Institution
University of Western Australia
Education•Perth, Western Australia, Australia•
About: University of Western Australia is a education organization based out in Perth, Western Australia, Australia. It is known for research contribution in the topics: Population & Poison control. The organization has 29613 authors who have published 87405 publications receiving 3064466 citations. The organization is also known as: UWA & University of WA.
Papers published on a yearly basis
Papers
More filters
••
University of Newcastle1, Woolcock Institute of Medical Research2, University of Queensland3, Princess Alexandra Hospital4, University of Adelaide5, Royal Adelaide Hospital6, Sir Charles Gairdner Hospital7, University of Western Australia8, The George Institute for Global Health9, Macquarie University10, University of New South Wales11, Flinders University12
TL;DR: Children and adults with persistent symptomatic asthma experience fewer asthma exacerbations and improved quality of life when treated with oral azithromycin for 48 weeks, suggesting it might be a useful add-on therapy in persistent asthma.
446 citations
••
TL;DR: In this paper, the relationship between rest-frame 8 μm luminosity (L_8) and star formation rate (SFR) for L* galaxies at z ~ 2 was investigated.
Abstract: We use a sample of 90 spectroscopically confirmed Lyman break galaxies with Hα measurements and Spitzer MIPS 24 μm observations to constrain the relationship between rest-frame 8 μm luminosity (L_8) and star formation rate (SFR) for L* galaxies at z ~ 2. We find a tight correlation with 0.24 dex scatter between L_8 and Hα luminosity/SFR for z ~ 2 galaxies with 10^(10) L_☉ ≲ L_(IR) ≲ 10^(12) L_☉. Employing this relationship with a larger sample of 392 galaxies with spectroscopic redshifts, we find that the UV slope β can be used to recover the dust attenuation of the vast majority of moderately luminous L* galaxies at z ~ 2 to within a 0.4 dex scatter using the local correlation. Separately, young galaxies with ages ≲100 Myr appear to be less dusty than their UV slopes would imply based on the local trend and may follow an extinction curve that is steeper than what is typically assumed. Consequently, very young galaxies at high redshift may be significantly less dusty than inferred previously. Our results provide the first direct evidence, independent of the UV slope, for a correlation between UV and bolometric luminosity (L_(bol)) at high redshift, in the sense that UV-faint galaxies are on average less infrared and less bolometrically luminous than their UV-bright counterparts. The L_(bol)-L_(UV) relation indicates that as the SFR increases, L_(UV) turns over (or "saturates") around the value of L* at z ~ 2, implying that dust obscuration may be largely responsible for modulating the bright end of the UV luminosity function. Finally, dust attenuation is found to correlate with oxygen abundance at z ~ 2. Accounting for systematic differences in local and high-redshift metallicity calibrations, we find that L* galaxies at z ~ 2, while at least an order of magnitude more bolometrically luminous, exhibit ratios of metals to dust that are similar to those of local starbursts. This result is expected if high-redshift galaxies are forming their stars in a less metal-rich environment compared to local galaxies of the same luminosity, thus naturally leading to a redshift evolution in both the bolometric luminosity-metallicity and bolometric luminosity-obscuration relations.
445 citations
••
TL;DR: In this paper, a proof-of-concept example for a method that allows the calculation of a similarity index between whole molecular crystal structures; this has been termed "structural genetic fingerprinting" is described.
Abstract: This paper describes a proof-of-concept example for a method that allows the calculation of a similarity index between whole molecular crystal structures; this has been termed ‘structural genetic fingerprinting’. It is based on the use of fingerprint plots derived from Hirshfeld surfaces coupled with cluster analysis and associated multivariate statistics. Using this formalism, it is possible to show quantitatively (using correlation coefficients) that, for example naphthalene is more similar to anthracene than to benzene, and moreover that benzodicoronene is more similar to anthrabenzonaphthopentacene than naphthalene is to anthracene. Whereas the correlation coefficients themselves obtained say nothing about the ways in which the patterns of intermolecular interactions are similar or different for two different structures, the fingerprint plots do contain such information. In principle this method for quantifying structural similarities of whole molecular crystal structures should be both robust and generally applicable. This method is potentially applicable to datasets consisting of many hundreds or even thousands of structures.
