Xiong, Yong

Accelerating Novel Candidate Gene Discovery in Neurogenetic Disorders via Whole-Exome Sequencing of Prescreened Multiplex Consanguineous Families

Alazami, A. M., Patel, N., Shamseldin, H. E., Anazi, S., Al-Dosari, M. S., Alzahrani, F., Hijazi, H., Alshammari, M., Aldahmesh, M. A., Salih, M. A., et al. (2015) · Cell Reports

Genomics and Rare DiseasesHereditary Neurological Disorders

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BRCA1–BARD1 promotes RAD51-mediated homologous DNA pairing

Zhao, W., Steinfeld, J. B., Liang, F., Chen, X., Maranon, D. G., Jian Ma, C., Kwon, Y., Rao, T., Wang, W., Sheng, C., et al. (2017) · Nature

DNA Repair MechanismsBRCA gene mutations in cancer

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Visualizing the translation landscape in human cells at high resolution

Zheng, W., Zhang, Y., Wang, J., Wang, S., Chai, P., Bailey, E. J., Guo, W., Devarkar, S. C., Wu, S., Lin, J., et al. (2024) · Nature Communications

RNA and protein synthesis mechanismsAdvanced Electron Microscopy Techniques and Applications

Cited by 32