Ann‐Christine Syvänen

Uppsala University — Sweden

Medicine · Health Sciences

40h-index8.2kcitations153works0.02yr avg
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Research Topics

Acute Lymphoblastic Leukemia research(23), Epigenetics and DNA Methylation(20), Salivary Gland Disorders and Functions(15), Genetic Associations and Epidemiology(13), Molecular Biology Techniques and Applications(12)

Publications146 total

From early methods for DNA diagnostics to genomes and epigenomes at high resolution during four decades – a personal perspective
Upsala Journal of Medical Sciences·2024Open Access
Multimodal classification of molecular subtypes in pediatric acute lymphoblastic leukemia
npj Precision Oncology·2023· 25 citedOpen Access
Distinct HLA associations with autoantibody-defined subgroups in idiopathic inflammatory myopathies
EBioMedicine·2023· 14 citedOpen Access
Multimodal <scp>Single‐Cell</scp> Sequencing of B Cells in Primary Sjögren's Syndrome
Arthritis & Rheumatology·2023· 41 citedOpen Access
OP0021 STRATIFICATION OF PATIENTS WITH SJÖGREN'S SYNDROME BY JOINT MULTI-MODAL ANALYSIS OF CIRCULATING B CELLS
Annals of the Rheumatic Diseases·2023· 1 citedOpen Access
Multimodal classification of molecular subtypes in pediatric acute lymphoblastic leukemia
2023· 6 citedOpen Access
Distinct HLA Associations with Autoantibody-Defined Subgroups in Idiopathic Inflammatory Myopathies
SSRN Electronic Journal·2023· 5 citedOpen Access
Mutational patterns and clonal evolution from diagnosis to relapse in pediatric acute lymphoblastic leukemia
Scientific Reports·2021· 13 citedOpen Access
DNA Methylation-Based Interferon Scores Associate With Sub-Phenotypes in Primary Sjögren’s Syndrome
Frontiers in Immunology·2021· 37 citedOpen Access
Higher magnesium intake is associated with lower fasting glucose and insulin, with no evidence of interaction with select genetic loci, in a meta-analysis of 15 CHARGE consortium studies 1-4
UNC Libraries·2020Open Access
Function of multiple sclerosis-protective HLA class I alleles revealed by genome-wide protein-quantitative trait loci mapping of interferon signalling
PLoS Genetics·2020· 24 citedOpen Access
Exome Sequencing Reveals Common and Rare Variants in <i>F5</i> Associated With ACE Inhibitor and Angiotensin Receptor Blocker–Induced Angioedema
Clinical Pharmacology & Therapeutics·2020· 22 citedOpen Access
O34 Variants in <i>BANK1</i> are associated with lupus nephritis
Oral Presentations·2020Open Access
Refined detection and phasing of structural aberrations in pediatric acute lymphoblastic leukemia by linked-read whole-genome sequencing
Scientific Reports·2020· 17 citedOpen Access
Variants in BANK1 are associated with lupus nephritis
2020Open Access
Protein and DNA methylation-based scores as surrogate markers for interferon system activation in patients with primary Sjögren’s syndrome
RMD Open·2020· 22 citedOpen Access
Overexpression of chromatin remodeling and tyrosine kinase genes in iAMP21-positive acute lymphoblastic leukemia
Leukemia & lymphoma/Leukemia and lymphoma·2019· 8 citedOpen Access
Interferon signature in patients with <i>STAT1</i> gain‐of‐function mutation is epigenetically determined
European Journal of Immunology·2019· 35 citedOpen Access
Author response for "Interferon signature in patients with &lt;i&gt;STAT1&lt;/i&gt; gain-of-function mutation is epigenetically determined"
2019
Exploring rare and low-frequency variants in the Saguenay–Lac-Saint-Jean population identified genes associated with asthma and allergy traits
European Journal of Human Genetics·2018· 12 citedOpen Access
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Frequent Co-authors

Jessica Nordlund(15), Gudmar Lönnerholm(9), Erik Forestier(7), Gunnel Nordmark(7), Mats Heyman(6), Lars Rönnblom(6), Johanna K. Sandling(6), Eva Berglund(5), Maija‐Leena Eloranta(5), Trond Flægstad(5), Kjeld Schmiegelow(5), Juliana Imgenberg‐Kreuz(5), Lili Milani(5), Hans Söderlund(5), Tomas Axelsson(5), Per Wahlberg(4), Johan Dahlberg(4), Anders Lundmark(4), Jukka Kanerva(4), Gisela Barbany(4)