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Pathogenesis and mechanisms of antibody-mediated hemolysis

Transfusion (Philadelphia, Pa.), 2015-07, Vol.55 (S2), p.S47-S58

Flegel, Willy A.

2015

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COVID‐19 insights from transfusion medicine

British journal of haematology, 2020-09, Vol.190 (5), p.715-717

Flegel, Willy A.

2020

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Molecular genetics and clinical applications for RH

Transfusion and apheresis science, 2011-02, Vol.44 (1), p.81-91

Flegel, Willy A

2011

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Serological weak D phenotypes: a review and guidance for interpreting the RhD blood type using the RHD genotype

British journal of haematology, 2017-10, Vol.179 (1), p.10-19

2017

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When recombinant proteins can replace rare red cells in immunohematology workups

Transfusion (Philadelphia, Pa.), 2021-07, Vol.61 (7), p.2204-2212

2021

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Treatment Strategies for Deficiency of Adenosine Deaminase 2

The New England journal of medicine, 2019-04, Vol.380 (16), p.1582-1584

2019

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Does prolonged storage of red blood cells cause harm?

British journal of haematology, 2014-04, Vol.165 (1), p.3-16

2014

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Frameshift variations in the RHD coding sequence: Molecular mechanisms permitting protein expression

Transfusion (Philadelphia, Pa.), 2020-11, Vol.60 (11), p.2737-2744

2020

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Does prolonged storage of red blood cells cause harm?

British journal of haematology, 2014-04, Vol.165 (1), p.3-16

2014

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COVID-19: risk of infection is high, independently of ABO blood group

Haematologica (Roma), 2020-12, Vol.105 (12), p.2706-2708

Flegel, Willy Albert

2020

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When should RhD‐negative recipients be spared the transfusion of DEL red cells to avoid anti‐D alloimmunization?

Transfusion (Philadelphia, Pa.), 2022-11, Vol.62 (11), p.2405-2408

2022

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HLA associations, somatic loss of HLA expression, and clinical outcomes in immune aplastic anemia

Blood, 2021-12, Vol.138 (26), p.2799-2809

2021

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Analyses of genome wide association data, cytokines, and gene expression in African-Americans with benign ethnic neutropenia

PloS one, 2018-03, Vol.13 (3), p.e0194400-e0194400

2018

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DEL in China: the D antigen among serologic RhD-negative individuals

Journal of translational medicine, 2021-10, Vol.19 (1), p.439-14, Article 439

2021

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NM_000148.4(FUT1):c.[229C>T;302C>T] with 2 missense variations in the FUT1 gene associated with a para‐Bombay phenotype

Transfusion (Philadelphia, Pa.), 2022-01, Vol.62 (1), p.E5-E7

2022

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Breakpoint regions of an RHD-CE(4-9)-D allele and a rare JK allele in a Pacific Islander individual

Blood transfusion = Trasfusione del sangue, 2024-05, Vol.22 (3), p.189-197

2024

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Red Blood Cell Transfusion: Precision vs Imprecision Medicine

JAMA : the journal of the American Medical Association, 2015-10, Vol.314 (15), p.1557

2015

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Implementing mass-scale red cell genotyping at a blood center

Transfusion (Philadelphia, Pa.), 2015-11, Vol.55 (11), p.2610-2615

2015

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Primary oxidative phosphorylation defects lead to perturbations in the human B cell repertoire

Frontiers in immunology, 2023-07, Vol.14, p.1142634-1142634

2023

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Autoantibodies Recognizing Specificity Protein 4 Co‐occur With Anti–Transcription Intermediary Factor 1 and Are Associated With Distinct Clinical Features and Immunogenetic Risk Factors in Juvenile Myositis

Arthritis & rheumatology (Hoboken, N.J.), 2023-09, Vol.75 (9), p.1668-1677

2023

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It's time to phase in RHD genotyping for patients with a serologic weak D phenotype

Transfusion (Philadelphia, Pa.), 2015-03, Vol.55 (3), p.680-689

2015

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Does transfusion of Asian‐type DEL red blood cells to D– recipients cause D alloimmunization?

Transfusion (Philadelphia, Pa.), 2019-07, Vol.59 (7), p.2455-2458

2019

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Norovirus gastroenteritis causes severe and lethal complications after chemotherapy and hematopoietic stem cell transplantation

Blood, 2011-06, Vol.117 (22), p.5850-5856

2011

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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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Pathogenesis and mechanisms of antibody-mediated hemolysis

COVID‐19 insights from transfusion medicine

Molecular genetics and clinical applications for RH

Serological weak D phenotypes: a review and guidance for interpreting the RhD blood type using the RHD genotype

When recombinant proteins can replace rare red cells in immunohematology workups

Treatment Strategies for Deficiency of Adenosine Deaminase 2

Does prolonged storage of red blood cells cause harm?

Frameshift variations in the RHD coding sequence: Molecular mechanisms permitting protein expression

Does prolonged storage of red blood cells cause harm?

COVID-19: risk of infection is high, independently of ABO blood group

When should RhD‐negative recipients be spared the transfusion of DEL red cells to avoid anti‐D alloimmunization?

HLA associations, somatic loss of HLA expression, and clinical outcomes in immune aplastic anemia

Analyses of genome wide association data, cytokines, and gene expression in African-Americans with benign ethnic neutropenia

DEL in China: the D antigen among serologic RhD-negative individuals

NM_000148.4(FUT1):c.[229C>T;302C>T] with 2 missense variations in the FUT1 gene associated with a para‐Bombay phenotype

Breakpoint regions of an RHD-CE(4-9)-D allele and a rare JK allele in a Pacific Islander individual

Red Blood Cell Transfusion: Precision vs Imprecision Medicine

Implementing mass-scale red cell genotyping at a blood center

Primary oxidative phosphorylation defects lead to perturbations in the human B cell repertoire

Autoantibodies Recognizing Specificity Protein 4 Co‐occur With Anti–Transcription Intermediary Factor 1 and Are Associated With Distinct Clinical Features and Immunogenetic Risk Factors in Juvenile Myositis

It's time to phase in RHD genotyping for patients with a serologic weak D phenotype

International Society of Blood Transfusion Working Party on Red Cell Immunogenetics and Blood Group Terminology: Report of the Dubai, Copenhagen and Toronto meetings

Does transfusion of Asian‐type DEL red blood cells to D– recipients cause D alloimmunization?

Norovirus gastroenteritis causes severe and lethal complications after chemotherapy and hematopoietic stem cell transplantation

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

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