A more accurate method for colocalisation analysis allowing for multiple causal variants

• Trans -eQTLs reveal the architecture of human gene regulatory networks

  2026 medRxiv preprint Biochemistry, Genetics and Molecular Biology Genetic Associations and Epidemiology Open access

  2

  citations
• Epigenome-wide association study of circulating interleukin-6 connects DNA methylation to immunometabolic and inflammatory health

  2026 Communications Biology article Biochemistry, Genetics and Molecular Biology Epigenetics and DNA Methylation Open access

  3

  citations
• Identification of SENP7 and UTF1/VENTX as new loci influencing clustered protocadherin methylation across blood and brain using a genome-wide association study

  2025 Molecular Psychiatry article Biochemistry, Genetics and Molecular Biology Epigenetics and DNA Methylation Open access

  1

  citations
• HNF1A and A1CF coordinate a beta cell transcription-splicing axis that is disrupted in type 2 diabetes

  2025 Cell Metabolism article Medicine Pancreatic function and diabetes Open access

  17

  citations
• MR-link-2: pleiotropy robust cis Mendelian randomization validated in three independent reference datasets of causality

  2025 Nature Communications article Biochemistry, Genetics and Molecular Biology Genetic Associations and Epidemiology Open access

  20

  citations
• Genome-wide association and multi-omics analyses provide insights into the disease mechanisms of central serous chorioretinopathy

  2025 Scientific Reports article Medicine Retinal Diseases and Treatments Open access

  4

  citations
• Genome-wide association study meta-analysis provides insights into the etiology of heart failure and its subtypes

  2025 Nature Genetics article Biochemistry, Genetics and Molecular Biology Genetic Associations and Epidemiology Open access

  57

  citations
• Partitioned polygenic risk scores identify distinct types of metabolic dysfunction-associated steatotic liver disease

  2024 Nature Medicine article Medicine Liver Disease Diagnosis and Treatment Open access

  134

  citations
• Genome-wide meta-analysis of myasthenia gravis uncovers new loci and provides insights into polygenic prediction

  2024 Nature Communications review Medicine Myasthenia Gravis and Thymoma Open access

  16

  citations
• eLife Assessment: Statistical examination of shared loci in neuropsychiatric diseases using genome-wide association study summary statistics

  2024 peer-review Biochemistry, Genetics and Molecular Biology Genetic Associations and Epidemiology Open access

  0

  citations
• Partitioned polygenic risk scores identify distinct types of metabolic dysfunction-associated steatotic liver disease

  2024 Research Square preprint Medicine Liver Disease Diagnosis and Treatment Open access

  3

  citations
• A multitrait genetic study of hemostatic factors and hemorrhagic transformation after stroke treatment

  2023 Journal of Thrombosis and Haemostasis article Biochemistry, Genetics and Molecular Biology Genetic Associations and Epidemiology Open access

  9

  citations
• Mapping the aetiological foundations of the heart failure spectrum using human genetics

  2023 medRxiv preprint Biochemistry, Genetics and Molecular Biology Genetic Associations and Epidemiology Open access

  6

  citations
• eLife Assessment: Statistical examination of shared loci in neuropsychiatric diseases using genome-wide association study summary statistics

  2023 peer-review Biochemistry, Genetics and Molecular Biology Genetic Associations and Epidemiology Open access

  0

  citations
• GWAS of random glucose in 476,326 individuals provide insights into diabetes pathophysiology, complications and treatment stratification

  2023 Nature Genetics article Biochemistry, Genetics and Molecular Biology Genetic Associations and Epidemiology Open access

  107

  citations
• Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk

  2023 Nature Genetics article Medicine Chronic Obstructive Pulmonary Disease (COPD) Research Open access

  201

  citations
• Stroke genetics informs drug discovery and risk prediction across ancestries

  2022 Nature article Biochemistry, Genetics and Molecular Biology Genetic Associations and Epidemiology Open access

  598

  citations
• Stroke genetics informs drug discovery and risk prediction across ancestries

  2022 Research Square preprint Biochemistry, Genetics and Molecular Biology Genetic Associations and Epidemiology Open access

  9

  citations

18 results