| Genomic Diagnosis of Rare Pediatric Disease in the United Kingdom and Ireland CF Wright, P Campbell, RY Eberhardt, S Aitken, D Perrett, S Brent, ... New England Journal of Medicine, 2023 | 68 | 2023 |
| Multi-ancestry genome-wide association study of major depression aids locus discovery, fine mapping, gene prioritization and causal inference X Meng, G Navoly, O Giannakopoulou, DF Levey, D Koller, GA Pathak, ... Nature Genetics, 1-12, 2024 | 8* | 2024 |
| Rare genetic variants underlie outlying levels of DNA methylation and gene-expression VK Chundru, RE Marioni, JGD Prendergast, T Lin, AJ Beveridge, ... Human Molecular Genetics 32 (11), 1912-1921, 2023 | 2 | 2023 |
| Examining the Impact of Imputation Errors on Fine-Mapping Using DNA Methylation QTL as a Model Trait VK Chundru, RE Marioni, JGD Prendergast, CL Vallerga, T Lin, ... Genetics 212 (3), 577-586, 2019 | 2 | 2019 |
| Whole genome sequencing analysis identifies rare, large-effect non-coding variants and regions associated with circulating protein levels G Hawkes, K Chundru, L Jackson, KA Patel, A Murray, AR Wood, ... bioRxiv, 2023.11. 04.565589, 2023 | 1 | 2023 |
| Investigating the role of common cis-regulatory variants in modifying penetrance of putatively damaging, inherited variants in severe neurodevelopmental disorders EM Wigdor, KE Samocha, RY Eberhardt, VK Chundru, HV Firth, CF Wright, ... medRxiv, 2023.04. 20.23288860, 2023 | 1 | 2023 |
| Dissecting the contribution of common variants to risk of rare neurodevelopmental conditions QQ Huang, EM Wigdor, P Campbell, DS Malawsky, KE Samocha, ... medRxiv, 2024.03. 05.24303772, 2024 | | 2024 |
| Federated analysis of the contribution of recessive coding variants to 29,745 developmental disorder patients from diverse populations VK Chundru, Z Zhang, K Walter, S Lindsay, P Danecek, RY Eberhardt, ... medRxiv, 2023.07. 24.23293070, 2023 | | 2023 |
