H. Hustinx

发表

P1/P2 genotyping of known and novel null alleles in the P1PK and GLOB histo‐blood group systems

T. Peyrard, Å. Hellberg, J. S. Westman, 2013, Transfusion.

New and unusual O alleles at the ABO locus are implicated in unexpected blood group phenotypes

C. Levene, T. Wagner, Å. Hellberg, 2005, Transfusion.

Assessing and mitigating the interference of ALX148, a novel CD47 blocking agent, in pretransfusion compatibility testing

H. Hustinx, J. Sim, M. Yoon, 2020, Transfusion.

Somatic mosaicisms of chromosome 1 at two different stages of ontogenetic development detected by Rh blood group discrepancies

M. König, O. Haas, W. Mayr, 2018, Haematologica.

The molecular diversity of Sema7A, the semaphorin that carries the JMH blood group antigens

D. DeLuca, A. Seltsam, R. Blasczyk, 2007, Transfusion.

Implementation of a mandatory donor RHD screening in Switzerland.

C. Gassner, B. M. Frey, S. Fontana, 2014, Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis.

Anti-D immunoglobulin in Rh(D) negative volunteers: clearance of Rh(D) positive red cells and kinetics of serum anti-D levels.

A. Halabi, P. Lerch, H. Hustinx, 1998, Transfusion clinique et biologique : journal de la Societe francaise de transfusion sanguine.

The Remarkable Journey of a Low-Frequency Alloantibody

A. Buser, L. Infanti, A. Holbro, 2019, Transfusion Medicine and Hemotherapy.

Novel alleles at the JK blood group locus explain the absence of the erythrocyte urea transporter in European families *

N. Eicher, J. Poole, M. Olsson, 2002, British journal of haematology.

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

M. Palcic, T. Peyrard, M. Yazer, 2010, Transfusion.

Donors with a rare pheno (geno) type

P. Sistonen, W. Flegel, C. Levene, 2008, Vox sanguinis.

Will Genotyping Replace Serology in Future Routine Blood Grouping? – Opinion 2

S. Fontana, H. Hustinx, C. Niederhauser, 2009, Transfusion Medicine and Hemotherapy.

Structural basis for red cell phenotypic changes in newly identified, naturally occurring subgroup mutants of the human blood group B glycosyltransferase

M. Palcic, E. Smart, M. Persson, 2007, Transfusion.

Rapid detection of antibodies to immunoglobulin A molecules by using the particle gel immunoassay

U. Nydegger, A. Salama, H. Hustinx, 2001, Vox sanguinis.

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

J. Cartron, T. Peyrard, Edmond Lee, 2015, Blood.

Acquired and transient RBC CD55 deficiency (Inab phenotype) and anti‐IFC

G. Daniels, J. Poole, F. Boehlen, 2002, Transfusion.

Sequence and Specificity Analysis of Recombinant Human Fab Anti–Rh D Isolated by Phage Display

S. Miescher, M. Vogel, B. Stadler, 1998, Vox Sanguinis.

A KEL gene encoding serine at position 193 of the Kell glycoprotein results in expression of KEL1 antigen

I. Bromilow, G. Daniels, J. Poole, 2006, Transfusion.

DGTI Register of Rare Donors

H. Hustinx, 2014, Transfusion Medicine and Hemotherapy.

MNSs genotyping by MALDI‐TOF MS shows high concordance with serology, allows gene copy number testing and reveals new St(a) alleles

A. Buser, C. Gassner, B. M. Frey, 2016, British journal of haematology.

Management of anti‐Coltona alloimmunisation in pregnancy: a case report

R. Zimmermann, N. Kimmich, B. Brand, 2016, Transfusion medicine.

A novel Bweak hybrid allele lacks three enhancer repeats but generates normal ABO transcript levels

M. Olsson, A. Hult, H. Hustinx, 2012, Vox sanguinis.

Identification of six new alleles at the FUT1 and FUT2 loci in ethnically diverse individuals with Bombay and Para‐Bombay phenotypes

C. Levene, J. Poole, V. Yahalom, 2006, Transfusion.

What Is the Best Technique for the Detection of Red Cell Alloantibodies?

W. Ouwehand, M. Overbeeke, H. Reesink, 1995, Vox sanguinis.

The RHCE allele ceSL: the second example for D antigen expression without D‐specific amino acids

W. Flegel, H. Hustinx, Qing Chen, 2006, Transfusion.

Molecular RHD screening of RhD negative donors can replace standard serological testing for RhD negative donors.

J. Tissot, C. Gassner, B. M. Frey, 2014, Transfusion and Apheresis Science.

A Low‐Incidence Red Cell Antigen JAL Associated with Two Unusual Rh Gene Complexes

J. Poole, C. Lomas, C. Green, 1990, Vox sanguinis.

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

W. Flegel, F. Wagner, I. von Zabern, 2006, Transfusion.

Serologic and molecular investigations of DAR1 (weak D Type 4.2), DAR1.2, DAR1.3, DAR2 (DARE), and DARA

L. Haer-Wigman, S. Fontana, H. Hustinx, 2013, Transfusion.

Management of a Pregnant Woman with Anti-Holley Alloantibody

A. Buser, T. Peyrard, L. Infanti, 2015, Transfusion Medicine and Hemotherapy.

Vox Sanguinis International Forum on typing and matching strategies in patients on anti‐CD38 monoclonal therapy: summary

V. Deneys, A. Buser, A. Greinacher, 2018, Vox Sanguinis.

International Forum on typing and matching strategies in patients on anti‐CD38 monoclonal therapy

V. Deneys, A. Buser, A. Greinacher, 2018, Vox Sanguinis.

The Red Cell Antigen JAL in the Swiss Population: Family Studies Showing That JAL Is an Rh Antigen (RH48)

Y. Liew, J. Poole, P. Tippett, 1990, Vox sanguinis.

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

J. Cartron, T. Peyrard, Edmond Lee, 2015, Blood.

Body-wide chimerism and mosaicism are predominant causes of naturally occurring ABO discrepancies.

H. Hustinx, K. Nebral, M. Schönbacher, 2024, British journal of haematology.