Author

Charlotte Engström

Observed names: C Engström, C. Engström, Engström, C.

Institution: Swiss Red Cross

Observed institution: Swiss Red Cross

ORCID: 0009-0003-9591-9406

Observed ORCID: 0009-0003-9591-9406

OpenAlex ID: A5031275941

Two Prevalent ∼100-kb GYPB Deletions Causative of the GPB-Deficient Blood Group MNS Phenotype S–s–U– in Black Africans

2020 · Christoph Gassner, Gregory A. Denomme, et al. · Transfusion Medicine and Hemotherapy · 17

Low-Frequency Blood Group Antigens in Switzerland

2018 · Christoph Gassner, Frauke Degenhardt, et al. · Transfusion Medicine and Hemotherapy · 15

Novel regulatory variant in ABO intronic RUNX1 binding site inducing A 3 phenotype

2024 · Gian Andri Thun, Morgan Gueuning, et al. · Vox Sanguinis · 12

Stepwise partitioning of Xp21: a profiling method for XK deletions causative of the McLeod syndrome

2017 · Christoph Gassner, Chantal Brönnimann, et al. · Transfusion · 12

Resolving Genotype–Phenotype Discrepancies of the Kidd Blood Group System Using Long-Read Nanopore Sequencing

2024 · M Gueuning, GA Thun, et al. · Biomedicines · 11

Proof-of-principle: nanopore adaptive sampling enables full blood group genome analysis and resolution of hybrid alleles

2025 · M. Gueuning, G. A. Thun, et al. · Blood Advances · 8

International multicentre evaluation of a new anti‐idiotypic anti‐daratumumab for resolving pre‐transfusion interferences

2026 · Arnaud Reggiani, Sofia Lejon Crottet, et al. · Vox Sanguinis · 4

Involuntary movements, vocalizations and cognitive decline

2019 · Olafur Sveinsson, Bjarne Udd, et al. · Parkinsonism & Related Disorders · 3

Multicenter evaluation of soluble CD38: neutralizing anti-CD38 pan-reactivity to enable alloantibody detection.

2026 · Charlotte Engström, Eliane Scherrer, et al. · Blood transfusion · 2

WITHDRAWN: Novel Xp21.1 deletion associated with unusual features in a large McLeod syndrome kindred

2018 · Olafur Sveinsson, Bjarne Udd, et al. · Parkinsonism & Related Disorders · 2

Non-cryopreserved Kx negative packed red cell concentrates to support hematopoietic stem cell transplantation in McLeod contiguous gene deletion syndrome

2025 · Julian Thalhammer, Charlotte Engström, et al. · Journal of Human Immunity

Auflösung einer KEL1 Diskrepanz als Fallbeispiel der haplotypspezifischen Nanopore-Sequenzierung von Blutgruppengenen

2024 · Gian-Andri Thun, Morgan Gueuning, et al. · Transfusionsmedizin

Supplementary Material for: Two Prevalent ∼100-kb GYPB Deletions Causative of the GPB-Deficient Blood Group MNS Phenotype S–s–U– in Black Africans

2020 · Gassner, C., Denomme, G.A., et al. · Figshare

Supplementary Material for: Low-Frequency Blood Group Antigens in Switzerland

2018 · Gassner, C., Degenhardt, F., et al. · Figshare

28 Serology helps moleculardiagnostics to solve a rare case of homozygous FY*X/FY*X - consequences for transfusion recommendations

2010 · C. Engström, B. Grossrieder, et al. · Transfusion and Apheresis Science

Works count: 15

Citation count: 86

H-index: 6

I10-index: 5