Absence of superconducting dome at the charge-density-wave quantum phase transition in 2<i>H</i>−NbSe₂

Superconductivity is often found in a dome around quantum critical points, i.e. 2nd-order quantum phase transitions. Here, we show that an enhancement of superconductivity is avoided at the critical pressure of the charge-density-wave (CDW) state in NbSe$_2$. We present comprehensive high-pressure Hall effect and magnetic susceptibility measurements of the CDW and superconducting state in NbSe$_2$. Initially, the 2nd-order CDW transition is suppressed smoothly but it drops to zero abruptly at PCDW = 4.4 GPa thus indicating a change to 1st order whilstthe superconducting transition temperature Tc rises continuously up to PCDW but is constant above. The putative 1st-order nature of the CDW transition is suggested as the cause for the absence of a superconducting dome at PCDW. Indeed, we show that the suppression of the superconducting state at low pressures is due to the loss of density of states inside the CDW phase whilst the initial suppression of the CDW state is accounted for by the stiffening of the underlying bare phonon mode.Comment: 16 pages, 5 figures, S

Trigonal to cubic structural transition in possibly N-doped LuH3 measured by Raman and X-ray diffraction

After the reported discovery of room-temperature superconductivity at only 1 GPa in nitrogendoped lutetium trihydride and the resulting heated discussions, there is an urgent need to reproduce the results and synthesis of this compound. Here, we report the synthesis of (potentially N-doped) cubic LuH3 starting from pure Lu to produce very stable trigonal LuH3 which was subsequently pressurised to 2 GPa with a dilute N2/He rich pressure medium. Raman spectroscopy and X-ray diffraction were used to characterise the structure throughout the synthesis process.Comment: 8 pages, 5 figure

Clean-limit superconductivity in Im3¯m H3S synthesized from sulfur and hydrogen donor ammonia borane

We present detailed studies of the superconductivity in high-pressure H$_3$S. X-ray diffraction measurements show that cubic Im$\bar{3}$m H3S was synthesized from elemental sulfur and hydrogen donor ammonia borane (NH$_3$BH$_3$). Our electrical transport measurements confirm superconductivity with a transition temperature T$_c$=197K at 153 GPa. From the analysis of both the normal-state resistivity and the slope of the critical field, we conclude that the superconductivity is described by clean-limit behavior. A significant broadening of the resistive transition in finite magnetic field is found, as expected for superconductors. We identify a linear temperature-over-field scaling of the resistance at the superconducting transition which is not described by existing theories

Fermi surface reconstruction and electron dynamics at the charge-density-wave transition in TiSe2

The evolution of the charge carrier concentrations and mobilities are examined across the charge-density-wave (CDW) transition in TiSe2. Combined quantum oscillation and magnetotransport measurements show that a small electron pocket dominates the electronic properties at low temperatures whilst an electron and hole pocket contribute at room temperature. At the CDW transition, an abrupt Fermi surface reconstruction and a minimum in the electron and hole mobilities are extracted from two-band and Kohler analysis of magnetotransport measurements. The minimum in the mobilities is associated with the overseen role of scattering from the softening CDW mode. With the carrier concentrations and dynamics dominated by the CDW and the associated bosonic mode, our results highlight TiSe2 as a prototypical system to study the Fermi surface reconstruction at a density-wave transition.Comment: 15 pages, 3 figures, including supplementary informatio

Generation of 3D retinal tissue from human pluripotent stem cells using a directed small molecule-based serum-free microwell platform

Retinal degenerative diseases are a leading cause of blindness worldwide with debilitating life-long consequences for the affected individuals. Cell therapy is considered a potential future clinical intervention to restore and preserve sight by replacing lost photoreceptors and/or retinal pigment epithelium. Development of protocols to generate retinal tissue from human pluripotent stem cells (hPSC), reliably and at scale, can provide a platform to generate photoreceptors for cell therapy and to model retinal disease in vitro. Here, we describe an improved differentiation platform to generate retinal organoids from hPSC at scale and free from time-consuming manual microdissection steps. The scale up was achieved using an agarose mould platform enabling generation of uniform self-assembled 3D spheres from dissociated hPSC in microwells. Subsequent retinal differentiation was efficiently achieved via a stepwise differentiation protocol using a number of small molecules. To facilitate clinical translation, xeno-free approaches were developed by substituting Matrigel™ and foetal bovine serum with recombinant laminin and human platelet lysate, respectively. Generated retinal organoids exhibited important features reminiscent of retinal tissue including correct site-specific localisation of proteins involved in phototransduction

