List of works - Thierry Peyrard

A functional AQP1 allele producing a Co(a-b-) phenotype revises and extends the Colton blood group system.

scientific article

A novel GYPB-A-B hybrid gene responsible for Ss and MN typing discrepancies.

scientific article

A review of the Colton blood group system.

scientific article published on January 2010

ABCB6 is dispensable for erythropoiesis and specifies the new blood group system Langereis

scientific article

Acute hemolytic transfusion reaction associated with anti-Mta : case report and review of the literature

scientific article published on 10 September 2019

Alloanti-c/ce in a c+ceAR/Ce patient suggests that the rare RHCE ceAR allele (ceAR) encodes a partial c antigen.

scientific article

Analysis of complement receptor type 1 expression on red blood cells in negative phenotypes of the Knops blood group system, according to CR1 gene allotype polymorphisms.

scientific article published on 19 February 2010

Anti-D investigations in individuals expressing weak D Type 1 or weak D Type 2: allo- or autoantibodies?

scientific article published on 9 June 2011

Anti-HI can cause a severe delayed hemolytic transfusion reaction with hyperhemolysis in sickle cell disease patients

scientific article published on 3 May 2016

Anti-HrB and anti-hrb revisited

scientific article published on 14 July 2009

Band 3 phosphorylation induces irreversible alterations of stored red blood cells.

scientific article published on 20 January 2018

Banking of pluripotent adult stem cells as an unlimited source for red blood cell production: potential applications for alloimmunized patients and rare blood challenges.

scientific article published on 04 March 2011

CORS (CROM20): A new high-prevalence antigen in the Cromer blood group system

scientific article published on 08 September 2020

Characterization of a new human monoclonal antibody directed against the Vel antigen.

scientific article published on 18 September 2015

Difficulties of the care of public antigen alloimmunization

scientific article published on 27 January 2016

Disruption of SMIM1 causes the Vel- blood type.

scientific article published on 15 April 2013

Donors with a rare pheno (geno) type

scientific article published on 01 October 2008

Enhanced calreticulin expression in red cells of polycythemia vera patients harboring the JAK2V617F mutation.

scientific article published on 6 April 2017

Family study of a Swiss patient uncovered a novel genetic basis for the S-s-U+(var) phenotype.

scientific article

Fatal hemolytic disease of the fetus and newborn associated with anti-Jr.

scientific article published on 2 June 2008

Gene conversion events between GYPB and GYPE abolish expression of the S and s blood group antigens

scientific article published on 04 March 2015

Genetic background of the rare Yus and Gerbich blood group phenotypes: homologous regions of the GYPC gene contribute to deletion alleles.

scientific article published on 8 March 2017

High immunogenicity of red blood cell antigens restricted to the population of African descent in a cohort of sickle cell disease patients

scientific article published on 29 April 2018

Identification of the Molecular and Genetic Basis of PX2, a Glycosphingolipid Blood Group Antigen Lacking on Globoside-deficient Erythrocytes.

scientific article published on 8 June 2015

Impact of hydroxycarbamide and interferon-α on red cell adhesion and membrane protein expression in polycythemia vera.

scientific article published on 29 March 2018

Lack of the human choline transporter‐like protein <scp>SLC44A2</scp> causes hearing impairment and a rare red blood phenotype

scientific article published in 2023

Lack of the nucleoside transporter ENT1 results in the Augustine-null blood type and ectopic mineralization

scientific article published on 20 April 2015

Large deletions involving the regulatory upstream regions of A4GALT give rise to principally novel P1PK-null alleles.

scientific article published on 14 January 2014

Live Brucella spp. fail to induce tumor necrosis factor alpha excretion upon infection of U937-derived phagocytes.

scientific article

Management of a pregnant woman with anti-holley alloantibody

scientific article published on 29 January 2015

Management of the blood supply for a Jk(a-b-) patient with an anti-Jk3 in preparation for an urgent heart transplant: An illustrative example of a successful international cooperation

scientific article published on 23 May 2018

Null alleles of ABCG2 encoding the breast cancer resistance protein define the new blood group system Junior

scientific article published on 15 January 2012

Prevalence and risk factors for red blood cell alloimmunization in 175 children with sickle cell disease in a French university hospital reference centre

scientific article published on 12 April 2017

Proof of principle for transfusion of in vitro-generated red blood cells.

scientific article

RHDDOL1 and RHDDOL2 encode a partial D antigen and are in cis with the rare RHCE*ceBI allele in people of African descent

scientific article published on 13 June 2012

Severe autoimmune hemolytic anemia in a liver transplanted child

scientific article published on 22 April 2008

Severe hemolytic disease of the fetus and the newborn associated with anti-Vw (Vw)

scientific article published on 01 September 2010

Short duplication within the RHCE gene associated with an in cis deleted RHD causing a Rhnull amorph phenotype in an immunized pregnant woman with anti-Rh29.

scientific article published on 21 November 2014

Structural Basis for the ABO Blood-Group Dependence of Plasmodium falciparum Rosetting

scientific article

The French national rare blood program

scientific article published on January 2016

The Gerbich blood group system: old knowledge, new importance.

scientific article published on 2 March 2018

The LAN blood group system:a review

scientific article published on December 2013

The Vel blood group system: a review

scientific article published on June 2017

The rare blood groups: a public health challenge

scientific article published on 10 April 2008

Transfusion of rare cryopreserved red blood cell units stored at -80 degrees C: the French experience.

