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| A recurrent PDGFRB mutation causes familial infantile myofibromatosis YH Cheung, T Gayden, PM Campeau, CA LeDuc, D Russo, VH Nguyen, ... The American Journal of Human Genetics 92 (6), 996-1000, 2013 | 158 | 2013 |
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| Hydrogen sulfide as a novel regulatory factor in liver health and disease DD Wu, DY Wang, HM Li, JC Guo, SF Duan, XY Ji Oxidative Medicine and Cellular Longevity 2019, 2019 | 74 | 2019 |
| New insights into the genetics of fetal megacystis: ACTG2 mutations, encoding γ-2 smooth muscle actin in megacystis microcolon intestinal hypoperistalsis syndrome (Berdon syndrome) L Tuzovic, S Tang, RS Miller, L Rohena, L Shahmirzadi, K Gonzalez, X Li, ... Fetal diagnosis and therapy 38 (4), 296-306, 2015 | 58 | 2015 |
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| Development of an Au-anchored Fe Single-atom nanozyme for biocatalysis and enhanced tumor photothermal therapy N Feng, Q Li, Q Bai, S Xu, J Shi, B Liu, J Guo Journal of colloid and interface science 618, 68-77, 2022 | 38 | 2022 |
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| Development of MOF “Armor‐Plated” Phycocyanin and Synergistic Inhibition of Cellular Respiration for Hypoxic Photodynamic Therapy in Patient‐Derived Xenograft Models D Chen, M Suo, J Guo, W Tang, W Jiang, Y Liu, Y Duo Advanced Healthcare Materials 10 (3), 2001577, 2021 | 28 | 2021 |
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