Publications by authors named "Hein Hustinx"

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Body-wide chimerism and mosaicism are predominant causes of naturally occurring ABO discrepancies.
Eva-Maria Dauber, Oskar A Haas, Karin Nebral, Christoph Gassner, Sabrina Haslinger, Hein Hustinx

Br J Haematol· September 2024

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Assessing and mitigating the interference of ALX148, a novel CD47 blocking agent, in pretransfusion compatibility testing.
Tae Yeul Kim, Mi Sook Yoon, Hein Hustinx, Janet Sim, Hong I Wan

Transfusion· October 2020

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The Remarkable Journey of a Low-Frequency Alloantibody.
Adrian Bachofner, Tanja Rüfli, Andreas Holbro, Hein Hustinx, Sofia Lejon Crottet

Transfus Med Hemother· October 2019

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Somatic mosaicisms of chromosome 1 at two different stages of ontogenetic development detected by Rh blood group discrepancies.
Eva-Maria Dauber, Wolfgang R Mayr, Hein Hustinx, Marlies Schönbacher, Holger Budde

Haematologica· March 2019

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MNSs genotyping by MALDI-TOF MS shows high concordance with serology, allows gene copy number testing and reveals new St(a) alleles.
Stefan Meyer, Caren Vollmert, Nadine Trost, Sonja Sigurdardottir, Claudia Portmann, Hein Hustinx

Br J Haematol· August 2016

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Rare donor programs in Switzerland, Germany, and Austria.
Hein Hustinx, Sofia Lejon Crottet, Erwin A Scharberg, Christof Weinstock

Immunohematology· June 2016

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Lack of the nucleoside transporter ENT1 results in the Augustine-null blood type and ectopic mineralization.
Geoff Daniels, Bryan A Ballif, Virginie Helias, Carole Saison, Shane Grimsley, Hein Hustinx

Blood· June 2015

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Management of a pregnant woman with anti-holley alloantibody.
Thomas Braschler, Cora Alexandra Vökt, Hein Hustinx, Thierry Peyrard, Laura Infanti

Transfus Med Hemother· March 2015

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DGTI Register of Rare Donors.
Hein Hustinx

Transfus Med Hemother· October 2014

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Molecular RHD screening of RhD negative donors can replace standard serological testing for RhD negative donors.
Peter Gowland, Christoph Gassner, Hein Hustinx, Martin Stolz, Jochen Gottschalk

Transfus Apher Sci· April 2014

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Implementation of a mandatory donor RHD screening in Switzerland.
Sofia Lejon Crottet, Christine Henny, Stefan Meyer, Franziska Still, Martin Stolz, Hein Hustinx

Transfus Apher Sci· April 2014

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Serologic and molecular investigations of DAR1 (weak D Type 4.2), DAR1.2, DAR1.3, DAR2 (DARE), and DARA.
Sofia Lejon Crottet, Lonneke Haer-Wigman, Peter Gowland, Stefano Fontana, Christoph Niederhauser, Hein Hustinx

Transfusion· November 2013

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P1/P2 genotyping of known and novel null alleles in the P1PK and GLOB histo-blood group systems.
Julia S Westman, Asa Hellberg, Thierry Peyrard, Hein Hustinx, Britt Thuresson

Transfusion· November 2013

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Weak A phenotypes associated with novel ABO alleles carrying the A2-related 1061C deletion and various missense substitutions.
Annika K Hult, Mark H Yazer, René Jørgensen, Asa Hellberg, Hein Hustinx

Transfusion· July 2010

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Will Genotyping Replace Serology in Future Routine Blood Grouping? - Opinion 2.
Hein Hustinx, Stefano Fontana, Peter Gowland, Christoph Niederhauser

Transfus Med Hemother· May 2009

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Structural basis for red cell phenotypic changes in newly identified, naturally occurring subgroup mutants of the human blood group B glycosyltransferase.
Bahram Hosseini-Maaf, James A Letts, Mattias Persson, Elizabeth Smart, Pierre-Yves LePennec, Hein Hustinx

Transfusion· May 2007

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The molecular diversity of Sema7A, the semaphorin that carries the JMH blood group antigens.
Axel Seltsam, Susanne Strigens, Cyril Levene, Vered Yahalom, Marilyn Moulds, Hein Hustinx

Transfusion· January 2007

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Identification of six new alleles at the FUT1 and FUT2 loci in ethnically diverse individuals with Bombay and Para-Bombay phenotypes.
Jill R Storry, Jannica S Johannesson, Joyce Poole, Johanna Strindberg, Maria J Rodrigues, Hein Hustinx

Transfusion· December 2006

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In-frame triplet deletions in RHD alter the D antigen phenotype.
Willy A Flegel, Nicole I Eicher, Andrea Doescher, Hein Hustinx, Peter Gowland

Transfusion· December 2006

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A KEL gene encoding serine at position 193 of the Kell glycoprotein results in expression of KEL1 antigen.
Joyce Poole, Nicole Warke, Hein Hustinx, Behrouz Mansouri Taleghani, Peter Martin

Transfusion· November 2006

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The RHCE allele ceSL: the second example for D antigen expression without D-specific amino acids.
Qing Chen, Hein Hustinx, Willy A Flegel

Transfusion· May 2006

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New and unusual O alleles at the ABO locus are implicated in unexpected blood group phenotypes.
Bahram Hosseini-Maaf, Nidal M Irshaid, Asa Hellberg, Thomas Wagner, Cyril Levene, Hein Hustinx

Transfusion· January 2005

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Acquired and transient RBC CD55 deficiency (Inab phenotype) and anti-IFC.
Thomas Matthes, Emanuelle Tullen, Joyce Poole, Jackie Banks, Monika Nagy, Hein Hustinx

Transfusion· November 2002

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Novel alleles at the JK blood group locus explain the absence of the erythrocyte urea transporter in European families.
Nidal M Irshaid, Nicole I Eicher, Hein Hustinx, Joyce Poole, Martin L Olsson

Br J Haematol· February 2002

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