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Elife|January 15, 2024
Design of the HPV-automated visual evaluation (PAVE) study: Validating a novel cervical screening strategySilvia de Sanjosé, Rebecca B Perkins, Nicole Campos, et al.Nature|March 16, 2023
The dietary sweetener sucralose is a negative modulator of T cell-mediated responsesFabio Zani, Julianna Blagih, Tim Gruber, et al.Clinical & Experimental Metastasis|October 17, 2025
Postoperative stereotactic radiotherapy for brain metastases: results from a single-center retrospective analysisE K M Lam, D K C Leung, V H F Lee, et al.European Journal of Haematology|May 30, 2021
A descriptive cost-analysis of MYX.1/MCRN003, a phase 2 clinical trial evaluating high-dose weekly carfilzomib, cyclophosphamide, and dexamethasone in relapsed and refractory multiple myelomaBethany E Monteith, Christopher P Venner, Matthew C Cheung, et al.Journal of Abnormal Psychology|January 14, 2020
Emotion-behavior decoupling in individuals with schizophrenia, bipolar disorder, and major depressive disorderYan-Yu Wang, Mao-Hong Ge, Guo-Hui Zhu, et al.The Journal of Nutrition|June 9, 2020
The Cardioprotective Role of Flaxseed in the Prevention of Doxorubicin- and Trastuzumab-Mediated Cardiotoxicity in C57BL/6 MiceChantal Y Asselin, Amy Lam, David Y C Cheung, et al.Spine|December 24, 2005
The TRP2 allele of COL9A2 is an age-dependent risk factor for the development and severity of intervertebral disc degenerationJeffrey J T Jim, Noora Noponen-Hietala, Kenneth M C Cheung, et al.Schizophrenia Research|July 29, 2017
Trajectories of schizotypy and their emotional and social functioning: An 18-month follow-up studyYi Wang, Hai-Song Shi, Wen-Hua Liu, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 16, 2009
Identification of neuroglycan C and interacting partners as potential susceptibility genes for schizophrenia in a Southern Chinese populationHon-Cheong So, Pui Y Fong, Ronald Y L Chen, et al.Journal of Orthopaedic Research : Official Publication of the Orthopaedic Research Society|September 28, 2010
A splice-site mutation leads to haploinsufficiency of EXT2 mRNA for a dominant trait in a large family with multiple osteochondromasLiu Yang, Wing Sum Hui, Wilson C W Chan, et al.Pageof 212