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Institution

St Thomas' Hospital

HealthcareLondon, United Kingdom
About: St Thomas' Hospital is a healthcare organization based out in London, United Kingdom. It is known for research contribution in the topics: Population & Pregnancy. The organization has 12105 authors who have published 15596 publications receiving 624309 citations. The organization is also known as: St Thomas's Hospital & St. Thomas's.


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Journal ArticleDOI
TL;DR: Results from analyses of opposite sex pairs showed evidence of sex-specific genetic effects suggesting there may be some differences between men and women in the genetic factors that influence variation in BMI, and encourage the continued search for genes of importance to the body composition and the development of obesity.
Abstract: Body mass index (BMI), a simple anthropometric measure, is the most frequently used measure of adiposity and has been instrumental in documenting the worldwide increase in the prevalence of obesity witnessed during the last decades. Although this increase in overweight and obesity is thought to be mainly due to environmental changes, i.e., sedentary lifestyles and high caloric diets, consistent evidence from twin studies demonstrates high heritability and the importance of genetic differences for normal variation in BMI. We analysed self-reported data on BMI from approximately 37,000 complete twin pairs (including opposite sex pairs) aged 20-29 and 30-39 from eight different twin registries participating in the GenomEUtwin project. Quantitative genetic analyses were conducted and sex differences were explored. Variation in BMI was greater for women than for men, and in both sexes was primarily explained by additive genetic variance in all countries. Sex differences in the variance components were consistently significant. Results from analyses of opposite sex pairs also showed evidence of sex-specific genetic effects suggesting there may be some differences between men and women in the genetic factors that influence variation in BMI. These results encourage the continued search for genes of importance to the body composition and the development of obesity. Furthermore, they suggest that strategies to identify predisposing genes may benefit from taking into account potential sex specific effects.

338 citations

Journal ArticleDOI
TL;DR: Belimumab treatment improved overall SLE disease activity in the most common musculoskeletal and mucocutaneous organ domains and less worsening occurred in the haematological, immunological and renal domains.
Abstract: Objective To evaluate the effects of belimumab versus placebo, plus standard systemic lupus erythematosus (SLE) therapy, on organ domain-specific SLE disease activity. Methods Data obtained after 52 weeks of treatment from two phase III trials (BLISS-52 and BLISS-76) comparing belimumab 1 and 10 mg/kg versus placebo, plus standard therapy, in 1684 autoantibody-positive patients were analysed post hoc for changes in British Isles Lupus Assessment Group (BILAG) and Safety of Estrogens in Lupus National Assessment–Systemic Lupus Erythematosus Disease Activity Index (SELENA–SLEDAI) organ domain scores. Results At baseline, the domains involved in the majority of patients were musculoskeletal and mucocutaneous by both BILAG and SELENA–SLEDAI, and immunological by SELENA–SLEDAI. At 52 weeks, significantly more patients treated with belimumab versus placebo had improvement in BILAG musculoskeletal and mucocutaneous domains (1 and 10 mg/kg), and in SELENA–SLEDAI mucocutaneous (10 mg/kg), musculoskeletal (1 mg/kg) and immunological (1 and 10 mg/kg) domains. Improvement was also observed in other organ systems with a low prevalence (≤16%) at baseline, including the SELENA–SLEDAI vasculitis and central nervous system domains. Significantly fewer patients treated with belimumab versus placebo had worsening in the BILAG haematological domain (1 mg/kg) and in the SELENA–SLEDAI immunological (10 mg/kg), haematological (10 mg/kg) and renal (1 mg/kg) domains. Conclusions Belimumab treatment improved overall SLE disease activity in the most common musculoskeletal and mucocutaneous organ domains. Less worsening occurred in the haematological, immunological and renal domains.

337 citations

Journal ArticleDOI
TL;DR: A guidelines group of the European Network for Hyperkinetic Disorders (EUNETHYDIS) has reviewed the literature, recruited renowned clinical subspecialists and consulted as a group to examine concerns about the safety of ADHD medications.
Abstract: The safety of ADHD medications is not fully known. Concerns have arisen about both a lack of contemporary-standard information about medications first licensed several decades ago, and signals of possible harm arising from more recently developed medications. These relate to both relatively minor adverse effects and extremely serious issues such as sudden cardiac death and suicidality. A guidelines group of the European Network for Hyperkinetic Disorders (EUNETHYDIS) has therefore reviewed the literature, recruited renowned clinical subspecialists and consulted as a group to examine these concerns. Some of the effects examined appeared to be minimal in impact or difficult to distinguish from risk to untreated populations. However, several areas require further study to allow a more precise understanding of these risks.

