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Arthritis and Rheumatism|July 13, 2002
Role of NOD2 variants in spondylarthritisAlison M Crane, Linda Bradbury, David A van Heel, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|November 7, 2017
Genetic Variants in ERAP1 and ERAP2 Associated With Immune-Mediated Diseases Influence Protein Expression and the Isoform ProfileAimee L Hanson, Thomas Cuddihy, Katelin Haynes, et al.
Frontiers in Genetics|June 27, 2022
Contribution of HLA and KIR Alleles to Systemic Sclerosis Susceptibility and Immunological and Clinical Disease SubtypesAimee L Hanson, Joanne Sahhar, Gene-Siew Ngian, et al.
Arthritis and Rheumatism|April 23, 2013
Brief report: high-throughput sequencing of IL23R reveals a low-frequency, nonsynonymous single-nucleotide polymorphism that is associated with ankylosing spondylitis in a Han Chinese populationStuart I Davidson, Lei Jiang, Adrian Cortes, et al.
Human Molecular Genetics|August 21, 2009
Investigating the genetic association between ERAP1 and ankylosing spondylitisDavid Harvey, Jennifer J Pointon, David M Evans, et al.
Diabetes Care|December 8, 2018
Cost-effectiveness Analysis of Routine Screening Using Massively Parallel Sequencing for Maturity-Onset Diabetes of the Young in a Pediatric Diabetes Cohort: Reduced Health System Costs and Improved Patient Quality of LifeStephanie R Johnson, Hannah E Carter, Paul Leo, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 22, 2011
Crystal structures of the endoplasmic reticulum aminopeptidase-1 (ERAP1) reveal the molecular basis for N-terminal peptide trimmingGrazyna Kochan, Tobias Krojer, David Harvey, et al.
Microbiome|February 19, 2018
Type 1 diabetes susceptibility alleles are associated with distinct alterations in the gut microbiotaJane A Mullaney, Juliette E Stephens, Mary-Ellen Costello, et al.
Plos One|April 11, 2015
N-ethyl-N-Nitrosourea (ENU) induced mutations within the klotho gene lead to ectopic calcification and reduced lifespan in mouse modelsChristopher T Esapa, Fadil M Hannan, Valerie N Babinsky, et al.
Clinical Endocrinology|October 10, 2013
Whole exome sequencing is an efficient and sensitive method for detection of germline mutations in patients with phaeochromcytomas and paragangliomasAideen M McInerney-Leo, Mhairi S Marshall, Brooke Gardiner, et al.
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