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Author Details
Full Name
Jessica Nordlund
Affiliation
Uppsala University
ORCID
Career Start Year
2009
Papers
58
H Index
21
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37610265
Multimodal Single-Cell Sequencing of B Cells in Primary Sjögren's Syndrome.
Arthritis Rheumatol
2024
37463882
Next generation pan-cancer blood proteome profiling using proximity extension assay.
Nat Commun
2023
37758813
Single-cell transcriptomics delineates the immune cell landscape in equine lower airways and reveals upregulation of FKBP5 in horses with asthma.
Sci Rep
2023
37664045
Feasibility to use whole-genome sequencing as a sole diagnostic method to detect genomic aberrations in pediatric B-cell acute lymphoblastic leukemia.
Front Oncol
2023
38012772
Quartet DNA reference materials and datasets for comprehensively evaluating germline variant calling performance.
Genome Biol
2023
38066241
Multimodal classification of molecular subtypes in pediatric acute lymphoblastic leukemia.
NPJ Precis Oncol
2023
37620373
Long-read whole-genome analysis of human single cells.
Nat Commun
2023
37218648
Increased MYB alternative promoter usage is associated with relapse in acute lymphoblastic leukemia.
Genes Chromosomes Cancer
2023
34647650
Transcriptome sequencing of archived lymphoma specimens is feasible and clinically relevant using exome capture technology.
Genes Chromosomes Cancer
2022
35406529
Next Generation Plasma Proteomics Identifies High-Precision Biomarker Candidates for Ovarian Cancer.
Cancers (Basel)
2022
35402448
A Study Protocol for Validation and Implementation of Whole-Genome and -Transcriptome Sequencing as a Comprehensive Precision Diagnostic Test in Acute Leukemias.
Front Med (Lausanne)
2022
35388090
scSPLAT, a scalable plate-based protocol for single cell WGBS library preparation.
Sci Rep
2022
36310597
Tackling the translational challenges of multi-omics research in the realm of European personalised medicine: A workshop report.
Front Mol Biosci
2022
36327219
Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative.
PLoS Genet
2022
34049715
Expression of BCL6 in paediatric B-cell acute lymphoblastic leukaemia and association with prognosis.
Pathology
2021
33837451
Immune cells lacking Y chromosome show dysregulation of autosomal gene expression.
Cell Mol Life Sci
2021
34949218
Author Correction: The SEQC2 epigenomics quality control (EpiQC) study.
Genome Biol
2021
34872606
The SEQC2 epigenomics quality control (EpiQC) study.
Genome Biol
2021
34504347
Establishing community reference samples, data and call sets for benchmarking cancer mutation detection using whole-genome sequencing.
Nat Biotechnol
2021
34504346
Toward best practice in cancer mutation detection with whole-genome and whole-exome sequencing.
Nat Biotechnol
2021
33987955
RAG1 co-expression signature identifies ETV6-RUNX1-like B-cell precursor acute lymphoblastic leukemia in children.
Cancer Med
2021
34362951
Mutational patterns and clonal evolution from diagnosis to relapse in pediatric acute lymphoblastic leukemia.
Sci Rep
2021
34200630
DNA Methylation Signatures Predict Cytogenetic Subtype and Outcome in Pediatric Acute Myeloid Leukemia (AML).
Genes (Basel)
2021
34312421
Leukocytes with chromosome Y loss have reduced abundance of the cell surface immunoprotein CD99.
Sci Rep
2021
32573712
Association of aberrant ASNS imprinting with asparaginase sensitivity and chromosomal abnormality in childhood BCP-ALL.
Blood
2020
34079956
The proliferative history shapes the DNA methylome of B-cell tumors and predicts clinical outcome.
Nat Cancer
2020
32029838
Clinicopathological features and prognostic value of SOX11 in childhood acute lymphoblastic leukemia.
Sci Rep
2020
32054878
Refined detection and phasing of structural aberrations in pediatric acute lymphoblastic leukemia by linked-read whole-genome sequencing.
Sci Rep
2020
31640433
Overexpression of chromatin remodeling and tyrosine kinase genes in iAMP21-positive acute lymphoblastic leukemia.
Leuk Lymphoma
2020
32605573
Genome assembly of the basket willow, Salix viminalis, reveals earliest stages of sex chromosome expansion.
BMC Biol
2020
30484860
CD99 expression is strongly associated with clinical outcome in children with B-cell precursor acute lymphoblastic leukaemia.
Br J Haematol
2019
30989628
Transcriptome and Proteome Profiling of Neural Induced Pluripotent Stem Cells from Individuals with Down Syndrome Disclose Dynamic Dysregulations of Key Pathways and Cellular Functions.
