Professor Chris Wallace
(she/her)About Professor Chris Wallace
I am a Wellcome Trust Senior Research Fellow at the University of Cambridge and joined the MRC Biostatistics Unit as an Honorary Group Leader in February 2016.
Prior to this, I held fellowships from the Wellcome Trust and the British Heart Foundation at other institutes in Cambridge and Queen Mary University of London, where I worked on various aspects of statistical genomics.
My focus is on the twin goals of using genomic analysis to make meaningful contributions to the understanding of human autoimmune disease and the development of statistical methodology to enable these contributions.
My research group has three complementary aims. First, to develop the statistical tools needed to identify genetic associations with disease, then robustly and empirically link each genetic association with a gene, cell type, stimulatory condition and ultimately a biological pathway. Specifically, this requires methods for:
- horizontal integration of different layers of omics data
- mapping the variants which regulate gene expression
- “fine mapping” causal genetic variants from amongst associated variants in genetic association data, typically using sparse variable selection
- “fine mapping” regulatory contacts in 3D maps of folded DNA from technologies such as promoter capture Hi-C
While the methods are broadly applicable across a range of common complex diseases, my second aim is to use the methods to understand the causes of autoimmune diseases, the links between different diseases, and identify pharmaceutical targets and opportunities for pharmaceutical re-purposing. Finally, a third strand of research aims to build upon what we have learnt about mechanisms underlying to disease to make stronger inference about the relationship of omics biomarkers and treatment outcomes in childhood arthritis, in order to aid treatment decisions.
For further details of my group’s research, including papers and code, see chr1swallace.github.io.
Publications
Showing 1 to 10 of 308 publications
Standardised Human Phenotype Ontology Annotation Enables High Quality Phenotypic Data Capture in a Real-World Common Variable Immunodeficiency Cohort.
Authors: LC Campos, É Favreau, D Greene, J Blach, M Thomas, K Alsehaim, L Mutlu, S Elhadari, A Herwadkar, J Payne, C Lever, D Mahmoud, F Moreira, M O'Sullivan, M Berry, G Twigg, ACJ Hart, N Joshi, S Fuller, INTREPID Consortium, KGC Smith, E Turro, MC Cook, C Wallace, SO Burns
Published:
Journal: J Allergy Clin Immunol
DOI: 10.1016/j.jaci.2026.08.027
Large-scale GWAS meta-analysis of serum antibody levels in healthy individuals reveals distinct genetic architectures.
Authors: TW Willis, E Gkrania-Klotsas, NJ Wareham, EF McKinney, PA Lyons, KGC Smith, C Wallace
Published:
Journal: Genes Immun
DOI: 10.1038/s41435-026-00408-z
Cell-type-resolved genetic variation shapes inflammatory bowel disease risk.
Authors: T Alegbe, BT Harris, L Fachal, L Ramirez-Navarro, M Tutert, M Krzak, M Ghouraba, M Strickland, M Ozols, CE Cohen, S Khullar, E Khabirova, NI Panousis, D Ochoa, N Wana, MX Hu, J Skelton, J Ostermayer, KAX Cheam, D Leland Taylor, Y Gu, C Dawson, T Thompson, K Arestang, N Nishad, B Brezina, CQ Caballes, W Garri, S Leonard, V Iyer, M Parkes, C Wallace, RE McIntyre, CC Martin, G-R Jones, T Raine, CA Anderson
Journal: Nature
DOI: 10.1038/s41586-026-10627-z
High-resolution promoter interaction analysis implicates genes involved in activation of type 3 innate lymphoid cells in immune disease risk.
Authors: V Malysheva, H Ray-Jones, N Lakes, RA Brown, TA Cazares, O Clay, DE Ohayon, P Artemov, JA Wayman, ZF Yang, M Della Rosa, C Petitjean, C Booth, JIJ Ellaway, JR Barnes, AW Dangel, A Saini, WR Orchard, X Chen, S Parameswaran, F Burden, M Frontini, T Nagano, P Fraser, S Schoenfelder, MT Weirauch, LC Kottyan, DF Smith, N Powell, JM Weimer, EM Oltz, C Wallace, ER Miraldi, SN Waggoner, M Spivakov
Journal: Nat Genet
DOI: 10.1038/s41588-026-02681-0
Correction: Eliciting priors and relaxing the single causal variant assumption in colocalisation analyses.
Authors: C Wallace
Journal: PLoS Genet
DOI: 10.1371/journal.pgen.1012155
Design and interpretation of eQTL-GWAS colocalisation studies: Lessons from a large-scale evaluation.
Authors: G Reales, JM Pullin, I Manipur, E Vigorito, C Wallace
Journal: PLoS Genet
DOI: 10.1371/journal.pgen.1012141
Standardised Human Phenotype Ontology Annotation Enables High Quality Phenotypic Data Capture in a Real-World Common Variable Immunodeficiency Cohort
Authors: LC Campos, É Favreau, D Greene, J Blach, M Thomas, K Alsehaim, L Mutlu, S Elhadari, A Herwadkar, J Payne, C Lever, D Mahmoud, F Moreira, M O’Sullivan, M Berry, G Twigg, ACJ Hart, N Joshi, S Fuller, I Consortium, KGC Smith, E Turro, MC Cook, C Wallace, SO Burns
Published:
DOI: 10.64898/2026.04.29.26350963
Altered B cell activation contributes to the immunopathogenesis of childhood arthritis-associated uveitis.
Authors: BR Jebson, B Ingledow, V Alexiou, J Kubiak, P Jenkins, Y Meng, M Kartawinata, R Restuadi, W-Y Lin, C Wallace, CJ Chu, AL Solebo, LR Wedderburn, EC Rosser, CLUSTER consortium
Published:
Journal: Nat Commun
DOI: 10.1038/s41467-025-68264-5
High-resolution promoter interaction analysis implicates genes involved in the activation of Type 3 Innate Lymphoid Cells in autoimmune disease risk.
Authors: V Malysheva, H Ray-Jones, N Lakes, RA Brown, TA Cazares, O Clay, DE Ohayon, P Artemov, JA Wayman, ZF Yang, M Della Rosa, C Petitjean, C Booth, JIJ Ellaway, JR Barnes, AW Dangel, A Saini, WR Orchard, X Chen, S Parameswaran, F Burden, M Frontini, T Nagano, P Fraser, S Schoenfelder, MT Weirauch, LC Kottyan, DF Smith, N Powell, JM Weimer, EM Oltz, C Wallace, ER Miraldi, S Waggoner, M Spivakov
Published:
DOI: 10.1101/2022.10.19.512842
Inflammation and Obesity Correlate in Pulmonary Hypertension but Associate with Diverging Outcomes.
Authors: E De Bie, P Correa-Jaque, R Jones, HJ Bogaard, J Chan, C Church, JG Coghlan, A Gaur, S Ghio, H-A Ghofrani, ZM Goh, LS Howard, M Humbert, G Kovacs, A Lawrie, J Lordan, W-Y Lin, D Neelam-Naganathan, J Newman, CJ Rhodes, K Sheares, O Sitbon, TW Willis, SJ Wort, S Gräf, DG Kiely, RL Benza, A Rothman, C Wallace, M Toshner
Published:
Journal: American Journal of Respiratory and Critical Care Medicine
DOI: 10.1164/rccm.202412-2393OC