Author

Jonathan Chung

Novartis (Switzerland)

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Bioinformatics· 1 Genetic & Genomic Medicine· 1 Genetics· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Approach:statistical model· 4 Organism:human· 3 Research Focus:GWAS / association mapping· 2 Assay:GWAS summary statistics· 2 Research Focus:cell type annotation· 1 Assay:CITE-seq· 1 Research Focus:clustering· 1 Research Focus:differential expression· 1

Frequent Co-Authors

Åsa K. HedmaniD· 2 shared Markus PerolaiD· 2 shared Aarno V. PalotieiD· 1 shared Abbas DehghaniD· 1 shared Adam E. Ziemann· 1 shared Adriana Huertas‐Vázquez· 1 shared Alaa A. ShalabyiD· 1 shared Alanna C. MorrisoniD· 1 shared

Activity by Year

2019-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 30 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Åsa K. HedmanORCID

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Author profile →

4 papers

Recent·Most cited

Large-scale genome-wide analyses with proteomics integration reveal novel loci and biological insights into frailty

Jonathan K. L. Mak, Chenxi Qin, Moritz Krüger, Anna Kuukka, FinnGen, Aarno V. Palotie, Mark J. Daly, Bridget Riley-Gillis, Howard J. Jacob, Dirk S. Paul, Slavé Petrovski, Heiko Runz, Sally John, George Okafo, Robert M. Plenge, , Ekaterina A. Khramtsova

This study identifies 1,242 novel genetic variants and 31 novel genes associated with frailty through genome-wide association and proteomics integration.

Nature Aging · Aug 5, 2025Peer-reviewedGenetic & Genomic Medicine

Patient brain organoids identify a link between the 16p11.2 copy number variant and the RBFOX1 gene.

Milos Kostic, Joseph J. Raymond, Christophe A. C. Freyre, Beata Henry, Tayfun Tumkaya, Jivan Khlghatyan, Jill Dvornik, Jingyao Li, Jack S. Hsiao, Seon Hye Cheon, Jonathan Chung, Yishan Sun, Ricardo E. Dolmetsch, Kathleen A. Worringer, Robert J. Ihry

The paper uses patient brain organoids to show that 16p11.2 CNVs affect RBFOX1 expression and link it to neurodevelopmental disorders.

ACS Chemical Neuroscience · Oct 30, 2023Peer-reviewedNeuroscience

TrackSOM: mapping immune response dynamics through sequential clustering of time- and disease-course single-cell cytometry data

Givanna Putri, Jonathan Chung, Davis N. Edwards, Felix Marsh‐Wakefield, Irena Koprinska, Suat Dervish, Nicholas J. C. King, Thomas M. Ashhurst, Mark Norman Read

TrackSOM maps immune response dynamics through sequential clustering of time- and disease-course single-cell cytometry data, revealing heterogeneous immune cell populations and their functional evolution in West Nile Virus infection.

Cytometry Part A · Jun 27, 2022Peer-reviewedBioinformatics

Genome-wide association study provides new insights into the genetic architecture and pathogenesis of heart failure

Sonia H Shah, Albert Henry, Carolina Roselli, Honghuang Lin, Garðar Sveinbjörnsson, Ghazaleh Fatemifar, Åsa K. Hedman, Jemma B. Wilk, Michael P. Morley, Mark D. Chaffin, Anna Helgadóttir, Niek Verweij, Abbas Dehghan, Peter Almgren, Charlotte Andersson, , David J. Stott

This study conducts a large GWAS on heart failure, identifying 12 genetic loci with associations to CAD, atrial fibrillation, and reduced left ventricular function, and provides causal evidence for several risk factors.

bioRxiv · Jul 10, 2019 · PreprintGenetics