| Harmonizing clinical sequencing and interpretation for the eMERGE III network H Zouk, E Venner, NJ Lennon, DM Muzny, D Abrams, S Adunyah, ... The American Journal of Human Genetics 105 (3), 588-605, 2019 | 93 | 2019 |
| Facilitating phenotype transfer using a common data model G Hripcsak, N Shang, PL Peissig, LV Rasmussen, C Liu, B Benoit, ... Journal of biomedical informatics 96, 103253, 2019 | 63 | 2019 |
| Characterization of genome-wide H3K27ac profiles reveals a distinct PM2.5-associated histone modification signature C Liu, J Xu, Y Chen, X Guo, Y Zheng, Q Wang, Y Chen, N Ni, Y Zhu, A ... Environmental Health 14, 65, 2015 | 58* | 2015 |
| Genome-wide polygenic score to predict chronic kidney disease across ancestries A Khan, MC Turchin, A Patki, V Srinivasasainagendra, N Shang, ... Nature medicine 28 (7), 1412-1420, 2022 | 56 | 2022 |
| Phen2Gene: rapid phenotype-driven gene prioritization for rare diseases M Zhao, JM Havrilla, L Fang, Y Chen, J Peng, C Liu, C Wu, M Sarmady, ... NAR genomics and Bioinformatics 2 (2), lqaa032, 2020 | 56 | 2020 |
| Doc2Hpo: a web application for efficient and accurate HPO concept curation C Liu, FS Peres Kury, Z Li, C Ta, K Wang, C Weng Nucleic acids research 47 (W1), W566-W570, 2019 | 51 | 2019 |
| Linking the genetic architecture of cytosine modifications with human complex traits X Zhang, EL Moen, C Liu, W Mu, ER Gamazon, SM Delaney, C Wing, ... Human molecular genetics 23 (22), 5893-5905, 2014 | 44 | 2014 |
| Returning integrated genomic risk and clinical recommendations: The eMERGE study JE Linder, A Allworth, HT Bland, PJ Caraballo, RL Chisholm, EW Clayton, ... Genetics in Medicine 25 (4), 100006, 2023 | 38 | 2023 |
| A retrospective analysis of COVID-19 mRNA vaccine breakthrough infections–risk factors and vaccine effectiveness C Liu, J Lee, C Ta, A Soroush, JR Rogers, JH Kim, K Natarajan, J Zucker, ... Medrxiv, 2021 | 38* | 2021 |
| Meta-analysis of sex differences in gene expression in schizophrenia W Qin, C Liu, M Sodhi, H Lu BMC systems biology 10, 99-106, 2016 | 38 | 2016 |
| Generalizability of polygenic risk scores for breast cancer among women with European, African, and Latinx ancestry C Liu, N Zeinomar, WK Chung, K Kiryluk, AG Gharavi, G Hripcsak, ... JAMA network open 4 (8), e2119084-e2119084, 2021 | 37 | 2021 |
| Making work visible for electronic phenotype implementation: lessons learned from the eMERGE network N Shang, C Liu, LV Rasmussen, CN Ta, RJ Caroll, B Benoit, T Lingren, ... Journal of biomedical informatics 99, 103293, 2019 | 35 | 2019 |
| Multi-omics facilitated variable selection in Cox-regression model for cancer prognosis prediction C Liu, X Wang, GZ Genchev, H Lu Methods 124, 100-107, 2017 | 32 | 2017 |
| The evolution of alternative splicing exons in vascular endothelial growth factor A J Xu, T Dou, C Liu, M Fu, Y Huang, S Gu, Y Zhou, Y Xie Gene 487 (2), 143-150, 2011 | 31 | 2011 |
| Ensembles of natural language processing systems for portable phenotyping solutions C Liu, CN Ta, JR Rogers, Z Li, J Lee, AM Butler, N Shang, FSP Kury, ... Journal of biomedical informatics 100, 103318, 2019 | 29 | 2019 |
| Epigenetic contribution of the myosin light chain kinase gene to the risk for acute respiratory distress syndrome KL Szilágyi, C Liu, X Zhang, T Wang, JD Fortman, W Zhang, JGN Garcia Translational Research 180, 12-21, 2017 | 28 | 2017 |
| SCAN database: facilitating integrative analyses of cytosine modification and expression QTL W Zhang, ER Gamazon, X Zhang, A Konkashbaev, C Liu, KL Szilagyi, ... Database 2015, bav025, 2015 | 28 | 2015 |
| Deep learning for rare disease: A scoping review J Lee, C Liu, J Kim, Z Chen, Y Sun, JR Rogers, WK Chung, C Weng Journal of Biomedical Informatics 135, 104227, 2022 | 24 | 2022 |
| Natural language processing (NLP) tools in extracting biomedical concepts from research articles: a case study on autism spectrum disorder J Peng, M Zhao, J Havrilla, C Liu, C Weng, W Guthrie, R Schultz, K Wang, ... BMC Medical Informatics and Decision Making 20, 1-9, 2020 | 23 | 2020 |
| A disease similarity matrix based on the uniqueness of shared genes MB Carson, C Liu, Y Lu, C Jia, H Lu BMC medical genomics 10, 27-32, 2017 | 23 | 2017 |
