(Q28658627)

3

object named as

Surakameth Mahasirimongkol

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author name string

Vorasuk Shotelersuk

1

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Chanin Limwongse

2

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Surakameth Mahasirimongkol

Molecular genetics & genomic medicine

3

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language of work or name

English

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publication date

May 2014

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published in

1 reference

Mapping human genetic diversity in Asia

volume

2

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issue

3

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page(s)

210-6

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cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4049361

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

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4049361

Using health technology assessment for informing coverage decisions in Thailand

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4049361

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

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4049361

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

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4049361

Clinical and molecular findings in Thai patients with isolated methylmalonic acidemia.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4049361

PDGFRa mutations in humans with isolated cleft palate.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4049361

HLA-A*3101 and carbamazepine-induced hypersensitivity reactions in Europeans

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4049361

A novel p.E276K IDUA mutation decreasing α-L-iduronidase activity causes mucopolysaccharidosis type I.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4049361

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

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4049361

p.D645E of acid α-glucosidase is the most common mutation in thai patients with infantile-onset pompe disease.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4049361

Detection of phenylketonuria by the newborn screening program in Thailand.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4049361

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

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4049361

TBX22 mutations are a frequent cause of non-syndromic cleft palate in the Thai population.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4049361

Heterozygous nonsense mutation SATB2 associated with cleft palate, osteoporosis, and cognitive defects.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4049361

Significant association between IRF6 820G->A and non-syndromic cleft lip with or without cleft palate in the Thai population

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4049361

Neonatal screening program in Thailand

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4049361

A variant in the CD209 promoter is associated with severity of dengue disease

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4049361

Maternal 677CT/1298AC genotype of the MTHFR gene as a risk factor for cleft lip

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4049361

Novel mutations in a Thai patient with methylmalonic acidemia.

3 June 2018

1 reference

A mutation of the p63 gene in non-syndromic cleft lip.

21 January 2018

1 reference

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

21 January 2018

1 reference

FOXE1 mutations in Thai patients with oral clefts.

21 January 2018

1 reference

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

21 January 2018

1 reference

Holocarboxylase synthetase deficiency: novel clinical and molecular findings

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

An exceptionally low percentage of Thai expectant mothers and medical personnel with folic acid knowledge and peri-conceptional consumption urges an urgent education program and/or food fortification.

21 January 2018

1 reference

A successful strategy for Preimplantation Genetic Diagnosis of beta-thalassemia and simultaneous detection of Down's syndrome using multiplex fluorescent PCR.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4049361

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

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4049361

Haemoglobin Synthesis in β-Thalassaemia

27 November 2018

1 reference

Hæmoglobin H Disease in Thailand: a Genetical Study

21 January 2018

1 reference

Studies of the Distribution of Haemoglobin E, Thalassaemias and Glucose-6-phosphate Dehydrogenase Deficiency in North-eastern Thailand

21 January 2018

1 reference

MSX1 mutations contribute to nonsyndromic cleft lip in a Thai population

21 January 2018

1 reference

12 December 2020

Application of geographic information system in TSH neonatal screening for monitoring of iodine deficiency areas in Thailand

1 reference

12 December 2020

Establishing gas chromatography-mass spectrometry to diagnose organic acidemias in Thailand

1 reference

12 December 2020

Risk factors associated with the occurrence of frontoethmoidal encephalomeningocele

1 reference

12 December 2020

Further Evidence for a Genetic Basis of Haemoglobin H Disease from Newborn Offspring of Patients

1 reference

12 December 2020

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

1 reference

12 December 2020

Exome sequencing of liver fluke-associated cholangiocarcinoma

1 reference

12 December 2020