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Author

Chunyan Mo

Observed names: Chun-Yan Mo, Chun-yan Mo, Mo Chunyan
Observed institutions: Leiden University Medical Center, Amsterdam UMC Location University of Amsterdam, Sanquin, Yale University, Guangzhou Blood Center, University of Amsterdam, Guangzhou Medical University
ORCID: 0009-0003-4943-9524
Observed ORCID: 0009-0003-4943-9524
OpenAlex ID: A5112516610
H 435‐containing immunoglobulin G 3 allotypes are transported efficiently across the human placenta: implications for alloantibody‐mediated diseases of the newborn
2013 · Helga Einarsdottir, Yanli Ji, et al. · Transfusion · 53
Hemolytic disease of the fetus and newborn due to alloanti‐M: three Chinese case reports and a review of the literature
2018 · Si Li, Chunyan Mo, et al. · Transfusion · 35
The summary of FUT 1 and FUT 2 genotyping analysis in C hinese para‐ B ombay individuals including additional nine probands from G uangzhou in C hina
2013 · Guangping Luo, Ling Wei, et al. · Transfusion · 25
Hyporegenerative anemia in anti‐M‐associated hemolytic disease of the fetus
2021 · Si Li, Zhiming He, et al. · Transfusion · 14
Transfused platelets enhance alloimmune responses to transfused KEL-expressing red blood cells in a murine model.
2019 · David J Madrid, Manjula Santhanakrishnan, et al. · Blood transfusion · 7
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Identification of a novel P1PK allele (A4GALT*c.1‐504_1044del1548) in two Chinese sisters with a history of recurrent spontaneous abortion
2022 · Shuangshuang Jia, Si Li, et al. · Transfusion · 4
A case of hyperhaemolysis syndrome in a pregnant Chinese woman with β‐thalassemia during perinatal transfusion
2020 · Yuanjun Wu, Yanli Ji, et al. · Transfusion Medicine · 4
[Serological and genetic study of a pedigree featuring a rare p phenotype].
2012 · Ling Wei, Yan-li Ji, et al. · PubMed · 4
Identification of a novel A4GALT * 299A allele associated with the rare p phenotype in one Chinese family
2024 · Chunyan Mo, Shuangshuang Jia, et al. · Transfusion · 2
[Anti-Mur screening and Mur antigen genotyping of voluntary blood donors in Guangzhou].
2012 · Ling Wei, Yanli Ji, et al. · PubMed · 2
Identification of a novel FUT1 variant ( c.696G>C , p.Trp232Cys ) associated with the para‐Bombay phenotype in a Chinese blood donor
2026 · Jing Xu, Chunyan Mo, et al. · Transfusion · 1
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[Identification of a novel ABO B(A)07 allele].
2017 · Hong Luo, Guangping Luo, et al. · PubMed · 1
An RHD gene variant, common in southern Chinese Han, involves a short 688 bp deletion and a long 21.8 kb insertion in the RHD exon 10 non-coding region, affecting the accuracy of red cell genotyping
2026 · Jizhi Wen, Fei He, et al. · Journal of Translational Medicine
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[Establishment of a genotyping method for the junior blood group and identification of a rare blood type with partial DVI.3 and Jr(a-)].
2024 · Shuang Liang, Chunyan Mo, et al. · PubMed
[Correlation between special A/O genotype and the O phenotype].
2019 · Hong Luo, Runqing Zhang, et al. · PubMed
特殊なa/o遺伝子型とo表現型の関係【jst・京大機械翻訳】
2019 · Luo Hong, Runqing Zhang, et al. · Zhonghua yixue yichuanxue zazhi
[Phenotype Types and Genetic Mutation Mechanism of Rhesus D Variant Individuals].
2017 · Hong Luo, Ji-Zhi Wen, et al. · PubMed
Application of multiple ligation-dependent probe amplification in allele detection of 2 cases with rare Rh partial D individuals
2015 · Hong Luo, Runqing Zhang, et al. · Guoji shuxue ji xueyexue zazhi
[High-throughput genotyping multiplex ligation-dependent probe amplification for assisting diagnosis in a case of anti-Di(a)-induced severe hemolytic disease of the newborn].
2012 · Yanli Ji, Chunyan Mo, et al. · PubMed
Works count: 19
Citation count: 152
H-index: 5
I10-index: 4
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