| Familial transmission of the FMR1 CGG repeat. SL Nolin, FA Lewis 3rd, LL Ye, GE Houck Jr, AE Glicksman, P Limprasert, ... American journal of human genetics 59 (6), 1252, 1996 | 259 | 1996 |
| β-synuclein gene alterations in dementia with Lewy bodies H Ohtake, P Limprasert, Y Fan, O Onodera, A Kakita, H Takahashi, ... Neurology 63 (5), 805-811, 2004 | 203 | 2004 |
| β-synuclein modulates α-synuclein neurotoxicity by reducing α-synuclein protein expression Y Fan, P Limprasert, IVJ Murray, AC Smith, VMY Lee, JQ Trojanowski, ... Human molecular genetics 15 (20), 3002-3011, 2006 | 111 | 2006 |
| Familial dementia with lewy bodies: a clinical and neuropathological study of 2 families DW Tsuang, AM Dalan, CJ Eugenio, P Poorkaj, P Limprasert, ... Archives of neurology 59 (10), 1622-1630, 2002 | 66 | 2002 |
| HLA-B*15:21 and carbamazepine-induced Stevens-Johnson syndrome: pooled-data and in silico analysis K Jaruthamsophon, V Tipmanee, A Sangiemchoey, C Sukasem, ... Scientific reports 7 (1), 45553, 2017 | 55 | 2017 |
| 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 P Limprasert, N Nouri, RA Heyman, C Nopparatana, M Kamonsilp, ... Human molecular genetics 5 (2), 207-213, 1996 | 54 | 1996 |
| Novel compound heterozygous mutations in the TRAPPC9 gene in two siblings with autism and intellectual disability A Hnoonual, P Graidist, S Kritsaneepaiboon, P Limprasert Frontiers in Genetics 10, 413583, 2019 | 36 | 2019 |
| De novo subtelomeric deletion of 15q associated with satellite translocation in a child with developmental delay and severe growth retardation S Rujirabanjerd, W Suwannarat, T Sripo, P Dissaneevate, ... American Journal of Medical Genetics Part A 143 (3), 271-276, 2007 | 36 | 2007 |
| Familial dementia with Lewy bodies with an atypical clinical presentation LT Bonner, DW Tsuang, MM Cherrier, CJ Eugenio, JQ Du, EJ Steinbart, ... Journal of geriatric psychiatry and neurology 16 (1), 59-64, 2003 | 35 | 2003 |
| Two Thai families with Norrie disease (ND): association of two novel missense mutations with severe ND phenotype, seizures, and a manifesting carrier K Yamada, P Limprasert, M Ratanasukon, S Tengtrisorn, ... American journal of medical genetics 100 (1), 52-55, 2001 | 32 | 2001 |
| Chromosomal microarray analysis in a cohort of underrepresented population identifies SERINC2 as a novel candidate gene for autism spectrum disorder A Hnoonual, W Thammachote, T Tim-Aroon, K Rojnueangnit, ... Scientific reports 7 (1), 12096, 2017 | 28 | 2017 |
| Significant changes in plasma alpha-synuclein and beta-synuclein levels in male children with autism spectrum disorder W Sriwimol, P Limprasert BioMed research international 2018, 2018 | 26 | 2018 |
| Mutation screening of the neurexin 1 gene in thai patients with intellectual disability and autism spectrum disorder S Yangngam, O Plong-On, T Sripo, R Roongpraiwan, T Hansakunachai, ... Genetic testing and molecular biomarkers 18 (7), 510-515, 2014 | 26 | 2014 |
| A case with a ring chromosome 13 in a cohort of 203 children with non-syndromic autism and review of the cytogenetic literature C Charalsawadi, W Maisrikhaw, V Praphanphoj, J Wirojanan, ... Cytogenetic and genome research 144 (1), 1-8, 2014 | 25 | 2014 |
| Mutation screening of the CDKL5 gene in cryptogenic infantile intractable epilepsy and review of clinical sensitivity U Intusoma, F Hayeeduereh, O Plong-On, T Sripo, P Vasiknanonte, ... european journal of paediatric neurology 15 (5), 432-438, 2011 | 23 | 2011 |
| A New Method for FMR1 Gene Methylation Screening by Multiplex Methylation-Specific Real-Time Polymerase Chain Reaction MH Elias, R Ankathil, AR Salmi, W Sudhikaran, P Limprasert, BA Zilfalil Genetic testing and molecular biomarkers 15 (6), 387-393, 2011 | 22 | 2011 |
| A genome wide pattern of population structure and admixture in peninsular Malaysia Malays WI Hatin, AR Nur-Shafawati, A Etemad, W Jin, P Qin, S Xu, L Jin, SG Tan, ... The HUGO journal 8, 1-18, 2014 | 20 | 2014 |
| Comparative studies of the CAG repeats in the spinocerebellar ataxia type 1 (SCA1) gene P Limprasert, N Nouri, C Nopparatana, PL Deininger, BJB Keats American journal of medical genetics 74 (5), 488-493, 1997 | 20 | 1997 |
| Whole-exome sequencing identifies a novel heterozygous missense variant of the EN2 gene in two unrelated patients with autism spectrum disorder A Hnoonual, T Sripo, P Limprasert Psychiatric Genetics 26 (6), 297-301, 2016 | 18 | 2016 |
| Mutation screening of the Aristaless-related homeobox (ARX) gene in Thai pediatric patients with delayed development: first report from Thailand S Rujirabanjerd, K Tongsippunyoo, T Sripo, P Limprasert European journal of medical genetics 50 (5), 346-354, 2007 | 18 | 2007 |