Sleep problems and associations with psychopathology and cognition in young people with 22q11.2 deletion syndrome (22q11.2DS)

Background: Young people with 22q11.2 deletion syndrome (22q11.2DS) are at high risk for neurodevelopmental disorders. Sleep problems may play a role in this risk but their prevalence, nature and links to psychopathology and cognitive function remain undescribed in this population. Method: Sleep problems, psychopathology, developmental coordination and cognitive function were assessed in 140 young people with 22q11.2DS (mean age=10.1, SD=2.46) and 65 unaffected sibling controls (mean age=10.8, SD=2.26). Primary carers completed questionnaires screening for the children’s developmental coordination and autism spectrum disorder. Results: Sleep problems were identified in 60% of young people with 22q11.2DS compared to 23% of sibling controls (OR=5.00, p<0.001). Two patterns best described sleep problems in 22q11.2DS: restless sleep and insomnia. Restless sleep was linked to increased ADHD symptoms (OR=1.16, p<0.001) and impaired executive function (OR=0.975, p=0.013). Both patterns were associated with elevated symptoms of anxiety disorder (restless sleep: OR=1.10, p=0.006 and insomnia: OR=1.07, p=0.045) and developmental coordination disorder (OR=0.968, p=0.0023, and OR=0.955, p=0.009). The insomnia pattern was also linked to elevated conduct disorder symptoms (OR=1.53, p=0.020). Conclusions: Clinicians and carers should be aware that sleep problems are common in 22q11.2DS and index psychiatric risk, cognitive deficits and motor coordination problems. Future studies should explore the physiology of sleep and the links with the neurodevelopment in these young peopl

Sleep EEG in young people with 22q11.2 deletion syndrome:a cross-sectional study of slow-waves, spindles and correlations with memory and neurodevelopmental symptoms

Background:: Young people living with 22q11.2 Deletion Syndrome (22q11.2DS) are at increased risk of schizophrenia, intellectual disability, attention-deficit hyperactivity disorder (ADHD) and autism spectrum disorder (ASD). In common with these conditions, 22q11.2DS is also associated with sleep problems. We investigated whether abnormal sleep or sleep-dependent network activity in 22q11.2DS reflects convergent, early signatures of neural circuit disruption also evident in associated neurodevelopmental conditions. Methods:: In a cross-sectional design, we recorded high-density sleep EEG in young people (6–20 years) with 22q11.2DS (n=28) and their unaffected siblings (n=17), quantifying associations between sleep architecture, EEG oscillations (spindles and slow waves) and psychiatric symptoms. We also measured performance on a memory task before and after sleep. Results:: 22q11.2DS was associated with significant alterations in sleep architecture, including a greater proportion of N3 sleep and lower proportions of N1 and REM sleep than in siblings. During sleep, deletion carriers showed broadband increases in EEG power with increased slow-wave and spindle amplitudes, increased spindle frequency and density, and stronger coupling between spindles and slow-waves. Spindle and slow-wave amplitudes correlated positively with overnight memory in controls, but negatively in 22q11.2DS. Mediation analyses indicated that genotype effects on anxiety, ADHD and ASD were partially mediated by sleep EEG measures. Conclusions:: This study provides a detailed description of sleep neurophysiology in 22q11.2DS, highlighting alterations in EEG signatures of sleep which have been previously linked to neurodevelopment, some of which were associated with psychiatric symptoms. Sleep EEG features may therefore reflect delayed or compromised neurodevelopmental processes in 22q11.2DS, which could inform our understanding of the neurobiology of this condition and be biomarkers for neuropsychiatric disorders. Funding:: This research was funded by a Lilly Innovation Fellowship Award (UB), the National Institute of Mental Health (NIMH 5UO1MH101724; MvdB), a Wellcome Trust Institutional Strategic Support Fund (ISSF) award (MvdB), the Waterloo Foundation (918-1234; MvdB), the Baily Thomas Charitable Fund (2315/1; MvdB), MRC grant Intellectual Disability and Mental Health: Assessing Genomic Impact on Neurodevelopment (IMAGINE) (MR/L011166/1; JH, MvdB and MO), MRC grant Intellectual Disability and Mental Health: Assessing Genomic Impact on Neurodevelopment 2 (IMAGINE-2) (MR/T033045/1; MvdB, JH and MO); Wellcome Trust Strategic Award ‘Defining Endophenotypes From Integrated Neurosciences’ Wellcome Trust (100202/Z/12/Z MO, JH). NAD was supported by a National Institute for Health Research Academic Clinical Fellowship in Mental Health and MWJ by a Wellcome Trust Senior Research Fellowship in Basic Biomedical Science (202810/Z/16/Z). CE and HAM were supported by Medical Research Council Doctoral Training Grants (C.B.E. 1644194, H.A.M MR/K501347/1). HMM and UB were employed by Eli Lilly & Co during the study; HMM is currently an employee of Boehringer Ingelheim Pharma GmbH & Co KG. The views and opinions expressed are those of the author(s), and not necessarily those of the NHS, the NIHR or the Department of Health funders

