Publications by authors named "Chanin Limwongse"

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Prevalence of genetic alterations in basal cell carcinoma patients resistant to Hedgehog pathway inhibitors: a systematic review.
Suvijak Untaaveesup, Pornteera Srichana, Gynna Techataweewan, Chanamon Pongphaew, Wichapol Dendumrongsup, Chanin Limwongse

Ann Med· December 2025

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Pharmacogenomic and Clinical Predictors of Deferasirox Response in Transfusion-Dependent Thalassemia Identified Using Whole-Genome Sequencing.
Kittika Yampayon, Watchara Sakares, Krittin Pitinanon, Chanin Limwongse, Somdet Srichairatanakool

Clin Transl Sci· December 2025

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Bridging Pharmacokinetics and Pharmacodynamics: A PBPK/PD Model-Based Approach for Deferasirox Dosing in Transfusion-Dependent Thalassemia.
Watchara Sakares, Udomsak Udomnilobol, Xian Pan, Kittika Yampayon, Supachai Ekwattanakit, Chanin Limwongse

Clin Transl Sci· September 2025

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Next-generation sequencing for pediatric-onset neuromuscular disorders unresolved by conventional diagnostic methods.
Pimchanok Kulsirichawaroj, Mongkol Chanvanichtrakool, Pish Wattanadilokchatkun, Theeraphong Pho-Iam, Chanin Limwongse

Pediatr Res· June 2025

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Prevalence and implications of fragile X premutation screening in Thailand.
Areerat Hnoonual, Sunita Kaewfai, Chanin Limwongse, Pornprot Limprasert

Sci Rep· November 2024

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Alleviated bleeding phenotypes in a child with severe haemophilia A and thalassemia disease.
Pongpak Pongphitcha, Werasak Sasanakul, Praguywan Kadegasem, Duantida Songdej, Chanin Limwongse

Haemophilia· July 2024

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Germline mutations of 4567 patients with hereditary breast-ovarian cancer spectrum in Thailand.
Chalermkiat Kansuttiviwat, Pongtawat Lertwilaiwittaya, Ekkapong Roothumnong, Panee Nakthong, Peerawat Dungort, Chanin Limwongse

NPJ Genom Med· February 2024

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Gene Distribution in Pediatric-Onset Inherited Peripheral Neuropathy: A Single Tertiary Center in Thailand.
Pimchanok Kulsirichawaroj, Yanin Suksangkharn, Da Eun Nam, Theeraphong Pho-Iam, Chanin Limwongse

J Neuromuscul Dis· January 2024

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Whole exome sequencing and rare variant association study to identify genetic modifiers, mutations, and a novel double mutation in Thai patients with hemoglobin E/beta-thalassemia.
Chattree Hantaweepant, Bhoom Suktitipat, Manop Pithukpakorn, Yingyong Chinthammitr, Chanin Limwongse

Hematology· December 2023

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How do we translate gaps and unmet needs of blood management for thalassemia into a collaborative implementation framework?
Chanin Limwongse, Ponlapat Rojnuckarin, Pawinee Kupatawintu, Aphisit Thongthaisin, Parichart Permpikul

Transfus Med· December 2023

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Familial clustering of nonalcoholic fatty liver disease in first-degree relatives of adults with lean nonalcoholic fatty liver disease.
Sorachat Niltwat, Chanin Limwongse, Natthinee Charatcharoenwitthaya, Duangkamon Bunditvorapoom, Wimolrak Bandidniyamanon

Liver Int· December 2023

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Identification of Genomic Alterations in Thai Patients With Colorectal Cancer Using Next-Generation Sequencing-Based Multigene Cancer Panel.
Worapoj Jinda, Hathaiwan Moungthard, Chanin Limwongse, Manop Pithukpakorn, Pensri Saelee

Cureus· May 2023

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STK11 Causative Variants and Copy Number Variations Identified in Thai Patients With Peutz-Jeghers Syndrome.
Wannasiri Chiraphapphaiboon, Wanna Thongnoppakhun, Thawornchai Limjindaporn, Sunisa Sawasdichai, Ekkapong Roothumnong, Chanin Limwongse

