Yu-Li Zhu (Yuli Zhu, YuLi Zhu)

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 12

Top Topics

Bioinformatics Analysis

Top Venues

This page only lists publications with an associated author ORCID identifier.

Publications

Yu-Li Zhu, Lihong Jiang, Zhi-Hui Feng, Aiying Wang
Novel RHD allele with c.487-2A>G (IVS3-2A>G) variant causing RhD negative phenotype. Transfusion (2024)
Run An, Zhi Jiang, Yu-Li Zhu, Shuxian Jiao, Shutao Pang
Genomic full-length sequence of the HLA-C*07:154 allele was identified by full-length group-specific sequencing. HLA 103 (2) (2024)
Run An, Zhi Jiang, Yu-Li Zhu, Shuxian Jiao, Shutao Pang
Genomic full-length sequence of the HLA-C*07:154 allele was identified by full-length group-specific sequencing. HLA 103 (2) (2024)
Yu-Li Zhu, Caixia Qiu, Yulin Wang, Zhi-Hui Feng
The c.254C>A change (p.Ala85Glu) in RHD causing a weak D phenotype. Transfusion (2024)
Yu-Li Zhu, Caixia Qiu, Yulin Wang, Zhi-Hui Feng
The c.254C>A change (p.Ala85Glu) in RHD causing a weak D phenotype. Transfusion 64 (8) (2024)
Yu-Li Zhu, Caixia Qiu, Yulin Wang, Zhi-Hui Feng
The c.254C>A change (p.Ala85Glu) in RHD causing a weak D phenotype. Transfusion 64 (8) (2024)
Yu-Li Zhu, Caixia Qiu, Yulin Wang, Zhi-Hui Feng
The c.254C>A change (p.Ala85Glu) in RHD causing a weak D phenotype. Transfusion 64 (8) (2024)
Yu-Li Zhu, Zhen Wang, Zhihui Feng, Shuhong Yu
Identification of a novel weak A allele with c.27delC in a Chinese individual. Transfusion (2023)
Yu-Li Zhu, Shu-Xian Jiao, Peng Chen, Shu-Tao Pang
A novel HLA-C*07 allele, HLA-C*07:1024, was identified in a Chinese individual. HLA (2022)
Bin Han, Jianfang Zhu, Yu-Li Zhu, Zhi-Hui Feng, Shaoqiang Zhang
A novel FUT1 variant allele was identified in a Chinese Para-Bombay individual. Transfusion (2021)
Yu-Li Zhu, Bin Du, Xiaomeng Huang, Zhihui Feng, Yingying Wang
Identification of a novel A allele with c.792_794delCTA in a Chinese individual. Transfusion 61 (11) (2021)
Yu-Li Zhu, Li Liu, Zhihui Feng, Yong Dong
A novel O allele in the ABO blood group system, a nine-base-pair deletion in an ABO*O.01.01 allele. Transfusion 61 (1) (2020)