Wilson B - Search Results

1

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. Among authors: wilson b. Vox Sang. 2015 Jan;108(1):52-7. doi: 10.1111/vox.12185. Epub 2014 Aug 4. Vox Sang. 2015. PMID: 25092430

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. Among authors: wilson b. 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

Quantitation of Lan antigen in Lan+, Lan+(w) and Lan- phenotypes.

McBean RS, Wilson B, Liew YW, Hyland CA, Flower RL. McBean RS, et al. Among authors: wilson b. Blood Transfus. 2015 Oct;13(4):662-5. doi: 10.2450/2015.0262-14. Epub 2015 Feb 26. Blood Transfus. 2015. PMID: 25761317 Free PMC article. No abstract available.

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. Among authors: wilson b. Vox Sang. 2015 Oct;109(3):296-303. doi: 10.1111/vox.12273. Epub 2015 Apr 20. Vox Sang. 2015. PMID: 25900316

5

Genotyping confirms inheritance of the rare At(a-) type in a case of haemolytic disease of the newborn.

McBean R, Liew YW, Wilson B, Kupatawintu P, Emthip M, Hyland C, Flower R. McBean R, et al. Among authors: wilson b. J Pathol Clin Res. 2015 Dec 11;2(1):53-5. doi: 10.1002/cjp2.33. eCollection 2016 Jan. J Pathol Clin Res. 2015. PMID: 27499913 Free PMC article.

6

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. Among authors: wilson b. Transfusion. 2017 Mar;57(3):716-717. doi: 10.1111/trf.13952. Epub 2016 Dec 4. Transfusion. 2017. PMID: 27917500 No abstract available.

7

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

Schoeman EM, Roulis EV, Liew YW, Martin JR, Powley T, Wilson B, Millard GM, McGowan EC, Lopez GH, O'Brien H, Condon JA, Flower RL, Hyland CA. Schoeman EM, et al. Among authors: wilson b. Transfusion. 2018 Feb;58(2):284-293. doi: 10.1111/trf.14393. Epub 2017 Nov 8. Transfusion. 2018. PMID: 29119571

8

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.

Millard GM, McGowan EC, Wilson B, Martin JR, Spooner M, Morris S, Farley R, James S, Liew YW, Schoeman EM, Dean MM, Flower RL, Hyland CA, Powley T, Roxby D. Millard GM, et al. Among authors: wilson b. Transfusion. 2018 May;58(5):1320-1322. doi: 10.1111/trf.14562. Epub 2018 Mar 5. Transfusion. 2018. PMID: 29504136 No abstract available.

9

Acute haemolytic reaction secondary to an ABO minor mismatched platelet transfusion from a group A blood donor.

Swain F, Daly J, Baidya S, Wilson B, Morrison J, Liew YW, Powley T, Jivan Y, Bryant S, Allen A, Crampton N. Swain F, et al. Among authors: wilson b. Transfus Med. 2019 Apr;29(2):133-135. doi: 10.1111/tme.12591. Epub 2019 Mar 21. Transfus Med. 2019. PMID: 30900358 No abstract available.

10

Frequency of Mi^a (MNS7) and Classification of Mi^a-Positive Hybrid Glycophorins in an Australian Blood Donor Population.

Lopez GH, Wilson B, Turner RM, Millard GM, Fraser NS, Roots NM, Liew YW, Hyland CA, Flower RL. Lopez GH, et al. Among authors: wilson b. Transfus Med Hemother. 2020 Jul;47(4):279-286. doi: 10.1159/000504026. Epub 2019 Nov 14. Transfus Med Hemother. 2020. PMID: 32884500 Free PMC article.

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