| Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use M Liu, Y Jiang, R Wedow, Y Li, DM Brazel, F Chen, G Datta, ... Nature Genetics, 1, 2019 | 1593 | 2019 |
| Genetic diversity fuels gene discovery for tobacco and alcohol use GRB Saunders, X Wang, F Chen, SK Jang, M Liu, C Wang, S Gao, ... Nature, 1-7, 2022 | 182 | 2022 |
| Phylogenetic analysis of CDK and cyclin proteins in premetazoan lineages L Cao, F Chen, X Yang, W Xu, J Xie, L Yu BMC evolutionary biology 14 (1), 10, 2014 | 165 | 2014 |
| Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci AM Erzurumluoglu, M Liu, VE Jackson, DR Barnes, G Datta, ... Molecular Psychiatry, 1, 2019 | 136 | 2019 |
| Linking the septin expression with carcinogenesis M Liu, S Shen, F Chen, W Yu, L Yu Molecular biology reports 37 (7), 3601-3608, 2010 | 61 | 2010 |
| The phosphorylation of SEPT2 on Ser218 by casein kinase 2 is important to hepatoma carcinoma cell proliferation W Yu, X Ding, F Chen, M Liu, S Shen, X Gu, L Yu Molecular and cellular biochemistry 325 (1-2), 61-67, 2009 | 41 | 2009 |
| Inferring genes that escape X-Chromosome inactivation reveals important contribution of variable escape genes to sex-biased diseases R Sauteraud, JM Stahl, J James, M Englebright, F Chen, X Zhan, L Carrel, ... Genome Research, 2021 | 33 | 2021 |
| BRSK2 is regulated by ER stress in protein level and involved in ER stress-induced apoptosis Y Wang, B Wan, D Li, J Zhou, R Li, M Bai, F Chen, L Yu Biochemical and biophysical research communications 423 (4), 813-818, 2012 | 27 | 2012 |
| Proper conditional analysis in the presence of missing data: Application to large scale meta-analysis of tobacco use phenotypes Y Jiang, S Chen, D McGuire, F Chen, M Liu, WG Iacono, JK Hewitt, ... PLOS Genetics 14 (7), e1007452, 2018 | 26 | 2018 |
| Model-based assessment of replicability for genome-wide association meta-analysis D McGuire, Y Jiang, M Liu, JD Weissenkampen, S Eckert, L Yang, F Chen, ... Nature Communications 12 (1), 1-14, 2021 | 25 | 2021 |
| Multi-ancestry transcriptome-wide association analyses yield insights into tobacco use biology and drug repurposing F Chen, X Wang, SK Jang, BC Quach, JD Weissenkampen, ... Nature Genetics, 1-10, 2023 | 24 | 2023 |
| GTP binding is required for SEPT12 to form filaments and to interact with SEPT11. X Ding, W Yu, M Liu, SQ Shen, F Chen, L Cao, B Wan, L Yu Molecules & Cells (Springer Science & Business Media BV) 25 (3), 2008 | 21 | 2008 |
| Integrating 3D genomic and epigenomic data to enhance target gene discovery and drug repurposing in transcriptome-wide association studies C Khunsriraksakul, D McGuire, R Sauteraud, F Chen, L Yang, L Wang, ... Nature Communications 13 (1), 1-15, 2022 | 18 | 2022 |
| T‐LAK cell‐originated protein kinase is essential for the proliferation of hepatocellular carcinoma SMMC‐7721 cells F Chen, R Li, C Wang, L Cao, Y Wang, L Yu Cell biochemistry and function 31 (8), 736-742, 2013 | 17 | 2013 |
| APC/C Cdh1 Targets Brain-Specific Kinase 2 (BRSK2) for Degradation via the Ubiquitin-Proteasome Pathway R Li, B Wan, J Zhou, Y Wang, T Luo, X Gu, F Chen, L Yu PloS one 7 (9), e45932, 2012 | 15 | 2012 |
| Meta-analysis shows significant association of the TP53 Arg72Pro with ovarian cancer risk SQ Shen, DK Jiang, GY Liu, F Chen, L Yu Molecular biology reports 39 (4), 4683-4690, 2012 | 13 | 2012 |
| Investigation of discordant phenotype in mild Hemophilia A using whole exome sequencing PH Cygan, SE Arnold-Croop, EA Weidman, F Chen, DJ Liu, ME Eyster, ... Thrombosis Research, 2020 | 1 | 2020 |
| Integrating single cell expression quantitative trait loci summary statistics to understand complex trait risk genes L Wang, C Khunsriraksakul, H Markus, D Chen, F Zhang, F Chen, X Zhan, ... Nature Communications 15 (1), 4260, 2024 | | 2024 |
| Prothrombotic variants as modifiers of clinical phenotype in four related individuals with haemophilia A L Carrel, S Arnold‐Croop, T Achtermann, F Chen, Y Cheng, D Liu, ... Haemophilia, 2021 | | 2021 |
| Bleeding in Mild Hemophilia A Due to a Splice-Site F8 Mutation May be Fully Abrogated By Prothrombotic Gene Variants PH Cygan, SE Arnold-Croop, EA Weidman, F Chen, DJ Liu, ME Eyster, ... Blood, The Journal of the American Society of Hematology 134 (Supplement_1 …, 2019 | | 2019 |
