Author

Ann‐Christine Syvänen

Uppsala UniversityORCID 0000-0002-9681-9146Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 4 Approach:statistical model· 3 Research Focus:differential expression· 2 Research Focus:gene regulatory network inference· 2 Assay:whole-genome sequencing· 2 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:database / resource· 1

Frequent Co-Authors

Jessica NordlundiD· 2 shared A. R. Rekha· 1 shared Adam AmeuriD· 1 shared Aditya Vailaya· 1 shared Amanda RaineiD· 1 shared Anders LundmarkiD· 1 shared Andreas KähäriiD· 1 shared Anne BordroniD· 1 shared

Activity by Year

2017-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 10 mutual co-author links

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2 shared papersImmunology

Jessica NordlundORCID

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Author profile →

4 papers

Recent·Most cited

Interferon-α-Driven Stratification of B Cell Reveals Metabolic Reprogramming of Double Negative, Naive and Transitional cell subsets and Refines Molecular Classification in Söjgren's Disease.

Cristian Iperi, A. R. Rekha, Gustav Arvidsson, Gunnel Nordmark, Éléonore Bettacchioli, Marie Frutoso, Marta Eugenia Alarcón-Riquelme, Jessica Nordlund, Ann‐Christine Syvänen, Valérie Devauchelle‐Pensec, Divi Cornec, Sophie Hillon, Anne Bordron

This paper identifies an IFN-α signature in B cells of Sjögren's disease patients, revealing metabolic reprogramming and refining molecular classification.

European Journal of Immunology · Sep 1, 2026Peer-reviewedImmunology

Refined detection and phasing of structural aberrations in pediatric acute lymphoblastic leukemia by linked-read whole genome sequencing

Jessica Nordlund, Yanara Marincevic-Zuniga, Lucia B. Cavelier, Amanda Raine, Tom Martin, Anders Lundmark, Jonas Abrahamsson, Ulrika Norén‐Nyström, Gudmar Lönnerholm, Ann‐Christine Syvänen

This study uses linked-read whole genome sequencing to detect and phase structural aberrations in pediatric ALL with higher resolution than traditional methods.

Scientific Reports · Feb 13, 2020Peer-reviewedGenomics

Haplotypes associated to gene expression in breast cancer: can they lead us to the susceptibility markers?

Hege Edvardsen, Bettina Kulle, Anya Tsalenko, Grethe Irene Grenaker Alnæs, Fredrik Ekeberg Johansen, Espen Enerly, Aditya Vailaya, Per Eystein Lønning, Åslaug Helland, Ann‐Christine Syvänen, Zohar Yakhini B, Anne‐Lise Børresen‐Dale, Arnoldo Frigessi, Vessela Nedelcheva Kristensen

The paper identifies haplotypes and LD patterns in 80 genes that differ between breast cancer patients and controls, and finds negative correlations in LD patterns for some genes.

bioRxiv · Feb 2, 2018 · PreprintGenomics

SweGen: A whole-genome map of genetic variability in a cross-section of the Swedish population

Adam Ameur, Johan Dahlberg, Pall I. Olason, Francesco Vezzi, Robert Karlsson, Marcel Martin, Johan Viklund, Andreas Kähäri, Pär Lundin, Huiwen Che, Jessada Thutkawkorapin, Jesper Eisfeldt, Samuel Lampa, Mats Dahlberg, Jonas Hagberg, , Ulf B Gyllensten

SweGen provides a high-quality whole-genome map of genetic variation in the Swedish population, useful for clinical genetics and association studies.

European Journal of Human Genetics · Aug 23, 2017Peer-reviewedGenetics