Mol Neurobiol
2019
30378076
Computational and Statistical Analysis of Array-Based DNA Methylation Data.
Methods Mol Biol
2019
28887175
Epigenetics in pediatric acute lymphoblastic leukemia.
Semin Cancer Biol
2018
30304863
De Novo Assembly of Two Swedish Genomes Reveals Missing Segments from the Human GRCh38 Reference and Improves Variant Calling of Population-Scale Sequencing Data.
Genes (Basel)
2018
29668744
Data quality of whole genome bisulfite sequencing on Illumina platforms.
PLoS One
2018
29515676
DNA methylation holds prognostic information in relapsed precursor B-cell acute lymphoblastic leukemia.
Clin Epigenetics
2018
29655283
Transcription profiling of peripheral B cells in antibody-positive primary Sjögren's syndrome reveals upregulated expression of CX3CR1 and a type I and type II interferon signature.
Scand J Immunol
2018
27786413
DNA methylation profiling of pediatric B-cell lymphoblastic leukemia with KMT2A rearrangement identifies hypomethylation at enhancer sites.
Pediatr Blood Cancer
2017
28649984
CD27 expression and its association with clinical outcome in children and adults with pro-B acute lymphoblastic leukemia.
Blood Cancer J
2017
28806978
Transcriptome sequencing in pediatric acute lymphoblastic leukemia identifies fusion genes associated with distinct DNA methylation profiles.
J Hematol Oncol
2017
27899585
SPlinted Ligation Adapter Tagging (SPLAT), a novel library preparation method for whole genome bisulphite sequencing.
Nucleic Acids Res
2017
26857698
Genome-wide DNA methylation analysis in multiple tissues in primary Sjögren's syndrome reveals regulatory effects at interferon-induced genes.
Ann Rheum Dis
2016
26553913
CopyNumber450kCancer: baseline correction for accurate copy number calling from the 450k methylation array.
Bioinformatics
2016
26494837
PAX5-ESRRB is a recurrent fusion gene in B-cell precursor pediatric acute lymphoblastic leukemia.
Haematologica
2016
27590521
Deep targeted sequencing in pediatric acute lymphoblastic leukemia unveils distinct mutational patterns between genetic subtypes and novel relapse-associated genes.
Oncotarget
2016
27620872
Genome-wide repression of eRNA and target gene loci by the ETV6-RUNX1 fusion in acute leukemia.
Genome Res
2016
27552300
DNA methylome analysis of acute lymphoblastic leukemia cells reveals stochastic de novo DNA methylation in CpG islands.
Epigenomics
2016
25355294
The mutational landscape in pediatric acute lymphoblastic leukemia deciphered by whole genome sequencing.
Hum Mutat
2015
26018335
The clinical impact of IKZF1 deletions in paediatric B-cell precursor acute lymphoblastic leukaemia is independent of minimal residual disease stratification in Nordic Society for Paediatric Haematology and Oncology treatment protocols used between 1992 and 2013.
Br J Haematol
2015
1 - 50 of 58
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Francine E Garrett-Bakelman
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Martin Hirst
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Charles G Mullighan
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Robert S Fulton
McDonnell Genome Institute, Washington University School of Medicine
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Jinghui Zhang
Changhai Hospital, Second Military Medical University
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Holger Heyn
Barcelona Institute of Science and Technology, Spain Universitat Pompeu Fabra
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Christoph Plass
German Cancer Research Center
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row(s) 1 - 30 of 30
Collaborators
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Co-authored papers
25
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Uppsala University
Co-authored papers
10
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Co-authored papers
6
Weida Tong
National Center for Toxicological Research
Co-authored papers
5
Ann Nordgren
Co-authored papers
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5
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Institute for Molecular Medicine Finland (FIMM), University of Helsinki
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Ulf Gyllensten
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Wenming Xiao
Human Phenome Institute and Shanghai Cancer Center, Fudan University
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Baitang Ning
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Ming Shi
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3
Jonathan Foox
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Adam Ameur
Co-authored papers
3
Lili Milani
Co-authored papers
3
Joshua Xu
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3
Daniel Sinnett
Sainte-Justine University Hospital Research Center
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Gunnel Nordmark
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Mathias Uhl??n
KTH Royal Institute of Technology
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Per-Henrik Edqvist
Uppsala University
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2
Zivana Tezak
Center for Devices and Radiological Health
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2
John M Greally
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Altuna Akalin
Berlin Institute for Medical Systems Biology
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Chongqing Aier Eye Hospital
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