Institut für Translationale Medizin

Gassner C. PIEZO1: now also featuring blood group antigens: Editorial. Blood in press.

Clausen FB, Hellberg Å, Bein G, Bugert P, Schwartz D, Drnovsek TD et al. Recommendation for validation and quality assurance of non-invasive prenatal testing for foetal blood groups and implications for IVD risk classification according to EU regulations. Vox Sang 2022; 117(2):157–65. 
PMID: 34155647 

Degenhardt F, Ellinghaus D, Juzenas S, Lerga-Jaso J, Wendorff M, Maya-Miles D et al. Detailed stratified GWAS analysis for severe COVID-19 in four European populations. Hum Mol Genet 2022.
PMID: 35848942

Gassner C, Olsson ML, Lane WJ, Hyland CA. Novel or not? Reference alleles, genes, and genomes to unmask the true nature of the ABO*AW.10 allele associated with weak A phenotype: Editorial. Transfusion 2022; 62(4):721–4.
PMID: 335383952

Gassner C, Scherer V, Zanolin-Purin D, Scharberg EA, Flesch B. Occurrence of Rare Deletional Yus and Gerbich Alleles in Syria and Neighbouring Countries. Transfusion medicine and hemotherapy 2022:1–9.
DOI: 10.1159/000524249 

Gassner C, Wagner FF. Blood Groups and Their Correlation with Hereditary Disease: Editorial. Transfusion medicine and hemotherapy 2022; 49(1):1–3. Available from: URL: https://www.karger.com/Article/FullText/521418.

Gueuning M, Schneider L, Thun GA, Trost N, Sigurdardottir S, Engstroem C et al. Nanopore sequencing to resolve KIDD blood group discrepancies: Abstract. Clin.Lab. 2022; Abstract No. 24(08):14–5.

Henny C, Engstroem C, Gassner C, Still F, Gottschalk J, Sigurdardottir S, Frey B.M., Niederhauser C., Hustinx H, Meyer S, Crotett S.L. Ten years of donor RHD Screening in Schwitzerland: Abtract. Clin.Lab. 2022; Abstract No.5(08):3–4.

Mattle-Greminger M, Gueuning M, Thun GA, Wittig M, Galati AL, Meyer S et al. Reference sequences for AB0 alleles by long-read sequencing reveal putative A1-diagnostic variants: Abstract. Clin.Lab. 2022; Abstract No. 26(08):15–6.
PMID: 34060100 

Steiert TA, Fuß J, Juzenas S, Wittig M, Hoeppner MP, Vollstedt M et al. High-throughput method for the hybridisation-based targeted enrichment of long genomic fragments for PacBio third-generation sequencing. NAR Genom Bioinform 2022; 4(3):lqac051.
PMID: 35855323

COVID-19 Host Genetics Initiative. Mapping the human genetic architecture of COVID-19. Nature 2021; 600(7889):472–7.
PMID: 34237774      PDF

Mattle-Greminger MP, Gueuning M, Thun GA, Wittig M,Galati AL, Meyer S, Fuss J, Sigurdardottir S Trost N, Merki Y, Neuenschwander K Gourri E, Busch Y, Gottschalk J, Franke A, Frey BM, Gassner C, Peter W. Complete reference sequences for ABO blood group gene alleles by long-read sequencing: Abstract. Vox Sang 2021; 116 Suppl 1:5–188.
PMID: 34060100    PDF 

Mattle-Greminger MP, Thun GA, Gueuning M, Wittig M, Galati AL, Meyer S, Fuss J, Sigurdardottir S Trost N, Merki Y, Neuenschwander K Gourri E, Busch Y, Gottschalk J, Franke A, Frey BM, Gassner C, Peter W. Fully-phased reference sequences for ABO blood group gene alleles by long-read Nanopore sequencing: putative ABO*A1-specific single-nucleotide variants revealed: Abstract. Transfusion medicine and hemotherapy 2021; 48(Suppl. 1):1–77.
DOI: 10.1159/000518751       Karger

Meyer S, Schneider L, Gueuning M, Trost N, Sigurdardottir S, Engström C, Rizzi G, Merki Y, Neuenschwander K Thun GA, Gassner C, Mattle-Greminger MP, Frey BM. From high-throughput genotyping to nanopore sequencing: resolving genotype/phenotype discrepancies of the kidd blood group system revealed novel null alleles and a large deletion variants revealed: Abstract. Transfusion medicine and hemotherapy 2021; 48(Suppl. 1):1-77.
DOI: 10.1159/000518751       Karger

Gassner C, Purin D. Erstellung eines Referenz-Genoms menschlicher Blutgruppen. «160 im Quadrat» Wissenschaftsmagazin des Liechtenstein-Instituts und der Universität Liechtenstein. 2021 [cited 2022 Jul 7]:64–5. Available from: URL: www.liechtenstein-institut.li/application/files/7016/3835/6661/Forschungsmagazin160_2_Web.pdf.

Boettcher S, Wilk CM, Singer J, Beier F, Burcklen E, Beisel C et al. Clonal hematopoiesis in donors and long-term survivors of related allogeneic hematopoietic stem cell transplantation. Blood 2020; 135(18):1548–59.
PMID: 32558485

Ellinghaus D, Degenhardt F, Bujanda L, Buti M, Albillos A, Invernizzi P et al. Genomewide Association Study of Severe Covid-19 with Respiratory Failure. N Engl J Med 2020; 383(16):1522–34.
PMID: 32558485

Engstroem C, Rizzi G, Trost N, Zorbas A, Neuenschwander K, Song Y, Meyer E, Gassner C, Frey BM, Meyer S. Bombay in-house: Highlight of a Molecular Employee Screening: Abstract. Vox Sang 2020; 115 Suppl 1:3–387.

Gassner C. Next-Generation Sequencing in Blood Group Genomics: State of the Art and Perspectives: Editorial. Transfus Med Hemother 2020; 47(1):2–3.
PMID: 32110188

Gassner C, Denomme GA, Portmann C, Bensing KM, Mattle-Greminger MP, Meyer S et al. Two Prevalent ∼100-kb GYPB Deletions Causative of the GPB-Deficient Blood Group MNS Phenotype S-s-U- in Black Africans. Transfus Med Hemother 2020; 47(4):326–36.

Hyland CA, Gassner C, Daly J, Flower R. Blood Group Antigens in the Genomic Era: Abstract. Vox Sang 2020; 115 Suppl 1:3–387.

Young-Lan Song, Pascal Weisser, Gabriella Rizzi, Nadine Trost, David Goslings, Yvonne Merki, Beat M. Frey, Christoph Gassner, Stefan Meyer, Charlotte Engström. Securing supply of HPA-1a negative platelet concentrates for FNAIT patients: Abstract. 53. Jahrestagung der Deutschen Gesellschaft für Transfusionsmedizin und Immunhämatologie e.V. (DGTI) 2020 [cited 2021 Jun 25].
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