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Chureerat Phokaew
Chureerat Phokaew
Lecturer at Faculty of Medicine, Chulalongkorn Univeristy, Thailand
Verified email at chula.ac.th
Title
Cited by
Cited by
Year
Whole-genome sequencing reveals host factors underlying critical COVID-19
A Kousathanas, E Pairo-Castineira, K Rawlik, A Stuckey, CA Odhams, ...
Nature 607 (7917), 97-103, 2022
2222022
Hypomethylation of intragenic LINE-1 represses transcription in cancer cells through AGO2
C Aporntewan, C Phokaew, J Piriyapongsa, C Ngamphiw, C Ittiwut, ...
PloS one 6 (3), e17934, 2011
1282011
LINE-1 methylation patterns of different loci in normal and cancerous cells
C Phokaew, S Kowudtitham, K Subbalekha, S Shuangshoti, ...
Nucleic acids research 36 (17), 5704-5712, 2008
1182008
Cyclin A1 promoter hypermethylation in human papillomavirus-associated cervical cancer
N Kitkumthorn, P Yanatatsanajit, S Kiatpongsan, C Phokaew, ...
BMC cancer 6, 1-9, 2006
972006
Detection of LINE-1s hypomethylation in oral rinses of oral squamous cell carcinoma patients
K Subbalekha, A Pimkhaokham, P Pavasant, S Chindavijak, C Phokaew, ...
Oral oncology 45 (2), 184-191, 2009
482009
Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative
G Butler-Laporte, G Povysil, JA Kosmicki, ET Cirulli, T Drivas, S Furini, ...
PLoS genetics 18 (11), e1010367, 2022
292022
SARS-CoV-2 susceptibility and COVID-19 disease severity are associated with genetic variants affecting gene expression in a variety of tissues
M D’Antonio, JP Nguyen, TD Arthur, H Matsui, BM Neale, M Daly, ...
Cell reports 37 (7), 2021
272021
The Thai reference exome (T‐REx) variant database
V Shotelersuk, D Wichadakul, C Ngamphiw, C Srichomthong, C Phokaew, ...
Clinical Genetics 100 (6), 703-712, 2021
232021
Whole exome sequencing revealed mutations in FBXL4, UNC80, and ADK in Thai patients with severe intellectual disabilities
C Kuptanon, C Srichomthong, C Ittiwut, T Wechapinan, S Sri-Udomkajorn, ...
Gene 696, 21-27, 2019
182019
Host genetic factors of COVID-19 susceptibility and disease severity in a Thai population
M Chamnanphon, M Pongpanich, TB Suttichet, W Jantarabenjakul, ...
Journal of human genetics 67 (5), 295-301, 2022
162022
Rapid exome sequencing as the first‐tier investigation for diagnosis of acutely and severely ill children and adults in Thailand
W Kamolvisit, P Phowthongkum, P Boonsimma, C Kuptanon, ...
Clinical Genetics 100 (1), 100-105, 2021
132021
Exome sequencing as first-tier genetic testing in infantile-onset pharmacoresistant epilepsy: Diagnostic yield and treatment impact
P Boonsimma, C Ittiwut, W Kamolvisit, R Ittiwut, W Chetruengchai, ...
European Journal of Human Genetics 31 (2), 179-187, 2023
112023
A Pathogenic Variant in ALPK3 Is Associated With an Autosomal Dominant Adult-onset Hypertrophic Cardiomyopathy
C Cheawsamoot, C Phokaew, W Chetruengchai, P Chantranuwat, ...
Circulation: Genomic and Precision Medicine 13 (6), e003127, 2020
112020
A patient with combined pituitary hormone deficiency and osteogenesis imperfecta associated with mutations in LHX4 and COL1A2
N Hemwong, C Phokaew, C Srichomthong, S Tongkobpetch, ...
Journal of Advanced Research 21, 121-127, 2020
112020
Severe neonatal haemolytic anaemia caused by compound heterozygous KLF1 mutations: report of four families and literature review
T Tangsricharoen, R Natesirinilkul, A Phusua, K Fanhchaksai, C Ittiwut, ...
British Journal of Haematology 194 (3), 626-634, 2021
102021
Prenatal sonographic features of CHARGE syndrome
K Traisrisilp, W Chankhunaphas, R Sittiwangkul, C Phokaew, ...
Diagnostics 11 (3), 415, 2021
92021
Age‐related dental phenotypes and tooth characteristics of FAM83H‐associated hypocalcified amelogenesis imperfecta
K Sriwattanapong, I Nitayavardhana, T Theerapanon, ...
Oral Diseases 28 (3), 734-744, 2022
62022
Expanding the genotypic spectrum of PYCR2 and a common ancestry in Thai patients with hypomyelinating leukodystrophy 10
C Manaspon, P Boonsimma, C Phokaew, T Theerapanon, ...
American Journal of Medical Genetics Part A 185 (10), 3068-3073, 2021
52021
A regulatory variant of CHRM3 is associated with cannabis-induced hallucinations in European Americans
Z Cheng, C Phokaew, YL Chou, D Lai, JL Meyers, A Agrawal, LA Farrer, ...
Translational psychiatry 9 (1), 309, 2019
52019
The association between Piwil2 expression and LINE-1 methylation in cancer cells
T Thanasupawat, C Phokaew, A Mutirangura
42010
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Articles 1–20