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Die wissenschaftlichen Publikationen des ZHBSD spiegeln unser Engagement für exzellente, praxisnahe Forschung wider. In enger Zusammenarbeit mit nationalen und internationalen Partnern leisten wir Beiträge zu aktuellen Themen der Transfusionsmedizin, Molekulargenetik und Immunhämatologie – von methodischen Entwicklungen bis hin zu klinisch relevanten Fragestellungen.
2025
- Mapping naturally presented T cell antigens in medulloblastoma based on integrative multi-omics
J. Velz, L. K. Freudenmann, G. Medici, M. Dubbelaar, M. Mohme, D. R. Ghasemi,
J. Scheid, D. J. Kowalewski, A. B. Patterson, A. M. Zeitlberger, K. Lamszus,
M. Westphal, M. Eyrich, M. Messing-Jünger, A. Röhrig, H. Reinhard, K. Beccaria,
R. B. Craveiro, B. M. Frey, M. Sill, S. Nahnsen, M. Gauder, K. Kapolou, M. Silginer,
T. Weiss, H.-G. Wirsching, P. Roth, M. Grotzer, N. Krayenbühl, O. Bozinov, L. Regli,
H.-G. Rammensee, E. J. Rushing, F. Sahm, J. S. Walz, M. Weller, M. C. Neidert - Sterility assessment of reclosable ophtioles with unpreserved autologous serum during single-day use
F. Blaser, I. Meneau, J. Wiedler, O. Lamprecht, D. Barthelmes, S. Zweifel, P. Perschak, M. R. J. Wiest, F. Fierz, S. Said, A. Bajka
- Multicenter evaluation of soluble CD38: neutralizing anti-CD38 pan-reactivity to enable alloantibody detection
Charlotte Engström, Eliane Scherrer, Jonathan Falconer, Donatella Londero, Carlos Penatejera, Isabelle Legoff, Nadine Dubosc Marchenay, Marine Le Bouar, Cosimo Nocera, Luigi Paesano, Salvatore De Martino, Marie-Edith Pettinelli, Ariane Caesar, Thomas Bise, Laziza Amniai
Article 2024
- Resolving genotype-phenotype discrepancies of the Kidd blood group system using long-read nanopore sequencing
M. Gueuning, G. A. Thun, N. Trost, L. Schneider, S. Sigurdardottir, C. Engström, N. Larbes, Y. Merki, B. M. Frey, S. Meyer, M. P. Mattle-Greminger
- Novel regulatory variant in ABO intronic RUNX1 binding site inducing A3 phenotype
G. A. Thun, M. Gueuning, S. Sigurdardottir, E. Meyer, E. Gourri, L. Schneider, Y. Merki, N. Trost, K. Neuenschwander, C. Engström, B. M. Frey, S. Meyer, M. P. Mattle-Greminger
- Prevalence of acute hepatitis E virus infections in Swiss blood donors 2018-2020
C. Niederhauser, P. Gowland, N. Widmer, S. Amar, M. P. Mattle-Greminger, J. Gottschalk, B. M. Frey
- Effects of CTLA-4 single nucleotide polymorphisms (SNPs) on toxicity of ipilimumab-containing regimens in patients with advanced stage melanoma
K. de Joode, A. Rojas Mora, R. H. N. van Schaik, A. Zippelius, A. van der Veldt, C. L. Gerard, H. Läubli, O. Michielin, R. von Moos, M. Jörger, M. P. Levesque, S. Aeppli, J. Mangana, C. Mangas, N. Trost, S. Meyer, S. L. Parvex, R. Mathijssen, Y. Metaxas
- Deciphering factors linked with reduced SARS-CoV2 susceptibility in the Swiss HIV Cohort Study
I. A. Abela, A. Hauser, M. Schwarzmüller, C. Pasin, K. Kusejko, S. Epp, M. Cavassini, M. Battegay, A. Rauch, A. Calmy, J. Notter, E. Bernasconi, C. A. Fux, K. Leuzinger, M. Perreau, A. Ramette, J. Gottschalk, E. Schindler, A. Wepf, M. Marconato, M. G. Manz , B. M. Frey, D. L. Braun, M. Huber, H. F. Günthard, A. Trkola, R. D. Kouyos, Swiss HIV Cohort Study
- Cellular architecture shapes the naïve T cell response
B. D. Hale, Y. Severin, F. Graebnitz, D. Stark, D. Guignard, J. Mena, Y. Festl, S. Lee, J. Hanimann, N. S. Zangger, M. Meier, D. Goslings, O. Lamprecht, B. M. Frey, A. Oxenius, B. Snijder
- The protean presentations of XK disease (McLeod syndrome): a case series with new observations and updates on previously reported families
