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Implications of dengue outbreaks for blood supply, Australia

Emerging infectious diseases, 2013-05, Vol.19 (5), p.787-789

2013

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RBCeq: A robust and scalable algorithm for accurate genetic blood typing

EBioMedicine, 2022-02, Vol.76, p.103759-103759, Article 103759

2022

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Frequency of Mia (MNS7) and Classification of Mia-Positive Hybrid Glycophorins in an Australian Blood Donor Population

Transfusion medicine and hemotherapy, 2020-07, Vol.47 (4), p.279-287

2020

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Approaches to Determination of a Full Profile of Blood Group Genotypes: Single Nucleotide Variant Mapping and Massively Parallel Sequencing

Computational and structural biotechnology journal, 2014-09, Vol.11 (19), p.147-151

2014

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Novel or not? Reference alleles, genes, and genomes to unmask the true nature of the ABOAW.10 allele associated with weak A phenotype

Transfusion (Philadelphia, Pa.), 2022-04, Vol.62 (4), p.721-724

2022

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Developments beyond blood group serology in the genomics era

British journal of haematology, 2019-03, Vol.184 (6), p.897-911

2019

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Predicting anti-RhD titers in donors: Boostering response and decline rates are personal

PloS one, 2018-04, Vol.13 (4), p.e0196382-e0196382

2018

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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, 2024-02, Vol.204 (2), p.694-705

2024

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Evaluation of targeted exome sequencing for 28 protein‐based blood group systems, including the homologous gene systems, for blood group genotyping

Transfusion (Philadelphia, Pa.), 2017-04, Vol.57 (4), p.1078-1088

2017

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Non-invasive prenatal testing for management of haemolytic disease of the fetus and newborn induced by maternal alloimmunisation

Transfusion and apheresis science, 2020-10, Vol.59 (5), p.102947-102947, Article 102947

2020

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A cold case of hemolytic disease of the fetus and newborn resolved by genomic sequencing and population studies to define a new antigen in the Rh system

Transfusion (Philadelphia, Pa.), 2024-06, Vol.64 (6), p.1171-1176

2024

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Recurrent pregnancy loss in a patient with anti-Rh17

Transfusion medicine (Oxford, England), 2024-02, Vol.34 (1), p.66-70

2024

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Hemolytic disease of the fetus and newborn caused by anti‐sD antibody in a GP.Mur/Mur Thai mother and review of the prevalence of sD in Thai blood donors

Transfusion (Philadelphia, Pa.), 2022-10, Vol.62 (10), p.2137-2142

2022

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Impact of transcription factors KLF1 and GATA1 on red blood cell antigen expression: a review

Immunohematology, 2024-04, Vol.40 (1), p.1

2024

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Comprehensive blood group antigen profile predictions for Western Desert Indigenous Australians from whole exome sequence data

Transfusion (Philadelphia, Pa.), 2019-02, Vol.59 (2), p.768-778

2019

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Genotyping analysis of MNS blood group GP(B‐A‐B) hybrid glycophorins in the Chinese Southern Han population using a high‐resolution melting assay

Transfusion (Philadelphia, Pa.), 2018-07, Vol.58 (7), p.1763-1771

2018

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Targeted exome sequencing defines novel and rare variants in complex blood group serology cases for a red blood cell reference laboratory setting

Transfusion (Philadelphia, Pa.), 2018-02, Vol.58 (2), p.284-293

2018

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A new high‐prevalence LW antigen detected by an antibody in an Indigenous Australian homozygous for LWA c.309C>A variant

Vox sanguinis, 2022-07, Vol.117 (7), p.958-965

2022

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An alloantibody in a homozygous GYPMur individual defines JENU (MNS49), a new high‐frequency antigen on glycophorin B

Transfusion (Philadelphia, Pa.), 2017-03, Vol.57 (3), p.716-717

2017

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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 RHD148+1T (RHD01EL.31)

Transfusion (Philadelphia, Pa.), 2018-10, Vol.58 (10), p.2260-2264

2018

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Noninvasive fetal RHD genotyping of RhD negative pregnant women for targeted anti‐D therapy in Australia: A cost‐effectiveness analysis

Prenatal diagnosis, 2017-12, Vol.37 (12), p.1245-1253

2017

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Anti‐D in a mother, hemizygous for the variant RHDDNB gene, associated with hemolytic disease of the fetus and newborn

Transfusion (Philadelphia, Pa.), 2017-08, Vol.57 (8), p.1938-1943

2017

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Investigation of the variable In(Lu) phenotype caused by KLF1 variants

Transfusion (Philadelphia, Pa.), 2018-10, Vol.58 (10), p.2414-2420

2018

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The RHD(1227G>A) DEL-associated allele is the most prevalent DEL allele in Australian D- blood donors with C+ and/or E+ phenotypes

Transfusion (Philadelphia, Pa.), 2014-11, Vol.54 (11), p.2931-2940

2014

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Implications of dengue outbreaks for blood supply, Australia

RBCeq: A robust and scalable algorithm for accurate genetic blood typing

Frequency of Mia (MNS7) and Classification of Mia-Positive Hybrid Glycophorins in an Australian Blood Donor Population

Approaches to Determination of a Full Profile of Blood Group Genotypes: Single Nucleotide Variant Mapping and Massively Parallel Sequencing

Novel or not? Reference alleles, genes, and genomes to unmask the true nature of the ABOAW.10 allele associated with weak A phenotype

Developments beyond blood group serology in the genomics era

Predicting anti-RhD titers in donors: Boostering response and decline rates are personal

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

Evaluation of targeted exome sequencing for 28 protein‐based blood group systems, including the homologous gene systems, for blood group genotyping

Non-invasive prenatal testing for management of haemolytic disease of the fetus and newborn induced by maternal alloimmunisation

A cold case of hemolytic disease of the fetus and newborn resolved by genomic sequencing and population studies to define a new antigen in the Rh system

Recurrent pregnancy loss in a patient with anti-Rh17

Hemolytic disease of the fetus and newborn caused by anti‐sD antibody in a GP.Mur/Mur Thai mother and review of the prevalence of sD in Thai blood donors

Impact of transcription factors KLF1 and GATA1 on red blood cell antigen expression: a review

Comprehensive blood group antigen profile predictions for Western Desert Indigenous Australians from whole exome sequence data

International Society of Blood Transfusion Working Party on Red Cell Immunogenetics and Blood Group Terminology Report of Basel and three virtual business meetings: Update on blood group systems

Genotyping analysis of MNS blood group GP(B‐A‐B) hybrid glycophorins in the Chinese Southern Han population using a high‐resolution melting assay

Targeted exome sequencing defines novel and rare variants in complex blood group serology cases for a red blood cell reference laboratory setting

A new high‐prevalence LW antigen detected by an antibody in an Indigenous Australian homozygous for LWA c.309C>A variant

An alloantibody in a homozygous GYPMur individual defines JENU (MNS49), a new high‐frequency antigen on glycophorin B

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 RHD148+1T (RHD01EL.31)

Noninvasive fetal RHD genotyping of RhD negative pregnant women for targeted anti‐D therapy in Australia: A cost‐effectiveness analysis

Anti‐D in a mother, hemizygous for the variant RHDDNB gene, associated with hemolytic disease of the fetus and newborn

Investigation of the variable In(Lu) phenotype caused by KLF1 variants

The RHD(1227G>A) DEL-associated allele is the most prevalent DEL allele in Australian D- blood donors with C+ and/or E+ phenotypes

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