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Developing an optimal stratification model for colorectal cancer screening and reducing racial disparities in multi-center population-based studies.
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- Genome Medicine, 2024, v. 16, n. 1, p. 1, doi. 10.1186/s13073-024-01355-y
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Prioritization of risk genes in colorectal cancer by integrative analysis of multi-omics data and gene networks.
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- SCIENCE CHINA Life Sciences, 2024, v. 67, n. 1, p. 132, doi. 10.1007/s11427-023-2439-7
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Risk SNP in a transcript of RP11-638I2.4 increases lncRNA–YY1 interaction and pancreatic cancer susceptibility.
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- Archives of Toxicology, 2023, v. 97, n. 10, p. 2799, doi. 10.1007/s00204-023-03564-7
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A variant in CYP26B1 associated with esophageal squamous cell carcinoma risk by affecting retinoic acid metabolism.
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- Molecular Carcinogenesis, 2023, v. 62, n. 7, p. 991, doi. 10.1002/mc.23540
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Aging Resistance of Multi-Walled Carbon Nano-tubes Reinforced Non-asbestos Gasket.
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- Lubrication Engineering (0254-0150), 2023, v. 48, n. 6, p. 175, doi. 10.3969/j.issn.0254-0150.2023.06.023
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Identification of specific susceptibility loci for the early-onset colorectal cancer.
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- Genome Medicine, 2023, v. 15, n. 1, p. 1, doi. 10.1186/s13073-023-01163-w
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In Utero and Childhood/Adolescence Exposure to Tobacco Smoke, Genetic Risk, and Lung Cancer Incidence and Mortality in Adulthood.
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- American Journal of Respiratory & Critical Care Medicine, 2023, v. 207, n. 2, p. 173, doi. 10.1164/rccm.202112-2758OC
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FOXA1 of regulatory variant associated with risk of breast cancer through allele-specific enhancer in the Chinese population.
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- Breast Cancer (13406868), 2022, v. 29, n. 2, p. 247, doi. 10.1007/s12282-021-01305-1
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Clinical characteristics and risk factors of COVID-19 patients with chronic hepatitis B: a multi-center retrospective cohort study.
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- Frontiers of Medicine, 2022, v. 16, n. 1, p. 111, doi. 10.1007/s11684-021-0854-5
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Integrated analysis and the identification of a circRNA-miRNA-mRNA network in the progression of abdominal aortic aneurysm.
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- PeerJ, 2021, p. 1, doi. 10.7717/peerj.12682
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Aberrant MCM10 SUMOylation induces genomic instability mediated by a genetic variant associated with survival of esophageal squamous cell carcinoma.
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- Clinical & Translational Medicine, 2021, v. 11, n. 6, p. 1, doi. 10.1002/ctm2.485
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Identification of genetic variants in m6A modification genes associated with pancreatic cancer risk in the Chinese population.
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- Archives of Toxicology, 2021, v. 95, n. 3, p. 1117, doi. 10.1007/s00204-021-02978-5
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Clinical characteristics of COVID‐19 in patients with preexisting ILD: A retrospective study in a single center in Wuhan, China.
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- Journal of Medical Virology, 2020, v. 92, n. 11, p. 2742, doi. 10.1002/jmv.26174
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The epidemiology and clinical characteristics of co‐infection of SARS‐CoV‐2 and influenza viruses in patients during COVID‐19 outbreak.
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- Journal of Medical Virology, 2020, v. 92, n. 11, p. 2870, doi. 10.1002/jmv.26163
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ABTB2 Regulatory Variant as Predictor of Epirubicin-Based Neoadjuvant Chemotherapy in Luminal A Breast Cancer.
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- Frontiers in Oncology, 2020, v. 10, p. N.PAG, doi. 10.3389/fonc.2020.571517
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Challenges and recommendations for cancer care in the COVID-19 pandemic.
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- Cancer Biology & Medicine, 2020, v. 17, n. 3, p. 515, doi. 10.20892/j.issn.2095-3941.2020.0300
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Copper alloy production in the Warring States period (475-221 BCE) of the Shu state: a metallurgical study on copper alloy objects of the Baishoulu cemetery in Chengdu, China.
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- Heritage Science, 2020, v. 8, n. 1, p. 1, doi. 10.1186/s40494-020-00412-0
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ANKLE1 N<sup>6</sup>‐Methyladenosine‐related variant is associated with colorectal cancer risk by maintaining the genomic stability.
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- International Journal of Cancer, 2020, v. 146, n. 12, p. 3281, doi. 10.1002/ijc.32677
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Functional characterization of a low-frequency V1937I variant in FASN associated with susceptibility to esophageal squamous cell carcinoma.
