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Institution

University of Amsterdam

EducationAmsterdam, Noord-Holland, Netherlands
About: University of Amsterdam is a education organization based out in Amsterdam, Noord-Holland, Netherlands. It is known for research contribution in the topics: Population & Randomized controlled trial. The organization has 59309 authors who have published 140894 publications receiving 5984137 citations. The organization is also known as: UvA & Universiteit van Amsterdam.


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Journal ArticleDOI
TL;DR: A mathematical expression is derived to compute PrediXcan results using summary data, and the effects of gene expression variation on human phenotypes in 44 GTEx tissues and >100 phenotypes are investigated.
Abstract: Scalable, integrative methods to understand mechanisms that link genetic variants with phenotypes are needed. Here we derive a mathematical expression to compute PrediXcan (a gene mapping approach) results using summary data (S-PrediXcan) and show its accuracy and general robustness to misspecified reference sets. We apply this framework to 44 GTEx tissues and 100+ phenotypes from GWAS and meta-analysis studies, creating a growing public catalog of associations that seeks to capture the effects of gene expression variation on human phenotypes. Replication in an independent cohort is shown. Most of the associations are tissue specific, suggesting context specificity of the trait etiology. Colocalized significant associations in unexpected tissues underscore the need for an agnostic scanning of multiple contexts to improve our ability to detect causal regulatory mechanisms. Monogenic disease genes are enriched among significant associations for related traits, suggesting that smaller alterations of these genes may cause a spectrum of milder phenotypes.

657 citations

Journal ArticleDOI
TL;DR: There is no significant overall survival benefit for either approach, however, compared with limited transhiatal resection extended transthoracic esophagectomy for type I esophageal adenocarcinoma shows an ongoing trend towards better 5-year survival.
Abstract: Objective: To determine whether extended transthoracic esophagectomy for adenocarcinoma of the mid/distal esophagus improves long-term survival. Background: A randomized trial was performed to compare surgical techniques. Complete 5-year survival data are now available. Methods: A total of 220 patients with adenocarcinoma of the distal esophagus (type I) or gastric cardia involving the distal esophagus (type II) were randomly assigned to limited transhiatal esophagectomy or to extended transthoracic esophagectomy with en bloc lymphadenectomy. Patients with peroperatively irresectable/incurable cancer were excluded from this analysis (n = 15). A total of 95 patients underwent transhiatal esophagectomy and 110 patients underwent transthoracic esophagectomy. Results: After transhiatal and transthoracic resection, 5-year survival was 34% and 36%, respectively (P = 0.71, per protocol analysis). In a subgroup analysis, based on the location of the primary tumor according to the resection specimen, no overall survival benefit for either surgical approach was seen in 115 patients with a type II tumor (P = 0.81). In 90 patients with a type I tumor, a survival benefit of 14% was seen with the transthoracic approach (51% vs. 37%, P = 0.33). There was evidence that the treatment effect differed depending on the number of positive lymph nodes in the resection specimen (test for interaction P = 0.06). In patients (n = 55) without positive nodes locoregional disease-free survival after transhiatal esophagectomy was comparable to that after transthoracic esophagectomy (86% and 89%, respectively). The same was true for patients (n = 46) with more than 8 positive nodes (0% in both groups). Patients (n = 104) with 1 to 8 positive lymph nodes in the resection specimen showed a 5-year locoregional disease-free survival advantage if operated via the transthoracic route (23% vs. 64%, P = 0.02). Conclusion: There is no significant overall survival benefit for either approach. However, compared with limited transhiatal resection extended transthoracic esophagectomy for type I esophageal adenocarcinoma shows an ongoing trend towards better 5-year survival. Moreover, patients with a limited number of positive lymph nodes in the resection specimen seem to benefit from an extended transthoracic esophagectomy.

