Sonja Sigurdardottir

Zurich, ZH, Switzerland

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 8 publications

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

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

Journal: Blood advances

Published: July 15, 2025

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

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

Journal: Biomedicines

Published: November 30, 2023

Novel regulatory variant in ABO intronic RUNX1 binding site inducing A3 phenotype.

Novel regulatory variant in ABO intronic RUNX1 binding site inducing A3 phenotype.

Journal: Vox sanguinis

Published: August 25, 2023

Haplotype sequence collection of ABO blood group alleles by long-read sequencing reveals putative A1-diagnostic variants.

Haplotype sequence collection of ABO blood group alleles by long-read sequencing reveals putative A1-diagnostic variants.

Journal: Blood advances

Published: February 11, 2022

Low-Frequency Blood Group Antigens in Switzerland.

Low-Frequency Blood Group Antigens in Switzerland.

Journal: Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie

Published: March 26, 2018

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

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

Journal: Transfusion

Published: September 08, 2016

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

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

Journal: British journal of haematology

Published: October 27, 2015

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

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

Journal: Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis

Published: March 25, 2014

Showing 1-8 of 8

Last Updated: 09/26/2026