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- Archives of Toxicology, 2020, v. 94, n. 6, p. 2039, doi. 10.1007/s00204-020-02738-x
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Genetic variants in m<sup>6</sup>A modification genes are associated with esophageal squamous-cell carcinoma in the Chinese population.
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- Carcinogenesis, 2020, v. 41, n. 6, p. 761, doi. 10.1093/carcin/bgaa012
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Fighting and burial: the production of bronze weapons in the Shu state based on a case study of Xinghelu cemetery, Chengdu, China.
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- Heritage Science, 2020, v. 8, n. 1, p. 1, doi. 10.1186/s40494-020-00379-y
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A functional variant in TNXB promoter associates with the risk of esophageal squamous‐cell carcinoma.
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- Molecular Carcinogenesis, 2020, v. 59, n. 4, p. 439, doi. 10.1002/mc.23166
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Evaluation of polymorphisms in microRNA‐binding sites and pancreatic cancer risk in Chinese population.
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- Journal of Cellular & Molecular Medicine, 2020, v. 24, n. 3, p. 2252, doi. 10.1111/jcmm.14906
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Three functional variants were identified to affect RPS24 expression and significantly associated with risk of colorectal cancer.
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- Archives of Toxicology, 2020, v. 94, n. 1, p. 295, doi. 10.1007/s00204-019-02600-9
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SLC10A1 S267F variant influences susceptibility to HBV infection and reduces cholesterol level by impairing bile acid uptake.
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- Journal of Viral Hepatitis, 2019, v. 26, n. 10, p. 1178, doi. 10.1111/jvh.13157
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Integrative analysis identifies genetic variant modulating MICA expression and altering susceptibility to persistent HBV infection.
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- Liver International, 2019, v. 39, n. 10, p. 1927, doi. 10.1111/liv.14127
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A functional variant in the boundary of a topological association domain is associated with pancreatic cancer risk.
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- Molecular Carcinogenesis, 2019, v. 58, n. 10, p. 1855, doi. 10.1002/mc.23077
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A genetic variant in PIK3R1 is associated with pancreatic cancer survival in the Chinese population.
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- Cancer Medicine, 2019, v. 8, n. 7, p. 3575, doi. 10.1002/cam4.2228
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A functional variant rs1537373 in 9p21.3 region is associated with pancreatic cancer risk.
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- Molecular Carcinogenesis, 2019, v. 58, n. 5, p. 760, doi. 10.1002/mc.22968
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AWESOME: a database of SNPs that affect protein post-translational modifications.
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- Nucleic Acids Research, 2019, v. 47, n. D1, p. D874, doi. 10.1093/nar/gky821
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CancerSplicingQTL: a database for genome-wide identification of splicing QTLs in human cancer.
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- Nucleic Acids Research, 2019, v. 47, n. D1, p. D909, doi. 10.1093/nar/gky954
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Integrative functional genomics identifies regulatory genetic variant modulating RAB31 expression and altering susceptibility to breast cancer.
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- Molecular Carcinogenesis, 2018, v. 57, n. 12, p. 1845, doi. 10.1002/mc.22902
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Exome-wide analysis identifies three low-frequency missense variants associated with pancreatic cancer risk in Chinese populations.
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- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-06136-x
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Identification of a functional polymorphism affecting microRNA binding in the susceptibility locus 1q25.3 for colorectal cancer.
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- Molecular Carcinogenesis, 2017, v. 56, n. 9, p. 2014, doi. 10.1002/mc.22649
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A low-frequency variant in SMAD7 modulates TGF-β signaling and confers risk for colorectal cancer in Chinese population.
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- Molecular Carcinogenesis, 2017, v. 56, n. 7, p. 1798, doi. 10.1002/mc.22637
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Breast cancer risk-associated variants at 6q25.1 influence risk of hepatocellular carcinoma in a Chinese population.
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- Carcinogenesis, 2017, v. 38, n. 4, p. 447, doi. 10.1093/carcin/bgx024
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A functional polymorphism located at transcription factor binding sites, rs6695837 near LAMC1 gene, confers risk of colorectal cancer in Chinese populations.
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- Carcinogenesis, 2017, v. 38, n. 2, p. 177, doi. 10.1093/carcin/bgw204
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Association between bilirubin and risk of Non-Alcoholic Fatty Liver Disease based on a prospective cohort study.
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- Scientific Reports, 2016, p. 31006, doi. 10.1038/srep31006
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A functional polymorphism in lnc-LAMC2-1:1 confers risk of colorectal cancer by affecting miRNA binding.
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- Carcinogenesis, 2016, v. 37, n. 5, p. 443, doi. 10.1093/carcin/bgw024
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The Associations between RNA Splicing Complex Gene SF3A1 Polymorphisms and Colorectal Cancer Risk in a Chinese Population.
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- PLoS ONE, 2015, v. 10, n. 6, p. 1, doi. 10.1371/journal.pone.0130377
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