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Blood Groups and Their Correlation with Hereditary Disease

Transfusion medicine and hemotherapy, 2022-02, Vol.49 (1), p.1-3

2022

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Six years' experience performing RHD genotyping to confirm D− red blood cell units in Germany for preventing anti-D immunizations

Transfusion (Philadelphia, Pa.), 2009-03, Vol.49 (3), p.465-471

2009

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Antibody testing in patients treated with anti-CD38: there is still room for improvement

Blood transfusion = Trasfusione del sangue, 2020-07, Vol.18 (4), p.244-246

Wagner, Franz F.

2020

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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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NG_007494.1(RHD):c.[4A>T;5G>C;6_7insG] with an RhD‐negative phenotype

Transfusion (Philadelphia, Pa.), 2020-11, Vol.60 (11), p.E45-E47

2020

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New ultraviolet C light‐based method for pathogen inactivation of red blood cell units

Transfusion (Philadelphia, Pa.), 2022-11, Vol.62 (11), p.2314-2323

2022

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D variants at the RhD vestibule in the weak D type 4 and Eurasian D clusters

Transfusion (Philadelphia, Pa.), 2009-06, Vol.49 (6), p.1059-1069

2009

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The Rhesus Site

Transfusion medicine and hemotherapy, 2014-10, Vol.41 (5), p.357-363

2014

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RHD PCR of D-Negative Blood Donors

Transfusion medicine and hemotherapy, 2013-06, Vol.40 (3), p.172-181

Wagner, Franz F.

2013

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Two novel antithetical KN blood group antigens may contribute to more than a quarter of all KN antisera in Europe

Transfusion (Philadelphia, Pa.), 2020-10, Vol.60 (10), p.2408-2418

2020

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Molecular typing for blood group antigens within 40 min by direct polymerase chain reaction from plasma or serum

British journal of haematology, 2017-03, Vol.176 (5), p.814-821

2017

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HBsAg non-reactive HBV infection in blood donors: Transmission and pathogenicity

Journal of medical virology, 2007, Vol.79 (S1), p.S32-S36

2007

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Optimized Antigen Matching - Chances and Challenges in Molecular Times

Transfusion medicine and hemotherapy, 2018-07, Vol.45 (4), p.216-217

2018

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Extended Donor Typing by Pooled Capillary Electrophoresis: Impact in a Routine Setting

Transfusion medicine and hemotherapy, 2018-07, Vol.45 (4), p.225-237

2018

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In-frame triplet deletions in RHD alter the D antigen phenotype

Transfusion (Philadelphia, Pa.), 2006-12, Vol.46 (12), p.2156-2161

2006

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D category IV: a group of clinically relevant and phylogenetically diverse partial D

Transfusion (Philadelphia, Pa.), 2013-11, Vol.53 (11pt2), p.2960-2973

2013

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Why do we use serological blood group phenotype determination in chronically transfused patients?

Blood transfusion = Trasfusione del sangue, 2014-01, Vol.12 (1), p.1-2

Wagner, Franz F

2014

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RHD gene deletion occurred in the Rhesus box

Blood, 2000-06, Vol.95 (12), p.3662-3668

2000

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The D category VI type 4 allele is prevalent in the Spanish population

Transfusion (Philadelphia, Pa.), 2006-04, Vol.46 (4), p.616-623

2006

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Evaluation of single-nucleotide polymorphisms as internal controls in prenatal diagnosis of fetal blood groups

Transfusion (Philadelphia, Pa.), 2013-02, Vol.53 (2), p.353-362

2013

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Terminologie der Blutgruppenantigene und -antikörper

Transfusionsmedizin, 2022-05, Vol.12 (2), p.103-107

2022

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Two molecular polymorphisms to detect the (C)ce(s) type 1 haplotype

Blood transfusion = Trasfusione del sangue, 2014-01, Vol.12 (1), p.136

2014

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Cost-efficient sequence-specific priming-polymerase chain reaction screening for blood donors with rare phenotypes

Transfusion (Philadelphia, Pa.), 2008-06, Vol.48 (6), p.1169-1173

2008

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Molecular testing in transfusion medicine

Expert opinion on medical diagnostics, 2010-09, Vol.4 (5), p.411-428

Wagner, Franz F

2010

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Weak D alleles express distinct phenotypes

Blood, 2000-04, Vol.95 (8), p.2699-2708

2000

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Blood Groups and Their Correlation with Hereditary Disease

Six years' experience performing RHD genotyping to confirm D− red blood cell units in Germany for preventing anti-D immunizations

Antibody testing in patients treated with anti-CD38: there is still room for improvement

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

NG_007494.1(RHD):c.[4A>T;5G>C;6_7insG] with an RhD‐negative phenotype

New ultraviolet C light‐based method for pathogen inactivation of red blood cell units

D variants at the RhD vestibule in the weak D type 4 and Eurasian D clusters

The Rhesus Site

RHD PCR of D-Negative Blood Donors

Two novel antithetical KN blood group antigens may contribute to more than a quarter of all KN antisera in Europe

Molecular typing for blood group antigens within 40 min by direct polymerase chain reaction from plasma or serum

HBsAg non-reactive HBV infection in blood donors: Transmission and pathogenicity

Optimized Antigen Matching - Chances and Challenges in Molecular Times

Extended Donor Typing by Pooled Capillary Electrophoresis: Impact in a Routine Setting

In-frame triplet deletions in RHD alter the D antigen phenotype

D category IV: a group of clinically relevant and phylogenetically diverse partial D

Why do we use serological blood group phenotype determination in chronically transfused patients?

RHD gene deletion occurred in the Rhesus box

The D category VI type 4 allele is prevalent in the Spanish population

Evaluation of single-nucleotide polymorphisms as internal controls in prenatal diagnosis of fetal blood groups

Terminologie der Blutgruppenantigene und -antikörper

Two molecular polymorphisms to detect the (C)ce(s) type 1 haplotype

Cost-efficient sequence-specific priming-polymerase chain reaction screening for blood donors with rare phenotypes

Molecular testing in transfusion medicine

Weak D alleles express distinct phenotypes

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