Genetic risk prediction in complex disease

por Jostins, Luke, Barrett, Jeffrey C.
Publicado 2011

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

por Morris, James A., Barrett, Jeffrey C.
Publicado 2012

Strategies for fine-mapping complex traits

por Spain, Sarah L., Barrett, Jeffrey C.
Publicado en Hum Mol Genet (2015)

Synthetic associations in the context of genome-wide association scan signals

por Orozco, Gisela, Barrett, Jeffrey C., Zeggini, Eleftheria
Publicado 2010

Imputation of low-frequency variants using the HapMap3 benefits from large, diverse reference sets

por Jostins, Luke, Morley, Katherine I, Barrett, Jeffrey C
Publicado 2011

Using Genetic Prediction from Known Complex Disease Loci to Guide the Design of Next-Generation Sequencing Experiments

por Jostins, Luke, Levine, Adam P., Barrett, Jeffrey C.
Publicado 2013

Synthetic Associations Are Unlikely to Account for Many Common Disease Genome-Wide Association Signals

por Anderson, Carl A., Soranzo, Nicole, Zeggini, Eleftheria, Barrett, Jeffrey C.
Publicado 2011

Evoker: a visualization tool for genotype intensity data

por Morris, James A., Randall, Joshua C., Maller, Julian B., Barrett, Jeffrey C.
Publicado 2010

Misuse of hierarchical linear models overstates the significance of a reported association between OXTR and prosociality

por Jostins, Luke, Pickrell, Joseph K., MacArthur, Daniel G., Barrett, Jeffrey C.
Publicado 2012

Characterization of Expression Quantitative Trait Loci in the Human Colon

por Singh, Tarjinder, Levine, Adam P., Smith, Philip J., Smith, Andrew M., Segal, Anthony W., Barrett, Jeffrey C.
Publicado en Inflamm Bowel Dis (2015)

Association of Fc receptor like 5 (FCRL5) with Graves’ disease is secondary to the effect of FCRL3

por Simmonds, Matthew J., Brand, Oliver J., Barrett, Jeffrey C., Newby, Paul R., Franklyn, Jayne A., Gough, Stephen C.L.
Publicado 2010

Biases and Reconciliation in Estimates of Linkage Disequilibrium in the Human Genome

por Pe’er, Itsik, Chretien, Yves R., de Bakker, Paul I. W., Barrett, Jeffrey C., Daly, Mark J., Altshuler, David M.
Publicado 2006

Evaluating the Effects of Imputation on the Power, Coverage, and Cost Efficiency of Genome-wide SNP Platforms

por Anderson, Carl A., Pettersson, Fredrik H., Barrett, Jeffrey C., Zhuang, Joanna J., Ragoussis, Jiannis, Cardon, Lon R., Morris, Andrew P.
Publicado 2008

Returning genome sequences to research participants: Policy and practice

por Wright, Caroline F., Middleton, Anna, Barrett, Jeffrey C., Firth, Helen V., FitzPatrick, David R., Hurles, Matthew E., Parker, Michael
Publicado en Wellcome Open Res (2017)

The intermediate filament protein vimentin is a regulator of NOD2 activity

por Stevens, Craig, Henderson, Paul, Nimmo, Elaine R., Soares, Dinesh C., Dogan, Belgin, Simpson, Kenneth W., Barrett, Jeffrey C., Wilson, David C., Satsangi, Jack
Publicado en Gut (2012)

Genetic Complexity of Crohn’s Disease in Two Large Ashkenazi Jewish Families

por Levine, Adam P., Pontikos, Nikolas, Schiff, Elena R., Jostins, Luke, Speed, Doug, Lovat, Laurence B., Barrett, Jeffrey C., Grasberger, Helmut, Plagnol, Vincent, Segal, Anthony W.
Publicado en Gastroenterology (2016)

Exome-wide assessment of the functional impact and pathogenicity of multinucleotide mutations

por Kaplanis, Joanna, Akawi, Nadia, Gallone, Giuseppe, McRae, Jeremy F., Prigmore, Elena, Wright, Caroline F., Fitzpatrick, David R., Firth, Helen V., Barrett, Jeffrey C., Hurles, Matthew E.
Publicado en Genome Res (2019)

Genetic association of fetal-hemoglobin levels in individuals with sickle cell disease in Tanzania maps to conserved regulatory elements within the MYB core enhancer

por Mtatiro, Siana N, Mgaya, Josephine, Singh, Tarjinder, Mariki, Harvest, Rooks, Helen, Soka, Deogratius, Mmbando, Bruno, Thein, Swee Lay, Barrett, Jeffrey C, Makani, Julie, Cox, Sharon E, Menzel, Stephan
Publicado en BMC Med Genet (2015)

Meta-analysis of genome-wide association study data identifies additional type 1 diabetes loci

por Cooper, Jason D, Smyth, Deborah J, Smiles, Adam M, Plagnol, Vincent, Walker, Neil M, Allen, James, Downes, Kate, Barrett, Jeffrey C, Healy, Barry, Mychaleckyj, Josyf C, Warram, James H, Todd, John A
Publicado 2008

Genome Wide Association Study of Fetal Hemoglobin in Sickle Cell Anemia in Tanzania

por Mtatiro, Siana Nkya, Singh, Tarjinder, Rooks, Helen, Mgaya, Josephine, Mariki, Harvest, Soka, Deogratius, Mmbando, Bruno, Msaki, Evarist, Kolder, Iris, Thein, Swee Lay, Menzel, Stephan, Cox, Sharon E., Makani, Julie, Barrett, Jeffrey C.
Publicado en PLoS One (2014)