers and multi-organ involvement, influenced by genetic factors associated with both HLA and non-HLA genes, including TNF-α and ERAP1. The...