Turnbull, Clare

Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores

Vilhjálmsson, B. J., Yang, J., Finucane, H. K., Gusev, A., Lindström, S., Ripke, S., Genovese, G., Loh, P.-R., Bhatia, G., Do, R., et al. (2015) · The American Journal of Human Genetics

Genetic Associations and EpidemiologyGenetic Mapping and Diversity in Plants and Animals

Cited by 1,303

Lung adenocarcinoma promotion by air pollutants

Hill, W., Lim, E. L., Weeden, C. E., Lee, C., Augustine, M., Chen, K., Kuan, F.-C., Marongiu, F., Evans, E. J., Moore, D. A., et al. (2023) · Nature

Air Quality and Health ImpactsCarcinogens and Genotoxicity Assessment

Cited by 808

Genome-wide association study identifies five new breast cancer susceptibility loci

The Breast Cancer Susceptibility Collaboration (UK), Turnbull, C., Ahmed, S., Morrison, J., Pernet, D., Renwick, A., Maranian, M., Seal, S., Ghoussaini, M., Hines, S., et al. (2010) · Nature Genetics

Genetic Associations and EpidemiologyBRCA gene mutations in cancer

Cited by 687

Estimated impact of the COVID-19 pandemic on cancer services and excess 1-year mortality in people with cancer and multimorbidity: near real-time data on cancer care, cancer deaths and a population-based cohort study

Lai, A. G., Pasea, L., Banerjee, A., Hall, G., Denaxas, S., Chang, W. H., Katsoulis, M., Williams, B., Pillay, D., Noursadeghi, M., et al. (2020) · BMJ Open

COVID-19 and healthcare impactsGlobal Cancer Incidence and Screening

Cited by 447

Diagnosis of Apert syndrome in the second‐trimester using 2D and 3D ultrasound

David, A. L., Turnbull, C., Scott, R., Freeman, J., Bilardo, C. M., van Maarle, M., & Chitty, L. S. (2007) · Prenatal Diagnosis

Prenatal Screening and DiagnosticsCraniofacial Disorders and Treatments

Cited by 61

High-resolution functional mapping of RAD51C by saturation genome editing

Olvera-León, R., Zhang, F., Offord, V., Zhao, Y., Tan, H. K., Gupta, P., Pal, T., Robles-Espinoza, C. D., Arriaga-González, F. G., Matsuyama, L. S. A. S., et al. (2024) · Cell

BRCA gene mutations in cancerGenomics and Rare Diseases

Cited by 44

Workshop report: the clinical application of data from multiplex assays of variant effect (MAVEs), 12 July 2023

Allen, S., Garrett, A., Muffley, L., Fayer, S., Foreman, J., Adams, D. J., Hurles, M., Rubin, A. F., Roth, F. P., Starita, L. M., et al. (2024) · European Journal of Human Genetics

Genomics and Rare DiseasesGenetic Associations and Epidemiology

Cited by 17

Availability of benign missense variant ‘truthsets’ for validation of functional assays: current status and a systematic approach

Rowlands, C. F., Allen, S., Garrett, A., Durkie, M., Burghel, G. J., Robinson, R., Callaway, A., Field, J., Frugtniet, B., Palmer-Smith, S., et al. (2025) · The American Journal of Human Genetics

Genomics and Rare DiseasesGenetic Associations and Epidemiology

Cited by 6