1. ScholarBank@NUS

Ene Choo Tan

rp05901

Collaboration Map View Statistics Email Alert RSS Feed

Publications

Results 1-20 of 23 (Search time: 0.011 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 
92017Correlation of cord blood telomere length with birth weightLee, S.-P; Hande, P ; Yeo, G.S; Tan, E.-C 
101-Jun-2018Dataset on gene expression in the elderly after Mindfulness Awareness Practice or Health Education ProgramLim, HW; Saw, WY ; Feng, L ; Lee, YK ; Mahendran, R ; Cheah, IKM ; Rawtaer, I ; Kumar, AP ; Kua, EH ; Mahendran, R ; Tan, EC 
112013De novo 2.3 Mb microdeletion of 1q32.2 involving the Van der Woude Syndrome locusTan, E.-C. ; Lim, E.C.; Lee, S.-T.
1215-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. 
13Jul-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. 
1423-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.
152007Functional 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. 
163-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.
17Mar-2011Methylenetetrahydrofolate reductase (MTHFR) C677T and A1298C polymorphisms and age of onset in schizophrenia: A combined analysis of independent samplesSaetre, P.; Vares, M.; Werge, T.; Andreassen, O.A.; Arinami, T.; Ishiguro, H.; Nanko, S.; Tan, E.C. ; Han, D.H.; Roffman, J.L.; Muntjewerff, J.-W.; Jagodzinski, P.P.; Kempisty, B.; Hauser, J.; Vilella, E.; Betcheva, E.; Nakamura, Y.; Regland, B.; Agartz, I.; Hall, H.; Terenius, L.; Jönsson, E.G.
181-Oct-2021Mindfulness Awareness Practice (MAP) to Prevent Dementia in Older Adults with Mild Cognitive Impairment: Protocol of a Randomized Controlled Trial and Implementation OutcomesNg, Ted Kheng Siang; Feng, Lei ; Fam, Johnson ; Rawtaer, Iris ; Kumar, Alan Prem ; Rane, Grishma ; Cheah, Irwin Kee-Mun ; Mahendran, Ratha ; Lee, Yuan Kun ; Tan, Ene Choo ; Goh, Lee Gan ; Kua, Ee Heok ; Mahendran, Rathi 
192015Next-generation sequencing using a pre-designed gene panel for the molecular diagnosis of congenital disorders in pediatric patientsLim, E.C; Brett, M; Lai, A.H ; Lee, S.-P; Tan, E.-S ; Jamuar, S.S ; Ng, I.S ; Tan, E.-C 
20Sep-1992Novel brain-specific bovine cDNA for a developmentally regulated mRNA encoding a putative new member of the leucine-rich glycoprotein (LRG) familyTan, E.-C. ; Lim, L.