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Browsing by Author NGEOW YUEN YIE JOANNE

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Showing results 6 to 15 of 15 < previous 
Issue DateTitleAuthor(s)
2015Germline and somatic SDHx alterations in apparently sporadic differentiated thyroid cancerNi, Y; Seballos, S; Ganapathi, S; Gurin, D; Fletcher, B; Ngeow, J ; Nagy, R; Kloos, R.T; Ringel, M.D; LaFramboise, T; Eng, C
2016Germline hemizygous deletion of CDKN2A-CDKN2B locus in a patient presenting with Li-Fraumeni syndromeChan, S.H; Lim, W.K ; Michalski, S.T; Lim, J.Q; Ishak, N.D.B; Met-Domestici, M; Young, C.N.C; Vikstrom, K; Esplin, E.D; Fulbright, J; Ang, M.K ; Wee, J ; Sittampalam, K; Farid, M ; Lincoln, S.E; Itahana, K ; Abdullah, S; Teh, B.T ; Ngeow, J 
2017Germline Mutations in Cancer Predisposition Genes are Frequent in Sporadic SarcomasChan, S.H; Lim, W.K ; Ishak, N.D.B; Li, S.-T; Goh, W.L; Tan, G.S; Lim, K.H ; Teo, M ; Young, C.N.C; Malik, S ; Tan, M.H ; Teh, J.Y.H; Chin, F.K.C ; Kesavan, S; Selvarajan, S ; Tan, P ; Teh, B.T ; Soo, K.C ; Farid, M ; Quek, R ; Ngeow, J 
2015Hereditary Syndromes Manifesting as Endometrial Carcinoma: How Can Pathological Features Aid Risk Assessment?Wong, A ; Ngeow, J 
2016Inherited breast cancer predisposition in Asians: Multigene panel testing outcomes from SingaporeWong, E.S.Y; Shekar, S; Met-Domestici, M; Chan, C; Sze, M; Yap, Y.S ; Rozen, S.G ; Tan, M.-H; Ang, P; Ngeow, J ; Lee, A.S.G 
2016Precision medicine in heritable cancer: When somatic tumour testing and germline mutations meetNgeow, J ; Eng, C
2018Predictors of next-generation sequencing panel selection using a shared decision-making approachCourtney, E; Li, S.-T; Shaw, T; Chen, Y; Allen, J.C ; Ngeow, J 
2019PRL3-zumab as an immunotherapy to inhibit tumors expressing PRL3 oncoproteinThura M.; Al-Aidaroos A.Q.; Gupta A. ; Chee C.E. ; Lee S.C. ; Hui K.M. ; Li J.; Guan Y.K. ; Yong W.P. ; So J. ; Chng W.J. ; Ng C.H. ; Zhou J. ; Wang L.Z. ; Yuen J.S.P. ; Ho H.S.S. ; Yi S.M.; Chiong E. ; Choo S.P. ; Ngeow J. ; Ng M.C.H. ; Chua C. ; Yeo E.S.A. ; Tan I.B.H. ; Sng J.X.E.; Tan N.Y.Z.; Thiery J.P. ; Goh B.C. ; Zeng Q. 
2018Whole exome sequencing identifies recessive germline mutations in FAM160A1 in familial NK/T cell lymphomaChan, J.Y ; Ng, A.Y.J; Cheng, C.L; Nairismägi, M.-L; Venkatesh, B ; Cheah, D.M.Z; Li, S.-T; Chan, S.H; Ngeow, J ; Laurensia, Y; Lim, J.Q; Pang, J.W.L; Nagarajan, S; Song, T; Chia, B; Tan, J; Huang, D; Goh, Y.T ; Poon, E; Somasundaram, N; Tao, M ; Quek, R.H.H ; Farid, M ; Khor, C.C ; Bei, J.-X; Tan, S.Y ; Lim, S.T ; Ong, C.K; Tang, T 
2015Whole-exome sequencing of breast cancer, malignant peripheral nerve sheath tumor and neurofibroma from a patient with neurofibromatosis type 1McPherson, J.R ; Ong, C.-K; Ng, C.C.-Y; Rajasegaran, V; Heng, H.-L; Yu, W.S.-S; Tan, B.K.-T ; Madhukumar, P ; Teo, M.C.-C ; Ngeow, J ; Thike, A.-A; Rozen, S.G ; Tan, P.-H; Lee, A.-G ; Teh, B.-T ; Yap, Y.-S 
Showing results 6 to 15 of 15 < previous