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High-throughput multiplex single-nucleotide polymorphism analysis for red cell and platelet antigen genotypes

Transfusion (Philadelphia, Pa.), 2005-05, Vol.45 (5), p.660-666

2005

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Cost‐effectiveness of implementing molecular immunohematology

ISBT science series, 2017-02, Vol.12 (1), p.223-226

Denomme, G. A.

2017

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Immunoglobulin G from patients with heparin-induced thrombocytopenia binds to a complex of heparin and platelet factor 4

Blood, 1994-06, Vol.83 (11), p.3232-3239

1994

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Maternal ABO-mismatched blood for intrauterine transfusion of severe hemolytic disease of the newborn due to anti-Rh17

Transfusion (Philadelphia, Pa.), 2004-09, Vol.44 (9), p.1357-1360

2004

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Unusual serological findings associated with ceftriaxone-induced immune hemolytic anemia in a child with disseminated low-grade glioma

Pediatric blood & cancer, 2016-10, Vol.63 (10), p.1852-1855

2016

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A diagnostic test for heparin‐induced thrombocytopenia: detection of platelet microparticles using flow cytometry

British journal of haematology, 1996-12, Vol.95 (4), p.724-731

1996

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ABO sequence analysis in a family with weak expression of blood group B

Transfusion (Philadelphia, Pa.), 2004-09, Vol.44 (9), p.1394-1395

2004

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Maternal immunization to Gov system alloantigens on human platelets

Transfusion (Philadelphia, Pa.), 1997-08, Vol.37 (8), p.823-828

1997

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Factor V Leiden and thrombotic complications in heparin-induced thrombocytopenia

Thrombosis and haemostasis, 1998-01, Vol.79 (1), p.50-53

1998

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An Adenine Trimer Precedes a C/G Polymorphism in the 3′-Amplimer Region of the Human Platelet Glycoprotein IIIa Intron 6 CT Repeat

Human heredity, 1998-03, Vol.48 (2), p.115-118

Denomme, G.A.

1998

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Consortium for Blood Group Genes (CBGG): 2009 report

Immunohematology, 2010-01, Vol.26 (2), p.47-50

2010

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Effect of cryopreservation on a rare McLeod donor red blood cell concentrate

Immunohematology, 2021-06, Vol.37 (2), p.78-83

2021

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RhD status of a fetus at risk for haemolytic disease with a discrepant maternal DNA-based RhD genotype

Prenatal diagnosis, 1999-05, Vol.19 (5), p.424-427

1999

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Consortium for Blood Group Genes (CBGG): 2008 report

Immunohematology, 2009-01, Vol.25 (2), p.75-78

2009

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Characterization and localization of the Gova/b alloantigens to the glycosylphosphatidylinositol-anchored protein CDw109 on human platelets

Blood, 1995-10, Vol.86 (7), p.2807-2814

1995

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The prenatal identification of fetal compatibility in neonatal alloimmune thrombocytopenia using amniotic fluid and variable number of tandem repeat (VNTR) analysis

British journal of haematology, 1995-11, Vol.91 (3), p.742-746

1995

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A human monoclonal autoantibody to platelet glycoprotein IIb derived from normal human lymphocytes

Blood, 1992-01, Vol.79 (2), p.447-451

1992

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Partial D, weak D types, and novel RHD alleles among 33,864 multiethnic patients: implications for anti-D alloimmunization and prevention

Transfusion (Philadelphia, Pa.), 2005-10, Vol.45 (10), p.1554-1560

2005

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Activation of platelets by sera containing IgG1 heparin-dependent antibodies : An explanation for the predominance of the FcγRIIa low responder (his131) gene in patients with heparin-induced thrombocytopenia

The Journal of laboratory and clinical medicine, 1997-09, Vol.130 (3), p.278-284

1997

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The production of human monoclonal antiplatelet auto‐antibodies derived from human lymphocytes of normal origin: reactivity to DNA, anionic phospholipids and platelet proteins

British journal of haematology, 1992-09, Vol.82 (1), p.99-106

1992

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Immunoglobulin V region sequences of two human antiplatelet monoclonal autoantibodies derived from B cells of normal origin

Journal of autoimmunity, 1994-08, Vol.7 (4), p.521-535

1994

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The Development of a Bacteriophage Expression Vector for Cloning Immunoglobulin Variable Region Genes from B-Cell Genomic DNA

Annals of the New York Academy of Sciences, 1995-09, Vol.764 (1), p.580-582

1995

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The structure and function of the molecules that carry human red blood cell and platelet antigens

Transfusion medicine reviews, 2004-07, Vol.18 (3), p.203-231

Denomme, Gregory A

2004

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Fcγ receptor IIa and IIIa polymorphisms in childhood immune thrombocytopenic purpura

British journal of haematology, 2003-01, Vol.120 (1), p.135-141

2003

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High-throughput multiplex single-nucleotide polymorphism analysis for red cell and platelet antigen genotypes

Cost‐effectiveness of implementing molecular immunohematology

Immunoglobulin G from patients with heparin-induced thrombocytopenia binds to a complex of heparin and platelet factor 4

Maternal ABO-mismatched blood for intrauterine transfusion of severe hemolytic disease of the newborn due to anti-Rh17

Unusual serological findings associated with ceftriaxone-induced immune hemolytic anemia in a child with disseminated low-grade glioma

A diagnostic test for heparin‐induced thrombocytopenia: detection of platelet microparticles using flow cytometry

ABO sequence analysis in a family with weak expression of blood group B

Maternal immunization to Gov system alloantigens on human platelets

Factor V Leiden and thrombotic complications in heparin-induced thrombocytopenia

An Adenine Trimer Precedes a C/G Polymorphism in the 3′-Amplimer Region of the Human Platelet Glycoprotein IIIa Intron 6 CT Repeat

Consortium for Blood Group Genes (CBGG): 2009 report

Effect of cryopreservation on a rare McLeod donor red blood cell concentrate

RhD status of a fetus at risk for haemolytic disease with a discrepant maternal DNA-based RhD genotype

Consortium for Blood Group Genes (CBGG): 2008 report

Characterization and localization of the Gova/b alloantigens to the glycosylphosphatidylinositol-anchored protein CDw109 on human platelets

The prenatal identification of fetal compatibility in neonatal alloimmune thrombocytopenia using amniotic fluid and variable number of tandem repeat (VNTR) analysis

A human monoclonal autoantibody to platelet glycoprotein IIb derived from normal human lymphocytes

Recommendation for validation and quality assurance of non‐invasive prenatal testing for foetal blood groups and implications for IVD risk classification according to EU regulations

Partial D, weak D types, and novel RHD alleles among 33,864 multiethnic patients: implications for anti-D alloimmunization and prevention

Activation of platelets by sera containing IgG1 heparin-dependent antibodies : An explanation for the predominance of the FcγRIIa low responder (his131) gene in patients with heparin-induced thrombocytopenia

The production of human monoclonal antiplatelet auto‐antibodies derived from human lymphocytes of normal origin: reactivity to DNA, anionic phospholipids and platelet proteins

Immunoglobulin V region sequences of two human antiplatelet monoclonal autoantibodies derived from B cells of normal origin

The Development of a Bacteriophage Expression Vector for Cloning Immunoglobulin Variable Region Genes from B-Cell Genomic DNA

The structure and function of the molecules that carry human red blood cell and platelet antigens

Fcγ receptor IIa and IIIa polymorphisms in childhood immune thrombocytopenic purpura

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