Lopez GH - Search Results

1

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.

McGowan EC, O'Brien H, Sarri ME, Lopez GH, Daly JJ, Flower RL, Gardener GJ, Hyland CA. McGowan EC, et al. Among authors: lopez gh. Br J Haematol. 2024 Feb;204(2):694-705. doi: 10.1111/bjh.19197. Epub 2023 Nov 20. Br J Haematol. 2024. PMID: 37984869

2

Molecular typing for the Indian blood group associated 252G>C single nucleotide polymorphism in a selected cohort of Australian blood donors.

Lopez GH, Mcbean RS, Wilson B, Irwin DL, Liew YW, Hyland CA, Flower RL. Lopez GH, et al. Blood Transfus. 2015 Jan;13(1):78-85. doi: 10.2450/2014.0336-13. Epub 2014 Jun 5. Blood Transfus. 2015. PMID: 24960658 Free PMC article.

3

A novel FY*A allele with the 265T and 298A SNPs formerly associated exclusively with the FY*B allele and weak Fy(b) antigen expression: implication for genotyping interpretative algorithms.

Lopez GH, Condon JA, Wilson B, Martin JR, Liew YW, Flower RL, Hyland CA. Lopez GH, et al. Vox Sang. 2015 Jan;108(1):52-7. doi: 10.1111/vox.12185. Epub 2014 Aug 4. Vox Sang. 2015. PMID: 25092430

4

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 sequencing in genotyping algorithms.

Lopez GH, Morrison J, Condon JA, Wilson B, Martin JR, Liew YW, Flower RL, Hyland CA. Lopez GH, et al. Vox Sang. 2015 Oct;109(3):296-303. doi: 10.1111/vox.12273. Epub 2015 Apr 20. Vox Sang. 2015. PMID: 25900316

5

Identification of six new RHCE variant alleles in individuals of diverse racial origin.

Goldman M, Cemborain A, Cote J, El Hamss R, Flower RL, Garaizar A, Garcia-Sanchez F, Hyland CA, Kalvelage M, Londero D, Lopez GH, Revelli N, Rodriguez-Wilhelmi P, Villa A, Ochoa-Garay G. Goldman M, et al. Among authors: lopez gh. Transfusion. 2016 Jan;56(1):244-8. doi: 10.1111/trf.13357. Epub 2015 Oct 4. Transfusion. 2016. PMID: 26435076

6

GYP*Kip, a novel GYP(B-A-B) hybrid allele, encoding the MNS48 (KIPP) antigen.

Lopez GH, Wei L, Ji Y, Condon JA, Luo G, Hyland CA, Flower RL. Lopez GH, et al. Transfusion. 2016 Feb;56(2):539-41. doi: 10.1111/trf.13450. Epub 2015 Dec 31. Transfusion. 2016. PMID: 26718482 No abstract available.

7

A D+ blood donor with a novel RHD*D-CE(5-6)-D gene variant exhibits the low-frequency antigen RH23 (D(W) ) characteristic of the partial DVa phenotype.

Lopez GH, McGowan EC, McGrath KA, Abaca-Cleopas ME, Schoeman EM, Millard GM, O'Brien H, Liew YW, Flower RL, Hyland CA. Lopez GH, et al. Transfusion. 2016 Sep;56(9):2322-30. doi: 10.1111/trf.13713. Epub 2016 Jul 8. Transfusion. 2016. PMID: 27390888

8

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 Spectrometry.

Wei L, Lopez GH, Ji Y, Condon JA, Irwin DL, Luo G, Hyland CA, Flower RL. Wei L, et al. Among authors: lopez gh. Mol Biotechnol. 2016 Oct;58(10):665-671. doi: 10.1007/s12033-016-9966-6. Mol Biotechnol. 2016. PMID: 27435823

9

An alloantibody in a homozygous GYP*Mur individual defines JENU (MNS49), a new high-frequency antigen on glycophorin B.

Lopez GH, Wilson B, Liew YW, Kupatawintu P, Emthip M, Hyland CA, Flower RL. Lopez GH, et al. Transfusion. 2017 Mar;57(3):716-717. doi: 10.1111/trf.13952. Epub 2016 Dec 4. Transfusion. 2017. PMID: 27917500 No abstract available.

10

Diverse and novel RHD variants in Australian blood donors with a weak D phenotype: implication for transfusion management.

McGowan EC, Lopez GH, Knauth CM, Liew YW, Condon JA, Ramadi L, Parsons K, Turner EM, Flower RL, Hyland CA. McGowan EC, et al. Among authors: lopez gh. Vox Sang. 2017 Apr;112(3):279-287. doi: 10.1111/vox.12488. Epub 2017 Feb 20. Vox Sang. 2017. PMID: 28220510

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