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Repeated Spinal Mobility Measures and Their Association With Radiographic Damage in Ankylosing Spondylitis
Free accessWiley | 2021| -
The opposing effect of butanol and butyric acid on the abundance of bromide and iodide at the aqueous solution–air interfaceElectronic supplementary information (ESI) available: Description of molecular dynamics simulations, their results and comparison to experimental data. See DOI: 10.1039/c8cp07448h
British Library Online Contents | 2019| -
Genome-wide association study of extreme high bone mass: Contribution of common genetic variation to extreme BMD phenotypes and potential novel BMD-associated genes
British Library Online Contents | 2018| -
MiR-137-derived polygenic risk: effects on cognitive performance in patients with schizophrenia and controls
Free accessDSpace@MIT | 2017| -
Bridging climate science to adaptation action in data sparse Tanzania
Online Contents | 2014|Contributors: BROWN, MATTHEW A. -
Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20
National licenceNature Publishing Group | 2009| -
Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region
National licenceNature Publishing Group | 2009| -
Corrigendum: A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva
National licenceNature Publishing Group | 2007| -
Replication of Genome-Wide Association Signals in UK Samples Reveals Risk Loci for Type 2 Diabetes
Online Contents | 2007|Contributors: Brown, Matthew A. -
Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants
National licenceNature Publishing Group | 2007| -
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
National licenceNature Publishing Group | 2007| -
Localization of type 1 diabetes susceptibility to the MHC class I genes HLA-B and HLA-A
National licenceNature Publishing Group | 2007| -
A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva
National licenceNature Publishing Group | 2006|
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