Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Sonja Sigurdardottir

Showing results (1-10 of 9) with videos related to

Pageof 1
Sort By:
Blood Advances|November 10, 2025
Proof-of-principle: Nanopore adaptive sampling enables full blood group genome analysis and resolution of hybrid allelesMorgan Gueuning, Gian Andri Thun, Samuel Koller, et al.
Transfusion|May 31, 2017
Stepwise partitioning of Xp21: a profiling method for XK deletions causative of the McLeod syndromeChristoph Gassner, Chantal Brönnimann, Yvonne Merki, et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis|March 25, 2014
Molecular RHD screening of RhD negative donors can replace standard serological testing for RhD negative donorsPeter Gowland, Christoph Gassner, Hein Hustinx, et al.
Biomedicines|January 26, 2024
Resolving Genotype-Phenotype Discrepancies of the Kidd Blood Group System Using Long-Read Nanopore SequencingMorgan Gueuning, Gian Andri Thun, Nadine Trost, et al.
Vox Sanguinis|January 16, 2024
Novel regulatory variant in ABO intronic RUNX1 binding site inducing A<sub>3</sub> phenotypeGian Andri Thun, Morgan Gueuning, Sonja Sigurdardottir, et al.
Journal of Neuroimmunology|October 25, 2003
A whole genome association study in Icelandic multiple sclerosis patients with 4804 markersAslaug Jonasdottir, Theodora Thorlacius, Ragnheidur Fossdal, et al.
Blood Advances|September 21, 2022
Haplotype sequence collection of ABO blood group alleles by long-read sequencing reveals putative A1-diagnostic variantsMorgan Gueuning, Gian Andri Thun, Michael Wittig, et al.
British Journal of Haematology|April 14, 2016
MNSs genotyping by MALDI-TOF MS shows high concordance with serology, allows gene copy number testing and reveals new St(a) allelesStefan Meyer, Caren Vollmert, Nadine Trost, et al.
Transfusion Medicine and Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie|October 5, 2018
Low-Frequency Blood Group Antigens in SwitzerlandChristoph Gassner, Frauke Degenhardt, Stefan Meyer, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Blood Advances|November 10, 2025
Proof-of-principle: Nanopore adaptive sampling enables full blood group genome analysis and resolution of hybrid allelesMorgan Gueuning, Gian Andri Thun, Samuel Koller, et al.
Transfusion|May 31, 2017
Stepwise partitioning of Xp21: a profiling method for XK deletions causative of the McLeod syndromeChristoph Gassner, Chantal Brönnimann, Yvonne Merki, et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis|March 25, 2014
Molecular RHD screening of RhD negative donors can replace standard serological testing for RhD negative donorsPeter Gowland, Christoph Gassner, Hein Hustinx, et al.
Biomedicines|January 26, 2024
Resolving Genotype-Phenotype Discrepancies of the Kidd Blood Group System Using Long-Read Nanopore SequencingMorgan Gueuning, Gian Andri Thun, Nadine Trost, et al.
Vox Sanguinis|January 16, 2024
Novel regulatory variant in ABO intronic RUNX1 binding site inducing A<sub>3</sub> phenotypeGian Andri Thun, Morgan Gueuning, Sonja Sigurdardottir, et al.
Journal of Neuroimmunology|October 25, 2003
A whole genome association study in Icelandic multiple sclerosis patients with 4804 markersAslaug Jonasdottir, Theodora Thorlacius, Ragnheidur Fossdal, et al.
Blood Advances|September 21, 2022
Haplotype sequence collection of ABO blood group alleles by long-read sequencing reveals putative A1-diagnostic variantsMorgan Gueuning, Gian Andri Thun, Michael Wittig, et al.
British Journal of Haematology|April 14, 2016
MNSs genotyping by MALDI-TOF MS shows high concordance with serology, allows gene copy number testing and reveals new St(a) allelesStefan Meyer, Caren Vollmert, Nadine Trost, et al.
Transfusion Medicine and Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie|October 5, 2018
Low-Frequency Blood Group Antigens in SwitzerlandChristoph Gassner, Frauke Degenhardt, Stefan Meyer, et al.
Pageof 1