Genetics and genomics in Thailand: challenges and opportunities

Health workforce contributions to health system development: a platform for universal health coverage

(2013) Viroj Tangcharoensathien et al.   BULLETIN OF THE WORLD HEALTH ORGANIZATION

Economic evaluation of HLA-B*15:02 screening for carbamazepine-induced severe adverse drug reactions in Thailand

(2013) Waranya Rattanavipapong et al.   EPILEPSIA

FOXE1 mutations in Thai patients with oral clefts

(2013) CHALURMPON SRICHOMTHONG et al.   Genetics Research

Disorders with similar clinical phenotypes reveal underlying genetic interaction: SATB2 acts as an activator of the UPF3B gene

(2013) Petcharat Leoyklang et al.   HUMAN GENETICS

A common and two novel GBA mutations in Thai patients with Gaucher disease

(2013) Rachaneekorn Tammachote et al.   JOURNAL OF HUMAN GENETICS

Primary hyperoxaluria type 1 and brachydactyly mental retardation syndrome caused by a novel mutation inAGXTand a terminal deletion of chromosome 2

(2012) Rachaneekorn Tammachote et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

A newly identified locus for benign adult familial myoclonic epilepsy on chromosome 3q26.32-3q28

(2012) Patra Yeetong et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

PDGFRa mutations in humans with isolated cleft palate

(2012) Sawitree Rattanasopha et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Clinical and molecular findings in Thai patients with isolated methylmalonic acidemia

(2012) Nithiwat Vatanavicharn et al.   MOLECULAR GENETICS AND METABOLISM

Exome sequencing of liver fluke–associated cholangiocarcinoma

(2012) Choon Kiat Ong et al.   NATURE GENETICS

Using health technology assessment for informing coverage decisions in Thailand

(2012) Adun Mohara et al.   Journal of Comparative Effectiveness Research

Health-financing reforms in southeast Asia: challenges in achieving universal coverage

(2011) Viroj Tangcharoensathien et al.   LANCET

HLA-A*3101 and Carbamazepine-Induced Hypersensitivity Reactions in Europeans

(2011) Mark McCormack et al.   NEW ENGLAND JOURNAL OF MEDICINE

p.D645E of Acid α-Glucosidase Is the Most Common Mutation in Thai Patients with Infantile-Onset Pompe Disease

(2010) Pramuk Amarinthnukrowh et al.   Genetic Testing and Molecular Biomarkers

Holocarboxylase synthetase deficiency: novel clinical and molecular findings

(2009) R Tammachote et al.   CLINICAL GENETICS

Prenatal diagnosis of a novel mutation, c.529C>T (p.Q177X), in the BCKDHA gene in a family with maple syrup urine disease

(2009) R. Tammachote et al.   JOURNAL OF INHERITED METABOLIC DISEASE

Mapping Human Genetic Diversity in Asia

(2009) et al.   SCIENCE

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

(2008) Chaichon Locharernkul et al.   EPILEPSIA

Study of the poliovirus receptor related-1 gene in Thai patients with non-syndromic cleft lip with or without cleft palate

(2008) S. Tongkobpetch et al.   INTERNATIONAL JOURNAL OF ORAL AND MAXILLOFACIAL SURGERY

Risk factors associated with the occurrence of frontoethmoidal encephalomeningocele

(2007) Kanya Suphapeetiporn et al.   EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY