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Institution

Pompeu Fabra University

EducationBarcelona, Spain
About: Pompeu Fabra University is a education organization based out in Barcelona, Spain. It is known for research contribution in the topics: Population & Gene. The organization has 8093 authors who have published 23570 publications receiving 858431 citations. The organization is also known as: Universitat Pompeu Fabra & UPF.


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Journal ArticleDOI
TL;DR: Lower job experience and knowledge of workplace hazards, measured by length of employment, is a possible mechanism to explain the consistent association between temporary workers and occupational injury.
Abstract: Objective: To determine whether observed higher risks of occupational injury among temporary workers are due to exposure to hazardous working conditions and/or to lack of job experience level. Methods: Data systematically recorded for 2000 and 2001 by the Spanish Ministry of Labour and Social Affairs on fatal and non-fatal traumatic occupational injuries were examined by type of employment and type of accident, while adjusting for gender, age, occupation, and length of employment in the company. In the study period there were 1500 fatal and 1 806 532 non-fatal traumatic occupational injuries that occurred at the workplace. Incidence rates and rate ratios (RR) were estimated using Poisson regression models. Results: Temporary workers showed a rate ratio of 2.94 for non-fatal occupational injuries (95% CI 2.40 to 3.61) and 2.54 for fatal occupational injuries (95% CI 1.88 to 3.42). When these associations were adjusted by gender, age, occupation, and especially length of employment, they loose statistic significance: 1.05 (95% CI 0.97 to 1.12) for non-fatal and 1.07 (95% CI 0.91 to 1.26) for fatal. Conclusions: Lower job experience and knowledge of workplace hazards, measured by length of employment, is a possible mechanism to explain the consistent association between temporary workers and occupational injury. The role of working conditions associated with temporary jobs should be assessed more specifically.

227 citations

Journal ArticleDOI
TL;DR: Inequalities in the use of cancer screening according to SEP are higher in countries without population-based cancer screening programmes and these results highlight the potential benefits of population- based screening programmes.
Abstract: Background The aim of this study was to describe inequalities in the use of breast and cervical cancer screening services according to educational level in European countries in 2002, and to determine the influence of the type of screening program on the extent of inequality. Methods A cross-sectional study was performed using individual-level data from the WHO World Health Survey (2002) and data regarding the implementation of cancer screening programmes. The study population consisted of women from 22 European countries, aged 25-69 years for cervical cancer screening (n =11 770) and 50-69 years for breast cancer screening (n = 4784). Dependent variables were having had a PAP smear and having had a mammography during the previous 3 years. The main independent variables were socio-economic position (SEP) and the type of screening program in the country. For each country the prevalence of screening was calculated, overall and for each level of education, and indices of relative (RII) and absolute (SII) inequality were computed by educational level. Multilevel logistic regression models were fitted. Results SEP inequalities in screening were found in countries with opportunistic screening [comparing highest with lowest educational level: RII = 1.28, 95% confidence interval (CI) 1.12-1.48 for cervical cancer; and RII = 3.11, 95% CI 1.78-5.42 for breast cancer] but not in countries with nationwide population-based programmes. Inequalities were also observed in countries with regional screening programs (RII = 1.35, 95% CI 1.10-1.65 for cervical cancer; and RII = 1.58, 95% CI 1.26-1.98 for breast cancer). Conclusions Inequalities in the use of cancer screening according to SEP are higher in countries without population-based cancer screening programmes. These results highlight the potential benefits of population-based screening programmes.

226 citations

Journal ArticleDOI
TL;DR: The basis for their functional specificity and the mechanisms of action of some of their characteristic protein domains are discussed.
Abstract: Specificity is key to biological regulation. Two families of RNA binding proteins, heterogeneous nuclear ribonucleoproteins and serine-arginine-rich proteins, were initially thought to have redundant or nonspecific biochemical functions. Recently, members of these families have been found as components of distinct regulatory complexes with highly specific and essential roles in mRNA metabolism. Here we discuss the basis for their functional specificity and the mechanisms of action of some of their characteristic protein domains.

