Author

Sunyoung Ham

QIMR Berghofer Medical Research Institute

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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Genetics· 1 Molecular Biology· 1

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Research Focus:differential expression· 2 Organism:human· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Assay:ChIP-seq· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Research Focus:GWAS / association mapping· 1

Frequent Co-Authors

Alison M. DunningiD· 2 shared Andreas MölleriD· 2 shared Douglas F. EastoniD· 2 shared Georgia Chenevix‐TrenchiD· 2 shared Haran SivakumaraniD· 2 shared Jonathan BeesleyiD· 2 shared Juliet D. FrenchiD· 2 shared Kristine M. HillmaniD· 2 shared

Activity by Year

2019-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersMolecular Biology

Alison M. DunningORCID

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2 papers

Recent·Most cited

Chromatin interactome mapping at 139 independent breast cancer risk signals

Jonathan Beesley, Haran Sivakumaran, Mahdi Moradi Marjaneh, Luize Goncalves Lima, Kristine M. Hillman, Susanne Kaufmann, Natasha Tuano, Nehal Hussein, Sunyoung Ham, Pamela Mukhopadhyay, Stephen H. Kazakoff, Jason S. Lee, Kyriaki Michailidou, Daniel R. Barnes, Antonis C. Antoniou, , Stacey L. Edwards

The paper maps chromatin interactions at 139 breast cancer risk signals using Capture Hi-C and identifies candidate target genes and functional mechanisms.

Genome biology · Jan 7, 2020Peer-reviewedMolecular Biology

High-throughput allelic expression imbalance analyses identify candidate breast cancer risk genes

Mahdi Moradi Marjaneh, Haran Sivakumaran, Kristine M. Hillman, Susanne Kaufmann, Nehal Hussein, Luize Goncalves Lima, Sunyoung Ham, Siddhartha Kar, Jonathan Beesley, Laura Fachal, Douglas F. Easton, Alison M. Dunning, Andreas Möller, Georgia Chenevix‐Trench, Stacey L. Edwards, Juliet D. French

The paper identifies 14 genes, including NTN4, associated with breast cancer risk variants through allelic expression imbalance analysis.

bioRxiv · Jan 16, 2019 · PreprintGenetics