Junwen Wang
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A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer
DJ Hunter, P Kraft, KB Jacobs, DG Cox, M Yeager, SE Hankinson, ...
Nature genetics 39 (7), 870-874, 2007
The support of human genetic evidence for approved drug indications
MR Nelson, H Tipney, JL Painter, J Shen, P Nicoletti, Y Shen, A Floratos, ...
Nature genetics 47 (8), 856-860, 2015
Genome-wide association analysis identifies new lung cancer susceptibility loci in never-smoking women in Asia
Q Lan, CA Hsiung, K Matsuo, YC Hong, A Seow, Z Wang, HD Hosgood III, ...
Nature Genetics, 2012
GWASdb: a database for human genetic variants identified by genome-wide association studies
MJ Li, P Wang, X Liu, EL Lim, Z Wang, M Yeager, MP Wong, PC Sham, ...
Nucleic Acids Research 40 (D1), D1047-D1054, 2012
Transcriptional genomics associates FOX transcription factors with human heart failure
S Hannenhalli, ME Putt, JM Gilmore, J Wang, MS Parmacek, JA Epstein, ...
Circulation 114 (12), 1269-1276, 2006
GWASdb v2: an update database for human genetic variants identified by genome-wide association studies
MJ Li, Z Liu, P Wang, MP Wong, MR Nelson, JPA Kocher, M Yeager, ...
Nucleic acids research 44 (D1), D869-D876, 2016
Analysis of heritability and shared heritability based on genome-wide association studies for 13 cancer types
JN Sampson, WA Wheeler, M Yeager, O Panagiotou, Z Wang, SI Berndt, ...
Journal of the National Cancer Institute 107 (12), djv279, 2015
Vitamin D inhibits COX-2 expression and inflammatory response by targeting thioesterase superfamily member 4
Q Wang, Y He, Y Shen, Q Zhang, D Chen, C Zuo, J Qin, H Wang, J Wang, ...
Journal of Biological Chemistry 289 (17), 11681-11694, 2014
Hyperglycemia-induced protein kinase C β2 activation induces diastolic cardiac dysfunction in diabetic rats by impairing caveolin-3 expression and Akt/eNOS signaling
S Lei, H Li, J Xu, Y Liu, X Gao, J Wang, KFJ Ng, WB Lau, X Ma, ...
Diabetes 62 (7), 2318-2328, 2013
Lumbar disc degeneration is linked to a carbohydrate sulfotransferase 3 variant
YQ Song, T Karasugi, KMC Cheung, K Chiba, DWH Ho, A Miyake, ...
The Journal of clinical investigation 123 (11), 4909-4917, 2013
Predictive models for protein crystallization
B Rupp, J Wang
Methods 34 (3), 390-407, 2004
Developments in blood-brain barrier penetrance and drug repurposing for improved treatment of glioblastoma
BG Harder, MR Blomquist, J Wang, AJ Kim, GF Woodworth, JA Winkles, ...
Frontiers in oncology 8, 462, 2018
GWAS3D: Detecting human regulatory variants by integrative analysis of genome-wide associations, chromosome interactions and histone modifications
MJ Li, LY Wang, Z Xia, PC Sham, J Wang
Nucleic acids research 41 (W1), W150-W158, 2013
Evaluation of tools for highly variable gene discovery from single-cell RNA-seq data
SH Yip, PC Sham, J Wang
Briefings in bioinformatics 20 (4), 1583-1589, 2019
Potent paracrine effects of human induced pluripotent stem cell-derived mesenchymal stem cells attenuate doxorubicin-induced cardiomyopathy
Y Zhang, X Liang, S Liao, W Wang, J Wang, X Li, Y Ding, Y Liang, F Gao, ...
Scientific reports 5 (1), 11235, 2015
N-Acetylcysteine and allopurinol up-regulated the Jak/STAT3 and PI3K/Akt pathways via adiponectin and attenuated myocardial postischemic injury in diabetes
T Wang, X Mao, H Li, S Qiao, A Xu, J Wang, S Lei, Z Liu, KFJ Ng, ...
Free Radical Biology and Medicine 63, 291-303, 2013
Lung cancer tumorigenicity and drug resistance are maintained through ALDHhiCD44hi tumor initiating cells
J Liu, Z Xiao, SKM Wong, VPC Tin, KY Ho, J Wang, MH Sham, MP Wong
Oncotarget 4 (10), 1698, 2013
Imputation and subset-based association analysis across different cancer types identifies multiple independent risk loci in the TERT-CLPTM1L region on …
Z Wang, B Zhu, M Zhang, H Parikh, J Jia, CC Chung, JN Sampson, ...
Human molecular genetics 23 (24), 6616-6633, 2014
Linnorm: improved statistical analysis for single cell RNA-seq expression data
SH Yip, P Wang, JPA Kocher, PC Sham, J Wang
Nucleic acids research 45 (22), e179-e179, 2017
Next generation sequencing has lower sequence coverage and poorer SNP-detection capability in the regulatory regions
W Wang, Z Wei, TW Lam, J Wang
Scientific Reports 1, 2011
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