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| 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 56 (2), 222-233, 2024 | 61 | 2024 |
| Examining the role of common variants in rare neurodevelopmental conditions QQ Huang, EM Wigdor, DS Malawsky, P Campbell, KE Samocha, ... Nature, 1-8, 2024 | 7* | 2024 |
| Federated analysis of autosomal recessive coding variants in 29,745 developmental disorder patients from diverse populations VK Chundru, Z Zhang, K Walter, SJ Lindsay, P Danecek, RY Eberhardt, ... Nature Genetics, 1-8, 2024 | 5* | 2024 |
| 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, ... Scientific Reports 14 (1), 8708, 2024 | 4 | 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 | 4 | 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 | 4 | 2019 |
| Trans-ancestry genome-wide study of depression identifies 697 associations implicating cell types and pharmacotherapies MJ Adams, F Streit, X Meng, S Awasthi, BN Adey, KW Choi, VK Chundru, ... Cell 188 (3), 640-652. e9, 2025 | 3 | 2025 |
| 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 | 2 | 2023 |
| Substantial role of rare inherited variation in individuals with developmental disorders KE Samocha, V Kartik Chundru, JM Fu, EJ Gardner, P Danecek, ... medRxiv, 2024.08. 28.24312746, 2024 | 1 | 2024 |
| An atlas of expressed transcripts in the prenatal and postnatal human cortex R Bamford, SK Leung, VK Chundru, AR Jeffries, J Davies, A Franklin, ... bioRxiv, 2024.05. 24.595768, 2024 | 1 | 2024 |
| Phenotypic spectrum of dual diagnoses in developmental disorders AM Ridsdale, A Dickerson, VK Chundru, HV Firth, CF Wright The American Journal of Human Genetics 111 (11), 2382-2391, 2024 | | 2024 |