Publications

Results 1-20 of 26 (Search time: 0.008 seconds).

Issue DateTitleAuthor(s)
110-May-2012A submicroscopic deletion involving part of the CREBBP gene detected by array-CGH in a patient with Rubinstein-Taybi syndromeLai, A.H.M.; Brett, M.S.; Chin, W.-H.; Lim, E.C.P.; Ng, J.S.H.; Tan, E.-C. 
22008A118G single nucleotide polymorphism of human μ-opioid receptor gene influences pain perception and patient-controlled intravenous morphine consumption after intrathecal morphine for postcesarean analgesiaSia, A.T. ; Goh, R.W.C.; Law, H.Y.; Landau, R.; Teo, Y.-Y.; Tan, E.C. ; Lim, Y.; Lim, E.C.P.
32010Alcohol and aldehyde dehydrogenase polymorphisms in chinese and indian populationsTan, E.-C. ; Lim, L.; Leong, J.-Y.; Lim, J.-Y.; Lee, A.; Yang, J.; Tan, C.-H.; Winslow, M.
42011An additional case of the recurrent 15q24.1 microdeletion syndrome and review of the literatureNg, I.S.L.; Chin, W.-H.; Lim, E.C.P.; Tan, E.-C. 
51-Jun-2014Association of premenstrual/menstrual symptoms with perinatal depression and a polymorphic repeat in the polyglutamine tract of the retinoic acid induced 1 geneTan, E.-C. ; Tan, H.-S.; Chua, T.-E.; Lee, T.; Ng, J.; Ch'Ng, Y.-C.; Choo, C.-H.; Chen, H.Y. 
62015Case-control study of glucocorticoid receptor and corticotrophin-releasing hormone receptor gene variants and risk of perinatal depressionTan, E.-C ; Chua, T.-E ; Lee, T.M.Y ; Tan, H.-S ; Ting, J.L; Chen, H.Y 
75-Jul-2006Characterization of frequencies and distribution of single nucleotide insertions/deletions in the human genomeTan, E.-C. ; Li, H.
82014Chromosome 15q11-q13 copy number gain detected by array-CGH in two cases with a maternal methylation patternTan, E.-S ; Yong, M.-H; Lim, E.C.P; Li, Z.-H; Brett, M.S.Y; Tan, E.-C 
92015Clinical application of next-generation sequencing for Mendelian diseasesJamuar, S.S ; Tan, E.-C 
102006Congenital long QT syndromes: Clinical features, molecular genetics and genetic testingChing, C.-K.; Tan, E.-C. 
112017Correlation of cord blood telomere length with birth weightLee, S.-P; Hande, P ; Yeo, G.S; Tan, E.-C 
122013De novo 2.3 Mb microdeletion of 1q32.2 involving the Van der Woude Syndrome locusTan, E.-C. ; Lim, E.C.; Lee, S.-T.
1315-Mar-2013De novo 3q22.1 q24 deletion associated with multiple congenital anomalies, growth retardation and intellectual disabilityBrett, M.S.; Ng, I.S.L.; Lim, E.C.P.; Yong, M.H.; Li, Z.; Lai, A.; Tan, E.-C. 
14Jul-2013De novo trisomy 12p in twin girls with different levels of mosaicismLim, E.C.P.; Ng, I.S.L.; Yong, M.-H.; Yon, H.-Y.; Brett, M.S.Y.; Tan, E.-C. 
152007Epidemiology of completed suicides in Singapore for 2001 and 2002Loh, M.; Mondry, A.; Tan, C.H. ; Leong, J.-Y.; Sim, K.; Tan, E.-C. ; Lau, G.
1623-Jun-2009Ethnicity and OPRM variant independently predict pain perception and patient-controlled analgesia usage for post-operative painTan, E.-C. ; Lim, E.C.P.; Teo, Y.-Y.; Lim, Y.; Law, H.-Y.; Sia, A.T.
171999Evidence for an association between heroin dependence and a VNTR polymorphism at the serotonin transporter locus [3]Tan, E.C. ; Yeo, B.K.L.; Ho, B.K.W.; Tay, A.H.N. ; Tan, C.H.
182007Functional polymorphisms of the cytochrome P450 1A2 (CYP1A2) gene and prolonged QTc interval in schizophreniaTay, J.K.X.; Tan, C.H. ; Chong, S.-A.; Tan, E.-C. 
193-Oct-2005Gender-specific association of insertion/deletion polymorphisms in the nogo gene and chronic schizophreniaTan, E.-C. ; Chong, S.-A.; Wang, H.; Lim, E.C.-P.; Teo, Y.-Y.
205-Oct-2009LRRK2 G2385R modulates age at onset in Parkinson's disease: A multi-center pooled analysisTan, E.K. ; Peng, R.; Wu, Y.R.; Wu, R.M.; Wu-Chou, Y.H.; Tan, L.C.; An, X.K.; Chen, C.M.; Fook-Chong, S.; Lu, C.S.