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Institution

Glenfield Hospital

HealthcareLeicester, United Kingdom
About: Glenfield Hospital is a healthcare organization based out in Leicester, United Kingdom. It is known for research contribution in the topics: Population & Extracorporeal membrane oxygenation. The organization has 1382 authors who have published 1812 publications receiving 99238 citations. The organization is also known as: Glenfield General Hospital.


Papers
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Journal ArticleDOI
Christina Loley1, Maris Alver2, Themistocles L. Assimes3, Andrew Bjonnes4, Anuj Goel5, Anuj Goel6, Stefan Gustafsson7, Jussi Hernesniemi8, Jemma C. Hopewell6, Stavroula Kanoni9, Marcus E. Kleber10, King Wai Lau6, Yingchang Lu11, Leo-Pekka Lyytikäinen8, Christopher P. Nelson12, Christopher P. Nelson13, Majid Nikpay14, Liming Qu15, Elias Salfati3, Markus Scholz16, Taru Tukiainen17, Taru Tukiainen4, Christina Willenborg1, Hong-Hee Won18, Lingyao Zeng19, Weihua Zhang20, Weihua Zhang21, Sonia S. Anand22, Frank Beutner16, Erwin P. Bottinger11, Robert Clarke6, George Dedoussis23, Ron Do, Tõnu Esko2, Tõnu Esko4, Markku Eskola8, Martin Farrall5, Martin Farrall6, Dominique Gauguier24, Vilmantas Giedraitis, Christopher B. Granger25, Alistair S. Hall26, Anders Hamsten27, Stanley A Hazen28, Jie Huang, Mika Kähönen8, Theodosios Kyriakou5, Theodosios Kyriakou6, Reijo Laaksonen8, Lars Lind29, Cecilia M. Lindgren5, Cecilia M. Lindgren30, Patrik K. E. Magnusson27, Eirini Marouli9, Evelin Mihailov2, Andrew P. Morris5, Andrew P. Morris31, Kjell Nikus8, Nancy L. Pedersen27, Loukianos S. Rallidis, Veikko Salomaa32, Svati H. Shah25, Alexandre F.R. Stewart14, John R. Thompson12, Pierre Zalloua4, Pierre Zalloua33, John C. Chambers34, John C. Chambers22, John C. Chambers21, Rory Collins6, Erik Ingelsson5, Erik Ingelsson7, Carlos Iribarren35, Pekka J. Karhunen8, Jaspal S. Kooner22, Jaspal S. Kooner34, Jaspal S. Kooner32, Terho Lehtimäki8, Ruth J. F. Loos11, Winfried März36, Winfried März10, Winfried März37, Ruth McPherson14, Andres Metspalu2, Muredach P. Reilly15, S. Ripatti38, S. Ripatti35, Dharambir K. Sanghera39, Joachim Thiery16, Hugh Watkins5, Hugh Watkins6, Panos Deloukas40, Panos Deloukas9, Panos Deloukas41, Sekar Kathiresan, Nilesh J. Samani13, Nilesh J. Samani12, Heribert Schunkert20, Jeanette Erdmann1, Inke R. König1 
TL;DR: A comprehensive X-chromosome-wide meta-analysis including more than 43,000 CAD cases and 58,000 controls from 35 international study cohorts found none of the investigated models revealed genome-wide significant associations for any variant.
Abstract: In recent years, genome-wide association studies have identified 58 independent risk loci for coronary artery disease (CAD) on the autosome. However, due to the sex-specific data structure of the X chromosome, it has been excluded from most of these analyses. While females have 2 copies of chromosome X, males have only one. Also, one of the female X chromosomes may be inactivated. Therefore, special test statistics and quality control procedures are required. Thus, little is known about the role of X-chromosomal variants in CAD. To fill this gap, we conducted a comprehensive X-chromosome-wide meta-analysis including more than 43,000 CAD cases and 58,000 controls from 35 international study cohorts. For quality control, sex-specific filters were used to adequately take the special structure of X-chromosomal data into account. For single study analyses, several logistic regression models were calculated allowing for inactivation of one female X-chromosome, adjusting for sex and investigating interactions between sex and genetic variants. Then, meta-analyses including all 35 studies were conducted using random effects models. None of the investigated models revealed genome-wide significant associations for any variant. Although we analyzed the largest-to-date sample, currently available methods were not able to detect any associations of X-chromosomal variants with CAD.

24 citations

Journal ArticleDOI
TL;DR: To study the reproducibility of the measurement of shoulder movement, a series of 64 patients with and without shoulder problems are examined, measuring active elevation, abduction, and external rotation in adduction using an inclinometer.
Abstract: To study the reproducibility of the measurement of shoulder movement, we have examined a series of 64 patients with and without shoulder problems, measuring active elevation, abduction, and external rotation in adduction using an inclinometer. The difference within which readings by different observers were expected to lie for 95% of the pairs of observations ranged from 24° to 33° for different movements in asymptomatic shoulders and from 24° to 41° in those with unilateral shoulder symptoms awaiting surgery.

