Eunike C McGowan (Eunike McGowan)

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 11

Top Topics

African American

Pluripotent Stem Cells

Top Venues

Proceedings of the National Academy of Sciences of the United States of America

British journal of haematology

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

Publications

Antoine Lewin, Eunike C McGowan, Jian Ou-Yang, Lilian Antwi Boateng, Carla Luana Dinardo, Saikat Mandal, Nour Almozain, Jannison Ribeiro, Syeldy Langi Sasongko, null null
The future of blood services amid a tight balance between the supply and demand of blood products: Perspectives from the ISBT Young Professional Council. Vox sanguinis 119 (5) (2024)
Eunike C McGowan, Jill R Storry, Martin L Olsson
An intronic polymorphism associated with 2,3-bisphosphoglycerate levels in human red cells is linked to expression of RhCE blood groups. Proceedings of the National Academy of Sciences of the United States of America 121 (36) (2024)
Antoine Lewin, Eunike C McGowan, Jian Ou-Yang, Lilian Antwi Boateng, Carla Luana Dinardo, Saikat Mandal, Nour Almozain, Jannison Ribeiro, Syeldy Langi Sasongko, null null
The future of blood services amid a tight balance between the supply and demand of blood products: Perspectives from the ISBT Young Professional Council. Vox sanguinis (2024)
Eunike C McGowan, Jill R Storry, Martin L Olsson
An intronic polymorphism associated with 2,3-bisphosphoglycerate levels in human red cells is linked to expression of RhCE blood groups. Proceedings of the National Academy of Sciences of the United States of America 121 (36) (2024)
Antoine Lewin, Eunike C McGowan, Jian Ou-Yang, Lilian Antwi Boateng, Carla Luana Dinardo, Saikat Mandal, Nour Almozain, Jannison Ribeiro, Syeldy Langi Sasongko, null null
The future of blood services amid a tight balance between the supply and demand of blood products: Perspectives from the ISBT Young Professional Council. Vox sanguinis 119 (5) (2024)
Eunike C McGowan, Helen O'Brien, Mia E Sarri, Genghis H Lopez, James J Daly, Robert L P Flower, Glenn J Gardener, Catherine A Hyland
Feasibility for non-invasive prenatal fetal blood group and platelet genotyping by massively parallel sequencing: A single test system for multiple atypical red cell, platelet and quality control markers. British journal of haematology (2023)
Elona Turley, Eunike C McGowan, Catherine A Hyland, Elizna M Schoeman, Robert L Flower, Amanda Skoll, Marie-France Delisle, Tanya Nelson, Gwen Clarke, Nicholas Au
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). Transfusion 58 (10) (2018)
Glenda M Millard, Eunike C McGowan, Brett Wilson, Jacqui R Martin, Michaela Spooner, Scott Morris, Ray Farley, Simon James, Yew-Wah Liew, Elizna M Schoeman, Melinda M Dean, Robert L Flower, Catherine A Hyland, Tanya Powley, David Roxby
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. Transfusion 58 (5) (2018)
Elizna M Schoeman, Eileen V Roulis, Yew-Wah Liew, Jacqueline R Martin, Tanya Powley, Brett Wilson, Glenda M Millard, Eunike C McGowan, Genghis H Lopez, Helen O'Brien, Jennifer A Condon, Robert L P Flower, Catherine A Hyland
Targeted exome sequencing defines novel and rare variants in complex blood group serology cases for a red blood cell reference laboratory setting. Transfusion 58 (2) (2017)
Genghis H Lopez, Eunike C McGowan, Jennifer A Condon, Elizna M Schoeman, Glenda M Millard, Helen O'Brien, Eileen V Roulis, Gorka Ochoa-Garay, Yew-Wah Liew, Robert L P Flower, Catherine A Hyland
Genotyping by sequencing defines independent novel RHD variants for an antenatal patient and a blood donor. Transfusion 57 (9) (2017)
Genghis H Lopez, Robyn M Turner, Eunike C McGowan, Elizna M Schoeman, Stacy A Scott, Helen O'Brien, Glenda M Millard, Eileen V Roulis, Amanda J Allen, Yew-Wah Liew, Robert L P Flower, Catherine A Hyland
A DEL phenotype attributed to RHD Exon 9 sequence deletion: slipped-strand mispairing and blood group polymorphisms. Transfusion 58 (3) (2017)