R. H. Walker, M. Barreto, J. R. Bateman, M. Leonor Bustamante, G. Chiu, S. Feitell, B. M. Frey, P. Guerra, S. Guerrero, H. H. Jung, F. Maldonado, E. Meyer, M. Miranda, E. McFarland, P. Oates, G. Ochoa, K. Olsson, M. Paucar, J. Alvarez Proschle, E. M. Sammler, M. Troncoso, R. Wu-Wallace, L. Young, S. Vege, C. M. Westhoff, A. Danek
- Plasma and patelet lipidome changes in Fabry Disease
B. Burla, J. Oh, A. Nowak, N.Piraud, E. Meyer, D. Mei, A. K. Bendt, J.-D. Studt, B. M. Frey,
M. R. Wenk, P.-A. Krayenbühl - Auflösung einer KEL1 Diskrepanz als Fallbeispiel der haplotyp-spezifischen Nanopore-Sequenzierung von Blutgruppengenen
G. A. Thun, M. Gueuning, Y. Merki, N. Niederberger, N. Trost, S. Sigurdardottir, C. Engström, M. P. Mattle-Greminger, S. Meyer
2023
- Inborn errors of type I interferon immunity in patients with symptomatic acute Hepatitis E
A. Saadat, J. Gouttenoire, P. Ripellino, D. Semela, S. Amar, B. M. Frey, S. Fontana, HEV Human Genetics Collab., E. Mdawar-Bailly, D. Moradpour, J. Fellay, M. Fraga
- First report of a low-frequency mosaic mutation in the hydroxymethylbilane synthase gene causing acute intermittent porphyria
A. Belosevic, A-E. Minder, M. Gueuning, F. van Breemen, G. A. Thun, M. P. Mattle-Greminger,S. Meyer, A. Baumer, I. E. Minder, X. Schneider-Yin, and J. Barman-Aksözen
- A T-cell antigen atlas for meningioma: novel options for immunotherapy
G. Medici, L. K. Freudenmann, J. Velz, S. Wang, K. Kapolou, N. Paramasivam, L. Mühlenbruch, D. J. Kowalewski, F. Vasella, T. Bilich, B. M. Frey, M. L. Dubbelaar, A. B. Patterson, A. M. Zeitlberger, M. Silginer, P. Roth, T. Weiss, H.-G. Wirsching, N. Krayenbühl, O. Bozinov, L. Regli, H.-G. Rammensee, E. J. Rushing, F. Sahm, J. S. Walz, M. Weller, M. C. Neidert
- Continuous population-level monitoring of SARS-CoV-2 seroprevalence in a large European metropolitan region
Marc Emmenegger, Elena De Cecco, David Lamparter, Raphaël P.B. Jacquat, Julien Riou, Dominik Menges, Tala Ballouz, Daniel Ebner, Matthias M. Schneider, Itzel Condado Morales, Berre Doğançay, Jingjing Guo, Anne Wiedmer, Julie Domange, Marigona Imeri, Rita Moos, Chryssa Zografou, Leyla Batkitar, Lidia Madrigal, Dezirae Schneider, Chiara Trevisan, Andres Gonzalez-Guerra, Alessandra Carrella, Irina L. Dubach, Catherine K. Xu, Georg Meisl, Vasilis Kosmoliaptsis, Tomas Malinauskas, Nicola Burgess-Brown, Ray Owens, Stephanie Hatch, Juthathip Mongkolsapaya, Gavin R. Screaton, Katharina Schubert, John D. Huck, Feimei Liu, Florence Pojer, Kelvin Lau, David Hacker, Elsbeth Probst-Müller, Carlo Cervia, Jakob Nilsson, Onur Boyman, Lanja Saleh, Katharina Spanaus, Arnold von Eckardstein, Dominik J. Schaer, Nenad Ban, Ching-Ju Tsai, Jacopo Marino, Gebhard F.X. Schertler, Nadine Ebert, Volker Thiel, Jochen Gottschalk, Beat M. Frey, Regina R. Reimann, Simone Hornemann, Aaron M. Ring, Tuomas P.J. Knowles, Milo A. Puhan, Christian L. Althaus, Ioannis Xenarios, David I. Stuart, and Adriano Aguzzi
- Long-Read Sequencing in Blood Group Genetics
Gian Andri Thun, Morgan Gueuning, and Maja P. Mattle-Greminger
- Haplotype sequence collection of ABO blood group alleles by long-read sequencing reveals putative A1-diagnostic variants
Morgan Gueuning, Gian Andri Thun, Michael Wittig, Anna-Lena Galati, Stefan Meyer, Nadine Trost, Elise Gourri, Janina Fuss, Sonja Sigurdardottir, Yvonne Merki,Kathrin Neuenschwander, Yannik Busch, Peter Trojok, Marco Schäfer, Jochen Gottschalk, Andre Franke, Christoph Gassner, Wolfgang Peter, Beat M. Frey, Maja P. Mattle-Greminger
2022
- Prevalence of Occult Hepatitis B Virus Infection in Blood Donors with Negative ID-NAT in Switzerland
