| dbNSFP v3. 0: A one‐stop database of functional predictions and annotations for human nonsynonymous and splice‐site SNVs X Liu, C Wu, C Li, E Boerwinkle Human mutation 37 (3), 235-241, 2016 | 993 | 2016 |
| dbNSFP v4: a comprehensive database of transcript-specific functional predictions and annotations for human nonsynonymous and splice-site SNVs X Liu, C Li, C Mou, Y Dong, Y Tu Genome medicine 12, 1-8, 2020 | 346 | 2020 |
| MetaRNN: differentiating rare pathogenic and rare benign missense SNVs and InDels using deep learning C Li, D Zhi, K Wang, X Liu Genome Medicine 14 (1), 115, 2022 | 50 | 2022 |
| SARS-COV-2 as potential microRNA sponge in COVID-19 patients C Li, R Wang, A Wu, T Yuan, K Song, Y Bai, X Liu BMC Medical Genomics 15 (Suppl 2), 94, 2022 | 26 | 2022 |
| The performance of deleteriousness prediction scores for rare non-protein-changing single nucleotide variants in human genes X Liu, C Li, E Boerwinkle Journal of medical genetics 54 (2), 134-144, 2017 | 17 | 2017 |
| Genome annotation of disease-causing microorganisms Y Dong, C Li, K Kim, L Cui, X Liu Briefings in Bioinformatics 22 (2), 845-854, 2021 | 15 | 2021 |
| dbMTS: a comprehensive database of putative human microRNA target site SNVs and their functional predictions C Li, C Mou, MD Swartz, B Yu, Y Bai, Y Tu, X Liu Human mutation 41 (6), 1123-1130, 2020 | 11 | 2020 |
| Iron Hack-A symposium/hackathon focused on porphyrias, Friedreich’s ataxia, and other rare iron-related diseases GC Ferreira, J Oberstaller, R Fonseca, TE Keller, SR Adapa, J Gibbons, ... F1000Research 8, 2019 | 9 | 2019 |
| Identifying putative causal links between MicroRNAs and severe COVID-19 using mendelian randomization C Li, A Wu, K Song, J Gao, E Huang, Y Bai, X Liu Cells 10 (12), 3504, 2021 | 8 | 2021 |
| Genetic variants in microRNA genes and targets associated with cardiovascular disease risk factors in the African-American population C Li, ML Grove, B Yu, BC Jones, A Morrison, E Boerwinkle, X Liu Human genetics 137, 85-94, 2018 | 7 | 2018 |
| Identification of microRNA-related tumorigenesis variants and genes in The Cancer Genome Atlas (TCGA) Data C Li, B Wu, H Han, J Zhao, Y Bai, X Liu Genes 11 (9), 953, 2020 | 6 | 2020 |
| MalariaSED: a deep learning framework to decipher the regulatory contributions of noncoding variants in malaria parasites C Wang, Y Dong, C Li, J Oberstaller, M Zhang, J Gibbons, CV Pires, ... Genome Biology 24 (1), 231, 2023 | | 2023 |
| Biomedical application of DNA modifications F Mao, H Baiyin, J Li, X Chen, Y Xu, C Wang, C Li Frontiers in Genetics 14, 1286185, 2023 | | 2023 |
| Orthogonal analysis of variants in APOE gene using in-silico approaches reveals novel disrupting variants C Li, I Hou, M Ma, G Wang, Y Bai, X Liu Frontiers in Bioinformatics 3, 1122559, 2023 | | 2023 |
| A Bioinformatics Pipeline for the identification of disease-causing variants in humans that can change protein structure M Ma, I Hou, J Gao, C Li, Y Bai, X Liu 2022 IEEE International Conference on Bioinformatics and Biomedicine (BIBM …, 2022 | | 2022 |
| Analysis of data consistency identifies measurement abnormality in Howells' craniometric test data set J Pang, Y Dong, C Turner, C Li, X Liu American Journal of Biological Anthropology 179 (4), 687-692, 2022 | | 2022 |
| SNPAAMapper-Python: A highly efficient genome-wide SNP variant analysis pipeline for Next-Generation Sequencing data C Li, K Ma, N Xu, C Fu, A He, X Liu, Y Bai Frontiers in Artificial Intelligence 5, 991733, 2022 | | 2022 |
| Uncovering host-microbiome interactions in global systems with collaborative programming: a novel approach integrating social and data sciences J Oberstaller, SR Adapa, GW Dayhoff II, J Gibbons, TE Keller, C Li, J Lim, ... F1000Research 9, 1478, 2020 | | 2020 |
| Iron Hack-A symposium/hackathon focused on porphyrias GC Ferreira, J Oberstaller, R Fonseca, TE Keller, SR Adapa, J Gibbons, ... | | |
| Friedreich’s ataxia, and other rare iron-related diseases GC Ferreira, J Oberstaller, R Fonseca, TE Keller, SR Adapa, J Gibbons, ... | | |
