Wuttichart Kamolvisit

Bangkok, Thailand

Last Updated: 09/26/2026

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Found 27 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

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

Novel TMEM63A mutation associated with transient hypomyelination of infancy - lessons from a previously negative whole-exome sequencing case: Three case reports.

Novel TMEM63A mutation associated with transient hypomyelination of infancy - lessons from a previously negative whole-exome sequencing case: Three case reports.

Journal: World journal of clinical pediatrics

Published: December 12, 2025

Blau syndrome initially manifested with hypercalcemia: a case report and literature review.

Blau syndrome initially manifested with hypercalcemia: a case report and literature review.

Journal: Annals of pediatric endocrinology & metabolism

Published: September 25, 2025

Blau syndrome initially presenting with hypercalcemia: a case report and literature review.

Blau syndrome initially presenting with hypercalcemia: a case report and literature review.

Journal: Annals of pediatric endocrinology & metabolism

Published: September 25, 2025

Expansion of Phenotyping and Genotypic Spectra of KIF7 -Related Intellectual Disability: Case Report and Review of Literature.

Expansion of Phenotyping and Genotypic Spectra of KIF7 -Related Intellectual Disability: Case Report and Review of Literature.

Journal: American journal of medical genetics. Part A

Published: April 19, 2025

Singleton rapid long-read genome sequencing as first tier genetic test for critically Ill children with suspected genetic diseases.

Singleton rapid long-read genome sequencing as first tier genetic test for critically Ill children with suspected genetic diseases.

Journal: European journal of human genetics : EJHG

Published: October 07, 2024

Unveiling Novel DSPP Variants and Dental Phenotypes in Dentinogenesis Imperfecta.

Unveiling Novel DSPP Variants and Dental Phenotypes in Dentinogenesis Imperfecta.

Journal: Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology

Published: May 08, 2024

Craniosynostosis: orofacial and oral health perspectives with masticatory insights.

Craniosynostosis: orofacial and oral health perspectives with masticatory insights.

Journal: BMC oral health

Published: April 21, 2024

Can knowledgeable experts assess costs and outcomes as if they were ignorant? An experiment within precision medicine evaluation.

Can knowledgeable experts assess costs and outcomes as if they were ignorant? An experiment within precision medicine evaluation.

Journal: International journal of technology assessment in health care

Published: November 16, 2023

Genetic, metabolic and clinical delineation of an MRPS23-associated mitochondrial disorder.

Genetic, metabolic and clinical delineation of an MRPS23-associated mitochondrial disorder.

Journal: Scientific reports

Published: July 25, 2023

Using an experiment among clinical experts to determine the cost and clinical impact of rapid whole exome sequencing in acute pediatric settings.

Using an experiment among clinical experts to determine the cost and clinical impact of rapid whole exome sequencing in acute pediatric settings.

Journal: Frontiers in pediatrics

Published: April 12, 2023

Showing 1-12 of 27

Last Updated: 09/26/2026