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Corneliu A Bodea , Benjamin M Neale , Stephan Ripke , Murray Barclay
American Journal of Human Genetics 98 ( 5) 857 -868

14
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Human SNP links differential outcomes in inflammatory and infectious disease to a FOXO3-regulated pathway

James C Lee , Marion Espeli , Carl A Anderson , Michelle A Linterman
Cell 155 ( 1) 57 -69

166
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18
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The intermediate filament protein, vimentin, is a regulator of NOD2 activity

Craig Stevens , Paul Henderson , Elaine R Nimmo , Dinesh C Soares
Gut 62 ( 5) 695 -707

50
2013
254
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Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders

Tarjinder Singh , Mitja I Kurki , David Curtis , Shaun M Purcell
Nature Neuroscience 19 ( 4) 571 -577

277
2016
Open Targets Genetics: systematic identification of trait-associated genes using large-scale genetics and functional genomics.

Maya Ghoussaini , Edward Mountjoy , Miguel Carmona , Gareth Peat
Nucleic Acids Research 49

170
2021
Evaluating coverage of genome-wide association studies

Jeffrey C Barrett , Lon R Cardon ,
Nature Genetics 38 ( 6) 659 -662

377
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Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility.

Miles Parkes , Jeffrey C Barrett , Natalie J Prescott , Mark Tremelling
Nature Genetics 39 ( 7) 830 -832

1,016
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To what extent do scans of non-synonymous SNPs complement denser genome-wide association studies?

David M Evans , Jeffrey C Barrett , Lon R Cardon ,
European Journal of Human Genetics 16 ( 6) 718 -723

21
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Genetic diagnosis of developmental disorders in the DDD study: a scalable analysis of genome-wide research data

Caroline F Wright , Tomas W Fitzgerald , Wendy D Jones , Stephen Clayton
The Lancet 385 ( 9975) 1305 -1314

713
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Imputation of low-frequency variants using the HapMap3 benefits from large, diverse reference sets

Luke Jostins , Katherine I Morley , Jeffrey C Barrett
European Journal of Human Genetics 19 ( 6) 662 -666

34
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Exome Sequencing and Genotyping Identify a Rare Variant in NLRP7 Gene Associated With Ulcerative Colitis.

Alexandros Onoufriadis , Kristina Stone , Antreas Katsiamides , Ariella Amar
Journal of Crohn's and Colitis 12 ( 3) 321 -326

6
2018
Exploring the genetic architecture of inflammatory bowel disease by whole-genome sequencing identifies association at ADCY7

Yang Luo , Katrina M de Lange , Luke Jostins , Loukas Moutsianas
Nature Genetics 49 ( 2) 186 -192

84
2017
Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease

Katrina M de Lange , Loukas Moutsianas , James C Lee , Christopher A Lamb
Nature Genetics 49 ( 2) 256 -261

891
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Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes

Jeffrey C Barrett , David G Clayton , Patrick Concannon , Beena Akolkar
Nature Genetics 41 ( 6) 703 -707

1,374
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The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability

Tarjinder Singh , , James T R Walters , Mandy Johnstone
Nature Genetics 49 ( 8) 1167 -1173

110
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Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci

Severine Vermeire , Richard H Duerr , Mark S Silverberg , Jack Satsangi
Nature Genetics 42 ( 12) 1118 -1125

2,912
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Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.

Carl A Anderson , Gabrielle Boucher , Charlie W Lees , Andre Franke
Nature Genetics 43 ( 3) 246 -252

1,552
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