Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease

Manuel A. Rivas, Mélissa Beaudoin, Agnès Gardet, +33

Nature Genetics

Genome-wide Association StudyMedicineGeneticsImmunologyGenetic Epidemiology +6

Genome-wide association identifies multiple ulcerative colitis susceptibility loci

Dermot McGovern, Agnès Gardet, Leif Törkvist, +51

Nature Genetics

Genome-wide Association StudyGenome-wide Association IdentifiesImmunologyGenetic EpidemiologyUlcerative Colitis

The All of Us Research Program: Data quality, utility, and diversity

Andrea H. Ramirez, Lina Sulieman, David J. Schlueter, +142

Patterns

IBD risk loci are enriched in multigenic regulatory modules encompassing putative causative genes

Yukihide Momozawa, Julia Dmitrieva, Emilie Théâtre, +191

Nature Communications

Supporting conditional mouse mutagenesis with a comprehensive cre characterization resource

Caleb Heffner, C. Herbert Pratt, Randal P. Babiuk, +5

Nature Communications

Deep Resequencing of GWAS Loci Identifies Rare Variants in CARD9, IL23R and RNF186 That Are Associated with Ulcerative Colitis

Mélissa Beaudoin, Philippe Goyette, Gabrielle Boucher, +31

PLoS Genetics

Mouse Gestation Length Is Genetically Determined

Stephen A. Murray, Judith L. Morgan, Coleen Kane, +4

PLoS ONE

A Pleiotropic Missense Variant in SLC39A8 Is Associated With Crohn’s Disease and Human Gut Microbiome Composition

Dalin Li, Jean-Paul Achkar, Talin Haritunians, +37

Gastroenterology

Chronic Inflammatory DiseasesDysbiosisMucosal ImmunologyPleiotropic Missense VariantPathogenesis +8

PPTGAL, a convenient Gal4 P‐element vector for testing expression of enhancer fragments in <i>drosophila</i>

Yashoda Sharma, Una S. Cheung, Ellen Larsen, +1

genesis

BiologyTranscriptional RegulationDevelopmental GeneticsGeneticsNatural Sciences +7

Comparative performances of machine learning methods for classifying Crohn Disease patients using genome-wide genotyping data

Alberto Romagnoni, Simon Jégou, Kristel Van Steen, +339

Scientific Reports