Singapore (SG)

Fine-scale mapping of 8q24 locus identifies multiple independent risk variants for breast cancer (2016) Shi J, Zhang Y, Zheng W, Michailidou K, Ghoussaini M, Bolla MK, Wang Q, et al. Journal article Association of genetic susceptibility variants for type 2 diabetes with breast cancer risk in women of European ancestry (2016) Zhao Z, Wen W, Michailidou K, Bolla MK, Wang Q, Zhang B, Long J, et al. Journal article Patient survival and tumor characteristics associated with CHEK2:p.I157T - findings from the Breast Cancer Association Consortium (2016) Muranen TA, Blomqvist C, Doerk T, Jakubowska A, Heikkila P, Fagerholm R, Greco D, et al. Journal article Look-Ahead Schemes for Nearest Neighbor Optimization of 1D and 2D Quantum Circuits (2016) Wille R, Keszocze O, Walter M, Rohrs P, Chattopadhyay A, Drechsler R Conference contribution, Conference Contribution Randomized, Double-Blind, Phase III Trial of Enzastaurin Versus Placebo in Patients Achieving Remission After First-Line Therapy for High-Risk Diffuse Large B-Cell Lymphoma (2016) Crump M, Leppa S, Fayad L, Lee JJ, Di Rocco A, Ogura M, Hagberg H, et al. Journal article Biphasic Squamoid Alveolar Renal Cell Carcinoma: A Distinctive Subtype of Papillary Renal Cell Carcinoma? (2016) Hes O, Condom Mundo E, Peckova K, Lopez JI, Martinek P, Vanecek T, Falconieri G, et al. Journal article Human lymphoid organ dendritic cell identity is predominantly dictated by ontogeny, not tissue microenvironment (2016) Heidkamp GF, Sander J, Lehmann C, Heger L, Eissing N, Baranska A, Lühr J, et al. Journal article Inappropriate cadherin switching in the mouse epiblast compromises proper signaling between the epiblast and the extraembryonic ectoderm during gastrulation (2016) Basilicata MF, Frank M, Solter D, Brabletz T, Stemmler M Journal article Influence of reviewers' clinical backgrounds on interpretation of confocal laser endomicroscopy findings (2016) Kobayashi M, Neumann H, Hino S, Abe S, Nakai Y, Nakajima K, Kiesslich R, et al. Journal article Angiopoietin receptor TEK mutations underlie primary congenital glaucoma with variable expressivity (2016) Souma T, Tompson SW, Thomson BR, Siggs OM, Kizhatil K, Yamaguchi S, Feng L, et al. Journal article