simGWAS: a fast method for simulation of large scale case–control GWAS summary statistics

od Fortune, Mary D, Wallace, Chris
Izdano u Bioinformatics (2019)

Integration of disease association and eQTL data using a Bayesian colocalisation approach highlights six candidate causal genes in immune-mediated diseases

od Guo, Hui, Fortune, Mary D., Burren, Oliver S., Schofield, Ellen, Todd, John A., Wallace, Chris
Izdano u Hum Mol Genet (2015)

Stochastic search and joint fine-mapping increases accuracy and identifies previously unreported associations in immune-mediated diseases

od Asimit, Jennifer L., Rainbow, Daniel B., Fortune, Mary D., Grinberg, Nastasiya F., Wicker, Linda S., Wallace, Chris
Izdano u Nat Commun (2019)

Diagnostic tool or screening programme? Asymptomatic testing for SARS-CoV-2 needs clear goals and protocols

od Skittrall, Jordan P, Fortune, Mary D, Jalal, Hamid, Zhang, Hongyi, Enoch, David A, Brown, Nicholas M, Swift, Anne
Izdano u Lancet Reg Health Eur (2020)

Specificity and positive predictive value of SARS-CoV-2 nucleic acid amplification testing in a low-prevalence setting

od Skittrall, Jordan P., Wilson, Michael, Smielewska, Anna A., Parmar, Surendra, Fortune, Mary D., Sparkes, Dominic, Curran, Martin D., Zhang, Hongyi, Jalal, Hamid
Izdano u Clin Microbiol Infect (2021)

Insight into Genotype-Phenotype Associations through eQTL Mapping in Multiple Cell Types in Health and Immune-Mediated Disease

od Peters, James E., Lyons, Paul A., Lee, James C., Richard, Arianne C., Fortune, Mary D., Newcombe, Paul J., Richardson, Sylvia, Smith, Kenneth G. C.
Izdano u PLoS Genet (2016)

A Method for Gene-Based Pathway Analysis Using Genomewide Association Study Summary Statistics Reveals Nine New Type 1 Diabetes Associations

od Evangelou, Marina, Smyth, Deborah J, Fortune, Mary D, Burren, Oliver S, Walker, Neil M, Guo, Hui, Onengut-Gumuscu, Suna, Chen, Wei-Min, Concannon, Patrick, Rich, Stephen S, Todd, John A, Wallace, Chris
Izdano u Genet Epidemiol (2014)

Statistical Colocalization of Genetic Risk Variants for Related Autoimmune Diseases in the Context of Common Controls

od Fortune, Mary D., Guo, Hui, Burren, Oliver, Schofield, Ellen, Walker, Neil M., Ban, Maria, Sawcer, Stephen J., Bowes, John, Worthington, Jane, Barton, Ann, Eyre, Steve, Todd, John A., Wallace, Chris
Izdano u Nat Genet (2015)

Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancers

od Onengut-Gumuscu, Suna, Chen, Wei-Min, Burren, Oliver, Cooper, Nick J., Quinlan, Aaron R., Mychaleckyj, Josyf C., Farber, Emily, Bonnie, Jessica K., Szpak, Michal, Schofield, Ellen, Achuthan, Premanand, Guo, Hui, Fortune, Mary D., Stevens, Helen, Walker, Neil M., Ward, Luke D., Kundaje, Anshul, Kellis, Manolis, Daly, Mark J., Barrett, Jeffrey C., Cooper, Jason D., Deloukas, Panos, Todd, John A., Wallace, Chris, Concannon, Patrick, Rich, Stephen S.
Izdano u Nat Genet (2015)

Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa

od Gurdasani, Deepti, Carstensen, Tommy, Fatumo, Segun, Chen, Guanjie, Franklin, Chris S., Prado-Martinez, Javier, Bouman, Heleen, Abascal, Federico, Haber, Marc, Tachmazidou, Ioanna, Mathieson, Iain, Ekoru, Kenneth, DeGorter, Marianne K., Nsubuga, Rebecca N., Finan, Chris, Wheeler, Eleanor, Chen, Li, Cooper, David N., Schiffels, Stephan, Chen, Yuan, Ritchie, Graham R.S., Pollard, Martin O., Fortune, Mary D., Mentzer, Alex J., Garrison, Erik, Bergström, Anders, Hatzikotoulas, Konstantinos, Adeyemo, Adebowale, Doumatey, Ayo, Elding, Heather, Wain, Louise V., Ehret, Georg, Auer, Paul L., Kooperberg, Charles L., Reiner, Alexander P., Franceschini, Nora, Maher, Dermot, Montgomery, Stephen B., Kadie, Carl, Widmer, Chris, Xue, Yali, Seeley, Janet, Asiki, Gershim, Kamali, Anatoli, Young, Elizabeth H., Pomilla, Cristina, Soranzo, Nicole, Zeggini, Eleftheria, Pirie, Fraser, Morris, Andrew P., Heckerman, David, Tyler-Smith, Chris, Motala, Ayesha A., Rotimi, Charles, Kaleebu, Pontiano, Barroso, Inês, Sandhu, Manj S.
Izdano u Cell (2019)