24 citations

Journal ArticleDOI
TL;DR: TRM provides regional quantitative information on changes in inhaled gas ventilation in response to therapy and could be used as a sensitive regional outcome metric for novel respiratory interventions.
Abstract: Purpose To assess the magnitude of regional response to respiratory therapeutic agents in the lungs by using treatment response mapping (TRM) with hyperpolarized gas magnetic resonance (MR) imaging. TRM was used to quantify regional physiologic response in adults with asthma who underwent a bronchodilator challenge. Materials and Methods This study was approved by the national research ethics committee and was performed with informed consent. Imaging was performed in 20 adult patients with asthma by using hyperpolarized helium 3 (3He) ventilation MR imaging. Two sets of baseline images were acquired before inhalation of a bronchodilating agent (salbutamol 400 μg), and one set was acquired after. All images were registered for voxelwise comparison. Regional treatment response, ΔR(r), was calculated as the difference in regional gas distribution (R[r] = ratio of inhaled gas to total volume of a voxel when normalized for lung inflation volume) before and after intervention. A voxelwise activation threshold from the variability of the baseline images was applied to ΔR(r) maps. The summed global treatment response map (ΔRnet) was then used as a global lung index for comparison with metrics of bronchodilator response measured by using spirometry and the global imaging metric percentage ventilated volume (%VV). Results ΔRnet showed significant correlation (P < .01) with changes in forced expiratory volume in 1 second (r = 0.70), forced vital capacity (r = 0.84), and %VV (r = 0.56). A significant (P < .01) positive treatment effect was detected with all metrics; however, ΔRnet showed a lower intersubject coefficient of variation (64%) than all of the other tests (coefficient of variation, ≥99%). Conclusion TRM provides regional quantitative information on changes in inhaled gas ventilation in response to therapy. This method could be used as a sensitive regional outcome metric for novel respiratory interventions. © RSNA, 2017 Online supplemental material is available for this article.

24 citations

Journal ArticleDOI
TL;DR: Fungal involvement in asthma is associated with severe disease and the full spectrum of fungal species in asthma are not well described and are derived largely from insensitive culture techniques.
Abstract: BACKGROUND:Fungal involvement in asthma is associated with severe disease. The full spectrum of fungal species in asthma is not well described and is derived largely from insensitive culture techniques. OBJECTIVES:To use high-throughput sequencing to describe the airway mycobiota in asthmatics with and without fungal-sensitisation and healthy controls; to compare samples representing different airway compartments; to determine if the mycobiota was influenced by the fungal composition of outdoor air, and to compare findings with clinically relevant outcomes. METHODS:We amplified the internal transcribed spacer region 2 of the nuclear ribosomal operon to identify the fungal species present. Ninety-seven subjects were recruited and provided sputum (83 asthmatics; 14 healthy subjects), with 29 also undergoing a bronchoscopy. A subset of airway samples were compared with matched outdoor air and mouthwash samples. RESULTS:Two hundred and six taxa at the species level were identified in sputum, most at low relative abundance. Aspergillus fumigatus, Candida albicans and Mycosphaerella tassiana had the highest relative abundances and were the most prevalent species across all subjects. The airway mycobiota consisted of a complex community with high diversity between individuals. Notable shifts in the balance of fungi detected in the lung were associated with asthma status, asthma duration and biomarkers of inflammation. Aspergillus tubingensis, a member of the Aspergillus niger species complex, was most prevalent from bronchoscopic protected brush samples and significantly associated with a low sputum neutrophilia. Cryptococcus pseudolongus, from the Cryptococcus humicola species complex, was more abundant from bronchoscopy samples than sputum, and differentially more abundant in asthma than health. CONCLUSIONS AND CLINICAL RELEVANCE:The airway mycobiota was dominated by a relatively small number of species, but was distinct from the oropharyngeal mycobiota and air samples. Members of the Aspergillus niger and Cryptococus humicola species complexes may play unexpected roles in the pathogenesis of asthma.

23 citations


Authors

Showing all 1385 results

NameH-indexPapersCitations
Nilesh J. Samani149779113545
Daniel I. Chasman13448472180
Massimo Mangino11636984902
Ian D. Pavord10857547691
Christopher E. Brightling10355244358
Ulf Gyllensten10036859219
Pim van der Harst9951742777
Andrew J. Wardlaw9231133721
Kenneth J. O'Byrne8762939193
Paul Burton8541842766
Bryan Williams8245440798
Marylyn D. Ritchie8045932559
John R. Thompson7820250475
Maria G. Belvisi7326916021
Martin D. Tobin7221834028
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
20228
2021124
2020104
201996
201891
201789