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| Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders T Wang, K Hoekzema, D Vecchio, H Wu, A Sulovari, BP Coe, ... Nature communications 11 (1), 4932, 2020 | 143 | 2020 |
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| SLC39A5 mutations interfering with the BMP/TGF-β pathway in non-syndromic high myopia H Guo, X Jin, T Zhu, T Wang, P Tong, L Tian, Y Peng, L Sun, A Wan, ... Journal of medical genetics 51 (8), 518-525, 2014 | 118 | 2014 |
| Plasmodium Genomics and Genetics: New Insights into Malaria Pathogenesis, Drug Resistance, Epidemiology, and Evolution X Su, KD Lane, L Xia, JM Sá, TE Wellems Clinical microbiology reviews 32 (4), 10.1128/cmr. 00019-19, 2019 | 109 | 2019 |
| Mutations of P4HA2 encoding prolyl 4-hydroxylase 2 are associated with nonsyndromic high myopia H Guo, P Tong, Y Liu, L Xia, T Wang, Q Tian, Y Li, Y Hu, Y Zheng, X Jin, ... Genetics in Medicine 17 (4), 300-306, 2015 | 79 | 2015 |
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| Type I interferons and malaria: A double-edge sword against a complex parasitic disease X He, L Xia, KC Tumas, J Wu, XZ Su Frontiers in cellular and infection microbiology 10, 594621, 2020 | 33 | 2020 |
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| The E3 ubiquitin ligase MARCH1 regulates antimalaria immunity through interferon signaling and T cell activation J Wu, L Xia, X Yao, X Yu, KC Tumas, W Sun, Y Cheng, X He, Y Peng, ... Proceedings of the National Academy of Sciences 117 (28), 16567-16578, 2020 | 29 | 2020 |
| Exome sequencing identifies POU4F3 as the causative gene for a large Chinese family with non-syndromic hearing loss XZ Cai, Y Li, L Xia, Y Peng, CF He, L Jiang, Y Feng, K Xia, XZ Liu, LY Mei, ... Journal of human genetics 62 (2), 317-320, 2017 | 27 | 2017 |
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