Eunike C. McGowan

Publications by Year

Research Areas

Blood groups and transfusion, Erythrocyte Function and Pathophysiology, Hemoglobinopathies and Related Disorders, Prenatal Screening and Diagnostics, Blood disorders and treatments

Most-Cited Works

• → Evaluation of targeted exome sequencing for 28 protein‐based blood group systems, including the homologous gene systems, for blood group genotyping(2017)72 cited
• → Targeted exome sequencing defines novel and rare variants in complex blood group serology cases for a red blood cell reference laboratory setting(2017)42 cited
• → Diverse and novel RHD variants in Australian blood donors with a weak D phenotype: implication for transfusion management(2017)26 cited
• → Non-invasive fetal RHD genotyping for RhD negative women stratified into RHD gene deletion or variant groups: comparative accuracy using two blood collection tube types(2017)25 cited
• → A proposed new low‐frequency antigen in the Augustine blood group system associated with a severe case of hemolytic disease of the fetus and newborn(2018)12 cited
• → A DEL phenotype attributed to RHD Exon 9 sequence deletion: slipped‐strand mispairing and blood group polymorphisms(2017)11 cited
• → Severe hemolytic disease of the fetus and newborn due to allo‐anti‐D in a patient with a partial DEL phenotype arising from the variant allele described as RHD*148+1T (RHD*01EL.31)(2018)10 cited
• → A D+ blood donor with a novel RHD*D‐CE(5‐6)‐D gene variant exhibits the low‐frequency antigen RH23 (DW) characteristic of the partial DVa phenotype(2016)9 cited
• → A Bioinformatically Initiated Approach to Evaluate GATA1 Regulatory Regions in Samples with Weak D, Del, or D– Phenotypes Despite Normal <i>RHD</i> Exons(2024)8 cited
• → Epigenetic dissection of human blood group genes reveals regulatory elements and detailed characteristics of KEL and four other loci(2024)6 cited