Author

Iain Goulding

Queen Mary University of London

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

Biology Disciplines

Click to filter author papers

Cancer Biology· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 2 Approach:statistical model· 2 Research Focus:cell-cell communication· 1 Assay:ChIP-seq· 1 Approach:deep learning· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Assay:Hi-C· 1

Frequent Co-Authors

Adam DowleiD· 1 shared Alisa ZverevaiD· 1 shared Andrea GillespieiD· 1 shared Andrew N. HoldingiD· 1 shared Aparna D Sinha· 1 shared Bruno M. SimõesiD· 1 shared Chloë Baldreki· 1 shared Chris Taylor· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

1 shared paperCancer Biology

Adam DowleORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintApr 10, 2026

Functional annotation of breast cancer risk loci implicates perturbation of FILIP1L expression in mammary fibroblasts in influencing breast cancer risk.

Alisa Zvereva, Harriet Kemp, Andrea Gillespie…·Nichola Johnson

The paper identifies a breast cancer risk locus by analyzing functional variants and target genes in mammary fibroblasts, showing their non-autonomous impact on breast cancer risk.

DOI 10.64898/2026.04.09.26350488

humanChIP-seq

Cancer BiologybioRxivPreprintAug 7, 2025

DIANNeR: label-free RIME resolves lineage-restricted Glucocorticoid Receptor interactomes in normal human tissues

Weiye Zhao, Thomas F. Grimes, Susanna F Rose…·Andrew N. Holding

DIANNeR improves detection of GR interactomes in normal tissues by integrating DIA, ion mobility, and library-free analysis, revealing context-specific networks and previously undetected interactions.

1 citation

humanproteomics