Chureerat Phokaew
Bangkok, 10330, Thailand
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 20 publications
Whole exome sequencing in relapsed or refractory childhood cancer: case series.
Journal: Asian biomedicine : research, reviews and news
Published: September 23, 2024
Exome sequencing as first-tier genetic testing in infantile-onset pharmacoresistant epilepsy: diagnostic yield and treatment impact.
Journal: European journal of human genetics : EJHG
Published: June 03, 2022
Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative.
Journal: PLoS genetics
Published: April 06, 2022
A LILRB1 variant with a decreased ability to phosphorylate SHP-1 leads to autoimmune diseases.
Journal: Scientific reports
Published: March 16, 2022
Host genetic factors of COVID-19 susceptibility and disease severity in a Thai population.
Journal: Journal of human genetics
Published: July 30, 2021
Whole genome sequencing identifies a homozygous nonsense mutation in the JPH2 gene in Shih Tzu dogs with progressive retinal atrophy.
Journal: Animal genetics
Published: June 24, 2021
Severe neonatal haemolytic anaemia caused by compound heterozygous KLF1 mutations: report of four families and literature review.
Journal: British journal of haematology
Published: April 12, 2021
Rapid exome sequencing as the first-tier investigation for diagnosis of acutely and severely ill children and adults in Thailand.
Journal: Clinical genetics
Published: March 28, 2021
Last Updated: 09/26/2026