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Dosage Optimization of Efavirenz Based on a Population Pharmacokinetic–Pharmacogenetic Model of HIV-infected Patients in Thailand

Clinical therapeutics, 2020-07, Vol.42 (7), p.1234-1245

2020

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A LILRB1 variant with a decreased ability to phosphorylate SHP-1 leads to autoimmune diseases

Scientific reports, 2022-09, Vol.12 (1), p.15420-15420, Article 15420

2022

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Generation of two human iPSC lines (MDCUi001-A and MDCUi001-B) from dermal fibroblasts of a Thai patient with X-linked osteogenesis imperfecta using integration-free Sendai virus

Stem cell research, 2019-08, Vol.39, p.101493-101493, Article 101493

2019

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Carbamazepine and phenytoin induced Stevens‐Johnson syndrome is associated with HLA‐B1502 allele in Thai population

Epilepsia (Copenhagen), 2008-12, Vol.49 (12), p.2087-2091

2008

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Long-read Amplicon Sequencing of the CYP21A2 in 48 Thai Patients With Steroid 21-Hydroxylase Deficiency

The journal of clinical endocrinology and metabolism, 2022-06, Vol.107 (7), p.1939-1947

2022

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PTPRF is disrupted in a patient with syndromic amastia

BMC medical genetics, 2011-03, Vol.12 (1), p.46-46, Article 46

2011

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Pentanucleotide Repeat Insertions in RAI1 Cause Benign Adult Familial Myoclonic Epilepsy Type 8

Movement disorders, 2024-01, Vol.39 (1), p.164-172

2024

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PTEN c.511C>T Nonsense Mutation in a BRRS Family Disrupts a Potential Exonic Splicing Enhancer and Causes Exon Skipping

Japanese journal of clinical oncology, 2006-12, Vol.36 (12), p.814-821

2006

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Pharmacogenetic testing can identify patients taking atazanavir at risk for hyperbilirubinemia

Journal of acquired immune deficiency syndromes (1999), 2015-05, Vol.69 (1), p.e36

2015

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Identification of a mitochondrial 12S rRNA A1555G mutation causing aminoglycoside-induced deafness in a large Thai family

Asian biomedicine, 2017-01, Vol.9 (2), p.211-215

2017

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Novel CTSK mutation resulting in an entire exon 2 skipping in a T hai girl with pycnodysostosis

Pediatrics international, 2013-10, Vol.55 (5), p.651-655

2013

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In vitro Correction of a Novel Splicing Alteration in the BTK Gene by Using Antisense Morpholino Oligonucleotides

Archivum Immunologiae et Therapiae Experimentalis, 2014-10, Vol.62 (5), p.431-436

2014

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DcR3 mutations in patients with juvenile-onset systemic lupus erythematosus lead to enhanced lymphocyte proliferation

Journal of rheumatology, 2013-08, Vol.40 (8), p.1316

2013

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Two novel EBP mutations in Conradi-Hünermann-Happle syndrome

EJD. European journal of dermatology, 2008-07, Vol.18 (4), p.391-393

2008

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Carbamazepine and phenytoin induced Stevens-Johnson syndrome is associated with HLA-B 1502 allele in Thai population

Epilepsia (Copenhagen), 2008, Vol.49 (12), p.2087-2091

2008

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ASA E382K disrupts a potential exonic splicing enhancer and causes exon skipping, but missense mutations in ASA are not associated with ESEs

International journal of molecular medicine, 2004-10, Vol.14 (4), p.683

2004

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Nonsense mutations of the CYBB gene in two Thai families with X-linked chronic granulomatous disease

Asian Pacific journal of allergy and immunology, 2007-12, Vol.25 (4), p.243

2007

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Clinical and molecular characteristics of Thai families with X-linked chronic granulomatous disease

The World Allergy Organization journal, 2007-11, p.S110-S111

2007

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Expressions of mammaglobins A and B are not different between nasal polyps with and without allergic rhinitis

The World Allergy Organization journal, 2007-11, p.S91

2007

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FGFR2 mutations among Thai children with Crouzon and Apert syndromes

The Journal of craniofacial surgery, 2003-01, Vol.14 (1), p.101-104

2003

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Compound Heterozygous PGM3 Mutations in a Thai Patient with a Specific Antibody Deficiency Requiring Monthly IVIG Infusions

Journal of clinical immunology, 2020, Vol.40 (1), p.227-231

2020

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Expression of mammaglobins A and B in nasal polyps is similar in patients with and without allergic rhinitis

American journal of rhinology, 2008-03, Vol.22 (2), p.135-138

2008

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Dosage Optimization of Efavirenz Based on a Population Pharmacokinetic–Pharmacogenetic Model of HIV-infected Patients in Thailand

A LILRB1 variant with a decreased ability to phosphorylate SHP-1 leads to autoimmune diseases

Generation of two human iPSC lines (MDCUi001-A and MDCUi001-B) from dermal fibroblasts of a Thai patient with X-linked osteogenesis imperfecta using integration-free Sendai virus

Carbamazepine and phenytoin induced Stevens‐Johnson syndrome is associated with HLA‐B1502 allele in Thai population

Long-read Amplicon Sequencing of the CYP21A2 in 48 Thai Patients With Steroid 21-Hydroxylase Deficiency

PTPRF is disrupted in a patient with syndromic amastia

Pentanucleotide Repeat Insertions in RAI1 Cause Benign Adult Familial Myoclonic Epilepsy Type 8

PTEN c.511C>T Nonsense Mutation in a BRRS Family Disrupts a Potential Exonic Splicing Enhancer and Causes Exon Skipping

Pharmacogenetic testing can identify patients taking atazanavir at risk for hyperbilirubinemia

Identification of a mitochondrial 12S rRNA A1555G mutation causing aminoglycoside-induced deafness in a large Thai family

Novel CTSK mutation resulting in an entire exon 2 skipping in a T hai girl with pycnodysostosis

In vitro Correction of a Novel Splicing Alteration in the BTK Gene by Using Antisense Morpholino Oligonucleotides

DcR3 mutations in patients with juvenile-onset systemic lupus erythematosus lead to enhanced lymphocyte proliferation

Two novel EBP mutations in Conradi-Hünermann-Happle syndrome

Carbamazepine and phenytoin induced Stevens-Johnson syndrome is associated with HLA-B 1502 allele in Thai population

ASA E382K disrupts a potential exonic splicing enhancer and causes exon skipping, but missense mutations in ASA are not associated with ESEs

Nonsense mutations of the CYBB gene in two Thai families with X-linked chronic granulomatous disease

Clinical and molecular characteristics of Thai families with X-linked chronic granulomatous disease

Expressions of mammaglobins A and B are not different between nasal polyps with and without allergic rhinitis

FGFR2 mutations among Thai children with Crouzon and Apert syndromes

Compound Heterozygous PGM3 Mutations in a Thai Patient with a Specific Antibody Deficiency Requiring Monthly IVIG Infusions

Expression of mammaglobins A and B in nasal polyps is similar in patients with and without allergic rhinitis

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