Institution
University of Barcelona
Education•Barcelona, Spain•
About: University of Barcelona is a(n) education organization based out in Barcelona, Spain. It is known for research contribution in the topic(s): Population & Transplantation. The organization has 46197 authors who have published 108576 publication(s) receiving 3723377 citation(s). The organization is also known as: Universitat de Barcelona & UB.
Topics: Population, Transplantation, Bipolar disorder, Cirrhosis, European union
Papers published on a yearly basis
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University of Manchester1, University of Barcelona2, St George's Hospital3, University of Marburg4, University of Texas Health Science Center at San Antonio5, Imperial College London6, University of Modena and Reggio Emilia7, University of Michigan8, Hokkaido University9, University of British Columbia10
TL;DR: It is recommended that spirometry is required for the clinical diagnosis of COPD to avoid misdiagnosis and to ensure proper evaluation of severity of airflow limitation.
Abstract: Chronic obstructive pulmonary disease (COPD) remains a major public health problem. It is the fourth leading cause of chronic morbidity and mortality in the United States, and is projected to rank fifth in 2020 in burden of disease worldwide, according to a study published by the World Bank/World Health Organization. Yet, COPD remains relatively unknown or ignored by the public as well as public health and government officials. In 1998, in an effort to bring more attention to COPD, its management, and its prevention, a committed group of scientists encouraged the U.S. National Heart, Lung, and Blood Institute and the World Health Organization to form the Global Initiative for Chronic Obstructive Lung Disease (GOLD). Among the important objectives of GOLD are to increase awareness of COPD and to help the millions of people who suffer from this disease and die prematurely of it or its complications. The first step in the GOLD program was to prepare a consensus report, Global Strategy for the Diagnosis, Management, and Prevention of COPD, published in 2001. The present, newly revised document follows the same format as the original consensus report, but has been updated to reflect the many publications on COPD that have appeared. GOLD national leaders, a network of international experts, have initiated investigations of the causes and prevalence of COPD in their countries, and developed innovative approaches for the dissemination and implementation of COPD management guidelines. We appreciate the enormous amount of work the GOLD national leaders have done on behalf of their patients with COPD. Despite the achievements in the 5 years since the GOLD report was originally published, considerable additional work is ahead of us if we are to control this major public health problem. The GOLD initiative will continue to bring COPD to the attention of governments, public health officials, health care workers, and the general public, but a concerted effort by all involved in health care will be necessary.
16,210 citations
University of California, Berkeley1, Lawrence Berkeley National Laboratory2, Instituto Superior Técnico3, Pierre-and-Marie-Curie University4, Stockholm University5, European Southern Observatory6, Collège de France7, University of Cambridge8, University of Barcelona9, Yale University10, Space Telescope Science Institute11, European Space Agency12, University of New South Wales13
Abstract: We report measurements of the mass density, Omega_M, and
cosmological-constant energy density, Omega_Lambda, of the universe based on
the analysis of 42 Type Ia supernovae discovered by the Supernova Cosmology
Project. The magnitude-redshift data for these SNe, at redshifts between 0.18
and 0.83, are fit jointly with a set of SNe from the Calan/Tololo Supernova
Survey, at redshifts below 0.1, to yield values for the cosmological
parameters. All SN peak magnitudes are standardized using a SN Ia lightcurve
width-luminosity relation. The measurement yields a joint probability
distribution of the cosmological parameters that is approximated by the
relation 0.8 Omega_M - 0.6 Omega_Lambda ~= -0.2 +/- 0.1 in the region of
interest (Omega_M <~ 1.5). For a flat (Omega_M + Omega_Lambda = 1) cosmology we
find Omega_M = 0.28{+0.09,-0.08} (1 sigma statistical) {+0.05,-0.04}
(identified systematics). The data are strongly inconsistent with a Lambda = 0
flat cosmology, the simplest inflationary universe model. An open, Lambda = 0
cosmology also does not fit the data well: the data indicate that the
cosmological constant is non-zero and positive, with a confidence of P(Lambda >
0) = 99%, including the identified systematic uncertainties. The best-fit age
of the universe relative to the Hubble time is t_0 = 14.9{+1.4,-1.1} (0.63/h)
Gyr for a flat cosmology. The size of our sample allows us to perform a variety
of statistical tests to check for possible systematic errors and biases. We
find no significant differences in either the host reddening distribution or
Malmquist bias between the low-redshift Calan/Tololo sample and our
high-redshift sample. The conclusions are robust whether or not a
width-luminosity relation is used to standardize the SN peak magnitudes.
15,392 citations
[...]
TL;DR: Version 5 implements a number of new features and analytical methods allowing extensive DNA polymorphism analyses on large datasets, including visualizing sliding window results integrated with available genome annotations in the UCSC browser.
Abstract: Motivation: DnaSP is a software package for a comprehensive analysis of DNA polymorphism data. Version 5 implements a number of new features and analytical methods allowing extensive DNA polymorphism analyses on large datasets. Among other features, the newly implemented methods allow for: (i) analyses on multiple data files; (ii) haplotype phasing; (iii) analyses on insertion/deletion polymorphism data; (iv) visualizing sliding window results integrated with available genome annotations in the UCSC browser.
Availability: Freely available to academic users from: http://www.ub.edu/dnasp
Contact: [email protected]
12,188 citations
TL;DR: The 1000 Genomes Project set out to provide a comprehensive description of common human genetic variation by applying whole-genome sequencing to a diverse set of individuals from multiple populations, and has reconstructed the genomes of 2,504 individuals from 26 populations using a combination of low-coverage whole-generation sequencing, deep exome sequencing, and dense microarray genotyping.
