Vorasuk Shotelersuk

254 Phayathai Road
Bangkok, 10330, Thailand

Last Updated: 09/26/2026

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Found 222 publications

Novel CHD7 Variants Associated with an Expanded Orofacial and Dental Phenotype.

Novel CHD7 Variants Associated with an Expanded Orofacial and Dental Phenotype.

Journal: European journal of dentistry
Published: July 15, 2026

Genetic diversity of clinical Mycobacterium bovis BCG isolates from an immunocompromised patient with BCG infection.

Genetic diversity of clinical Mycobacterium bovis BCG isolates from an immunocompromised patient with BCG infection.

Journal: Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases
Published: May 21, 2026

Metagenome and Metabolic Pathways in Plaque Biofilms of Thai ELANE-Associated Neutropenic Patients: An Original Study and Scoping Review.

Metagenome and Metabolic Pathways in Plaque Biofilms of Thai ELANE-Associated Neutropenic Patients: An Original Study and Scoping Review.

Journal: European journal of dentistry
Published: March 25, 2026

Correction: Somatic mutations in the TG and RELA genes specific for radioiodine-refractory thyroid cancer.

Correction: Somatic mutations in the TG and RELA genes specific for radioiodine-refractory thyroid cancer.

Journal: Scientific reports
Published: January 21, 2026

Long-read genome sequencing increases diagnostic yield in a short-read sequencing unsolved developmental epileptic encephalopathy (DEE) cohort.

Long-read genome sequencing increases diagnostic yield in a short-read sequencing unsolved developmental epileptic encephalopathy (DEE) cohort.

Journal: Journal of medical genetics
Published: January 19, 2026

Pentanucleotide repeat instability and transmission in benign adult familial myoclonic epilepsy types 1, 4, and 8.

Pentanucleotide repeat instability and transmission in benign adult familial myoclonic epilepsy types 1, 4, and 8.

Journal: Epilepsia
Published: November 19, 2025

Exercise-induced lactic acidemia associated with a SLC16A13 biallelic variant.

Exercise-induced lactic acidemia associated with a SLC16A13 biallelic variant.

Journal: NPJ genomic medicine
Published: October 22, 2025

Dopaminergic neurons are vulnerable to dysregulation of YEATS2-dependent calcium homeostasis.

Dopaminergic neurons are vulnerable to dysregulation of YEATS2-dependent calcium homeostasis.

Journal: iScience
Published: September 13, 2025

Multi-ancestral genome-wide association study of clinically defined nicotine dependence reveals strong genetic correlations with other substance use disorders and health-related traits.

Multi-ancestral genome-wide association study of clinically defined nicotine dependence reveals strong genetic correlations with other substance use disorders and health-related traits.

Journal: Psychological medicine
Published: August 20, 2025

The ASEAN genome consortium: advancing equitable precision medicine through regional solidarity.

The ASEAN genome consortium: advancing equitable precision medicine through regional solidarity.

Journal: The Lancet regional health. Western Pacific
Published: June 05, 2025

Genome sequencing identifies uniparental isodisomy of chromosome 2p and a homozygous ABCG5 variant, enabling effective treatment of pediatric hypercholesterolemia after 13 years of therapeutic resistance: A case report.

Genome sequencing identifies uniparental isodisomy of chromosome 2p and a homozygous ABCG5 variant, enabling effective treatment of pediatric hypercholesterolemia after 13 years of therapeutic resistance: A case report.

Journal: Biomedical reports
Published: May 07, 2025

FAM20A Deficiency Drives Transcriptomic Dysregulation and Functional Impairment in Gingival Fibroblasts.

FAM20A Deficiency Drives Transcriptomic Dysregulation and Functional Impairment in Gingival Fibroblasts.

Journal: Cell proliferation
Published: April 30, 2025
Showing 1-12 of 222

Last Updated: 09/26/2026