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Influence of genetic and non-genetic factors on phenytoin-induced severe cutaneous adverse drug reactions

European journal of clinical pharmacology, 2017-07, Vol.73 (7), p.855-865

2017

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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

Breast cancer research and treatment, 2021-07, Vol.188 (1), p.237-248

2021

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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 VKORC1 gene: a randomized controlled trial

Hematology (Luxembourg), 2022-12, Vol.27 (1), p.95-104

2022

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Deficient DNA mismatch repair is associated with favorable prognosis in Thai patients with sporadic colorectal cancer

World journal of gastroenterology : WJG, 2015-01, Vol.21 (3), p.926-934

2015

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Medical genetic services in a developing country: lesson from Thailand

Current opinion in pediatrics, 2017-12, Vol.29 (6), p.634-639

Limwongse, Chanin

2017

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Tumor mutational profile of triple negative breast cancer patients in Thailand revealed distinctive genetic alteration in chromatin remodeling gene

PeerJ (San Francisco, CA), 2019-02, Vol.7, p.e6501-e6501, Article e6501

2019

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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

Molecular genetics & genomic medicine, 2021-07, Vol.9 (7), p.e1727-n/a

2021

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Identification of Genomic Alterations in Thai Patients With Colorectal Cancer Using Next-Generation Sequencing-Based Multigene Cancer Panel

Curēus (Palo Alto, CA), 2023-05

2023

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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

International ophthalmology, 2021, Vol.41 (1), p.121-134

2021

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STK11 Causative Variants and Copy Number Variations Identified in Thai Patients With Peutz-Jeghers Syndrome

Curēus (Palo Alto, CA), 2023-02

2023

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Germline mutations of 4567 patients with hereditary breast-ovarian cancer spectrum in Thailand

Npj genomic medicine, 2024-02, Vol.9 (1), p.9-9, Article 9

2024

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P069: Clinical and genomic spectrum of Lynch syndrome in Thailand: A 7-year experience of cancer genetic testing at Siriraj Genomics

Genetics in Medicine Open, 2024, Vol.2, p.100951, Article 100951

2024

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Orientia tsutsugamushi stimulates an original gene expression program in monocytes: relationship with gene expression in patients with scrub typhus

PLoS neglected tropical diseases, 2011-05, Vol.5 (5), p.e1028-e1028

2011

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Combination of multiplex PCR and DHPLC-based strategy for CYP2D6 genotyping scheme in Thais

Clinical biochemistry, 2011-09, Vol.44 (13), p.1144-1152

2011

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Iron overload in the Asian community

Blood, 2009-07, Vol.114 (1), p.20-25

2009

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Etiology of Dementia in Thai Patients

Dementia and geriatric cognitive disorders extra, 2021-01, Vol.11 (1), p.64-70

2021

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Detecting purely epistatic multi-locus interactions by an omnibus permutation test on ensembles of two-locus analyses

BMC bioinformatics, 2009-09, Vol.10 (1), p.294-294, Article 294

2009

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Case series: Childhood Charcot-Marie-Tooth: Predominance of axonal subtype

eNeurologicalSci, 2019-09, Vol.16, p.100200, Article 100200

2019

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Genetics and genomics in Thailand: challenges and opportunities

Molecular genetics & genomic medicine, 2014-05, Vol.2 (3), p.210-216

2014

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Pathogenic PSEN1 Glu184Gly Mutation in a Family from Thailand with Probable Autosomal Dominant Early Onset Alzheimer's Disease

Diagnostics (Basel), 2020-03, Vol.10 (3), p.135

2020

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Activation of indoleamine 2,3-dioxygenase in patients with scrub typhus and its role in growth restriction of Orientia tsutsugamushi

PLoS neglected tropical diseases, 2012-07, Vol.6 (7), p.e1731-e1731

2012

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Novel Mutation of the TINF2 Gene in a Patient with Dyskeratosis Congenita

Case reports in dermatology, 2015-08, Vol.7 (2), p.212-219

2015

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Sa1550 FAMILIAL CLUSTERING OF NONALCOHOLIC FATTY LIVER DISEASE IN FIRST-DEGREE RELATIVES OF ADULTS WITH LEAN NONALCOHOLIC FATTY LIVER DISEASE

Gastroenterology (New York, N.Y. 1943), 2023-05, Vol.164 (6), p.S-1288-S-1289

2023

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A Novel Mutation of the GNE Gene in Distal Myopathy with Rimmed Vacuoles: A Case with Inflammation

Case reports in neurology, 2014-03, Vol.6 (1), p.55-59

2014

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Influence of genetic and non-genetic factors on phenytoin-induced severe cutaneous adverse drug reactions

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

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 VKORC1 gene: a randomized controlled trial

Deficient DNA mismatch repair is associated with favorable prognosis in Thai patients with sporadic colorectal cancer

Medical genetic services in a developing country: lesson from Thailand

Tumor mutational profile of triple negative breast cancer patients in Thailand revealed distinctive genetic alteration in chromatin remodeling gene

Whole exome sequencing and rare variant association study to identify genetic modifiers, KLF1 mutations, and a novel double mutation in Thai patients with hemoglobin E/beta-thalassemia

Identification of novel mutation in RANKL by whole‐exome sequencing in a Thai family with osteopetrosis; a case report and review of RANKL osteopetrosis

Identification of Genomic Alterations in Thai Patients With Colorectal Cancer Using Next-Generation Sequencing-Based Multigene Cancer Panel

Molecular and clinical characterization of Thai patients with achromatopsia: identification of three novel disease-associated variants in the CNGA3 and CNGB3 genes

STK11 Causative Variants and Copy Number Variations Identified in Thai Patients With Peutz-Jeghers Syndrome

Germline mutations of 4567 patients with hereditary breast-ovarian cancer spectrum in Thailand

P069: Clinical and genomic spectrum of Lynch syndrome in Thailand: A 7-year experience of cancer genetic testing at Siriraj Genomics

Orientia tsutsugamushi stimulates an original gene expression program in monocytes: relationship with gene expression in patients with scrub typhus

Combination of multiplex PCR and DHPLC-based strategy for CYP2D6 genotyping scheme in Thais

Iron overload in the Asian community

Etiology of Dementia in Thai Patients

Detecting purely epistatic multi-locus interactions by an omnibus permutation test on ensembles of two-locus analyses

Case series: Childhood Charcot-Marie-Tooth: Predominance of axonal subtype

Genetics and genomics in Thailand: challenges and opportunities

Pathogenic PSEN1 Glu184Gly Mutation in a Family from Thailand with Probable Autosomal Dominant Early Onset Alzheimer's Disease

Activation of indoleamine 2,3-dioxygenase in patients with scrub typhus and its role in growth restriction of Orientia tsutsugamushi

Novel Mutation of the TINF2 Gene in a Patient with Dyskeratosis Congenita

Sa1550 FAMILIAL CLUSTERING OF NONALCOHOLIC FATTY LIVER DISEASE IN FIRST-DEGREE RELATIVES OF ADULTS WITH LEAN NONALCOHOLIC FATTY LIVER DISEASE

A Novel Mutation of the GNE Gene in Distal Myopathy with Rimmed Vacuoles: A Case with Inflammation

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