How next-generation sequencing is transforming complex disease geneticsKILPINEN, Helena; BARRETT, Jeffrey C.Trends in genetics (Regular ed.). 2013, Vol 29, Num 1, pp 23-30, issn 0168-9525, 8 p.Article

Genetic risk prediction in complex diseaseJOSTINS, Luke; BARRETT, Jeffrey C.Human molecular genetics (Print). 2011, Vol 20, Num 2, issn 0964-6906, R182-R188, NSArticle

Evaluating coverage of genome-wide association studiesBARRETT, Jeffrey C; CARDON, Lon R.Nature genetics. 2006, Vol 38, Num 6, pp 659-662, issn 1061-4036, 4 p.Article

Imputation of low-frequency variants using the HapMap3 benefits from large, diverse reference setsJOSTINS, Luke; MORLEY, Katherine I; BARRETT, Jeffrey C et al.European journal of human genetics. 2011, Vol 19, Num 6, pp 662-666, issn 1018-4813, 5 p.Article

Synthetic associations in the context of genome-wide association scan signalsOROZCO, Gisela; BARRETT, Jeffrey C; ZEGGINI, Eleftheria et al.Human molecular genetics (Print). 2010, Vol 19, issn 0964-6906, R137-R144, NS2Article

Olorin: combining gene flow with exome sequencing in large family studies of complex diseaseMORRIS, James A; BARRETT, Jeffrey C.Bioinformatics (Oxford. Print). 2012, Vol 28, Num 24, pp 3320-3321, issn 1367-4803, 2 p.Article

Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetesBARRETT, Jeffrey C; CLAYTON, David G; PLAGNOL, Vincent et al.Nature genetics. 2009, Vol 41, Num 6, pp 703-707, issn 1061-4036, 5 p.Article

Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetesZEGGINI, Eleftheria; WEEDON, Michael N; BARRETT, Jeffrey C et al.Science (Washington, D.C.). 2007, Vol 316, Num 5829, pp 1336-1341, issn 0036-8075, 6 p.Article

Biases and reconciliation in estimates of linkage disequilibrium in the human genomePE'ER, Itsik; CHRETIEN, Yves R; DE BAKKER, Paul I. W et al.American journal of human genetics. 2006, Vol 78, Num 4, pp 588-603, issn 0002-9297, 16 p.Article

To what extent do scans of non-synonymous SNPs complement denser genome-wide association studies?EVANS, David M; BARRETT, Jeffrey C; CARDON, Lon R et al.European journal of human genetics. 2008, Vol 16, Num 6, pp 718-723, issn 1018-4813, 6 p.Article

Association of the thyroid stimulating hormone receptor gene (TSHR) with Graves' diseaseBRAND, Oliver J; BARRETT, Jeffrey C; WIERSINGA, Wilmar M et al.Human molecular genetics (Print). 2009, Vol 18, Num 9, pp 1704-1713, issn 0964-6906, 10 p.Article

Genetic determinants of ulcerative colitis include the ECM1 locus and five loci implicated in Crohn's diseaseFISHER, Sheila A; TREMELLING, Mark; BARRETT, Jeffrey C et al.Nature genetics. 2008, Vol 40, Num 6, pp 710-712, issn 1061-4036, 3 p.Article

A common variant in the FT0 gene is associated with body mass index and predisposes to childhood and adult obesityFRAYHNG, Timothy M; TIMPSON, Nicholas J; SHIELDS, Beverley et al.Science (Washington, D.C.). 2007, Vol 316, Num 5826, pp 889-894, issn 0036-8075, 6 p.Article

Common deletion polymorphisms in the human genomeMCCARROLL, Steven A; HADNOTT, Tracy N; ALTSHULER, David M et al.Nature genetics. 2006, Vol 38, Num 1, pp 86-92, issn 1061-4036, 7 p.Article

Evaluating the Effects of Imputation on the Power, Coverage, and Cost Efficiency of Genome-wide SNP PlatformsANDERSON, Carl A; PETTERSSON, Fredrik H; BARRETT, Jeffrey C et al.American journal of human genetics. 2008, Vol 83, Num 1, pp 112-119, issn 0002-9297, 8 p.Article

Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk lociCOOPER, Jason D; SMYTH, Deborah J; WARRAM, James H et al.Nature genetics. 2008, Vol 40, Num 12, pp 1399-1401, issn 1061-4036, 3 p.Article

A Systematic Survey of Loss-of-Function Variants in Human Protein-Coding GenesMACARTHUR, Daniel G; BALASUBRAMANIAN, Suganthi; ALBERS, Cornelis A et al.Science (Washington, D.C.). 2012, Vol 335, Num 6070, pp 823-828, issn 0036-8075, 6 p.Article

Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility lociFRANKE, Andre; MCGOVERN, Dermot P. B; ANDERSON, Carl A et al.Nature genetics. 2010, Vol 42, Num 12, pp 1118-1125, issn 1061-4036, 8 p.Article

Association of PTPN22 haplotypes with graves' diseaseHEWARD, Joanne M; BRAND, Oliver J; BARRETT, Jeffrey C et al.The Journal of clinical endocrinology and metabolism. 2007, Vol 92, Num 2, pp 685-690, issn 0021-972X, 6 p.Article

Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosisLIU, Jimmyz; ALMARRI, Mohameda; DONALDSON, Peter T et al.Nature genetics. 2012, Vol 44, Num 10, pp 1137-1141, issn 1061-4036, 5 p.Article

Association of Fc receptor-like 5 (FCRL5) with Graves' disease is secondary to the effect of FCRL3SIMMONDS, Matthew J; BRAND, Oliver J; BARRETT, Jeffrey C et al.Clinical endocrinology (Oxford. Print). 2010, Vol 73, Num 5, pp 654-660, issn 0300-0664, 7 p.Article

Evoker: a visualization tool for genotype intensity dataMORRIS, James A; RANDALL, Joshua C; MALLER, Julian B et al.Bioinformatics (Oxford. Print). 2010, Vol 26, Num 14, pp 1786-1787, issn 1367-4803, 2 p.Article

Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's diseaseBARRETT, Jeffrey C; HANSOUL, Sarah; BITTON, Alain et al.Nature genetics. 2008, Vol 40, Num 8, pp 955-962, issn 1061-4036, 8 p.Article

Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibilityPARKES, Miles; BARRETT, Jeffrey C; DRUMMOND, Hazel et al.Nature genetics. 2007, Vol 39, Num 7, pp 830-832, issn 1061-4036, 3 p.Article