Björn Nilsson

15PUBLICATIONS
109CO-AUTHORS
Gene and molecular therapyGene expression (incl. microarray and other genome-wide approaches)Immunogenetics (incl. genetic immunology)Medical infection agents (incl. prions)Gene mapping
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Publications (15)

|Sep 30, 2026
Human genetics implicates a BACH2-NRF2 axis in fetal haemoglobin activation.

|Nov 18, 2025
Putative multiple myeloma susceptibility genes identified by exome sequencing of 347 familial and early-onset cases.

Maroulio Pertesi, Delphine Demangel, Abhishek Niroula

|Sep 14, 2024
Sequence variants influencing the regulation of serum IgG subclass levels.

Thorunn A Olafsdottir, Gudmar Thorleifsson, Aitzkoa Lopez de Lapuente Portilla

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

Molly Went, Laura Duran-Lozano, Gisli H Halldorsson

|Jun 10, 2023
Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality.

Asmundur Oddsson, Patrick Sulem, Gardar Sveinbjornsson

|Jan 11, 2022
Functional dissection of inherited non-coding variation influencing multiple myeloma risk.

Ram Ajore, Abhishek Niroula, Maroulio Pertesi

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Frequent Collaborators

8 joint publications

Gisli H Halldorsson

7 joint publications

Thorunn Rafnar

6 joint publications

Ingileif Jonsdottir

6 joint publications

Kari Stefansson