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Poh San Lai

rp01459

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Full Name
Poh San Lai
Variants
Lai, P.
Lai, P.-S.
Poh, S.L.
San, L.P.
Lai, P.S.
 
Main Affiliation
 
Faculty
 
Email
paelaips@nus.edu.sg
 

Publications

Results 21-40 of 50 (Search time: 0.008 seconds).

Issue DateTitleAuthor(s)
212022Expanding the genetic causes of small‐fiber neuropathy: SCN genes and beyondChan, Amanda CY ; Kumar, Shivaram; Tan, Grace; Wong, Hiu Yi ; Ong, Jonathan JY ; Chandra, Bharatendu ; Huang, Hua ; Sharma, Vijay Kumar ; Lai, Poh San 
222018Genetic Variation in the Maternal Oxytocin System Affects Cortisol Responsiveness to Breastfeeding in Infants and MothersKrol K.M.; Monakhov M. ; Lai P.S. ; Ebstein R.P. ; Heinrichs M.; Grossmann T.
231-Sep-2021Genetic variation in the oxytocin system and its link to social motivation in human infantsKrol, Kathleen M.; Namaky, Nauder; Monakhov, Mikhail, V ; Lai Poh San ; Ebstein, Richard ; Grossmann, Tobias
242009High incidence of allelic loss at 16q12.2 region spanning RBL2/p130 gene in retinoblastomaPriya, K. ; Jada, S.R. ; Poh, S.L. ; Boon, L.Q.; Thuan, C.Q.
52009High incidence of allelic loss at 16q12.2 region spanning RBL2/p130 gene in retinoblastomaPriya, K.; Jada, S.R. ; Poh, S.L. ; Boon, L.Q.; Thuan, C.Q. 
62009Identification and characterisation of human dysferlin transcript variants: Implications for dysferlin mutational screening and isoformsPramono, Z.A.D.; Yee, W.C.; Tan, C.L.; Seah, I.A.L.; See, J.S.L.; Kam, S.Y.; Lai, P.S. 
72006Identification and characterization of a novel human dysferlin transcript: Dysferlin_v1Pramono, Z.A.D.; Tan, C.L.; Yee, W.C.; Lai, P.S. ; Takeda, S.
8Jun-2010Identification of single nucleotide polymorphism (SNP) 153104 (A to G) of RB1 gene in Malaysian retinoblastoma children and its association with laterality and staging of the diseaseYusof, H.A.; Ramlee, N.; Ishak, S.R.; Ab Rajab, N.S.; Ghani, S.A.; Bachok, N.S.; Aziz, S.H.S.A.; Tajudin, L.-S.A.; Alagaratnam, J.V.; San, L.P. ; Nishio, H.; Alwi, Z.B.
92003IL-10 synergistically enhances GM-CSF-induced CCR1 expression in myelomonocytic cellsLi, H.; Choo, H.H. ; Chan, J.H.P.; Fred, Wong W.S. ; Cheung, W.; Lai, P.S. 
101-Dec-2022J’Accuse…. Or The Plight of pro-bono Volunteer Scientists in Academic PublishingReichardt, JKV; Patrinos, GP; Lai, PS ; Novelli, G
