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Eriksson D

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Family name Eriksson
Given name Daniel
Initials D
ORCID

ORCID 0000-0001-5473-3312
Affiliations Department of Medicine (Solna), Center for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden. daniel.eriksson@ki.se.
Department of Endocrinology, Metabolism and Diabetes Karolinska University Hospital, Stockholm, Sweden. daniel.eriksson@ki.se.

6 publications

PubMed DOI Crossref
Incontinentia pigmenti underlies thymic dysplasia, autoantibodies to type I IFNs, and viral diseases.
Rosain J, Le Voyer T, Liu X, ..., Anderson MS, Casanova JL
J. Exp. Med. 221 (11) - [2024-11-04; online 2024-10-01]
Autoimmunity and Serology Profiling [Service]
PubMed DOI Crossref
Integrating a Polygenic Risk Score into a clinical setting would impact risk predictions in familial breast cancer.
Baliakas P, Munters AR, Kämpe A, ..., Ladenvall C, Eriksson D
J. Med. Genet. - (-) - [2023-08-14; online 2023-08-14]
Bioinformatics Support for Computational Resources [Service] Clinical Genomics Uppsala [Collaborative]
PubMed DOI Crossref
GWAS for autoimmune Addison's disease identifies multiple risk loci and highlights AIRE in disease susceptibility.
Eriksson D, Røyrvik EC, Aranda-Guillén M, ..., Kämpe O, Husebye ES
Nat Commun 12 (1) 959 [2021-02-11; online 2021-02-11]
Bioinformatics Support for Computational Resources [Service]
PubMed DOI Crossref
Comment on 'AIRE-deficient patients harbor unique high-affinity disease-ameliorating autoantibodies'.
Landegren N, Rosen LB, Freyhult E, ..., Anderson M, Kämpe O
Elife 8 (-) - [2019-06-27; online 2019-06-27]
Autoimmunity and Serology Profiling [Service] Bioinformatics Support and Infrastructure [Service] Bioinformatics Support, Infrastructure and Training [Service]
PubMed DOI Crossref
Common genetic variation in the autoimmune regulator (AIRE) locus is associated with autoimmune Addison's disease in Sweden.
Eriksson D, Bianchi M, Landegren N, ..., Rosengren Pielberg G, Kämpe O
Sci Rep 8 (1) 8395 [2018-05-30; online 2018-05-30]
Bioinformatics Support for Computational Resources [Service] NGI Uppsala (SNP&SEQ Technology Platform) [Service] National Genomics Infrastructure [Service]
PubMed DOI Crossref
Extended exome sequencing identifies BACH2 as a novel major risk locus for Addison's disease.
Eriksson D, Bianchi M, Landegren N, ..., Kämpe O, Pielberg GR
J. Intern. Med. 280 (6) 595-608 [2016-12-00; online 2016-11-02]
Bioinformatics Support for Computational Resources [Service] NGI Uppsala (SNP&SEQ Technology Platform) [Service] National Genomics Infrastructure [Service]
SciLifeLab Data Centre
Publications 9.5.1