Mina Yang - Publications

Serum procalcitonin as an independent diagnostic markers of bacteremia in febrile patients with hematologic malignancies.

Journal: PloS one

Published: June 10, 2019

Development and Validation of a Novel Warfarin Dosing Algorithm for Korean Patients With VKORC1 1173C.

Journal: Annals of laboratory medicine

Published: April 19, 2019

EDTA Treatment for Overcoming the Prozone Effect and for Predicting C1q Binding in HLA Antibody Testing.

Journal: Annals of laboratory medicine

Published: January 04, 2019

Analysis of hematologic parameters of donors, patients, and granulocyte concentrates to predict successful granulocyte transfusion.

Journal: Blood research

Published: August 07, 2018

Transient loss of A1 phenotype in a patient with passenger lymphocyte syndrome after ABO minor incompatible liver transplantation: The first case report.

Journal: Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis

Published: July 03, 2018

Principles of Genetic Counseling in the Era of Next-Generation Sequencing.

Journal: Annals of laboratory medicine

Published: September 29, 2017

Comparative evaluation of the AdvanSure Mycobacteria GenoBlot assay and the GenoType Mycobacterium CM/AS assay for the identification of non-tuberculous mycobacteria.

Journal: Journal of medical microbiology

Published: December 01, 2016

Intrachromosomal amplification of chromosome 21 in Korean pediatric patients with B-cell precursor acute lymphoblastic leukemia in a single institution.

Journal: Blood research

Published: September 05, 2016

Laboratory Identification of Leptotrichia Species Isolated From Bacteremia Patients at a Single Institution.

Journal: Annals of laboratory medicine

Published: July 22, 2016

Evaluation of 16 genotype-guided Warfarin Dosing Algorithms in 310 Korean Patients Receiving Warfarin Treatment: Poor Prediction Performance in VKORC1 1173C Carriers.

Journal: Clinical therapeutics

Published: July 15, 2016

Clinical, biochemical and molecular characterization of Korean patients with mucolipidosis II/III and successful prenatal diagnosis.

Journal: Orphanet journal of rare diseases

Published: July 08, 2016

Novel Pathogenic Variant (c.580C>T) in the CPS1 Gene in a Newborn With Carbamoyl Phosphate Synthetase 1 Deficiency Identified by Whole Exome Sequencing.

Journal: Annals of laboratory medicine

Published: March 28, 2016