Mutation screening of Beta-Neurexin 1 (β-NRXN1), Neuroligin 3 (NLGN3) and Neuroligin 4X (NLGN4X) genes in Thai Children with autism spectrum disorder

by Pornprot Limprasert, Vincent, John B
Published 2015

Unique AGG interruption in the CGG repeats of the FMR1 gene exclusively found in asians linked to a specific SNP haplotype

by Pornprot Limprasert, Janpen Thanakitgosate, Kanoot Jaruthamsophon, Thanya Sripo
Published 2018

Comparison of a new in-house and three published HLA-B∗15:02 screening methods for prevention of carbamazepine-induced severe drug reactions

by Kanoot Jaruthamsophon, Thanya Sripo, Chonlaphat Sukasem, Pornprot Limprasert
Published 2018

Molecular screening for fragile x syndrome in Thailand

by Pornprot Limprasert, Nichara Ruangdaraganon, thanyachai Sura, Punnee Vasiknanonte, Uraiwan Jinorose
Published 1999

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

by Tippawan Hansakunachai, Rawiwan Roongpraiwan, Tasnawat Sombuntham, Pornprot Limprasert, Nichara Ruangdaraganon
Published 2018

Molecular screening for fragile X syndrome in Thailand

by Pornprot Limprasert, Nichara Ruangdaraganon, Thanyachai Sura, Punnee Vasiknanonte, Uraiwan Jinorose
Published 2018

Prevalence and clinical characteristics of fragile X syndrome at Child Development Clinic, Ramathibodi Hospital

by Nichara Ruangdaraganon, Thanyachai Sura, Noppawan Sriwongpanich, Pornprot Limprasert, Tasanawat Sombuntham, Nittaya Kotchabhakdi
Published 2018

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

by Pornprot Limprasert, Punnee Vasiknanonte, Somchit Jaruratanasirikul, Hutcha Sriplung, Nichara Ruangdaraganon, Thanyachai Sura, Noppawon Sriwongpanich
Published 2018

Haplotype analysis at the FRAXA locus in Thai subjects

by Pornprot Limprasert, Vannarat Saechan, Nichara Ruangdaraganon, Thanyachai Sura, Punnee Vasiknanote, Somchit Jaruratanasirikul, W. Ted Brown
Published 2018

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

by Chuphong Thongnak, Pornprot Limprasert, Duangkamol Tangviriyapaiboon, Suchaya Silvilairat, Apichaya Puangpetch, Ekawat Pasomsub, Chonlaphat Sukasem, Wasun Chantratita
Published 2018

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

by Chuphong Thongnak, Pornprot Limprasert, Duangkamol Tangviriyapaiboon, Suchaya Silvilairat, Apichaya Puangpetch, Ekawat Pasomsub, Chonlaphat Sukasem, Wasun Chantratita
Published 2018

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

by Chuphong Thongnak, Areerat Hnoonual, Duangkamol Tangviriyapaiboon, Suchaya Silvilairat, Apichaya Puangpetch, Ekawat Pasomsub, Wasun Chantratita, Pornprot Limprasert, Chonlaphat Sukasem
Published 2019

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

by Supaporn Yangngam, Oradawan Plong-On, Thanya Sripo, Rawiwan Roongpraiwan, Tippawan Hansakunachai, Juthamas Wirojanan, Tasnawat Sombuntham, Nichara Ruangdaraganon, Pornprot Limprasert
Published 2018

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

by Utcharee Intusoma, Fadell Hayeeduereh, Oradawan Plong-On, Thanya Sripo, Punnee Vasiknanonte, Supachai Janjindamai, Apasri Lusawat, Sasipa Thammongkol, Anannit Visudtibhan, Pornprot Limprasert
Published 2018

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

by Anna Mikhailov, Alanna Fennell, Oradawan Plong-On, Thanya Sripo, Tippawan Hansakunachai, Rawiwan Roongpraiwan, Tasnawat Sombuntham, Nichara Ruangdaraganon, John B. Vincent, Pornprot Limprasert
Published 2018