Selected Publications

Year 2023

  • Li, X., Quick, C., Zhou, H., Gaynor, S., Liu, Y., Chen, H., Selvaraj, M., Sun, R., Dey, R., Arnett D., Bielak, L., Bis, J., Blangero, J., Boerwinkle, E., Bowden, D., Brody, J., Cade, B., Correa, A., Cupples, L.A., Curran, J., De Vries, P., Duggirala, R., Freedman, B., Goring, H., Guo, X., Haessler, J., Kalyani, R., Kooperberg, C., Kral, B., Lange, L., Manichaikul, A., Martin, L., McGarvey, S., Mitchell, B., Montasser, M., Morrison, A., Naseri, T., O¡¯Connell, J., Palmer, N., Peyser, P., Psaty, B., Raffield, L., Redline, S., Reiner, A., Reupena, M., Rice, K., Rich, S., Sitlani, C., Smith, J., Taylor, K., Vasan, R., Wilson, J., Willer, C., Yanek, L., Zhao, W., NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, TOPMed Lipids Working Group, Rotter, J., Natarajan, P., Peloso, G., Li, Z., Lin, X. (2023) Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies.Nature Genetics 55(1), 154-164
  • Zhou, H., Arapoglou, T., Li, X., Li, Z., Zheng, X., Moore, J., Asok, A., Kumar, S., Blue, E.E., Buyske, S., Cox, N., Felsenfeld, A., Gerstein, M., Kenny, E., Li, B., Matise, T., Philippakis, A., Rehm, H.L., Sofia, H.J., Snyder, G., NHGRI Genome Sequencing Program Variant Functional Annotation Working Group, Weng, Z., Neale, B., Sunyaev, S.R., Lin, X. (2023). FAVOR: functional annotation of variants online resource and annotator for variation across the human genome.Nucleic Acids Research 51(D1), D1300-D1311

Year 2022

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