Author

Konain Bhatti

Imperial College 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

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Genetics· 1 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Assay:imaging· 1 Assay:spatial transcriptomics· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Bin LiuiD· 2 shared Gisli R. JenkinsiD· 2 shared Iain D. StewartiD· 2 shared Louise V. WainiD· 2 shared Simon R. JohnsoniD· 2 shared Alison E. JohniD· 1 shared Amanda L. TatleriD· 1 shared Andressa Alves Bordignon· 1 shared

Activity by Year

2024-2024 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 41 mutual co-author links

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2 shared papersMolecular Biology

Bin LiuORCID

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Author profile →

2 papers

Recent·Most cited

Spatial multiomic profiling reveals distinct fibrotic epithelial niches in idiopathic pulmonary fibrosis

Bin Liu, Konain Bhatti, Iain D. Stewart, James Michael May, Maria Concetta Zarcone, Nathalie Lambie, Nik Matthews, Rachel L. Clifford, Charlotte H. Dean, Peter Myles George, Richard J Hewitt, Elena Ana López-Jiménez, Maddy Parsons, Simon R. Johnson, Anna K. Reed, , Alison E. John

The paper uses spatial multiomic profiling to identify distinct fibrotic epithelial niches in IPF, revealing a KRT5low/KRT17 epithelial population and its association with SPP1 macrophages.

bioRxiv · Dec 10, 2024 · PreprintMolecular Biology

Burden of rare pathogenic variants suggests disrupted cytoskeletal organisation in the pathogenesis of pulmonary fibrosis

Konain Bhatti, Dapeng Wang, Hernan Fainberg, Andressa Alves Bordignon, Yujie Ni, Bin Liu, Simon R. Johnson, Richard Allen, Louise V. Wain, Toby M. Maher, Philip L Molyneaux, Elisabetta Renzoni, Gauri Saini, Deborah Morris-Rosendahl, Gisli R. Jenkins, Iain D. Stewart

The paper identifies rare pathogenic variants associated with pulmonary fibrosis by analyzing whole genome sequencing data and linking them to cytoskeletal dysfunction.

bioRxiv · Jun 10, 2024 · PreprintGenetics