追蹤
Fan Wang
標題
引用次數
引用次數
年份
Genome-wide association identifies a susceptibility locus for coronary artery disease in the Chinese Han population
F Wang, CQ Xu, Q He, JP Cai, XC Li, D Wang, X Xiong, YH Liao, QT Zeng, ...
Nature genetics 43 (4), 345-349, 2011
2792011
Sex-biased methylome and transcriptome in human prefrontal cortex
H Xu, F Wang, Y Liu, Y Yu, J Gelernter, H Zhang
Human molecular genetics 23 (5), 1260-1270, 2014
1502014
Assessment of association of rs2200733 on chromosome 4q25 with atrial fibrillation and ischemic stroke in a Chinese Han population
L Shi, C Li, C Wang, Y Xia, G Wu, F Wang, C Xu, P Wang, X Li, D Wang, ...
Human genetics 126, 843-849, 2009
1182009
Regulation of CARD8 Expression by ANRIL and Association of CARD8 Single Nucleotide Polymorphism rs2043211 (p.C10X) With Ischemic Stroke
Y Bai, S Nie, G Jiang, Y Zhou, M Zhou, Y Zhao, S Li, F Wang, Q Lv, ...
Stroke 45 (2), 383-388, 2014
1102014
A large-scale meta-analysis of the association between the ANKK1/DRD2 Taq1A polymorphism and alcohol dependence
F Wang, A Simen, A Arias, QW Lu, H Zhang
Human genetics 132, 347-358, 2013
1092013
Plasma angiopoietin-2 as a potential causal marker in sepsis-associated ARDS development: evidence from Mendelian randomization and mediation analysis
JP Reilly, F Wang, TK Jones, JA Palakshappa, BJ Anderson, ...
Intensive care medicine 44, 1849-1858, 2018
1042018
Paracrine action of mesenchymal stem cells revealed by single cell gene profiling in infarcted murine hearts
Y Yao, J Huang, Y Geng, H Qian, F Wang, X Liu, M Shang, S Nie, N Liu, ...
PloS one 10 (6), e0129164, 2015
942015
Significant association of SNP rs2106261 in the ZFHX3 gene with atrial fibrillation in a Chinese Han GeneID population
C Li, F Wang, Y Yang, F Fu, C Xu, L Shi, S Li, Y Xia, G Wu, X Cheng, H Liu, ...
Human genetics 129, 239-246, 2011
922011
Sexually dimorphic BDNF signaling directs sensory innervation of the mammary gland
Y Liu, M Rutlin, S Huang, CA Barrick, F Wang, KR Jones, L Tessarollo, ...
Science 338 (6112), 1357-1360, 2012
892012
A de novo mutation in NKX2. 5 associated with atrial septal defects, ventricular noncompaction, syncope and sudden death
P Ouyang, E Saarel, Y Bai, C Luo, Q Lv, Y Xu, F Wang, C Fan, ...
Clinica Chimica Acta 412 (1-2), 170-175, 2011
862011
DNA co-methylation modules in postmortem prefrontal cortex tissues of European Australians with alcohol use disorders
F Wang, H Xu, H Zhao, J Gelernter, H Zhang
Scientific reports 6 (1), 19430, 2016
852016
The IL-33-ST2L pathway is associated with coronary artery disease in a Chinese Han population
X Tu, S Nie, Y Liao, H Zhang, Q Fan, C Xu, Y Bai, F Wang, X Ren, T Tang, ...
The American Journal of Human Genetics 93 (4), 652-660, 2013
762013
Identification of NPPA variants associated with atrial fibrillation in a Chinese GeneID population
X Ren, C Xu, C Zhan, Y Yang, L Shi, F Wang, C Wang, Y Xia, B Yang, ...
Clinica chimica acta 411 (7-8), 481-485, 2010
762010
Molecular basis of gene-gene interaction: cyclic cross-regulation of gene expression and post-GWAS gene-gene interaction involved in atrial fibrillation
Y Huang, C Wang, Y Yao, X Zuo, S Chen, C Xu, H Zhang, Q Lu, L Chang, ...
PLoS genetics 11 (8), e1005393, 2015
732015
Superovulation alters the expression of endometrial genes critical to tissue remodeling and placentation
S Senapati, F Wang, T Ord, C Coutifaris, R Feng, M Mainigi
Journal of assisted reproduction and genetics 35, 1799-1808, 2018
712018
Genetic association and transcriptome integration identify contributing genes and tissues at cystic fibrosis modifier loci
J Gong, F Wang, B Xiao, N Panjwani, F Lin, K Keenan, J Avolio, ...
PLoS genetics 15 (2), e1008007, 2019
692019
Inhibition, not excitation, drives rhythmic whisking
M Deschênes, J Takatoh, A Kurnikova, JD Moore, M Demers, M Elbaz, ...
Neuron 90 (2), 374-387, 2016
692016
The same chromosome 9p21. 3 locus is associated with type 2 diabetes and coronary artery disease in a Chinese Han population
X Cheng, L Shi, S Nie, F Wang, X Li, C Xu, P Wang, B Yang, Q Li, Z Pan, ...
Diabetes 60 (2), 680-684, 2011
602011
Plasma sRAGE acts as a genetically regulated causal intermediate in sepsis-associated acute respiratory distress syndrome
TK Jones, R Feng, VE Kerchberger, JP Reilly, BJ Anderson, ...
American journal of respiratory and critical care medicine 201 (1), 47-56, 2020
572020
Minor allele C of chromosome 1p32 single nucleotide polymorphism rs11206510 confers risk of ischemic stroke in the Chinese Han population
C Xu, F Wang, B Wang, X Li, C Li, D Wang, X Xiong, P Wang, Q Lu, ...
Stroke 41 (8), 1587-1592, 2010
572010
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