| Evaluation of targeted exome sequencing for 28 protein‐based blood group systems, including the homologous gene systems, for blood group genotyping EM Schoeman, GH Lopez, EC McGowan, GM Millard, H O'Brien, ... Transfusion 57 (4), 1078-1088, 2017 | 70 | 2017 |
| Clinical scale ex vivo manufacture of neutrophils from hematopoietic progenitor cells NE Timmins, E Palfreyman, F Marturana, S Dietmair, S Luikenga, G Lopez, ... Biotechnology and bioengineering 104 (4), 832-840, 2009 | 58 | 2009 |
| Targeted exome sequencing defines novel and rare variants in complex blood group serology cases for a red blood cell reference laboratory setting EM Schoeman, EV Roulis, YW Liew, JR Martin, T Powley, B Wilson, ... Transfusion 58 (2), 284-293, 2018 | 41 | 2018 |
| 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 CA Hyland, GM Millard, H O'Brien, EM Schoeman, GH Lopez, ... Pathology 49 (7), 757-764, 2017 | 36 | 2017 |
| Diverse and novel RHD variants in Australian blood donors with a weak D phenotype: implication for transfusion management EC McGowan, GH Lopez, CM Knauth, YW Liew, JA Condon, L Ramadi, ... Vox Sanguinis 112 (3), 279-287, 2017 | 26 | 2017 |
| Molecular typing for the Indian blood group associated 252G>C single nucleotide polymorphism in a selected cohort of Australian blood donors GH Lopez, RS McBean, B Wilson, DL Irwin, YW Liew, CA Hyland, ... Blood Transfusion 13 (1), 78, 2015 | 26 | 2015 |
| An alloantibody in a homozygous GYP*Mur individual defines JENU (MNS49), a new high‐frequency antigen on glycophorin B GH Lopez, B Wilson, YW Liew, P Kupatawintu, M Emthip, CA Hyland, ... Transfusion 57 (3), 716-717, 2017 | 24 | 2017 |
| A novel FY*A allele with the 265T and 298A SNPs formerly associated exclusively with the FY*B allele and weak Fyb antigen expression: implication for … GH Lopez, JA Condon, B Wilson, JR Martin, YW Liew, RL Flower, ... Vox Sanguinis 108 (1), 52-57, 2015 | 22 | 2015 |
| Duffy blood group phenotype–genotype correlations using high‐resolution melting analysis PCR and microarray reveal complex cases including a new null FY* A allele: The role for … GH Lopez, J Morrison, JA Condon, B Wilson, JR Martin, YW Liew, ... Vox Sanguinis 109 (3), 296-303, 2015 | 21 | 2015 |
| Glycophorins and the MNS blood group system: a narrative review GH Lopez, CA Hyland, RL Flower Ann Blood 2021;6:39, 2021 | 20 | 2021 |
| Frequency of Mia (MNS7) and Classification of Mia-Positive Hybrid Glycophorins in an Australian Blood Donor Population GH Lopez, B Wilson, RM Turner, GM Millard, NS Fraser, NM Roots, ... Transfusion Medicine and Hemotherapy 47 (4), 279-287, 2020 | 19 | 2020 |
| GYP*Kip, a novel GYP(B‐A‐B) hybrid allele, encoding the MNS48 (KIPP) antigen GH Lopez, L Wei, Y Ji, JA Condon, G Luo, CA Hyland, RL Flower Transfusion 56 (2), 539-541, 2016 | 19 | 2016 |
| Genotyping analysis of MNS blood group GP (B‐A‐B) hybrid glycophorins in the Chinese Southern Han population using a high‐resolution melting assay L Wei, GH Lopez, Y Zhang, J Wen, Z Wang, Y Fu, CA Hyland, RL Flower, ... Transfusion 58 (7), 1763-1771, 2018 | 17 | 2018 |
| A DEL phenotype attributed to RHD Exon 9 sequence deletion: slipped‐strand mispairing and blood group polymorphisms GH Lopez, RM Turner, EC McGowan, EM Schoeman, SA Scott, H O'Brien, ... Transfusion 58 (3), 685-691, 2018 | 14 | 2018 |
| Genotyping for Glycophorin GYP(B-A-B) Hybrid Genes Using a Single Nucleotide Polymorphism-Based Algorithm by Matrix-Assisted Laser Desorption/Ionisation, Time-of-Flight Mass … L Wei, GH Lopez, Y Ji, JA Condon, DL Irwin, G Luo, CA Hyland, ... Molecular biotechnology 58 (10), 665-671, 2016 | 13 | 2016 |
| Anti‐D in a mother, hemizygous for the variant RHD*DNB gene, associated with hemolytic disease of the fetus and newborn KM Quantock, GH Lopez, CA Hyland, YW Liew, RL Flower, FJ Niemann, ... Transfusion 57 (8), 1938-1943, 2017 | 12 | 2017 |
| 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 GH Lopez, EC McGowan, KA McGrath, ME Abaca‐Cleopas, ... Transfusion 56 (9), 2322-2330, 2016 | 11 | 2016 |
| Identification of six new RHCE variant alleles in individuals of diverse racial origin M Goldman, A Cemborain, J Cote, R El Hamss, RL Flower, A Garaizar, ... Transfusion 56 (1), 244-248, 2016 | 11 | 2016 |
| Genotyping by sequencing defines independent novel RHD variants for an antenatal patient and a blood donor GH Lopez, EC McGowan, JA Condon, EM Schoeman, GM Millard, ... Transfusion 57 (9), 2281-2283, 2017 | 8 | 2017 |
| A new high‐prevalence LW antigen detected by an antibody in an Indigenous Australian homozygous for LW*A c.309C>A variant GH Lopez, B Wilson, GM Millard, TL Cawthorne, DE Grey, EA Fong, ... Vox Sanguinis 117 (7), 958-965, 2022 | 6 | 2022 |
Catherine A HylandAustralian Red Cross Blood ServiceEmail được xác minh tại redcrossblood.org.au