Cureus· February 2023

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The efficacy of low-dose warfarin initiation (3 mg versus 5 mg) in newly diagnosed venous thromboembolism patients among a population with a high prevalence of warfarin-sensitive haplotype of the gene: a randomized controlled trial.
Bundarika Suwanawiboon, Wannaphorn Rotchanapanya, Komkrit Mahaprom, Wanna Thongnoppakhun, Yupaporn Lalerd, Chanin Limwongse

Hematology· December 2022

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Association study identifies genetic determinants and non-genetic factors on steady-state plasma and therapeutic outcome of galantamine in mixed dementia.
Thitipon Yaowaluk, Vorapun Senanarong, Chanin Limwongse, Rasda Boonprasert, Duangkamon Bunditvorapoom

Eur J Clin Pharmacol· August 2022

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Single-Tube Screen for Rapid Detection of Repeat Expansions in Seven Common Spinocerebellar Ataxias.
Mulias Lian, Chanin Limwongse, Chui-Sheun Yoon, Caroline G Lee, Hai-Yang Law

Clin Chem· June 2022

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Sleep Disorder: An Overlooked Manifestation of Glucose Transporter Type-1 Deficiency Syndrome.
Kingthong Anurat, Chaiyos Khongkhatithum, Thipwimol Tim-Aroon, Chanin Limwongse, Lunliya Thampratankul

Neuropediatrics· April 2022

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Thai patients who fulfilled NCCN criteria for breast/ovarian cancer genetic assessment demonstrated high prevalence of germline mutations in cancer susceptibility genes: implication to Asian population testing.
Pongtawat Lertwilaiwittaya, Ekkapong Roothumnong, Panee Nakthong, Peerawat Dungort, Chutima Meesamarnpong, Chanin Limwongse

Breast Cancer Res Treat· July 2021

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Identification of novel mutation in RANKL by whole-exome sequencing in a Thai family with osteopetrosis; a case report and review of RANKL osteopetrosis.
Pongtawat Lertwilaiwittaya, Bhoom Suktitipat, Phongphak Khongthon, Warut Pongsapich, Chanin Limwongse

Mol Genet Genomic Med· July 2021

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Etiology of Dementia in Thai Patients.
Pornpatr A Dharmasaroja, Jintana Assanasen, Sunsanee Pongpakdee, Kankamol Jaisin, Praween Lolekha, Chanin Limwongse

Dement Geriatr Cogn Dis Extra· April 2021

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Molecular and clinical characterization of Thai patients with achromatopsia: identification of three novel disease-associated variants in the CNGA3 and CNGB3 genes.
Worapoj Jinda, Aekkachai Tuekprakhon, Wanna Thongnoppakhun, Chanin Limwongse, Adisak Trinavarat

Int Ophthalmol· January 2021

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Genotype and age at diagnosis in Thai boys with Duchenne muscular dystrophy (DMD).
Pattareeya Yamputchong, Theeraphong Pho-Iam, Chanin Limwongse, Duangrurdee Wattanasirichaigoon, Oranee Sanmaneechai

Neuromuscul Disord· October 2020

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Incidence and risk factors of vascular dementia in Thai stroke patients.
Pornpatr A Dharmasaroja, Chanin Limwongse, Thammanard Charernboon

J Stroke Cerebrovasc Dis· August 2020

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Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) in a Thai Patient: The Classic Clinical Manifestations, Funduscopic Feature, and Brain Imaging Findings with a Novel Mutation in the Gene.
Jindapa Srikajon, Yuvadee Pitakpatapee, Chanin Limwongse, Niphon Chirapapaisan, Prachaya Srivanitchapoom

Tremor Other Hyperkinet Mov (N Y)· June 2020

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Pathogenic PSEN1 Glu184Gly Mutation in a Family from Thailand with Probable Autosomal Dominant Early Onset Alzheimer's Disease.
Vorapun Senanarong, Seong Soo A An, Giau Vo Van, Chanin Limwongse, Eva Bagyinszky

Diagnostics (Basel)· March 2020

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