Lista de obras - Catherine A. Hyland - Dominio Público Uruguay

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

artículo científico publicado en 2016

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

artículo científico publicado en 2017

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.

artículo científico publicado en 2014

An ELISA for the detection of antibody to the core antigen of hepatitis C virus: use in diagnosis and analysis of indeterminate samples

artículo científico publicado en 1996

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

artículo científico publicado en 2016

Anti-D in pregnant women with the RHD(IVS3+1G>A)-associated DEL phenotype.

artículo científico publicado en 2012

Approaches to determination of a full profile of blood group genotypes: single nucleotide variant mapping and massively parallel sequencing.

artículo científico publicado en 2014

Biobanks of blood from donors and recipients of blood products

artículo científico publicado en 2008

Comprehensive blood group antigen profile predictions for Western Desert Indigenous Australians from whole exome sequence data

scientific article published on 06 December 2018

Dengue viremia in blood donors from Honduras, Brazil, and Australia

artículo científico publicado en 2008

Developments beyond blood group serology in the genomics era

artículo científico publicado en 2019

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

artículo científico publicado en 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.

artículo científico publicado en 2015

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

artículo científico publicado en 2017

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

artículo científico publicado en 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

artículo científico publicado en 2018

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

artículo científico publicado en 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

artículo científico publicado en 2016

Hepatitis C antibody and transaminase activities in blood donors

artículo científico publicado en 1990

Hepatitis C virus antibody seroconversion in a volunteer blood donor ⬇️

artículo científico publicado el 1 de agosto de 1994

Identification and analysis of Rh genes: application of PCR and RFLP typing tests.

artículo científico publicado en 1995

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

artículo científico publicado en 2015

Implementation of donor screening for infectious agents transmitted by blood by nucleic acid technology: update to 2003.

artículo científico publicado en 2005

Implications of dengue outbreaks for blood supply, Australia

artículo científico publicado en 2013

International Society of Blood Transfusion Working Party on red cell immunogenetics and blood group terminology: Cancun report (2012).

artículo científico publicado en 2013

Investigation of the variable In(Lu) phenotype caused by KLF1 variants

artículo científico publicado en 2018

Is there evidence for vector transmission of GBV-C?

artículo científico publicado en 1998

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

artículo científico publicado en 2014

Non-invasive prenatal testing (NIPT) for fetal Kell, Duffy and Rh blood group antigen prediction in alloimmunised pregnant women: power of droplet digital PCR

artículo científico publicado en 2020

Noninvasive fetal RHD genotyping by microfluidics digital PCR using maternal plasma from two alloimmunized women with the variant RHD(IVS3+1G>A) allele

artículo científico publicado en 2013

Nucleic acid technology screening of Australian blood donors for hepatitis C and human immunodeficiency virus-1 RNA: comparison of two high-throughput testing strategies.

artículo científico publicado en 2003

Predictive markers for hepatitis C antibody ELISA specificity in Australian blood donors

artículo científico publicado el 1 de septiembre de 1992

Prenatal RHD gene determination and dosage analysis by PCR: clinical evaluation

article

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

artículo científico publicado en 2015

SARA: a "new" low-frequency MNS antigen (MNS47) provides further evidence of the extreme diversity of the MNS blood group system

artículo científico publicado en 2014

Sensitivities of radioimmunoassay and enzyme-linked immunosorbent assay for detection of hepatitis B surface antigen

artículo científico publicado el 1 de enero de 1979

Seroprevalence of 2009 pandemic influenza A(H1N1) virus in Australian blood donors, October - December 2009.

artículo científico publicado en 2010

Strategy for managing maternal variant RHD alleles in Rhesus D negative obstetric populations during fetal RHD genotyping

artículo científico publicado en 2013

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

artículo científico publicado en 2017

The RHD(1227G>A) DEL-associated allele is the most prevalent DEL allele in Australian D- blood donors with C+ and/or E+ phenotypes

artículo científico publicado en 2014

The challenge and paradox in serology RhD typing for blood donors and patients

artículo científico publicado en 2012

The risk of dengue transmission by blood during a 2004 outbreak in Cairns, Australia.

artículo científico publicado en 2009

Lista de obras de Catherine A. Hyland

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.

An ELISA for the detection of antibody to the core antigen of hepatitis C virus: use in diagnosis and analysis of indeterminate samples

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

Anti-D in pregnant women with the RHD(IVS3+1G>A)-associated DEL phenotype.

Approaches to determination of a full profile of blood group genotypes: single nucleotide variant mapping and massively parallel sequencing.

Biobanks of blood from donors and recipients of blood products

Comprehensive blood group antigen profile predictions for Western Desert Indigenous Australians from whole exome sequence data

Dengue viremia in blood donors from Honduras, Brazil, and Australia

Developments beyond blood group serology in the genomics era

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

Hepatitis C antibody and transaminase activities in blood donors

Hepatitis C virus antibody seroconversion in a volunteer blood donor ⬇️

Identification and analysis of Rh genes: application of PCR and RFLP typing tests.

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

Implementation of donor screening for infectious agents transmitted by blood by nucleic acid technology: update to 2003.

Implications of dengue outbreaks for blood supply, Australia

International Society of Blood Transfusion Working Party on red cell immunogenetics and blood group terminology: Cancun report (2012).

Investigation of the variable In(Lu) phenotype caused by KLF1 variants

Is there evidence for vector transmission of GBV-C?

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

Non-invasive prenatal testing (NIPT) for fetal Kell, Duffy and Rh blood group antigen prediction in alloimmunised pregnant women: power of droplet digital PCR

Noninvasive fetal RHD genotyping by microfluidics digital PCR using maternal plasma from two alloimmunized women with the variant RHD(IVS3+1G>A) allele

Nucleic acid technology screening of Australian blood donors for hepatitis C and human immunodeficiency virus-1 RNA: comparison of two high-throughput testing strategies.

Predictive markers for hepatitis C antibody ELISA specificity in Australian blood donors

Prenatal RHD gene determination and dosage analysis by PCR: clinical evaluation

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

SARA: a "new" low-frequency MNS antigen (MNS47) provides further evidence of the extreme diversity of the MNS blood group system

Sensitivities of radioimmunoassay and enzyme-linked immunosorbent assay for detection of hepatitis B surface antigen

Seroprevalence of 2009 pandemic influenza A(H1N1) virus in Australian blood donors, October - December 2009.

Strategy for managing maternal variant RHD alleles in Rhesus D negative obstetric populations during fetal RHD genotyping

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

The RHD(1227G>A) DEL-associated allele is the most prevalent DEL allele in Australian D- blood donors with C+ and/or E+ phenotypes

The challenge and paradox in serology RhD typing for blood donors and patients

The risk of dengue transmission by blood during a 2004 outbreak in Cairns, Australia.

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.