657 citations

Journal ArticleDOI
David T.W. Jones1, Barbara Hutter1, Natalie Jäger1, Andrey Korshunov2, Andrey Korshunov1, Marcel Kool1, Hans-Jörg Warnatz3, Thomas Zichner, Sally R. Lambert4, Marina Ryzhova5, Dong Anh Khuong Quang6, Adam M. Fontebasso6, Adrian M. Stütz, Sonja Hutter1, Marc Zuckermann1, Dominik Sturm1, Jan Gronych1, Bärbel Lasitschka1, Sabine Schmidt1, Huriye Seker-Cin1, Hendrik Witt2, Hendrik Witt1, Marc Sultan3, Meryem Ralser3, Paul A. Northcott1, Volker Hovestadt1, Sebastian Bender1, Elke Pfaff1, Sebastian Stark1, Damien Faury6, Jeremy Schwartzentruber6, Jacek Majewski6, Ursula D. Weber1, Marc Zapatka1, Benjamin Raeder, Matthias Schlesner1, Catherine L. Worth3, Cynthia C. Bartholomae1, Christof von Kalle1, Charles D. Imbusch1, S. Radomski2, S. Radomski1, Chris Lawerenz1, Peter van Sluis7, Jan Koster7, Richard Volckmann7, Rogier Versteeg7, Hans Lehrach3, Camelia M. Monoranu8, Beate Winkler8, Andreas Unterberg2, Christel Herold-Mende9, Till Milde2, Till Milde1, Andreas E. Kulozik2, Martin Ebinger10, Martin U. Schuhmann10, Yoon Jae Cho11, Scott L. Pomeroy12, Scott L. Pomeroy13, Andreas von Deimling1, Andreas von Deimling2, Olaf Witt2, Olaf Witt1, Michael D. Taylor14, Stephan Wolf1, Matthias A. Karajannis15, Charles G. Eberhart16, Wolfram Scheurlen17, Martin Hasselblatt18, Keith L. Ligon13, Mark W. Kieran13, Jan O. Korbel, Marie-Laure Yaspo3, Benedikt Brors1, Jörg Felsberg19, Guido Reifenberger19, V. Peter Collins4, Nada Jabado20, Nada Jabado6, Roland Eils1, Roland Eils2, Peter Lichter1 
TL;DR: Recurrent activating mutations in FGFR1 and PTPN11 and new NTRK2 fusion genes in non-cerebellar tumors and new BRAF-activating changes were observed, indicating that pilocytic astrocytoma is predominantly a single-pathway disease.
Abstract: Pilocytic astrocytoma, the most common childhood brain tumor, is typically associated with mitogen-activated protein kinase (MAPK) pathway alterations. Surgically inaccessible midline tumors are therapeutically challenging, showing sustained tendency for progression and often becoming a chronic disease with substantial morbidities. Here we describe whole-genome sequencing of 96 pilocytic astrocytomas, with matched RNA sequencing (n = 73), conducted by the International Cancer Genome Consortium (ICGC) PedBrain Tumor Project. We identified recurrent activating mutations in FGFR1 and PTPN11 and new NTRK2 fusion genes in non-cerebellar tumors. New BRAF-activating changes were also observed. MAPK pathway alterations affected all tumors analyzed, with no other significant mutations identified, indicating that pilocytic astrocytoma is predominantly a single-pathway disease. Notably, we identified the same FGFR1 mutations in a subset of H3F3A-mutated pediatric glioblastoma with additional alterations in the NF1 gene. Our findings thus identify new potential therapeutic targets in distinct subsets of pilocytic astrocytoma and childhood glioblastoma.