Lifshitz transition enabling superconducting dome around the quantum critical point in TiSe2_2

Superconductivity often emerges as a dome around a quantum critical point (QCP) where long-range order is suppressed to zero temperature. So far, this has been mostly studied in magnetically ordered materials. By contrast, the interplay between charge order and superconductivity at a QCP is not fully understood. Here, we present resistance measurements proving that a dome of superconductivity surrounds the charge-density-wave (CDW) QCP in pristine samples of 1$T$-TiSe$_2$ tuned with hydrostatic pressure. Furthermore, we use quantum oscillation measurements to show that the superconductivity sets in at a Lifshitz transition in the electronic band structure. We use density functional theory to identify the Fermi pockets enabling superconductivity: large electron and hole pockets connected by the CDW wave vector $\vec{Q}$ which emerge upon partial suppression of the zero-pressure CDW gap. Hence, we conclude that superconductivity is of interband type enabled by the presence of hole and electron bands connected by the CDW $\vec{Q}$ vector. Earlier calculations show that interband interactions are repulsive, which suggests that unconventional s$_{\pm}$ superconductivity is realised in TiSe$_2$ - similar to the iron pnictides. These results highlight the importance of Lifshitz transitions in realising unconventional superconductivity and help understand its interaction with CDW order in numerous materials.Comment: 21 pages, 5 figure

Psychopathology in mothers of children with pathogenic copy number variants

Background: Caring for children with pathogenic neurodevelopmental Copy Number Variants (CNVs) (i.e., deletions and duplications of genetic material) can place a considerable burden on parents, and their quality of life. Our study is the first to examine the frequency of psychiatric diagnoses in mothers of children with CNVs compared to the frequency of psychiatric problems in age-matched mothers from a large community study. Methods: Case-control study. 268 mothers of children with a CNV diagnosed in a medical genetics clinic and 2,680 age-matched mothers taking part in the ALSPAC study. Results: Mothers of children with CNVs reported higher frequency of depression, anorexia, bulimia, alcohol abuse and drug addiction problems compared to the age-matched mothers from the community sample. Focusing on psychiatric problems arising immediately after the birth of the index child, the levels of depression symptoms were similar between the two groups (48% in mothers of children with CNVs vs. 44% in mothers of the community sample, p=0.43), but mothers of children with CNVs had higher frequency of anxiety symptoms (55%) compared to mothers from the community sample (30%, p=0.03). Conclusion: Our study highlights the need for health-care providers to devise treatment plans that not only focus on meeting the child’s needs, but also assessing and if needed, addressing the mental health needs of the parent