Andrea Zbinden, Judith Ries, Patrick M. Redli, Cyril Shah, Andreas Glauser, David Goslings, Daniela Huzly, Jürg Böni, Jochen Gottschalk, Beat M. Frey
- Antibodies from convalescent plasma promote SARS-CoV-2 clearance in individuals with and without endogenous antibody response
Maddalena Marconato, Irene A. Abela, Anthony Hauser, Magdalena Schwarzmüller, Rheliana Katzensteiner, Dominique L. Braun, Selina Epp, Annette Audigé, Jacqueline Weber, Peter Rusert, Eméry Schindler, Chloé Pasin, Emily West, Jürg Böni, Verena Kufner, Michael Huber, Maryam Zaheri, Stefan Schmutz, Beat M. Frey, Roger D. Kouyos,Huldrych F. Günthard, Markus G. Manz and Alexandra Trkola
- Basic characteristics and safety of donation in related and unrelated haematopoietic progenitor cell donors - first 10 years of prospective donor follow-up of Swiss donors
M Rüesch, S Amar El Dusouqui, E Buhrfeind, A Buser, Y Chalandon, B M Frey, T Güngör, A Holbro, S Huguet, L Infanti, G Nair, G Nicoloso, J R Passweg, U Schanz, J-M Tiercy, I Widmer, U Zeilhofer, L Zurkinden, J P Halter.
- The effect of a natural polyphenol supplement on iron absorption in adults with hereditary hemochromatosis
Simone Buerkli, Laura Salvioni, Natalie Koller, Christophe Zeder, Maria José Teles, Graça Porto, Jana Helena Habermann, Irina Léa Dubach, Florence Vallelian, Beat M. Frey, Diego Moretti, Jeannine Baumgartner, Michael B. Zimmermann
- ATMPs: New Challenge for Transfusion Services
- Multiplexed high-throughput immune cell imaging reveals molecular health-associated phenotypes
Y. Severin, B. D. Hale, J. Mena, D. Goslings, B. M. Frey, B. Snijder
2021
- Microfluidic Characterisation reveals Broad Range of SARS-CoV-2 Antibody Affinity in Human Plasma
Matthias M Schneider, Marc Emmenegger, Catherine K Xu, Itzel Condado Morales, Georg Meisl, Priscilla Rurelli, Chriyssa Zografou, Manuela R Zimmermann, Beat M Frey, Sebastian Fiedler, Viola Denninger, Raphaël PB Jacquat, Lidia Madrigal, Alison Illsley, Vasilis Kosmoliaptsis, Heike Fiegler, Didier Trono, Tuomas PJ Knowles, Adriano Aguzzi
- Multifactorial seroprofiling dissects the contribution of pre-existing human coronaviruses responses to SARS-CoV-2 immunity
Irene A. Abela, Chloé Pasin, Magdalena Schwarzmüller Selina Epp, Michèle E. Sickmann, Merle M. Schanz, Peter Rusert, Jacqueline Weber, Stefan Schmutz, Annette Audigé, Liridona Maliqi,Annika Hunziker, Maria C. Hesselman, Cyrille R. Niklaus, Jochen Gottschalk, Eméry Schindler, Alexander Wepf, Urs Karrer, Aline Wolfensberger, Silvana K. Rampini, Patrick M. Meyer Sauteur, Christoph Berger, Michael Huber, Jürg Böni, Dominique L. Braun, Maddalena Marconato, Markus G. Manz , Beat M. Frey , Huldrych F. Günthard Roger D. Kouyos, Alexandra Trkola
- McLeod Neuroacanthocytosis Syndrome
Hans H Jung, Adrian Danek, Ruth H Walker, Beat M Frey, and Kevin Peikert
Created: December 3, 2004; Updated: September 16, 2021.
2020
- Clonal hematopoiesis in donors and long-term survivors of related allogeneic hematopoietic stem cell transplantation
Steffen Boettcher, C. Matthias Wilk,, Jochen Singer, Fabian Beier, Elodie Burcklen, Christian Beisel, Monica S. Ventura Ferreira,Elise Gourri,Christoph Gassner, Beat M. Frey, Urs Schanz, Radek C. Skoda, Benjamin L. Ebert,Tim H. Brummendorf,Niko Beerenwinkel, and Markus G. Manz
- Two Prevalent ∼100-kb GYPB deletions in S–s–U– phenotypes of Black Africans
Christoph Gassner, Gregory A. Denomme, Claudia Portmann, Kathleen M. Bensing, Maja P. Mattle-Greminger, Stefan Meyer, Nadine Trost, Young-Lan Song, Charlotte Engström, Christof Jungbauer, Burkhard Just, Jill R. Storry, Michael Forster, Andre Franke, Beat M. Frey
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