657 citations

Journal ArticleDOI
28 Mar 2012-JAMA
TL;DR: Among statin-treated patients, on-treatment levels of LDL-C, non-HDL-C and apoB were each associated with risk of future major cardiovascular events, but the strength of this association was greater for non- HDL-C than for LDL-B and apolipoproteins.
Abstract: Context The associations of low-density lipoprotein cholesterol (LDL-C), non–high-density lipoprotein cholesterol (non–HDL-C), and apolipoprotein B (apoB) levels with the risk of cardiovascular events among patients treated with statin therapy have not been reliably documented. Objective To evaluate the relative strength of the associations of LDL-C, non–HDL-C, and apoB with cardiovascular risk among patients treated with statin therapy. Design Meta-analysis of individual patient data from randomized controlled statin trials in which conventional lipids and apolipoproteins were determined in all study participants at baseline and at 1-year follow-up. Data Sources Relevant trials were identified by a literature search updated through December 31, 2011. Investigators were contacted and individual patient data were requested and obtained for 62 154 patients enrolled in 8 trials published between 1994 and 2008. Data Extraction Hazard ratios (HRs) and corresponding 95% CIs for risk of major cardiovascular events adjusted for established risk factors by 1-SD increase in LDL-C, non–HDL-C, and apoB. Results Among 38 153 patients allocated to statin therapy, 158 fatal myocardial infarctions, 1678 nonfatal myocardial infarctions, 615 fatal events from other coronary artery disease, 2806 hospitalizations for unstable angina, and 1029 fatal or nonfatal strokes occurred during follow-up. The adjusted HRs for major cardiovascular events per 1-SD increase were 1.13 (95% CI, 1.10-1.17) for LDL-C, 1.16 (95% CI, 1.12-1.19) for non–HDL-C, and 1.14 (95% CI, 1.11-1.18) for apoB. These HRs were significantly higher for non–HDL-C than LDL-C (P = .002) and apoB (P = .02). There was no significant difference between apoB and LDL-C (P = .21). Conclusion Among statin-treated patients, on-treatment levels of LDL-C, non–HDL-C, and apoB were each associated with risk of future major cardiovascular events, but the strength of this association was greater for non–HDL-C than for LDL-C and apoB.

656 citations

Journal ArticleDOI
TL;DR: In this article, the authors draw on the original job characteristics model (JCM) and on an elaborated model of work design to examine relationships between ethical leadership, task significance, job autonomy, effort, and job performance.
Abstract: Summary In the current study, we draw on the original job characteristics model (JCM) and on an elaborated model of work design to examine relationships between ethical leadership, task significance, job autonomy, effort, and job performance. We suggest that leaders with strong ethical commitments who regularly demonstrate ethically normative behavior can have an impacton the JCM elementsof tasksignificance and autonomy, thereby affecting anemployee’s motivation (willingness to exert effort), which in turn will be evidenced by indications of enhanced task performance and organizational citizenship behavior. We conducted a field study by surveying pairs of co-workers in a diverse set of organizations. Results provide support for a fully mediated model whereby task significance and effort fully mediate relationships between ethical leadership and subordinates’ job performance. Implications for future research on job design are discussed. Copyright # 2010 John Wiley & Sons, Ltd. At the heart of the job characteristics model (JCM, Hackman & Oldham, 1976) is the premise that leaders canshape intrinsic motivation bytheway inwhich theystructuretheobjectivecharacteristics of the work itself. 1 The theoretical model of job design was rooted in an examination of the ‘‘basic conditions that promote high performance motivation and satisfaction at work,’’ in order ‘‘to determine how those conditions can be created’’ (Hackman & Oldham, 1976; p. 71). We argue that the conceptual and empirical developments of the JCM to date can be expanded to encompass a broader role for leaders. In particular, we suggest that leaders with strong ethical commitments who regularly demonstrate ethically normative behavior can have an impact on the JCM elements of task significance and autonomy, thereby affecting an employee’s motivation (willingness to exert effort), which in turn will be evidenced by indications of enhanced task performance and organizational citizenship behaviors.

655 citations


Authors

Showing all 59759 results

NameH-indexPapersCitations
Richard A. Flavell2311328205119
Scott M. Grundy187841231821
Stuart H. Orkin186715112182
Kenneth C. Anderson1781138126072
David A. Weitz1781038114182
Dorret I. Boomsma1761507136353
Brenda W.J.H. Penninx1701139119082
Michael Kramer1671713127224
Nicholas J. White1611352104539
Lex M. Bouter158767103034
Wolfgang Wagner1562342123391
Jerome I. Rotter1561071116296
David Cella1561258106402
David Eisenberg156697112460
Naveed Sattar1551326116368
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
2023198
2022698
20219,648
20208,534
20197,822
20186,407