De novo genic mutations among a Chinese autism spectrum disorder cohort T Wang, H Guo, B Xiong, HAF Stessman, H Wu, BP Coe, TN Turner, Y Liu, ... Nature communications 7 (1), 13316, 2016 | 396 | 2016 |
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 | 178 | 2020 |
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 | 152 | 2019 |
Inherited and multiple de novo mutations in autism/developmental delay risk genes suggest a multifactorial model H Guo, T Wang, H Wu, M Long, BP Coe, H Li, G Xun, J Ou, B Chen, ... Molecular autism 9, 1-12, 2018 | 152 | 2018 |
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 | 127 | 2014 |
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 | 80 | 2015 |
Genome-wide copy number variation analysis in a Chinese autism spectrum disorder cohort H Guo, Y Peng, Z Hu, Y Li, G Xun, J Ou, L Sun, Z Xiong, Y Liu, T Wang, ... Scientific reports 7 (1), 44155, 2017 | 70 | 2017 |
Gene4Denovo: an integrated database and analytic platform for de novo mutations in humans G Zhao, K Li, B Li, Z Wang, Z Fang, X Wang, Y Zhang, T Luo, Q Zhou, ... Nucleic acids research 48 (D1), D913-D926, 2020 | 69 | 2020 |
Mutation analysis of the NRXN1 gene in a Chinese autism cohort Y Liu, Z Hu, G Xun, Y Peng, L Lu, X Xu, Z Xiong, L Xia, D Liu, W Li, J Zhao, ... Journal of psychiatric research 46 (5), 630-634, 2012 | 52 | 2012 |
RTP4 inhibits IFN-I response and enhances experimental cerebral malaria and neuropathology X He, AW Ashbrook, Y Du, J Wu, HH Hoffmann, C Zhang, L Xia, YC Peng, ... Proceedings of the National Academy of Sciences 117 (32), 19465-19474, 2020 | 48 | 2020 |
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 | 46 | 2020 |
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 | 35 | 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 |
New ZNF644 mutations identified in patients with high myopia X Xiang, T Wang, P Tong, Y Li, H Guo, A Wan, L Xia, Y Liu, Y Li, Q Tian, ... Molecular Vision 20, 939, 2014 | 23 | 2014 |
Detection of host pathways universally inhibited after Plasmodium yoelii infection for immune intervention L Xia, J Wu, S Pattaradilokrat, K Tumas, X He, Y Peng, R Huang, ... Scientific Reports 8 (1), 15280, 2018 | 22 | 2018 |
Biallelic loss-of-function variants in NEMF cause central nervous system impairment and axonal polyneuropathy A Ahmed, M Wang, G Bergant, R Maroofian, R Zhao, M Alfadhel, ... Human Genetics 140, 579-592, 2021 | 20 | 2021 |
Genome‐wide association analysis of autism identified multiple loci that have been reported as strong signals for neuropsychiatric disorders L Xia, J Ou, K Li, H Guo, Z Hu, T Bai, J Zhao, K Xia, F Zhang Autism Research 13 (3), 382-396, 2020 | 19 | 2020 |
Performance comparison of computational methods for the prediction of the function and pathogenicity of non-coding variants Z Wang, G Zhao, B Li, Z Fang, Q Chen, X Wang, T Luo, Y Wang, Q Zhou, ... Genomics, Proteomics & Bioinformatics 21 (3), 649-661, 2023 | 17 | 2023 |
Plasmodium yoelii erythrocyte-binding-like protein modulates host cell membrane structure, immunity, and disease severity Y Peng, Y Qi, C Zhang, X Yao, J Wu, S Pattaradilokrat, L Xia, KC Tumas, ... MBio 11 (1), 10.1128/mbio. 02995-19, 2020 | 17 | 2020 |
GPCards: An integrated database of genotype–phenotype correlations in human genetic diseases B Li, Z Wang, Q Chen, K Li, X Wang, Y Wang, Q Zeng, Y Han, B Lu, ... Computational and Structural Biotechnology Journal 19, 1603-1611, 2021 | 15 | 2021 |