Thorunn Rafnar

36PUBLICATIONS
204CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Medical infection agents (incl. prions)Epigenetics (incl. genome methylation and epigenomics)HaematologyPharmacogenomics
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Publications (36)

|Oct 30, 2024
Gene-based burden tests of rare germline variants identify six cancer susceptibility genes.

Erna V Ivarsdottir, Julius Gudmundsson, Vinicius Tragante

|Aug 27, 2024
Homozygosity for a stop-gain variant in CCDC201 causes primary ovarian insufficiency.

Asmundur Oddsson, Valgerdur Steinthorsdottir, Gudjon R Oskarsson

|Aug 05, 2024
Deciphering the genetics and mechanisms of predisposition to multiple myeloma.

Molly Went, Laura Duran-Lozano, Gisli H Halldorsson

|Jul 24, 2024
The correlation between CpG methylation and gene expression is driven by sequence variants.

Olafur Andri Stefansson, Brynja Dogg Sigurpalsdottir, Solvi Rognvaldsson

|Jul 09, 2024
Start codon variant in LAG3 is associated with decreased LAG-3 expression and increased risk of autoimmune thyroid disease.

Saedis Saevarsdottir, Kristbjörg Bjarnadottir, Thorsteinn Markusson

|May 22, 2024
Author Correction: Large-scale plasma proteomics comparisons through genetics and disease associations.

Grimur Hjorleifsson Eldjarn, Egil Ferkingstad, Sigrun H Lund

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