Jeffrey C. Barrett

According to our database, Jeffrey C. Barrett authored at least 6 papers between 2005 and 2021.

Collaborative distances:

• Dijkstra number of three.
• Erdős number of three.

2021

Open Targets Genetics: systematic identification of trait-associated genes using large-scale genetics and functional genomics.

Maya Ghoussaini, Edward Mountjoy, Miguel Carmona, Gareth Peat, Ellen M. Schmidt, Andrew Hercules, Luca Fumis, Alfredo Miranda, Denise Carvalho-Silva, Annalisa Buniello, Tony Burdett, James D. Hayhurst, Jarrod Baker, Javier Ferrer, Asier Gonzalez-Uriarte, Simon Jupp, Mohd Anisul Karim, Gautier Koscielny, Sandra Machlitt-Northen, Cinzia Malangone, Zoë May Pendlington, Paola Roncaglia, Daniel Suveges, Daniel Wright, Olga Vrousgou, Eliseo Papa, Helen E. Parkinson, Jacqueline A. L. MacArthur, John A. Todd, Jeffrey C. Barrett, Jeremy Schwartzentruber, David G. Hulcoop, David Ochoa, Ellen M. McDonagh, Ian Dunham

Nucleic Acids Res., 2021

2017

Fine-mapping inflammatory bowel disease loci to single-variant resolution.

Hailiang Huang, Ming Fang, Luke Jostins, Masa Umicevic Mirkov, Gabrielle Boucher, Carl A. Anderson, Vibeke Andersen, Isabelle Cleynen, Adrian Cortes, François Crins, Mauro D'Amato, Valérie Deffontaine, Julia Dmitrieva, Elisa Docampo, Mahmoud Elansary, Kyle Kai-How Farh, Andre Franke, Ann-Stephan Gori, Philippe Goyette, Jonas Halfvarson, Talin Haritunians, Jo Knight, Ian C. Lawrance, Charlie W. Lees, Edouard Louis, Rob Mariman, Theo H. E. Meuwissen, Myriam Mni, Yukihide Momozawa, Miles Parkes, Sarah L. Spain, Emilie Théâtre, Gosia Trynka, Jack Satsangi, Suzanne van Sommeren, Severine Vermeire, Ramnik J. Xavier, Rinse K. Weersma, Richard H. Duerr, Christopher G. P. Mathew, John D. Rioux, Dermot P. B. McGovern, Judy H. Cho, Michel Georges, Mark J. Daly, Jeffrey C. Barrett

Nat., 2017

2012

optiCall: a robust genotype-calling algorithm for rare, low-frequency and common variants.

T. S. Shah, J. Z. Liu, J. A. B. Floyd, James A. Morris, N. Wirth, Jeffrey C. Barrett, Carl A. Anderson

Bioinform., 2012

Olorin: combining gene flow with exome sequencing in large family studies of complex disease.

James A. Morris, Jeffrey C. Barrett

Bioinform., 2012

2010

Evoker: a visualization tool for genotype intensity data.

James A. Morris, Joshua C. Randall, Julian B. Maller, Jeffrey C. Barrett

Bioinform., 2010

2005

Haploview: analysis and visualization of LD and haplotype maps.

Jeffrey C. Barrett, B. Fry, Julian B. Maller, Mark J. Daly

Bioinform., 2005