List of works - Genghis H Lopez

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

scientific article published on 8 July 2016

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

scientific article

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

scientific article published on 4 August 2014

A standardized immunofluorescence test method with human neutrophil antigen-expressing cell lines to enhance antibody detection.

scientific article

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

scientific article

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

scientific article published on 21 June 2017

Clinical scale ex vivo manufacture of neutrophils from hematopoietic progenitor cells

scientific article published on 01 November 2009

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

scientific article published on 20 February 2017

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.

scientific article published on 20 April 2015

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

scientific article published on 24 March 2017

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

scientific article published on 31 December 2015

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

scientific article published on 13 June 2018

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

scientific article published on 16 July 2017

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

scientific article

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

scientific article published on 4 October 2015

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

scientific article published on 26 December 2018

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

scientific article

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.

scientific article published on 30 October 2017

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

scientific article published on 8 November 2017

List of works by Genghis H Lopez

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

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

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.

A standardized immunofluorescence test method with human neutrophil antigen-expressing cell lines to enhance antibody detection.

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

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

Clinical scale ex vivo manufacture of neutrophils from hematopoietic progenitor cells

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

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.

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

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

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

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

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

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

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

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

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.

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

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