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University of Zagreb

EducationZagreb, Grad Zagreb, Croatia
About: University of Zagreb is a education organization based out in Zagreb, Grad Zagreb, Croatia. It is known for research contribution in the topics: Population & European union. The organization has 21769 authors who have published 50267 publications receiving 783239 citations. The organization is also known as: Zagreb University & Sveučilište u Zagrebu.


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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. Magnani3, 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. Wang3, 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. Harris3, Elsayed Z. Soliman22, Patricia B. Munroe17, Bruce M. Psaty, Ben A. Oostra2, L. Adrienne Cupples14, L. Adrienne Cupples3, 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 Levy3, H-Erich Wichmann6, Wiek H. van Gilst5, Jacqueline C.M. Witteman2, Heyo K. Kroemer, W. H. Linda Kao16, Susan R. Heckbert1, Susan R. Heckbert26, Thomas Meitinger15, Albert Hofman2, Harry Campbell18, Aaron R. Folsom7, Dirk J. van Veldhuisen5, Christine Schwienbacher27, Christine Schwienbacher8, Christopher J. O'Donnell3, Claudia B. Volpato8, Mark J. Caulfield17, John M. C. Connell28, Lenore J. Launer3, 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 Rudan30, Igor Rudan18, Harold Snieder23, Harold Snieder5, James F. Wilson18, Peter P. Pramstaller8, David S. Siscovick1, Thomas J. Wang3, Thomas J. Wang4, 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
Gary Davies1, Nicola J. Armstrong2, J. C. Bis3, Jan Bressler4  +148 moreInstitutions (51)
TL;DR: In hypothesis-driven tests, there was significant association between general cognitive function and four genes previously associated with Alzheimer’s disease: TOMM40, APOE, ABCG1 and MEF2C.
Abstract: General cognitive function is substantially heritable across the human life course from adolescence to old age. We investigated the genetic contribution to variation in this important, health- and well-being-related trait in middle-aged and older adults. We conducted a meta-analysis of genome-wide association studies of 31 cohorts (N=53,949) in which the participants had undertaken multiple, diverse cognitive tests. A general cognitive function phenotype was tested for, and created in each cohort by principal component analysis. We report 13 genome-wide significant single-nucleotide polymorphism (SNP) associations in three genomic regions, 6q16.1, 14q12 and 19q13.32 (best SNP and closest gene, respectively: rs10457441, P=3.93 × 10(-9), MIR2113; rs17522122, P=2.55 × 10(-8), AKAP6; rs10119, P=5.67 × 10(-9), APOE/TOMM40). We report one gene-based significant association with the HMGN1 gene located on chromosome 21 (P=1 × 10(-6)). These genes have previously been associated with neuropsychiatric phenotypes. Meta-analysis results are consistent with a polygenic model of inheritance. To estimate SNP-based heritability, the genome-wide complex trait analysis procedure was applied to two large cohorts, the Atherosclerosis Risk in Communities Study (N=6617) and the Health and Retirement Study (N=5976). The proportion of phenotypic variation accounted for by all genotyped common SNPs was 29% (s.e.=5%) and 28% (s.e.=7%), respectively. Using polygenic prediction analysis, ~1.2% of the variance in general cognitive function was predicted in the Generation Scotland cohort (N=5487; P=1.5 × 10(-17)). In hypothesis-driven tests, there was significant association between general cognitive function and four genes previously associated with Alzheimer's disease: TOMM40, APOE, ABCG1 and MEF2C.

335 citations

Journal ArticleDOI
TL;DR: Surfactants in the Environment Surfactants are a diverse group of chemicals that are best known for their wide use in detergents and other cleaning products and most of them end up dispersed in different environmental compartments such as soil, water or sediment.
Abstract: Surfactants are a diverse group of chemicals that are best known for their wide use in detergents and other cleaning products. After use, residual surfactants are discharged into sewage systems or directly into surface waters, and most of them end up dispersed in different environmental compartments such as soil, water or sediment. The toxic effects of surfactants on various aquatic organisms are well known. In general, surfactants are present in the environment at levels below toxicity and in Croatia below the national limit. Most surfactants are readily biodegradable and their amount is greatly reduced with secondary treatment in wastewater treatment plants. The highest concern is the release of untreated wastewater or wastewater that has undergone primary treatment alone. The discharge of wastewater polluted with massive quantities of surfactants could have serious effects on the ecosystem. Future studies of surfactant toxicities and biodegradation are necessary to withdraw highly toxic and non-biodegradable compounds from commercial use and replace them with more environmentally friendly ones.

334 citations

Journal ArticleDOI
TL;DR: These guidelines provide clinically useful points to guide the management of UC in children and offer a standardized protocol that allows effective, timely management and monitoring of the disease course, while acknowledging that each patient is unique.
Abstract: Background and Aims: Pediatric ulcerative colitis (UC) shares many features with adult-onset disease but there are some unique considerations; therefore, therapeutic approaches have to be adapted to these particular needs. We aimed to formulate guidelines for managing UC in children based on a systematic review (SR) of the literature and a robust consensus process. The present article is a product of a joint effort of the European Crohn’s and Colitis Organization (ECCO) and the European Society for Paediatric Gastroenterology, Hepatology, and Nutrition (ESPGHAN). Methods: A group of 27 experts in pediatric IBD participated in an iterative consensus process including 2 face-to-face meetings, following an open call to ESPGHAN and ECCO members. A list of 23 predefined questions were addressed by working subgroups based on a SR of the literature. Results: A total of 40 formal recommendations and 68 practice points were endorsed with a consensus rate of at least 89% regarding initial evaluation, how to monitor disease activity, the role of endoscopic evaluation, medical and surgical therapy, timing and choice of each medication, the role of combined therapy, and when to stop medications. A management flowchart, based on the Pediatric Ulcerative Colitis Activity Index (PUCAI), is presented.

