Angkana Charoenyingwattana
Overview
Explore the profile of Angkana Charoenyingwattana including associated specialties, affiliations and a list of published articles.
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Articles
16
Citations
208
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Recent Articles
1.
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,...
2.
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...
3.
Trachoo O, Yingchoncharoen T, Ngernsritrakul T, Iemwimangsa N, Panthan B, Klumsathian S, et al.
PLoS One
. 2022 Sep;
17(9):e0267770.
PMID: 36166435
Hypertrophic cardiomyopathy (HCM) and dilated cardiomyopathy (DCM) are the most common referrals in the Inherited Cardiovascular Condition (ICC) Genetics Service. Several issues must be discussed with patients and their families...
4.
Saifon W, Sensorn I, Trachu N, Oranratnachai S, Charoenyingwattana A, Runcharoen C, et al.
BMC Cancer
. 2022 Sep;
22(1):963.
PMID: 36076157
Introduction: Difference in clinical responses to cancer therapy in each patient is from several factors. Gastrointestinal microbiota is one of the reasons. However, this correlation remains unknown. This study aims...
5.
Chanhom N, Jittikoon J, Wattanapokayakit S, Mahasirimongkol S, Charoenyingwattana A, Udomsinprasert W, et al.
J Pers Med
. 2022 Jun;
12(6).
PMID: 35743726
Glutathione s-transferase (GST) is a family of drug-metabolizing enzymes responsible for metabolizing and detoxifying drugs and xenobiotic substances. Therefore, deletion polymorphisms of s can be implicated in developing several pathological...
6.
Runcharoen C, Fukunaga K, Sensorn I, Iemwimangsa N, Klumsathian S, Tong H, et al.
Hum Genome Var
. 2021 Feb;
8(1):7.
PMID: 33542200
Pharmacogenomics can enhance the outcome of treatment by adopting pharmacogenomic testing to maximize drug efficacy and lower the risk of serious adverse events. Next-generation sequencing (NGS) is a cost-effective technology...
7.
Satirapod C, Sukprasert M, Panthan B, Charoenyingwattana A, Chitayanan P, Chantratita W, et al.
PLoS One
. 2019 Nov;
14(11):e0225457.
PMID: 31751397
Thalassemia and hemoglobinopathy is a group of hereditary blood disorder with diverse clinical manifestation inherited by autosomal recessive manner. The Beta thalassemia/Hemoglobin E disease (HbE/βthal) causes a variable degree of...
8.
Chumnumwat S, Lu Z, Sukasem C, Winther M, Capule F, Abdul Hamid A, et al.
Public Health Genomics
. 2019 Oct;
22(3-4):132-139.
PMID: 31587001
Pharmacogenomics (PGx) is increasingly being recognized as a potential tool for improving the efficacy and safety of drug therapy. Therefore, several efforts have been undertaken globally to facilitate the implementation...
9.
Trachoo O, Satirapod C, Panthan B, Sukprasert M, Charoenyingwattana A, Chantratita W, et al.
J Assist Reprod Genet
. 2016 Nov;
34(1):109-116.
PMID: 27815806
Purpose: We aim to present a case of a healthy infant born after intracytoplasmic sperm injection-in vitro fertilization (ICSI-IVF) with a preimplantation genetic diagnosis (PGD) for pantothenate kinase-associated neurodegeneration (PKAN)...
10.
Jittikoon J, Mahasirimongkol S, Charoenyingwattana A, Chaikledkaew U, Tragulpiankit P, Mangmool S, et al.
J Hum Genet
. 2015 Oct;
61(2):119-27.
PMID: 26423926
The objectives of this study are to investigate allele frequencies of drug absorption, distribution, metabolism and elimination (ADME)-related genes in the Thai population and to compare these genes to HapMap...