Publications by authors named "Chanatjit Cheawsamoot"

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Genome sequencing identifies uniparental isodisomy of chromosome 2p and a homozygous variant, enabling effective treatment of pediatric hypercholesterolemia after 13 years of therapeutic resistance: A case report.
Hannah Kassaie, Chanatjit Cheawsamoot, Sunisa Kanchanasutthiyakorn, Kanokwan Santawong, Sirinuch Chomtho

Biomed Rep· November 2025

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Generation of human induced pluripotent stem cell lines from patients with PHACE syndrome.
Rohin Ramchandani, Chanatjit Cheawsamoot, Giovanni A Torres, Jennifer Arthur Ataam, Dawn Siegel

Stem Cell Res· September 2025

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Singleton rapid long-read genome sequencing as first tier genetic test for critically Ill children with suspected genetic diseases.
Wuttichart Kamolvisit, Chanatjit Cheawsamoot, Wanna Chetruengchai, Phawin Kor-Anantakul, Rungroj Thangpong

Eur J Hum Genet· June 2025

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Corrigendum to "Generation of human induced pluripotent stem cell lines derived from four patients with a pathogenic ALPK3 variant associated with adult-onset hypertrophic cardiomyopathy (HCM)" [Stem Cell Res. 73 (2023) 103233].
Chanatjit Cheawsamoot, Rohin Ramchandani, Mohamed Ameen, Jennifer Ataam Arthur, Apichai Khongphatthanayothin

Stem Cell Res· February 2024

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Generation of human induced pluripotent stem cell lines derived from four patients with a pathogenic ALPK3 variant associated with adult-onset hypertrophic cardiomyopathy (HCM).
Chanatjit Cheawsamoot, Rohin Ramchandani, Mohamed Ameen, Jennifer Arthur Ataam, Apichai Khongphatthanayothin

Stem Cell Res· December 2023

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A Pathogenic Variant in Is Associated With an Autosomal Dominant Adult-onset Hypertrophic Cardiomyopathy.
Chanatjit Cheawsamoot, Chureerat Phokaew, Wanna Chetruengchai, Poonchavist Chantranuwat, Sarinya Puwanant

Circ Genom Precis Med· December 2020

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