31 research outputs found

    Recovery from Addiction on a University Campus – a UK Perspective

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    Between 30 and 40% of 18-year olds in England, Wales and Northern Ireland enter tertiary education (university) each year. Young adulthood (ages 15 to 25) is the usual period in which problems with alcohol, drugs or other behaviors begin to emerge, and yet these issues have received limited study in the UK. Government policy dictates that a full continuum of treatment and recovery services should be available in each area of the country, but uptake of these services by university students appears to be limited. In this discussion paper we describe the background to, and components of, the Collegiate Recovery Program (CRP), an initiative that has grown rapidly in the USA in the past decade. We then describe how the first UK University-led CRP was set up, before outlining what has been learnt so far and the potential challenges facing this approach

    Microwave-optical double resonance in a erbium-doped whispering-gallery-mode resonator

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    We showcase an erbium-doped whispering-gallery-mode resonator with optical modes that display intrinsic quality factors better than 10810^8 (linewidths less than 2 MHz), and coupling strengths to collective erbium transitions of up to 2π×\pi\times1.2 GHz - enough to reach the ensemble strong coupling regime. Our optical cavity sits inside a microwave resonator, allowing us to probe the spin transition which is tuned by an external magnetic field. We show a modified optically detected magnetic resonance measurement that measures population transfer by a change in coupling strength rather than absorption coefficient. This modification was enabled by the strong coupling to our modes, and allows us to optically probe the spin transition detuned by more than the inhomogeneous linewidth. We contrast this measurement with electron paramagnetic resonance to experimentally show that our optical modes are confined in a region of large microwave magnetic field and we explore how such a geometry could be used for coherent microwave-optical transduction.Comment: 8 pages, 6 figure

    Ultra-low Threshold Titanium doped sapphire Whispering-gallery Laser

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    Titanium doped sapphire (Ti:sapphire) is a laser gain material with broad gain bandwidth benefiting from the material stability of sapphire. These favorable characteristics of Ti:sapphire have given rise to femtosecond lasers and optical frequency combs. Shaping a single Ti:sapphire crystal into a millimeter sized high quality whispering gallery mode resonator (Q∼108Q\sim10^8) reduces the lasing threshold to 14.2 mW and increases the laser slope efficiency to 34%. The observed lasing can be both multi-mode and single-mode. This is the first demonstration of a Ti:sapphire whispering-gallery laser. Furthermore, a novel method of evaluating the gain in Ti:sapphire in the near infrared region is demonstrated by introducing a probe laser with a central wavelength of 795 nm. This method results in decreasing linewidth of the modes excited with the probe laser, consequently increasing their QQ. These findings open avenues for the usage of whispering gallery mode resonators as cavities for the implementation of compact Ti:sapphire lasers. Moreover, Ti:sapphire can also be utilized as an amplifier inside its gain bandwidth by implementing a pump-probe configuration.Comment: Main text (13 pages, 7 figures) Supplemental document (11 pages, 9 figures

    Neuromuscular disease genetics in under-represented populations: increasing data diversity

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    Neuromuscular diseases (NMDs) affect ∼15 million people globally. In high income settings DNA-based diagnosis has transformed care pathways and led to gene-specific therapies. However, most affected families are in low-to-middle income countries (LMICs) with limited access to DNA-based diagnosis. Most (86%) published genetic data is derived from European ancestry. This marked genetic data inequality hampers understanding of genetic diversity and hinders accurate genetic diagnosis in all income settings. We developed a cloud-based transcontinental partnership to build diverse, deeply-phenotyped and genetically characterized cohorts to improve genetic architecture knowledge, and potentially advance diagnosis and clinical management. We connected 18 centres in Brazil, India, South Africa, Turkey, Zambia, Netherlands and the UK. We co-developed a cloud-based data solution and trained 17 international neurology fellows in clinical genomic data interpretation. Single gene and whole exome data were analysed via a bespoke bioinformatics pipeline and reviewed alongside clinical and phenotypic data in global webinars to inform genetic outcome decisions. We recruited 6001 participants in the first 43 months. Initial genetic analyses ‘solved’ or ‘possibly solved’ ∼56% probands overall. In-depth genetic data review of the four commonest clinical categories (limb girdle muscular dystrophy, inherited peripheral neuropathies, congenital myopathy/muscular dystrophies and Duchenne/Becker muscular dystrophy) delivered a ∼59% ‘solved’ and ∼13% ‘possibly solved’ outcome. Almost 29% of disease causing variants were novel, increasing diverse pathogenic variant knowledge. Unsolved participants represent a new discovery cohort. The dataset provides a large resource from under-represented populations for genetic and translational research. In conclusion, we established a remote transcontinental partnership to assess genetic architecture of NMDs across diverse populations. It supported DNA-based diagnosis, potentially enabling genetic counselling, care pathways and eligibility for gene-specific trials. Similar virtual partnerships could be adopted by other areas of global genomic neurological practice to reduce genetic data inequality and benefit patients globally

    Quantifying Sources of Variability in Infancy Research Using the Infant-Directed-Speech Preference

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    Psychological scientists have become increasingly concerned with issues related to methodology and replicability, and infancy researchers in particular face specific challenges related to replicability: For example, high-powered studies are difficult to conduct, testing conditions vary across labs, and different labs have access to different infant populations. Addressing these concerns, we report on a large-scale, multisite study aimed at (a) assessing the overall replicability of a single theoretically important phenomenon and (b) examining methodological, cultural, and developmental moderators. We focus on infants’ preference for infant-directed speech (IDS) over adult-directed speech (ADS). Stimuli of mothers speaking to their infants and to an adult in North American English were created using seminaturalistic laboratory-based audio recordings. Infants’ relative preference for IDS and ADS was assessed across 67 laboratories in North America, Europe, Australia, and Asia using the three common methods for measuring infants’ discrimination (head-turn preference, central fixation, and eye tracking). The overall meta-analytic effect size (Cohen’s d) was 0.35, 95% confidence interval = [0.29, 0.42], which was reliably above zero but smaller than the meta-analytic mean computed from previous literature (0.67). The IDS preference was significantly stronger in older children, in those children for whom the stimuli matched their native language and dialect, and in data from labs using the head-turn preference procedure. Together, these findings replicate the IDS preference but suggest that its magnitude is modulated by development, native-language experience, and testing procedure
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