226 citations

Journal ArticleDOI
Mark P. Purdue1, Mattias Johansson, Diana Zelenika, Jorge R. Toro1, Ghislaine Scelo, Lee E. Moore1, Egor Prokhortchouk2, Xifeng Wu3, Lambertus A. Kiemeney4, Valerie Gaborieau, Kevin B. Jacobs1, Wong-Ho Chow1, David Zaridze, Vsevolod Matveev, Jan Lubinski, Joanna Trubicka, Neonila Szeszenia-Dabrowska5, Jolanta Lissowska, Peter Rudnai, Eleonora Fabianova, Alexandru Bucur, Vladimir Bencko6, Lenka Foretova7, Vladimir Janout8, Paolo Boffetta9, Joanne S. Colt1, Faith G. Davis10, Kendra Schwartz11, Rosamonde E. Banks12, Peter Selby12, Patricia Harnden, Christine D. Berg1, Ann W. Hsing1, Robert L. Grubb13, Heiner Boeing, Paolo Vineis14, Françoise Clavel-Chapelon15, Domenico Palli, Rosario Tumino, Vittorio Krogh, Salvatore Panico16, Eric J. Duell, José Ramón Quirós, María José Sánchez17, Carmen Navarro17, Eva Ardanaz17, M. Dorronsoro17, Kay-Tee Khaw18, Naomi E. Allen19, H. Bas Bueno-de-Mesquita, Petra H.M. Peeters20, Petra H.M. Peeters14, Dimitrios Trichopoulos21, Jakob Linseisen22, Börje Ljungberg23, Kim Overvad24, Anne Tjønneland, Isabelle Romieu, Elio Riboli14, Anush Mukeria, Oxana Shangina, Victoria L. Stevens24, Michael J. Thun, W. Ryan Diver24, Susan M. Gapstur, Paul D.P. Pharoah18, Douglas F. Easton18, Demetrius Albanes1, Stephanie J. Weinstein1, Jarmo Virtamo, Lars J. Vatten25, Kristian Hveem25, Inger Njølstad26, Grethe S. Tell27, Camilla Stoltenberg, Rajesh Kumar22, Kvetoslava Koppova, Olivier Cussenot28, Simone Benhamou29, Simone Benhamou15, Egbert Oosterwijk4, Sita H. Vermeulen4, Katja K.H. Aben4, Saskia S. L. van der Marel4, Yuanqing Ye3, Christopher G. Wood3, Xia Pu3, Alexander M. Mazur2, Eugenia S. Boulygina, Nikolai N. Chekanov2, Mario Foglio, Doris Lechner, Ivo Gut, Simon Heath, Hélène Blanché30, Amy Hutchinson1, Gilles Thomas1, Zhaoming Wang1, Meredith Yeager1, Joseph F. Fraumeni1, Konstantin G. Skryabin2, James McKay, Nathaniel Rothman1, Stephen J. Chanock1, Mark Lathrop, Paul Brennan 
TL;DR: A two-stage genome-wide association study of renal cell carcinoma in 3,772 affected individuals and 8,505 controls of European background and followed up 6 SNPs in 3 replication studies reports previously unidentified genomic regions associated with RCC risk that may lead to new etiological insights.
Abstract: We conducted a two-stage genome-wide association study of renal cell carcinoma (RCC) in 3,772 affected individuals (cases) and 8,505 controls of European background from 11 studies and followed up 6 SNPs in 3 replication studies of 2,198 cases and 4,918 controls. Two loci on the regions of 2p21 and 11q13.3 were associated with RCC susceptibility below genome-wide significance. Two correlated variants (r² = 0.99 in controls), rs11894252 (P = 1.8 × 10⁻⁸) and rs7579899 (P = 2.3 × 10⁻⁹), map to EPAS1 on 2p21, which encodes hypoxia-inducible-factor-2 alpha, a transcription factor previously implicated in RCC. The second locus, rs7105934, at 11q13.3, contains no characterized genes (P = 7.8 × 10⁻¹⁴). In addition, we observed a promising association on 12q24.31 for rs4765623, which maps to SCARB1, the scavenger receptor class B, member 1 gene (P = 2.6 × 10⁻⁸). Our study reports previously unidentified genomic regions associated with RCC risk that may lead to new etiological insights.

225 citations

Journal ArticleDOI
TL;DR: The Met66 variant is strongly associated to all ED subtypes, and the -270C BDNF variant has an effect on BN and late age at onset of weight loss, the first two variants associated with the pathophysiology of ED in different populations and support a role for BDNF in the susceptibility to aberrant eating behaviors.
Abstract: Several genes with an essential role in the regulation of eating behavior and body weight are considered candidates involved in the etiology of eating disorders (ED), but no relevant susceptibility genes with a major effect on anorexia nervosa (AN) or bulimia nervosa (BN) have been identified. Brain-derived neurotrophic factor (BDNF) has been implicated in the regulation of food intake and body weight in rodents. We previously reported a strong association of the Met66 allele of the Val66Met BDNF variant with restricting AN (ANR) and low minimum body mass index in Spanish patients. Another single nucleotide polymorphism located in the promoter region of the BDNF gene (-270C > T) showed lack of association with any ED phenotype. In order to replicate these findings in a larger sample, we performed a case-control study in 1142 Caucasian patients with ED consecutively recruited in six different centers from five European countries (France, Germany, Italy, Spain and UK) participating in the 'Factors in Healthy Eating' project. We have found that the Met66 variant is strongly associated to all ED subtypes (AN, ANR, binge-eating/purging AN and BN), and that the -270C BDNF variant has an effect on BN and late age at onset of weight loss. These are the first two variants associated with the pathophysiology of ED in different populations and support a role for BDNF in the susceptibility to aberrant eating behaviors.

225 citations


Authors

Showing all 8248 results

NameH-indexPapersCitations
Andrei Shleifer171514271880
Paul Elliott153773103839
Bert Brunekreef12480681938
Philippe Aghion12250773438
Anjana Rao11833761395
Jordi Sunyer11579857211
Kenneth J. Arrow113411111221
Xavier Estivill11067359568
Roderic Guigó108304106914
Mark J. Nieuwenhuijsen10764749080
Jordi Alonso10752364058
Alfonso Valencia10654255192
Luis Serrano10545242515
Vadim N. Gladyshev10249034148
Josep M. Antó10049338663
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
202349
2022248
20211,903
20201,930
20191,763
20181,660