Wenhui Ma (W-H Ma)

Publication Activity (10 Years)

Years Active: 2017-2022
Publications (10 Years): 9

Top Topics

Genome Wide Association Study

Intellectual Disability

Top Venues

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

Publications

Wenhui Ma, Wei Zhao, Zhihui Feng, Xiangmao Bu
Identification of a novel a variant at the ABO locus in Chinese Han individuals with a A2 phenotype. Transfusion (2022)
Wenhui Ma, Wei Zhao, Zhihui Feng, Xiangmao Bu
Identification of a novel a variant at the ABO locus in Chinese Han individuals with a A2 phenotype. Transfusion 63 (1) (2022)
Wenhui Ma, Wei Zhao, Zhihui Feng, Xiangmao Bu
Identification of a novel a variant at the ABO locus in Chinese Han individuals with a A2 phenotype. Transfusion 63 (1) (2022)
Wenhui Ma, Wei Zhao, Zhihui Feng, Xiangmao Bu
Identification of a novel a variant at the ABO locus in Chinese Han individuals with a A2 phenotype. Transfusion 63 (1) (2022)
Wenhui Ma, Wei Zhao, Zhihui Feng, Xiangmao Bu
Identification of a novel a variant at the ABO locus in Chinese Han individuals with a A2 phenotype. Transfusion 63 (1) (2022)
Shuhong Yu, Zhi-Hui Feng, Wenhui Ma, Ping Yan
A new missense mutation c.692C>A caused a weak Ael phenotype in a Chinese individual. Transfusion 59 (10) (2020)
Hongjuan Lyu, Shuxian Jiao, Wenhui Ma, Bin Hu
A novel RHD allele caused by c.739 G> C mutation was identified in a Chinese individual. Transfusion 61 (1) (2020)
Wenhui Ma, Shuchao Zhang, Shuxian Jiao, Zhihui Feng
A novel A allele with c.287G > T mutation identified in a Chinese family. Transfusion 60 (7) (2020)
Z-H Feng, Z-X Yang, Wenhui Ma, S-T Pang
A novel HLA class II allele, HLA-DRB1*04:01:17, identified in a Chinese volunteer donor for China Marrow Donor Program. HLA 91 (1) (2017)