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Journal of Medical Virology|July 21, 2022
Concordance of B- and T-cell responses to SARS-CoV-2 infection, irrespective of symptoms suggestive of COVID-19Marc F Österdahl, Eleni Christakou, Deborah Hart, et al.
The Review of Scientific Instruments|August 2, 2013
A new endstation at the Swiss Light Source for ultraviolet photoelectron spectroscopy, X-ray photoelectron spectroscopy, and X-ray absorption spectroscopy measurements of liquid solutionsMatthew A Brown, Amaia Beloqui Redondo, Inga Jordan, et al.
Orphanet Journal of Rare Diseases|May 5, 2019
Natural history of fibrodysplasia ossificans progressiva: cross-sectional analysis of annotated baseline phenotypesRobert J Pignolo, Geneviève Baujat, Matthew A Brown, et al.
Human Mutation|April 3, 2016
Fryns Syndrome Associated with Recessive Mutations in PIGN in two Separate FamiliesAideen M McInerney-Leo, Jessica E Harris, Michael Gattas, et al.
Journal of Medical Genetics|April 13, 2016
Mutations in LTBP3 cause acromicric dysplasia and geleophysic dysplasiaAideen M McInerney-Leo, Carine Le Goff, Paul J Leo, et al.
Arthritis Research & Therapy|April 8, 2011
Whole blood transcriptional profiling in ankylosing spondylitis identifies novel candidate genes that might contribute to the inflammatory and tissue-destructive disease aspectsFernando M Pimentel-Santos, Dário Ligeiro, Mafalda Matos, et al.
Plos Genetics|December 15, 2010
Association of variants at 1q32 and STAT3 with ankylosing spondylitis suggests genetic overlap with Crohn's diseasePatrick Danoy, Karena Pryce, Johanna Hadler, et al.
American Journal of Human Genetics|August 17, 2004
The interleukin 1 gene cluster contains a major susceptibility locus for ankylosing spondylitisAndrew E Timms, Alison M Crane, Anne-Marie Sims, et al.
JCI Insight|May 25, 2021
A KCNK16 mutation causing TALK-1 gain of function is associated with maturity-onset diabetes of the youngSarah M Graff, Stephanie R Johnson, Paul J Leo, et al.
BMC Musculoskeletal Disorders|March 29, 2014
The IFITM5 mutation c.-14C > T results in an elongated transcript expressed in human bone; and causes varying phenotypic severity of osteogenesis imperfecta type VSyndia Lazarus, Aideen M McInerney-Leo, Fiona A McKenzie, et al.
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