Works matching AU Lopez, Genghis H.

Results: 21

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.

Published in:

Transfusion, 2024, v. 64, n. 6, p. 1171, doi. 10.1111/trf.17205

By:

Wilson, Brett;
Davison, Candice L.;
Lopez, Genghis H.;
Millard, Glenda M.;
Liew, Yew‐Wah;
Powley, Tanya;
Campbell, Tamika;
Jadhao, Sudhir S.;
Nagaraj, Shivashankar H.;
Perry, Maree;
Roulis, Eileen V.;
Toombs, Maree;
Irving, David O.;
Flower, Robert L.;
Hyland, Catherine A.

Publication type:

Article

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.

Published in:

2022

By:

Lopez, Genghis H.;
Emthip, Morakot;
Suwanwootichai, Ploymanee;
Millard, Glenda M.;
Wilson, Brett;
Onpuns, Sunisa;
Laemsri, Kanchana;
Chiewsilp, Pimol;
Flower, Robert L.;
Hyland, Catherine A.;
Liew, Yew‐Wah;
Liew, Yew-Wah

Publication type:

Case Study

Modified expression of the KEL2 (k) blood group antigen attributed to p.Leu196Val amino acid change three residues from the K/k antigen polymorphism site: implications for donor screening.

Published in:

2019

By:

Millard, Glenda M.;
Lopez, Genghis H.;
Turner, Elise M.;
Lizarazu, Maria E.;
Roots, Naomi M.;
Liew, Yew‐Wah;
Flower, Robert L.;
Hyland, Catherine A.;
Liew, Yew-Wah

Publication type:

journal article

A Bioinformatically Initiated Approach to Evaluate GATA1 Regulatory Regions in Samples with Weak D, Del, or D– Phenotypes Despite Normal RHD Exons.

Published in:

Transfusion Medicine & Hemotherapy, 2024, v. 51, n. 4, p. 252, doi. 10.1159/000538469

By:

McGowan, Eunike C.;
Wu, Ping Chun;
Hellberg, Åsa;
Lopez, Genghis H.;
Hyland, Catherine A.;
Olsson, Martin L.

Publication type:

Article

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

Published in:

Transfusion Medicine & Hemotherapy, 2020, v. 47, n. 4, p. 279, doi. 10.1159/000504026

By:

Lopez, Genghis H.;
Wilson, Brett;
Turner, Robyn M.;
Millard, Glenda M.;
Fraser, Nicole S.;
Roots, Naomi M.;
Liew, Yew-Wah;
Hyland, Catherine A.;
Flower, Robert L.

Publication type:

Article

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.

Published in:

British Journal of Haematology, 2024, v. 204, n. 2, p. 694, doi. 10.1111/bjh.19197

By:

McGowan, Eunike C.;
O'Brien, Helen;
Sarri, Mia E.;
Lopez, Genghis H.;
Daly, James J.;
Flower, Robert L.;
Gardener, Glenn J.;
Hyland, Catherine A.

Publication type:

Article

Application of targeted long-read sequencing on RHD gene structural variants.

Published in:

Australian Journal of Medical Science, 2024, v. 45, n. 2, p. 87

By:

Lopez, Genghis H.;
Sarri, Mia E.;
Flower, Robert L.;
Hyland, Catherine A.

Publication type:

Article

Recurrent pregnancy loss in a patient with anti‐Rh17.

Published in:

Transfusion Medicine, 2024, v. 34, n. 1, p. 66, doi. 10.1111/tme.13014

By:

Moiz, Bushra;
Salman, Muhammed;
Rasheed, Seher;
Qudus, Ruhul;
Millard, Glenda;
Hyland, Catherine A.;
Flower, Robert L.;
Wilson, Brett;
Turner, Robyn;
Lopez, Genghis H.;
Liew, Yew‐Wah

Publication type:

Article

Fatal haemolytic transfusion reaction due to anti‐Ena and identification of a novel GYPA c.295delG variant in a Thai family.

Published in:

Vox Sanguinis, 2022, v. 117, n. 11, p. 1327, doi. 10.1111/vox.13358

By:

Suwanwootichai, Ploymanee;
Lopez, Genghis H.;
Emthip, Morakot;
Wilson, Brett;
Millard, Glenda M.;
Onpuns, Sunisa;
Laemsri, Kanchana;
Bejrachandra, Sasitorn;
Liew, Yew‐Wah

Publication type:

Article

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

Published in:

Vox Sanguinis, 2022, v. 117, n. 7, p. 958, doi. 10.1111/vox.13276

By:

Lopez, Genghis H.;
Wilson, Brett;
Millard, Glenda M.;
Cawthorne, Tanya L.;
Grey, Dianne E.;
Fong, Elizabeth A.;
Flower, Robert L.;
Hyland, Catherine A.;
Liew, Yew‐Wah

Publication type:

Article

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

Published in:

2018

By:

Wei, Ling;
Lopez, Genghis H.;
Zhang, Yang;
Wen, Jizhi;
Wang, Zhen;
Fu, Yongshui;
Hyland, Catherine A.;
Flower, Robert L.;
Luo, Guangping;
Ji, Yanli

Publication type:

journal article

A DEL phenotype attributed to RHD Exon 9 sequence deletion: slipped-strand mispairing and blood group polymorphisms.