445 citations
••
Mahidol University1, University of California, San Francisco2, University of Cape Town3, University of Tübingen4, Wellcome Trust5, University of Oxford6, University of Western Australia7, University of Paris8, World Health Organization9, University of Bamako10, University of Lausanne11, Swiss Tropical and Public Health Institute12, Pasteur Institute13, Novartis14, Liverpool School of Tropical Medicine15, Karolinska Institutet16, Walter and Eliza Hall Institute of Medical Research17, Drugs for Neglected Diseases Initiative18, University of Southern Denmark19, National University of Laos20, Mahosot Hospital21, International Military Sports Council22, Muhimbili University of Health and Allied Sciences23, Yale University24, Uppsala University25, University of Washington26, University of Amsterdam27
TL;DR: Higher, more frequent, or prolonged dosage regimens should now be evaluated in very young children, particularly if malnourished, and in patients with hyperparasitemia, as well as patients in very low transmission intensity areas with emerging parasite resistance.
Abstract: Background: Achieving adequate antimalarial drug exposure is essential for curing malaria. Day 7 blood or plasma lumefantrine concentrations provide a simple measure of drug exposure that correlates well with artemether-lumefantrine efficacy. However, the 'therapeutic' day 7 lumefantrine concentration threshold needs to be defined better, particularly for important patient and parasite sub-populations. Methods: The WorldWide Antimalarial Resistance Network (WWARN) conducted a large pooled analysis of individual pharmacokinetic-pharmacodynamic data from patients treated with artemether-lumefantrine for uncomplicated Plasmodium falciparum malaria, to define therapeutic day 7 lumefantrine concentrations and identify patient factors that substantially alter these concentrations. A systematic review of PubMed, Embase, Google Scholar, ClinicalTrials.gov and conference proceedings identified all relevant studies. Risk of bias in individual studies was evaluated based on study design, methodology and missing data. Results: Of 31 studies identified through a systematic review, 26 studies were shared with WWARN and 21 studies with 2,787 patients were included. Recrudescence was associated with low day 7 lumefantrine concentrations (HR 1.59 (95 % CI 1.36 to 1.85) per halving of day 7 concentrations) and high baseline parasitemia (HR 1.87 (95 % CI 1.22 to 2.87) per 10-fold increase). Adjusted for mg/kg dose, day 7 concentrations were lowest in very young children (98 % cure rates (if parasitemia <135,000/μL). Conclusions: Current artemether-lumefantrine dosing recommendations achieve day 7 lumefantrine concentrations ≥200 ng/ml and high cure rates in most uncomplicated malaria patients. Three groups are at increased risk of treatment failure: very young children (particularly those underweight-for-age); patients with high parasitemias; and patients in very low transmission intensity areas with emerging parasite resistance. In these groups, adherence and treatment response should be monitored closely. Higher, more frequent, or prolonged dosage regimens should now be evaluated in very young children, particularly if malnourished, and in patients with hyperparasitemia.
445 citations
••
TL;DR: Having considered issues of accuracy, repeatability and utility, the multi-component model might be employed as a performance or selection criterion, provided the selected model accounts for variability in the density of fat-free mass in its computation.
Abstract: Quantifying human body composition has played an important role in monitoring all athlete performance and training regimens, but especially so in gravitational, weight class and aesthetic sports wherein the tissue composition of the body profoundly affects performance or adjudication. Over the past century, a myriad of techniques and equations have been proposed, but all have some inherent problems, whether in measurement methodology or in the assumptions they make. To date, there is no universally applicable criterion or 'gold standard' methodology for body composition assessment. Having considered issues of accuracy, repeatability and utility, the multi-component model might be employed as a performance or selection criterion, provided the selected model accounts for variability in the density of fat-free mass in its computation. However, when profiling change in interventions, single methods whose raw data are surrogates for body composition (with the notable exception of the body mass index) remain useful.
445 citations
Authors
Showing all 29972 results
Name | H-index | Papers | Citations |
---|---|---|---|
Nicholas G. Martin | 192 | 1770 | 161952 |
Cornelia M. van Duijn | 183 | 1030 | 146009 |
Kay-Tee Khaw | 174 | 1389 | 138782 |
Steven N. Blair | 165 | 879 | 132929 |
David W. Bates | 159 | 1239 | 116698 |
Mark E. Cooper | 158 | 1463 | 124887 |
David Cameron | 154 | 1586 | 126067 |
Stephen T. Holgate | 142 | 870 | 82345 |
Jeremy K. Nicholson | 141 | 773 | 80275 |
Xin Chen | 139 | 1008 | 113088 |
Graeme J. Hankey | 137 | 844 | 143373 |
David Stuart | 136 | 1665 | 103759 |
Joachim Heinrich | 136 | 1309 | 76887 |
Carlos M. Duarte | 132 | 1173 | 86672 |
David Smith | 129 | 2184 | 100917 |