Yanling Ying - Publications

c.98 + 3A>G and c.155 + 1G>T splice-site variants in the ABO*B.01 allele lead to weak antigen expression in the Chinese individuals.

Journal: Frontiers in immunology

Published: November 05, 2025

Clinical and genetic analysis of an individual with Lan-negative rare blood group due to variant of ABCB6 gene

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: May 15, 2025

RH gene inversion-recombination as a major mechanism of the D phenotype in China.

Journal: Blood transfusion = Trasfusione del sangue

Published: May 04, 2025

Generation of Enucleated Erythrocytes From Lin-CD45-CD133+ Cells Isolated From Human Umbilical Cord Blood In Vitro.

Journal: Stem cells international

Published: August 27, 2024

Bacterial Analysis of the Whole Blood in Chinese Healthy Donors Using 16S rDNA-Targeted Metagenomic Sequencing.

Journal: The Canadian journal of infectious diseases & medical microbiology = Journal canadien des maladies infectieuses et de la microbiologie medicale

Published: July 15, 2024

Identification of a novel RHAG allele with a c.500A>G variation associated with Rhmod phenotype.

Journal: Transfusion

Published: June 11, 2024

Comprehensive Annotation of Complete ABO Alleles and Resolution of ABO Variants by an Improved Full-Length ABO Haplotype Sequencing.

Journal: Clinical chemistry

Published: May 29, 2024

Simultaneous high throughput genotyping of 36 blood group systems using NGS based on probe capture technology.

Journal: Heliyon

Published: April 10, 2024

Genetic and mechanistic evaluation of an individual with para-Bombay phenotype associated with a compound heterozygote comprising two novel FUT1 variants.

Journal: Blood transfusion = Trasfusione del sangue

Published: March 21, 2023

Full annotation of viral metagenomics in different components from Chinese blood donors using next-generation sequencing.

Journal: Blood transfusion = Trasfusione del sangue

Published: February 03, 2023

Study of the molecular characteristics of a Bweak phenotype due to a novel c.398T>C variant of the ABO gene

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: December 30, 2022

A case of McLeod syndrome caused by a nonsense variation c.942G>A in the XK gene: A case report.

Journal: Frontiers in genetics

Published: October 20, 2022