112009Mapping human genetic diversity in AsiaAbdulla, M.A.; Edo, J.; Jinam, T.A.; Phipps, M.E.; Ahmed, I.; Brahmachari, S.K.; Chaurasia, A.; Jha, P.; Mukerji, M.; Scaria, V.; Sinha, A.; Assawamakin, A.; Fuchareon, S.; Kulawonganunchai, S.; Ngamphiw, C.; Tongsima, S.; Bhak, J.; Ghang, H.; Kim, W.-Y.; Lee, S.; Oh, S.; Yang, J.O.; Yoo, H.-S.; Calacal, G.C.; De, Ungria M.C.A.; Delfin, F.C.; Perdigon, H.B.; Salvador, J.M.; Tabbada, K.A.; Villamor, L.P.; Chen, C.-H.; Chen, Y.-T.; Ho, S.-F.; Wu, J.-Y.; Chen, J.; Kumar, V.; Liu, E.T.; Ong, R.; Png, E.; Seielstad, M.; Tan, A.; Chu, J.; Cutiongco-de, La Paz E.M.C.; Padilla, C.D.; Gojobori, T.; Koike, T.; Suzuki, Y.; Han, J.; Xiao, H.; Hoh, B.P.; Sidek, M.R.; Zilfalil, B.A.; Huang, W.; Wang, Y.; Wang, H.; Yuan, W.; Zhao, G.; Inoko, H.; Oka, A.; Jin, L.; Jung, J.; Kim, H.-L.; Kim, K.; Lee, J.-Y.; Oh, B.; Kangwanpong, D.; Kampuansai, J.; Srikummool, M.; Kennedy, G.C.; Wang, E.; Khurana, P.; Mandapati, K.K.; Kim, S.; Kimm, K.; Kimura, R.; Nishida, N.; Ohashi, J.; Tokunaga, K.; Lai, P.S. ; Majumder, P.P.; Marzuki, S.; Sandraling, Y.; Sudoyo, H.; Suryadi, H.; Mitchell, W.; Naritomi, K.; Palittapongarnpim, P.; Sakaki, Y.; Sugano, S.; Jin, L.; Xu, S.; Shugart, Y.Y.; Niikawa, N.
121993Molecular characterization of β-thalassaemia in Singaporean Chinese: Application to prenatal diagnosisTan, J.A.M.A. ; Tay, J.S.H. ; Kham, S.; Chin, T.M.; Wong, H.B. ; Lai, P.S. 
131996Molecular diagnosis of duchenne muscular dystrophy in SingaporeLow, P.S. ; Lai, P.S. ; Lee, W.L. ; Chin, S.M.; Tay, J.S.H. ; Ong, H.T.
142005Molecular diagnosis of neurogenetic disorders involving trinucleotide repeat expansionsTan, E.-C.; Poh, S.L. 
151997Molecular Studies of Loss of Heterozygosity in RetinoblastomaChiu, L.L.; Lai, P.S. ; Low, P.S.; Chee, C.K.L.; Wong, P.K.; Ling, Y.L.F.; Cheong, P.Y.Y.; Lim, A.S.M. 
162017Mutation spectrum of RB1 mutations in retinoblastoma cases from Singapore with implications for genetic management and counsellingTomar S. ; Sethi R. ; Sundar G.; Quah T.C. ; Quah B.L. ; Lai P.S. 
171-Jun-2019Mutational spectrum of dystrophinopathies in Singapore: Insights for genetic diagnosis and precision therapyTomar, Swati ; Moorthy, Vikaesh; Sethi, Raman; Chai, Josiah; Low, Poh Sim ; Hong, Stacey Tay Kiat; Lai, Poh San 
181-Dec-2022Novel frameshift variant in the PCNT gene associated with Microcephalic Osteodysplastic Primordial Dwarfism (MOPD) Type II and small kidneysHettiarachchi, D; Subasinghe, SMV; Anandagoda, GG; Panchal, H; Lai, PS ; Dissanayake, VHW
192018NRG1 variant effects in patients with Hirschsprung diseaseGunadi, Budi N.Y.P.; Sethi R. ; Fauzi A.R.; Kalim A.S.; Indrawan T.; Iskandar K.; Makhmudi A.; Adrianto I.; San L.P.LL 
201-Sep-2006Overexpression of RB1 transcript is significantly correlated with 13q14 allelic imbalance in colorectal carcinomasLai, P.-S. ; Cheah, P.Y.; Kadam, P.; Chua, C.L.-M.; Lie, D.K.H.; Li, H.-H.; Eu, K.-W.; Seow-Choen, F.; Lee, A.S.-G.