Yang MY, Zhong JD, Li X, Tian G, Bai WY, Fang YH, Qiu MC, Yuan CD, Yu CF, Li N, Yang JJ, Liu YH, Yu SH, Zhao WW, Liu JQ, Sun Y, Cong PK, Khederzadeh S, Zhao PP, Qian Y, Guan PL, Gu JX, Gai SR, Yi XJ, Tao JG, Chen X, Miao MM, Lei LX, Xu L, Xie SY, Li JC, Guo JF, Karasik D, Yang L, Tang BS, Huang F, Zheng HF. SEAD reference panel with 22,134 haplotypes boosts rare variant imputation and genome-wide association analysis in Asian populations. Nat Commun. 2024 Dec 30;15(1):10839.doi: 10.1038/s41467-024-55147-4.PMID: 39738056

Cong PK, Bai WY, Li JC, Yang MY, Khederzadeh S, Gai SR, Li N, Liu YH, Yu SH, Zhao WW, Liu JQ, Sun Y, Zhu XW, Zhao PP, Xia JW, Guan PL, Qian Y, Tao JG, Xu L, Tian G, Wang PY, Xie SY, Qiu MC, Liu KQ, Tang BS, Zheng HF. Genomic analyses of 10,376 individuals in the Westlake BioBank for Chinese (WBBC) pilot project. Nat Commun. 2022 May 26;13(1):2939. doi: 10.1038/s41467-022-30526-x. PMID: 35618720

Cong PK, Khederzadeh S, Yuan CD, Ma RJ, Zhang YY, Liu JQ, Yu SH, Xu L, Gao JH, Pan HX, Li JC, Xie SY, Liu KQ, Tang BS, Zheng HF. Identification of clinically actionable secondary genetic variants from whole-genome sequencing in a large-scale Chinese population. Clin Transl Med. 2022 May;12(5):e866. doi: 10.1002/ctm2.866. PMID: 35538921.

Zhu XW, Liu KQ, Wang PY, Liu JQ, Chen JY, Xu XJ, Xu JJ, Qiu MC, Sun Y, Liu C, Bai WY, Zhao PP, Xia J, Gai SR, Guan PL, Qian Y, Cong PK, Xie SY, Zheng HF. Cohort profile: the Westlake BioBank for Chinese (WBBC) pilot project. BMJ Open. 2021 Jun 28;11(6):e045564. doi: 10.1136/bmjopen-2020-045564. PMID: 34183340.

Bai WY, Zhu XW, Cong PK, Zhang XJ, Richards JB, Zheng HF. Genotype imputation and reference panel: a systematic evaluation on haplotype size and diversity. Brief Bioinform. 2019 Nov 6:bbz108. doi: 10.1093/bib/bbz108. Epub ahead of print. PMID: 32002535.

Full publications can be found here: https://scholar.google.com/citations?user=IO3IhW8AAAAJ&hl=en