Tailored interventions to overcome identified barriers to change: effects on professional practice and health care outcomes
…, F Cheater, S Flottorp, N Robertson - Cochrane database …, 2010 - cochranelibrary.com
Background In the previous version of this review, the effectiveness of interventions tailored
to barriers to change was found to be uncertain. Objectives To assess the effectiveness of …
to barriers to change was found to be uncertain. Objectives To assess the effectiveness of …
Image-guided prostate biopsy using magnetic resonance imaging–derived targets: a systematic review
CM Moore, NL Robertson, N Arsanious, T Middleton… - European urology, 2013 - Elsevier
CONTEXT: Technical improvements in prostate magnetic resonance imaging (MRI) have
resulted in the use of MRI to target prostate biopsies. OBJECTIVE: To systematically review …
resulted in the use of MRI to target prostate biopsies. OBJECTIVE: To systematically review …
[HTML][HTML] Intrapartum-related neonatal encephalopathy incidence and impairment at regional and global levels for 2010 with trends from 1990
Background: Intrapartum hypoxic events (“birth asphyxia”) may result in stillbirth, neonatal or
postneonatal mortality, and impairment. Systematic morbidity estimates for the burden of …
postneonatal mortality, and impairment. Systematic morbidity estimates for the burden of …
Hundreds of variants clustered in genomic loci and biological pathways affect human height
H Lango Allen, K Estrada, G Lettre, SI Berndt… - Nature, 2010 - nature.com
Most common human traits and diseases have a polygenic pattern of inheritance: DNA
sequence variants at many genetic loci influence the phenotype. Genome-wide association …
sequence variants at many genetic loci influence the phenotype. Genome-wide association …
Rising prevalence of multiple sclerosis worldwide: Insights from the Atlas of MS
…, E Leray, RA Marrie, N Robertson… - Multiple Sclerosis …, 2020 - journals.sagepub.com
Background: High-quality epidemiologic data worldwide are needed to improve our
understanding of disease risk, support health policy to meet the diverse needs of people …
understanding of disease risk, support health policy to meet the diverse needs of people …
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis
By combining genome-wide association data from 8,130 individuals with type 2 diabetes
(T2D) and 38,987 controls of European descent and following up previously unidentified …
(T2D) and 38,987 controls of European descent and following up previously unidentified …
Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps
We expanded GWAS discovery for type 2 diabetes (T2D) by combining data from 898,130
European-descent individuals (9% cases), after imputation to high-density reference panels …
European-descent individuals (9% cases), after imputation to high-density reference panels …
Laser interferometer space antenna
…, E Porter, J Reiche, D Robertson, N Robertson… - arXiv preprint arXiv …, 2017 - arxiv.org
Following the selection of The Gravitational Universe by ESA, and the successful flight of
LISA Pathfinder, the LISA Consortium now proposes a 4 year mission in response to ESA's …
LISA Pathfinder, the LISA Consortium now proposes a 4 year mission in response to ESA's …
The genetic architecture of type 2 diabetes
The genetic architecture of common traits, including the number, frequency, and effect sizes
of inherited variants that contribute to individual risk, has been long debated. Genome-wide …
of inherited variants that contribute to individual risk, has been long debated. Genome-wide …
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis
International IBD Genetics Consortium (IIBDGC)… - Nature …, 2013 - nature.com
Using the ImmunoChip custom genotyping array, we analyzed 14,498 subjects with multiple
sclerosis and 24,091 healthy controls for 161,311 autosomal variants and identified 135 …
sclerosis and 24,091 healthy controls for 161,311 autosomal variants and identified 135 …