V. Kartik Chundru

Genomic Diagnosis of Rare Pediatric Disease in the United Kingdom and Ireland

Caroline F. Wright, Patrick Campbell, Ruth Y. Eberhardt et al. · New England Journal of Medicine · 2023 · 223 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Multi-ancestry genome-wide association study of major depression aids locus discovery, fine mapping, gene prioritization and causal inference

Xiangrui Meng, Georgina Navoly, Olga Giannakopoulou et al. · Nature Genetics · 2024 · 170 citations · Full text

Life Sciences, Genetics, Psychiatry +17

Examining the role of common variants in rare neurodevelopmental conditions

Qin Qin Huang, Emilie M. Wigdor, Daniel Malawsky et al. · Nature · 2024 · 55 citations · Full text

Life Sciences, Genetics, Genetic Epidemiology +16

Common genetic variants modify disease risk and clinical presentation in monogenic diabetes

Robin N. Beaumont, Ankit M Arni, V. Kartik Chundru et al. · Nature Metabolism · 2025 · 18 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Whole-genome sequencing analysis identifies rare, large-effect noncoding variants and regulatory regions associated with circulating protein levels

Gareth Hawkes, V. Kartik Chundru, Leigh Jackson et al. · Nature Genetics · 2025 · 14 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17