335 citations

Journal ArticleDOI
Nona Sotoodehnia1, Aaron Isaacs2, Paul I.W. de Bakker, Marcus Dörr, Christopher Newton-Cheh3, Christopher Newton-Cheh4, Ilja M. Nolte5, Pim van der Harst5, Martina Müller6, Mark Eijgelsheim2, Alvaro Alonso7, Andrew A. Hicks8, Sandosh Padmanabhan9, Caroline Hayward10, Albert V. Smith11, Ozren Polasek12, Steven Giovannone13, Jingyuan Fu5, Jared W. Magnani14, Jared W. Magnani4, Kristin D. Marciante1, Arne Pfeufer8, Arne Pfeufer15, Sina A. Gharib1, Alexander Teumer, Man Li16, Joshua C. Bis1, Fernando Rivadeneira2, Thor Aspelund11, Anna Köttgen16, Toby Johnson17, Kenneth Rice1, Mark P.S. Sie2, Ying A. Wang14, Ying A. Wang4, Norman Klopp, Christian Fuchsberger8, Sarah H. Wild18, Irene Mateo Leach5, Karol Estrada2, Uwe Völker, Alan F. Wright10, Folkert W. Asselbergs5, Folkert W. Asselbergs19, Jiaxiang Qu13, Aravinda Chakravarti20, Moritz F. Sinner6, Jan A. Kors2, Astrid Petersmann21, Tamara B. Harris4, Elsayed Z. Soliman22, Patricia B. Munroe17, Bruce M. Psaty, Ben A. Oostra2, L. Adrienne Cupples4, L. Adrienne Cupples14, Siegfried Perz, Rudolf A. de Boer5, André G. Uitterlinden2, Henry Völzke, Tim D. Spector23, Fangyu Liu13, Eric Boerwinkle24, Anna F. Dominiczak9, Jerome I. Rotter25, Gé van Herpen2, Daniel Levy4, H-Erich Wichmann6, Wiek H. van Gilst5, Jacqueline C.M. Witteman2, Heyo K. Kroemer, W. H. Linda Kao16, Susan R. Heckbert26, Susan R. Heckbert1, Thomas Meitinger15, Albert Hofman2, Harry Campbell18, Aaron R. Folsom7, Dirk J. van Veldhuisen5, Christine Schwienbacher27, Christine Schwienbacher8, Christopher J. O'Donnell4, Claudia B. Volpato8, Mark J. Caulfield17, John M. C. Connell28, Lenore J. Launer4, Xiaowen Lu5, Lude Franke17, Lude Franke5, Rudolf S N Fehrmann5, Gerard J. te Meerman5, Harry J.M. Groen5, Rinse K. Weersma5, Leonard H. van den Berg19, Cisca Wijmenga5, Roel A. Ophoff29, Roel A. Ophoff19, Gerjan Navis5, Igor Rudan18, Igor Rudan30, Harold Snieder5, Harold Snieder23, James F. Wilson18, Peter P. Pramstaller8, David S. Siscovick1, Thomas J. Wang4, Thomas J. Wang3, Vilmundur Gudnason11, Cornelia M. van Duijn2, Stephan B. Felix, Glenn I. Fishman13, Yalda Jamshidi31, Yalda Jamshidi23, Bruno H. Stricker, Nilesh J. Samani32, Nilesh J. Samani33, Stefan Kääb6, Dan E. Arking20 
TL;DR: It is demonstrated that SCN10A, a candidate gene at the most significantly associated locus in this study, is expressed in the mouse ventricular conduction system, and treatment with a selective SCN 10A blocker prolongs QRS duration.
Abstract: The QRS interval, from the beginning of the Q wave to the end of the S wave on an electrocardiogram, reflects ventricular depolarization and conduction time and is a risk factor for mortality, sudden death and heart failure. We performed a genome-wide association meta-analysis in 40,407 individuals of European descent from 14 studies, with further genotyping in 7,170 additional Europeans, and we identified 22 loci associated with QRS duration (P < 5 × 10(-8)). These loci map in or near genes in pathways with established roles in ventricular conduction such as sodium channels, transcription factors and calcium-handling proteins, but also point to previously unidentified biologic processes, such as kinase inhibitors and genes related to tumorigenesis. We demonstrate that SCN10A, a candidate gene at the most significantly associated locus in this study, is expressed in the mouse ventricular conduction system, and treatment with a selective SCN10A blocker prolongs QRS duration. These findings extend our current knowledge of ventricular depolarization and conduction.

335 citations

Journal ArticleDOI
18 Feb 2017-BMJ
TL;DR: It is confirmed that Rosamund Snow will not be attending this year's T in the Park.
Abstract: 这是一系列来自患者的零星文章中的最后一篇,他们的经历为医生提供了生动教程。关于"你的患者在想什么"系列的更多信息,请联系患者编辑Rosamund Snow (rsnow@bmj.com)。

335 citations


Authors

Showing all 12132 results

NameH-indexPapersCitations
David J. Hunter2131836207050
Rory Collins162489193407
Steven Williams144137586712
Geoffrey Burnstock141148899525
Nick C. Fox13974893036
Christopher D.M. Fletcher13867482484
David A. Jackson136109568352
Paul Harrison133140080539
Roberto Ferrari1331654103824
David Taylor131246993220
Keith Hawton12565755138
Nicole Soranzo12431674494
Roger Williams122145572416
John C. Chambers12264571028
Derek M. Yellon12263854319
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
20237
202235
2021654
2020595
2019485
2018462