Published in:

2018

By:

Lopez, Genghis H.;
Turner, Robyn M.;
McGowan, Eunike C.;
Schoeman, Elizna M.;
Scott, Stacy A.;
O'Brien, Helen;
Millard, Glenda M.;
Roulis, Eileen V.;
Allen, Amanda J.;
Liew, Yew‐Wah;
Flower, Robert L.;
Hyland, Catherine A.;
O'Brien, Helen;
Liew, Yew-Wah

Publication type:

journal article

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

Published in:

2018

By:

Schoeman, Elizna M.;
Roulis, Eileen V.;
Liew, Yew‐Wah;
Martin, Jacqueline R.;
Powley, Tanya;
Wilson, Brett;
Millard, Glenda M.;
McGowan, Eunike C.;
Lopez, Genghis H.;
O'Brien, Helen;
Condon, Jennifer A.;
Flower, Robert L.;
Hyland, Catherine A.;
Liew, Yew-Wah;
O'Brien, Helen

Publication type:

journal article

Genotyping by sequencing defines independent novel RHD variants for an antenatal patient and a blood donor.

Published in:

2017

By:

Lopez, Genghis H.;
McGowan, Eunike C.;
Condon, Jennifer A.;
Schoeman, Elizna M.;
Millard, Glenda M.;
O'Brien, Helen;
Roulis, Eileen V.;
Ochoa‐Garay, Gorka;
Liew, Yew‐Wah;
Flower, Robert L.;
Hyland, Catherine A.

Publication type:

journal article

Anti-D in a mother, hemizygous for the variant RHD*DNB gene, associated with hemolytic disease of the fetus and newborn.

Published in:

2017

By:

Quantock, Kelli M.;
Lopez, Genghis H.;
Hyland, Catherine A.;
Liew, Yew‐Wah;
Flower, Robert L.;
Niemann, Frans J.;
Joyce, Arthur

Publication type:

Case Study

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

Published in:

2017

By:

Schoeman, Elizna M.;
Lopez, Genghis H.;
McGowan, Eunike C.;
Millard, Glenda M.;
O'Brien, Helen;
Roulis, Eileen V.;
Liew, Yew ‐ Wah;
Martin, Jacqueline R.;
McGrath, Kelli A.;
Powley, Tanya;
Flower, Robert L.;
Hyland, Catherine A.

Publication type:

journal article

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

Published in:

2017

By:

Lopez, Genghis H.;
Wilson, Brett;
Liew, Yew‐Wah;
Kupatawintu, Pawinee;
Emthip, Morakot;
Hyland, Catherine A.;
Flower, Robert L.

Publication type:

journal article

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.

Published in:

2016

By:

Lopez, Genghis H.;
McGowan, Eunike C.;
McGrath, Kelli A.;
Abaca‐Cleopas, Maria E.;
Schoeman, Elizna M.;
Millard, Glenda M.;
O'Brien, Helen;
Liew, Yew‐Wah;
Flower, Robert L.;
Hyland, Catherine A.

Publication type:

journal article

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

Published in:

2016

By:

Lopez, Genghis H.;
Wei, Ling;
Ji, Yanli;
Condon, Jennifer A.;
Luo, Guangping;
Hyland, Catherine A.;
Flower, Robert L.

Publication type:

journal article

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

Published in:

2016

By:

Goldman, Mindy;
Cemborain, Arantxa;
Cote, Jacqueline;
El Hamss, Rachid;
Flower, Robert L.;
Garaizar, Adirane;
Garcia‐Sanchez, Felix;
Hyland, Catherine A.;
Kalvelage, Monica;
Londero, Donatella;
Lopez, Genghis H.;
Revelli, Nicoletta;
Rodriguez‐Wilhelmi, Pablo;
Villa, Antonietta;
Ochoa‐Garay, Gorka

Publication type:

journal article

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

Published in:

Blood Transfusion (17232007), 2015, v. 13, n. 1, p. 78, doi. 10.2450/2014.0336-13

By:

Lopez, Genghis H.;
McBean, Rhiannon S.;
Wilson, Brett;
Irwin, Darryl L.;
Yew-Wah Liew;
Hyland, Catherine A.;
Flower, Robert L.

Publication type:

Article

Works matching AU Lopez, Genghis H.

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.

Hemolytic disease of the fetus and newborn caused by anti-s<sup>D</sup> antibody in a GP.Mur/Mur Thai mother and review of the prevalence of s<sup>D</sup> in Thai blood donors.

Modified expression of the KEL2 (k) blood group antigen attributed to p.Leu196Val amino acid change three residues from the K/k antigen polymorphism site: implications for donor screening.

A Bioinformatically Initiated Approach to Evaluate GATA1 Regulatory Regions in Samples with Weak D, Del, or D– Phenotypes Despite Normal RHD Exons.

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

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.

Application of targeted long-read sequencing on RHD gene structural variants.

Recurrent pregnancy loss in a patient with anti‐Rh17.

Fatal haemolytic transfusion reaction due to anti‐En<sup>a</sup> and identification of a novel GYPA c.295delG variant in a Thai family.

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

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

A DEL phenotype attributed to RHD Exon 9 sequence deletion: slipped-strand mispairing and blood group polymorphisms.

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

Genotyping by sequencing defines independent novel RHD variants for an antenatal patient and a blood donor.

Anti-D in a mother, hemizygous for the variant RHD*DNB gene, associated with hemolytic disease of the fetus and newborn.

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

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

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.

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

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

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