scientific article

Transfusion-associated hazards: A revisit of their presentation

scientific article published on 04 April 2018

Weak A phenotypes associated with novel ABO alleles carrying the A2-related 1061C deletion and various missense substitutions.

scientific article published on 7 May 2010

[A KEL*02mod allele responsible for an apparent maternity exclusion]

scientific article published on 30 May 2013

[Genotyping of blood group systems at the CNRGS. I: FY, JK, MNS systems]

scientific article published on 21 April 2009

[Quality control of labile blood products. Why and howto properly take a specimen? Labile Blood Products Group of the French Blood Transfusion Society]

scientific article published on 01 December 1999

[Transfusion safety, time for a new partnership between stake-holders]

scientific article published on 01 November 2006

List of works by Thierry Peyrard

A functional AQP1 allele producing a Co(a-b-) phenotype revises and extends the Colton blood group system.

A novel GYPB-A-B hybrid gene responsible for Ss and MN typing discrepancies.

A review of the Colton blood group system.

ABCB6 is dispensable for erythropoiesis and specifies the new blood group system Langereis

Acute hemolytic transfusion reaction associated with anti-Mta : case report and review of the literature

Alloanti-c/ce in a c+ceAR/Ce patient suggests that the rare RHCE ceAR allele (ceAR) encodes a partial c antigen.

Analysis of complement receptor type 1 expression on red blood cells in negative phenotypes of the Knops blood group system, according to CR1 gene allotype polymorphisms.

Anti-D investigations in individuals expressing weak D Type 1 or weak D Type 2: allo- or autoantibodies?

Anti-HI can cause a severe delayed hemolytic transfusion reaction with hyperhemolysis in sickle cell disease patients

Anti-HrB and anti-hrb revisited

Band 3 phosphorylation induces irreversible alterations of stored red blood cells.

Banking of pluripotent adult stem cells as an unlimited source for red blood cell production: potential applications for alloimmunized patients and rare blood challenges.

CORS (CROM20): A new high-prevalence antigen in the Cromer blood group system

Characterization of a new human monoclonal antibody directed against the Vel antigen.

Difficulties of the care of public antigen alloimmunization

Disruption of SMIM1 causes the Vel- blood type.

Donors with a rare pheno (geno) type

Enhanced calreticulin expression in red cells of polycythemia vera patients harboring the JAK2V617F mutation.

Family study of a Swiss patient uncovered a novel genetic basis for the S-s-U+(var) phenotype.

Fatal hemolytic disease of the fetus and newborn associated with anti-Jr.

Gene conversion events between GYPB and GYPE abolish expression of the S and s blood group antigens

Genetic background of the rare Yus and Gerbich blood group phenotypes: homologous regions of the GYPC gene contribute to deletion alleles.

High immunogenicity of red blood cell antigens restricted to the population of African descent in a cohort of sickle cell disease patients

Identification of the Molecular and Genetic Basis of PX2, a Glycosphingolipid Blood Group Antigen Lacking on Globoside-deficient Erythrocytes.

Impact of hydroxycarbamide and interferon-α on red cell adhesion and membrane protein expression in polycythemia vera.

Lack of the human choline transporter‐like protein <scp>SLC44A2</scp> causes hearing impairment and a rare red blood phenotype

Lack of the nucleoside transporter ENT1 results in the Augustine-null blood type and ectopic mineralization

Large deletions involving the regulatory upstream regions of A4GALT give rise to principally novel P1PK-null alleles.

Live Brucella spp. fail to induce tumor necrosis factor alpha excretion upon infection of U937-derived phagocytes.

Management of a pregnant woman with anti-holley alloantibody

Management of the blood supply for a Jk(a-b-) patient with an anti-Jk3 in preparation for an urgent heart transplant: An illustrative example of a successful international cooperation

Null alleles of ABCG2 encoding the breast cancer resistance protein define the new blood group system Junior

Prevalence and risk factors for red blood cell alloimmunization in 175 children with sickle cell disease in a French university hospital reference centre

Proof of principle for transfusion of in vitro-generated red blood cells.

RHD*DOL1 and RHD*DOL2 encode a partial D antigen and are in cis with the rare RHCE*ceBI allele in people of African descent

Severe autoimmune hemolytic anemia in a liver transplanted child

Severe hemolytic disease of the fetus and the newborn associated with anti-Vw (Vw)

Short duplication within the RHCE gene associated with an in cis deleted RHD causing a Rhnull amorph phenotype in an immunized pregnant woman with anti-Rh29.

Structural Basis for the ABO Blood-Group Dependence of Plasmodium falciparum Rosetting

The French national rare blood program

The Gerbich blood group system: old knowledge, new importance.

The LAN blood group system:a review

The Vel blood group system: a review

The rare blood groups: a public health challenge

Transfusion of rare cryopreserved red blood cell units stored at -80 degrees C: the French experience.

Transfusion-associated hazards: A revisit of their presentation

Weak A phenotypes associated with novel ABO alleles carrying the A2-related 1061C deletion and various missense substitutions.

[A KEL*02mod allele responsible for an apparent maternity exclusion]

[Genotyping of blood group systems at the CNRGS. I: FY, JK, MNS systems]

[Quality control of labile blood products. Why and howto properly take a specimen? Labile Blood Products Group of the French Blood Transfusion Society]

[Transfusion safety, time for a new partnership between stake-holders]

RHDDOL1 and RHDDOL2 encode a partial D antigen and are in cis with the rare RHCE*ceBI allele in people of African descent