334 citations

Journal ArticleDOI
Jérôme Avouac1, Jaap Fransen2, Ulrich A. Walker3, Valeria Riccieri4, Vanessa Smith5, Carolina de Souza Müller6, I. Miniati7, Ingo H. Tarner8, S. Bellando Randone6, Maurizio Cutolo9, Yannick Allanore1, Oliver Distler10, Gabriele Valentini11, L. Czirják12, Ulf Müller-Ladner8, Daniel E. Furst13, A Tyndall3, Marco Matucci-Cerinic7, F De Keyser5, Alberto Sulli9, Carmen Pizzorni9, Britta Maurer10, Stanislaw Sierakowsky14, Otylia Kowal-Bielecka14, P. Coelho, G. Riemekasten15, Simona Rednic16, Ileana Nicoara16, Roberto Caporali, Jiri Stork17, Murat Inanc18, Patricia Carreira19, Srdan Novak, Cecília Varjú12, Carlo Chizzolini20, Camillo Ribi20, Eugeniusz J. Kucharz21, AT Kotulska21, Małgorzata Widuchowska21, Jutta G Richter22, A. Sipek-Dolnicar23, Blaž Rozman23, Armando Gabrielli24, Gianluca Moroncini24, Dominique Farge1, C. Durant1, Hans P. Kiener25, E. Rath25, Paolo Airò, Frank A. Wollheim26, Nicolas Hunzelmann27, Stefano Bombardieri28, A. Della Rossa28, Laura Bazzichi28, Raffaele Pellerito, M. Saracco, Christopher P. Denton29, Madelon C. Vonk, F.H.J. van den Hoogen, Nemanja Damjanov, Ina Kötter30, Stefan Heitmann, Matthias Seidel, Paul Hasler, J.M. van Laar31, Maria João Salvador32, J.A. Pereira da Silva32, Søren Jacobsen33, Margitta Worm15, Annegret Kuhn34, Tatiana Nevskaya35, Evgeny Nasonov35, Raffaella Scorza, Henrik Nielsen, Richard M. Silver, Eric Hachulla, D. Launay, Guido Valesini4, Ruxandra Ionescu36, Daniela Opris36, N. Del Papa, Wanda Maglione, D. Comina, G. Udrea, Coziana Ciurtin, R. Ionitescu, C. Mihai, Cord Sunderkötter34, Jae Bum Jun37, Chris T. Derk38, S. Alhasani, L. Alhajjar, Evelien Ton39, James R. Seibold40, Peter Nash, Luc Mouthon1, C. A. Von Mühlen, Brigitte Krummel-Lorenz, P. Eilbacher, Rene Westhovens41, E. De Langhe41, Miroslav Mayer42, Branimir Anić42, M. Baresic42, F. Stoeckl43, Maria Uprus, S. Popa, M. Buslau, B. Granel, Thierry Zenone, Alessandro Mathieu44, Alessandra Vacca44, Paolo Amerio, T. Tourinho, L. Lonzetti, M. Lemos Lopes, R. E. de Souza45, D. Vealex46, Paola Caramaschi47, Alexandra Balbir-Gurman, Y. Braun, Susanne Ullman33, Magdalena Szmyrka-Kaczmarek48, Ewa Morgiel48, Marie Vanthuyne49, M. Meurer50, P. Rehberger50, Percival D. Sampaio-Barros45 
TL;DR: A core set of preliminary items considered as important for the very early diagnosis of systemic sclerosis were identified in a Delphi exercise among 110 experts in the field of SSc.
Abstract: Objective: To identify a core set of preliminary items considered as important for the very early diagnosis of systemic sclerosis (SSc). Methods: A list of items provided by European League Against Rheumatism (EULAR) Scleroderma Trial and Research(EUSTAR) centres were subjected to a Delphi exercise among 110 experts in the field of SSc. In round 1, experts were asked to choose the items they considered as the most important for the very early diagnosis of SSc. In round 2, experts were asked to reconsider the items accepted after the first stage. In round 3, the clinical relevance of selected items and their importance as measures that would lead to an early referral process were rated using appropriateness scores. Results: Physicians from 85 EUSTAR centres participated in the study and provided an initial list of 121 items. After three Delphi rounds, the steering committee, with input from external experts, collapsed the 121 items into three domains containing seven items, developed as follows: skin domain (puffy fingers/puffy swollen digits turning into sclerodactily);vascular domain (Raynaud's phenomenon, abnormal capillaroscopy with scleroderma pattern) and laboratory domain (antinuclear, anticentromere and antitopoisomerase-I antibodies). Finally, the whole assembly of EUSTAR centres ratified with a majority vote the results in a final face-to-face meeting. Conclusion: The three Delphi rounds allowed us to identify the items considered by experts as necessary for the very early diagnosis of SSc. The validation of these items to establish diagnostic criteria is currently ongoing in a prospective observational cohort.

334 citations


Authors

Showing all 22096 results

NameH-indexPapersCitations
Harry Campbell150897115457
Joseph R. Ecker14838194860
Igor Rudan142658103659
Nikola Godinovic1381469100018
Ivica Puljak134143697548
Damir Lelas133135493354
Željko Ivezić12934484365
Piotr Ponikowski120762131682
Marin Soljacic11776451444
Ivan Dikic10735952088
Ozren Polasek10243652674
Mordechai Segev9972940073
Srdan Verstovsek96104538936
Segev BenZvi9548232127
Mirko Planinic9446731957
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
2023119
2022525
20213,277
20203,360
20193,176
20183,042