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Jonas Mattisson

Observed name: Mattisson, Jonas
ORCID: 0000-0002-4456-9667
Observed ORCID: 0000-0002-4456-9667
OpenAlex ID: A5090656528
Genetic predisposition to mosaic Y chromosome loss in blood
2019 · Deborah J. Thompson, The Kidney Cancer GWAS Meta-Analysis Project, et al. · Nature · 337
Hematopoietic loss of Y chromosome leads to cardiac fibrosis and heart failure mortality
2022 · Soichi Sano, Keita Horitani, et al. · Science · 261
Immune cells lacking Y chromosome show dysregulation of autosomal gene expression
2021 · Jan P. Dumanski, Jonatan Halvardson, et al. · Cellular and Molecular Life Sciences · 117
Longitudinal changes in the frequency of mosaic chromosome Y loss in peripheral blood cells of aging men varies profoundly between individuals
2019 · Marcus Danielsson, Jonatan Halvardson, et al. · European Journal of Human Genetics · 97
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Mosaic loss of chromosome Y in leukocytes matters
2018 · Lars A. Forsberg, Jonatan Halvardson, et al. · Nature Genetics · 74
Loss of Y and clonal hematopoiesis in blood—two sides of the same coin?
2021 · Viktor Ljungström, Jonas Mattisson, et al. · Leukemia · 49
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Leukocytes with chromosome Y loss have reduced abundance of the cell surface immunoprotein CD99
2021 · Jonas Mattisson, Marcus Danielsson, et al. · Scientific Reports · 48
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Loss of chromosome Y in regulatory T cells
2024 · Jonas Mattisson, Jonatan Halvardson, et al. · BMC Genomics · 32
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Loss of Y in regulatory T lymphocytes in the tumor micro-environment of primary colorectal cancers and liver metastases
2024 · Magdalena Wójcik, Ulana Juhas, et al. · Scientific Reports · 22
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A polygenic risk score predicts mosaic loss of chromosome Y in circulating blood cells
2021 · Moeen Riaz, Jonas Mattisson, et al. · Cell & Bioscience · 15
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Mosaic loss of chromosome Y in blood is associated with male susceptibility for idiopathic pulmonary fibrosis
2025 · Josefin Bjurling, Nicholas W. Chavkin, et al. · Communications Medicine · 13
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Genetic predisposition to mosaic Y chromosome loss in blood is associated with genomic instability in other tissues and susceptibility to non-haematological cancers
2019 · Deborah J. Thompson, Giulio Genovese, et al. · bioRxiv (Cold Spring Harbor Laboratory) · 6
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Genetic predisposition to mosaic Y chromosome loss in blood.
2019 · Thompson, Deborah J, Genovese, Giulio, et al. · Apollo (University of Cambridge) · 5
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Intra-individual changes in the frequency of mosaic loss of chromosome Y over time estimated with a new method
2019 · Marcus Danielsson, Jonatan Halvardson, et al. · bioRxiv (Cold Spring Harbor Laboratory) · 3
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Loss of chromosome Y in regulatory T cells
2023 · Jonas Mattisson, Jonatan Halvardson, et al. · medRxiv · 2
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Whole genome sequencing of familial isolated oesophagus atresia uncover shared structural variants
2020 · Joakim Klar, Helene Engstrand-Lilja, et al. · BMC Medical Genomics · 2
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Framtagning av unika gemensamma sekvenser hos koagulasnegativa stafylokocker
2016 · Jonas Mattisson, Sofia Gräsberg, et al. · KTH Publication Database DiVA (KTH Royal Institute of Technology) · 1
Reply to Veitia
2021 · Marcus Danielsson, Jonatan Halvardson, et al. · European Journal of Human Genetics
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Additional file 5 of Whole genome sequencing of familial isolated oesophagus atresia uncover shared structural variants
2020 · Klar, Joakim, Engstrand-Lilja, Helene, et al. · Figshare
Additional file 2 of Whole genome sequencing of familial isolated oesophagus atresia uncover shared structural variants
2020 · Klar, Joakim, Engstrand-Lilja, Helene, et al. · Figshare
Additional file 4 of Whole genome sequencing of familial isolated oesophagus atresia uncover shared structural variants
2020 · Klar, Joakim, Engstrand-Lilja, Helene, et al. · Figshare
Additional file 7 of Whole genome sequencing of familial isolated oesophagus atresia uncover shared structural variants
2020 · Klar, Joakim, Engstrand-Lilja, Helene, et al. · Figshare
Additional file 6 of Whole genome sequencing of familial isolated oesophagus atresia uncover shared structural variants
2020 · Klar, Joakim, Engstrand-Lilja, Helene, et al. · Figshare
Additional file 8 of Whole genome sequencing of familial isolated oesophagus atresia uncover shared structural variants
2020 · Klar, Joakim, Engstrand-Lilja, Helene, et al. · Figshare
Additional file 3 of Whole genome sequencing of familial isolated oesophagus atresia uncover shared structural variants
2020 · Klar, Joakim, Engstrand-Lilja, Helene, et al. · Figshare
Works count: 36
Citation count: 1,083
H-index: 11
I10-index: 11
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