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List of works by Pornprot Limprasert

A case with a ring chromosome 13 in a cohort of 203 children with non-syndromic autism and review of the cytogenetic literature

scientific article

A clinical checklist for fragile X syndrome: screening of Thai boys with developmental delay of unknown cause

2000 scientific article

A genome wide pattern of population structure and admixture in peninsular Malaysia Malays

scientific article

A new method for FMR1 gene methylation screening by multiplex methylation-specific real-time polymerase chain reaction

scientific article published on 17 February 2011

A new structured interview for children with autism spectrum disorder based on the DSM-IV.

scientific article published in August 2014

Analysis of CAG repeat of the Machado-Joseph gene in human, chimpanzee and monkey populations: a variant nucleotide is associated with the number of CAG repeats.

scientific article

Association of ABO Blood Group Phenotype and Allele Frequency with Chikungunya Fever

scientific article published on 21 April 2015

Beta-synuclein gene alterations in dementia with Lewy bodies

scientific article

Beta-synuclein modulates alpha-synuclein neurotoxicity by reducing alpha-synuclein protein expression

scientific article

Chromosomal microarray analysis in a cohort of underrepresented population identifies SERINC2 as a novel candidate gene for autism spectrum disorder.

scientific article published on 21 September 2017

Clinical abnormalities, intervention program, and school attendance of Down syndrome children in southern Thailand.

scientific article published in October 2004

Common Clinical Characteristics and Rare Medical Problems of Fragile X Syndrome in Thai Patients and Review of the Literature

scientific article

Comparative studies of the CAG repeats in the spinocerebellar ataxia type 1 (SCA1) gene

scientific article published in September 1997

Comparison of a New In-House and Three Published HLA-B*15:02 Screening Methods for Prevention of Carbamazepine-Induced Severe Drug Reactions

scientific article

De novo subtelomeric deletion of 15q associated with satellite translocation in a child with developmental delay and severe growth retardation

scientific article published on 01 February 2007

Exome Sequencing Identifies Compound Heterozygous Mutations in SCN5A Associated with Congenital Complete Heart Block in the Thai Population.

scientific article

Familial dementia with Lewy bodies with an atypical clinical presentation

scientific article

Familial dementia with lewy bodies: a clinical and neuropathological study of 2 families

scientific article published in October 2002

Familial transmission of the FMR1 CGG repeat.

scientific article published in December 1996

HLA-B*15:21 and carbamazepine-induced Stevens-Johnson syndrome: pooled-data and in silico analysis

scientific article

Haplotype analysis at the FRAXA locus in Thai subjects

scientific article published in January 2001

Maternal Age-Specific Rates for Trisomy 21 and Common Autosomal Trisomies in Fetuses from a Single Diagnostic Center in Thailand

scientific article

Molecular screening for fragile X syndrome in Thailand

scientific article published in January 1999

Multiplex methylation specific PCR analysis of fragile X syndrome: experience in Songklanagarind Hospital.

scientific article published in August 2005

Mutation screening of the Aristaless-related homeobox (ARX) gene in Thai pediatric patients with delayed development: first report from Thailand

scientific article published on 27 May 2007

Mutation screening of the CDKL5 gene in cryptogenic infantile intractable epilepsy and review of clinical sensitivity

scientific article published on 20 July 2011

Mutation screening of the neurexin 1 gene in thai patients with intellectual disability and autism spectrum disorder

scientific article

No association of Val158Met variant in the COMT gene with autism spectrum disorder in Thai children

scientific article

Novel Compound Heterozygous Mutations in the Gene in Two Siblings With Autism and Intellectual Disability

article

Polymorphism of FXR1 showing lack of association with autism

scientific article published in July 1997

Possible founder effects for FRAXE alleles

scientific article published on 01 May 1999

Prenatal diagnosis of deletion of chromosome 6p presenting with hydrops fetalis

scientific article published on 01 November 2004

Screening for Subtelomeric Rearrangements in Thai Patients with Intellectual Disabilities Using FISH and Review of Literature on Subtelomeric FISH in 15,591 Cases with Intellectual Disabilities.

scientific article published on 16 October 2016

Screening of NLGN3 and NLGN4X genes in Thai children with autism spectrum disorder

scientific article published in February 2014

Significant Changes in Plasma Alpha-Synuclein and Beta-Synuclein Levels in Male Children with Autism Spectrum Disorder.

scientific article published on 8 April 2018

The frequency of fragile X syndrome among selected patients at Songklanagarind Hospital during 1991-1996, studied by cytogenetic and molecular methods

scientific article published on January 1, 1997

Two Thai families with Norrie disease (ND): association of two novel missense mutations with severe ND phenotype, seizures, and a manifesting carrier

scientific article published in April 2001

Unilateral macroorchidism in fragile X syndrome

scientific article published on 01 December 2000

Unique AGG Interruption in the CGG Repeats of the FMR1 Gene Exclusively Found in Asians Linked to a Specific SNP Haplotype

scientific article published on 2 March 2016

Whole-Exome Sequencing Identifies One De Novo Variant in the FGD6 Gene in a Thai Family with Autism Spectrum Disorder.

scientific article published on 17 May 2018

Whole-exome sequencing identifies a novel heterozygous missense variant of the EN2 gene in two unrelated patients with autism spectrum disorder.

scientific article published on 14 October 2016

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