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1.
Systematic Functional Interrogation of Genes in GWAS Loci Identified ATF1 as a Key Driver in Colorectal Cancer Modulated by a Promoter-Enhancer Interaction.
Am J Hum Genet
; 105(1): 29-47, 2019 07 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-31204011
2.
A functional variant rs1537373 in 9p21.3 region is associated with pancreatic cancer risk.
Mol Carcinog
; 58(5): 760-766, 2019 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-30604909
3.
Integrative functional genomics identifies regulatory genetic variant modulating RAB31 expression and altering susceptibility to breast cancer.
Mol Carcinog
; 57(12): 1845-1854, 2018 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-30182384
4.
A functional polymorphism located at transcription factor binding sites, rs6695837 near LAMC1 gene, confers risk of colorectal cancer in Chinese populations.
Carcinogenesis
; 38(2): 177-183, 2017 02 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-28039327
5.
A low-frequency variant in SMAD7 modulates TGF-ß signaling and confers risk for colorectal cancer in Chinese population.
Mol Carcinog
; 56(7): 1798-1807, 2017 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-28218435
6.
[Effect of Bushen Huoxue Recipe on Paracrine Gene Expression Profiling of Uterine Natural Killer Cells and Uterine Stromal Cells].
Zhongguo Zhong Xi Yi Jie He Za Zhi
; 37(4): 485-489, 2017 04.
Artículo
en Zh
| MEDLINE | ID: mdl-30650511
7.
A functional polymorphism in lnc-LAMC2-1:1 confers risk of colorectal cancer by affecting miRNA binding.
Carcinogenesis
; 37(5): 443-51, 2016 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-26905585
8.
Genetic variant in DIP2A gene is associated with developmental dyslexia in Chinese population.
Am J Med Genet B Neuropsychiatr Genet
; 171B(2): 203-8, 2016 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-26452339
9.
Genetic variants in the SWI/SNF complex and smoking collaborate to modify the risk of pancreatic cancer in a Chinese population.
Mol Carcinog
; 54(9): 761-8, 2015 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-24585446
10.
Reelin gene variants and risk of autism spectrum disorders: an integrated meta-analysis.
Am J Med Genet B Neuropsychiatr Genet
; 165B(2): 192-200, 2014 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-24453138
11.
Genetic variations in the TGFß signaling pathway, smoking and risk of colorectal cancer in a Chinese population.
Carcinogenesis
; 34(4): 936-42, 2013 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-23275154
12.
Risk of GWAS-identified genetic variants for breast cancer in a Chinese population: a multiple interaction analysis.
Breast Cancer Res Treat
; 142(3): 637-44, 2013 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-24265035
13.
A functional polymorphism, rs28493229, in ITPKC and risk of Kawasaki disease: an integrated meta-analysis.
Mol Biol Rep
; 39(12): 11137-44, 2012 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-23065250
14.
Association of candidate genetic variations with gastric cardia adenocarcinoma in Chinese population: a multiple interaction analysis.
Carcinogenesis
; 32(3): 336-42, 2011 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-21148629
15.
Risk SNP-Mediated Enhancer-Promoter Interaction Drives Colorectal Cancer through Both FADS2 and AP002754.2.
Cancer Res
; 80(9): 1804-1818, 2020 05 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-32127356
16.
Integrative expression quantitative trait locus-based analysis of colorectal cancer identified a functional polymorphism regulating SLC22A5 expression.
Eur J Cancer
; 93: 1-9, 2018 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-29428571
17.
A Rare Missense Variant in TCF7L2 Associates with Colorectal Cancer Risk by Interacting with a GWAS-Identified Regulatory Variant in the MYC Enhancer.
Cancer Res
; 78(17): 5164-5172, 2018 09 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-30026326
18.
Educational and Behavioral Counseling in a Methadone Maintenance Treatment Program in China: A Randomized Controlled Trial.
Front Psychiatry
; 9: 113, 2018.
Artículo
en Inglés
| MEDLINE | ID: mdl-29670549
19.
Exome-wide analysis identifies three low-frequency missense variants associated with pancreatic cancer risk in Chinese populations.
Nat Commun
; 9(1): 3688, 2018 09 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-30206226
20.
Exome-wide analyses identify low-frequency variant in CYP26B1 and additional coding variants associated with esophageal squamous cell carcinoma.
Nat Genet
; 50(3): 338-343, 2018 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-29379198