Abstract: The 1000 Genomes Project set out to provide a comprehensive description of common human genetic variation by applying whole-genome sequencing to a diverse set of individuals from multiple populations. Here we report completion of the project, having reconstructed the genomes of 2,504 individuals from 26 populations using a combination of low-coverage whole-genome sequencing, deep exome sequencing, and dense microarray genotyping. We characterized a broad spectrum of genetic variation, in total over 88 million variants (84.7 million single nucleotide polymorphisms (SNPs), 3.6 million short insertions/deletions (indels), and 60,000 structural variants), all phased onto high-quality haplotypes. This resource includes >99% of SNP variants with a frequency of >1% for a variety of ancestries. We describe the distribution of genetic variation across the global sample, and discuss the implications for common disease studies.
9,821 citations
Theo Vos1, Amanuel Alemu Abajobir, Kalkidan Hassen Abate2, Cristiana Abbafati3 +775 more•Institutions (305)
Abstract: Summary Background As mortality rates decline, life expectancy increases, and populations age, non-fatal outcomes of diseases and injuries are becoming a larger component of the global burden of disease. The Global Burden of Diseases, Injuries, and Risk Factors Study 2016 (GBD 2016) provides a comprehensive assessment of prevalence, incidence, and years lived with disability (YLDs) for 328 causes in 195 countries and territories from 1990 to 2016. Methods We estimated prevalence and incidence for 328 diseases and injuries and 2982 sequelae, their non-fatal consequences. We used DisMod-MR 2.1, a Bayesian meta-regression tool, as the main method of estimation, ensuring consistency between incidence, prevalence, remission, and cause of death rates for each condition. For some causes, we used alternative modelling strategies if incidence or prevalence needed to be derived from other data. YLDs were estimated as the product of prevalence and a disability weight for all mutually exclusive sequelae, corrected for comorbidity and aggregated to cause level. We updated the Socio-demographic Index (SDI), a summary indicator of income per capita, years of schooling, and total fertility rate. GBD 2016 complies with the Guidelines for Accurate and Transparent Health Estimates Reporting (GATHER). Findings Globally, low back pain, migraine, age-related and other hearing loss, iron-deficiency anaemia, and major depressive disorder were the five leading causes of YLDs in 2016, contributing 57·6 million (95% uncertainty interval [UI] 40·8–75·9 million [7·2%, 6·0–8·3]), 45·1 million (29·0–62·8 million [5·6%, 4·0–7·2]), 36·3 million (25·3–50·9 million [4·5%, 3·8–5·3]), 34·7 million (23·0–49·6 million [4·3%, 3·5–5·2]), and 34·1 million (23·5–46·0 million [4·2%, 3·2–5·3]) of total YLDs, respectively. Age-standardised rates of YLDs for all causes combined decreased between 1990 and 2016 by 2·7% (95% UI 2·3–3·1). Despite mostly stagnant age-standardised rates, the absolute number of YLDs from non-communicable diseases has been growing rapidly across all SDI quintiles, partly because of population growth, but also the ageing of populations. The largest absolute increases in total numbers of YLDs globally were between the ages of 40 and 69 years. Age-standardised YLD rates for all conditions combined were 10·4% (95% UI 9·0–11·8) higher in women than in men. Iron-deficiency anaemia, migraine, Alzheimer's disease and other dementias, major depressive disorder, anxiety, and all musculoskeletal disorders apart from gout were the main conditions contributing to higher YLD rates in women. Men had higher age-standardised rates of substance use disorders, diabetes, cardiovascular diseases, cancers, and all injuries apart from sexual violence. Globally, we noted much less geographical variation in disability than has been documented for premature mortality. In 2016, there was a less than two times difference in age-standardised YLD rates for all causes between the location with the lowest rate (China, 9201 YLDs per 100 000, 95% UI 6862–11943) and highest rate (Yemen, 14 774 YLDs per 100 000, 11 018–19 228). Interpretation The decrease in death rates since 1990 for most causes has not been matched by a similar decline in age-standardised YLD rates. For many large causes, YLD rates have either been stagnant or have increased for some causes, such as diabetes. As populations are ageing, and the prevalence of disabling disease generally increases steeply with age, health systems will face increasing demand for services that are generally costlier than the interventions that have led to declines in mortality in childhood or for the major causes of mortality in adults. Up-to-date information about the trends of disease and how this varies between countries is essential to plan for an adequate health-system response. Funding Bill & Melinda Gates Foundation, and the National Institute on Aging and the National Institute of Mental Health of the National Institutes of Health.
8,768 citations
Authors
Showing all 46197 results
Name | H-index | Papers | Citations |
---|---|---|---|
Joan Massagué | 189 | 408 | 149951 |
Michael Snyder | 169 | 840 | 130225 |
Michael R. Stratton | 161 | 443 | 142586 |
Johan Auwerx | 158 | 653 | 95779 |
Bart Staels | 152 | 824 | 86638 |
David D'Enterria | 150 | 1592 | 116210 |
Thomas E. Starzl | 150 | 1625 | 91704 |
Manel Esteller | 146 | 713 | 96429 |
Peter B. Jones | 145 | 1857 | 94641 |
Carlos Cordon-Cardo | 144 | 589 | 84862 |
Kjell Fuxe | 142 | 1479 | 89846 |
Kenneth M. Yamada | 139 | 446 | 72136 |
John G.F. Cleland | 137 | 1172 | 110227 |
António Amorim | 136 | 1477 | 96519 |
Elias Campo | 135 | 761 | 85160 |