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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 & Context (language use). The organization has 59309 authors who have published 140894 publications receiving 5984137 citations. The organization is also known as: UvA & Universiteit van Amsterdam.


Papers
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Journal ArticleDOI
TL;DR: This paper performed a meta-analysis of 14 genome-wide association studies of coronary artery disease (CAD) comprising 22,233 individuals with CAD (cases) and 64,762 controls of European descent followed by genotyping of top association signals in 56,682 additional individuals.
Abstract: We performed a meta-analysis of 14 genome-wide association studies of coronary artery disease (CAD) comprising 22,233 individuals with CAD (cases) and 64,762 controls of European descent followed by genotyping of top association signals in 56,682 additional individuals. This analysis identified 13 loci newly associated with CAD at P < 5 - 10'8 and confirmed the association of 10 of 12 previously reported CAD loci. The 13 new loci showed risk allele frequencies ranging from 0.13 to 0.91 and were associated with a 6% to 17% increase in the risk of CAD per allele. Notably, only three of the new loci showed significant association with traditional CAD risk factors and the majority lie in gene regions not previously implicated in the pathogenesis of CAD. Finally, five of the new CAD risk loci appear to have pleiotropic effects, showing strong association with various other human diseases or traits.

1,705 citations

Journal ArticleDOI
Serena Nik-Zainal1, Serena Nik-Zainal2, Helen Davies1, Johan Staaf3, Manasa Ramakrishna1, Dominik Glodzik1, Xueqing Zou1, Inigo Martincorena1, Ludmil B. Alexandrov1, Sancha Martin1, David C. Wedge1, Peter Van Loo1, Young Seok Ju1, Michiel M. Smid4, Arie B. Brinkman5, Sandro Morganella6, Miriam Ragle Aure7, Ole Christian Lingjærde7, Anita Langerød8, Markus Ringnér3, Sung-Min Ahn9, Sandrine Boyault, Jane E. Brock, Annegien Broeks10, Adam Butler1, Christine Desmedt11, Luc Dirix12, Serge Dronov1, Aquila Fatima13, John A. Foekens4, Moritz Gerstung1, Gerrit Gk Hooijer14, Se Jin Jang15, David Jones1, Hyung-Yong Kim16, Tari Ta King17, Savitri Krishnamurthy18, Hee Jin Lee15, Jeong-Yeon Lee16, Yang Li1, Stuart McLaren1, Andrew Menzies1, Ville Mustonen1, Sarah O’Meara1, Iris Pauporté, Xavier Pivot19, Colin Ca Purdie20, Keiran Raine1, Kamna Ramakrishnan1, Germán Fg Rodríguez-González4, Gilles Romieu21, Anieta M. Sieuwerts4, Peter Pt Simpson22, Rebecca Shepherd1, Lucy Stebbings1, Olafur Oa Stefansson23, Jon W. Teague1, Stefania Tommasi, Isabelle Treilleux, Gert Van den Eynden12, Peter B. Vermeulen12, Anne Vincent-Salomon24, Lucy R. Yates1, Carlos Caldas25, Laura Van't Veer10, Andrew Tutt26, Andrew Tutt27, Stian Knappskog28, Benita Kiat Tee Bk Tan29, Jos Jonkers10, Åke Borg3, Naoto T. Ueno18, Christos Sotiriou11, Alain Viari, P. Andrew Futreal1, Peter J. Campbell1, Paul N. Span5, Steven Van Laere12, Sunil R. Lakhani22, Jorunn E. Eyfjord23, Alastair M Thompson, Ewan Birney6, Hendrik G. Stunnenberg5, Marc J. van de Vijver14, John W.M. Martens4, Anne Lise Børresen-Dale8, Andrea L. Richardson13, Gu Kong16, Gilles Thomas, Michael R. Stratton1 
02 Jun 2016-Nature
TL;DR: This analysis of all classes of somatic mutation across exons, introns and intergenic regions highlights the repertoire of cancer genes and mutational processes operative, and progresses towards a comprehensive account of the somatic genetic basis of breast cancer.
Abstract: We analysed whole-genome sequences of 560 breast cancers to advance understanding of the driver mutations conferring clonal advantage and the mutational processes generating somatic mutations. We found that 93 protein-coding cancer genes carried probable driver mutations. Some non-coding regions exhibited high mutation frequencies, but most have distinctive structural features probably causing elevated mutation rates and do not contain driver mutations. Mutational signature analysis was extended to genome rearrangements and revealed twelve base substitution and six rearrangement signatures. Three rearrangement signatures, characterized by tandem duplications or deletions, appear associated with defective homologous-recombination-based DNA repair: one with deficient BRCA1 function, another with deficient BRCA1 or BRCA2 function, the cause of the third is unknown. This analysis of all classes of somatic mutation across exons, introns and intergenic regions highlights the repertoire of cancer genes and mutational processes operating, and progresses towards a comprehensive account of the somatic genetic basis of breast cancer.

1,696 citations

Journal ArticleDOI
TL;DR: These guidelines are intended for use by physicians in all medical specialties who perform direct patient care, with an emphasis on the care of patients in hospitals and long-term care facilities.
Abstract: Guidelines for the diagnosis, prevention, and management of persons with catheter-associated urinary tract infection (CA-UTI), both symptomatic and asymptomatic, were prepared by an Expert Panel of the Infectious Diseases Society of America. The evidence-based guidelines encompass diagnostic criteria, strategies to reduce the risk of CA-UTIs, strategies that have not been found to reduce the incidence of urinary infections, and management strategies for patients with catheter-associated asymptomatic bacteriuria or symptomatic urinary tract infection. These guidelines are intended for use by physicians in all medical specialties who perform direct patient care, with an emphasis on the care of patients in hospitals and long-term care facilities.

1,682 citations

Journal ArticleDOI
TL;DR: This article developed, measured, and tested two types of intergroup prejudice (blatant and subtle) and reported the properties, structure and correlates of both scales across the seven samples, and make initial checks on their validity.
Abstract: This paper develops, measures, and tests two types of intergroup prejudice—blatant and subtle. Blatant prejudice is the traditional, often studied form; it is hot, close and direct. Subtle prejudice is the modern form; it is cool, distant and indirect. Using data from seven independent national samples from western Europe, we constructed 10-item scales in four languages to measure each of these varieties of prejudice. We report the properties, structure and correlates of both scales across the seven samples, and make initial checks on their validity. The cross-nationally consistent results support the value of the blatant-subtle distinction as two varieties of prejudice. While they share many correlates, their distinctive differences suggest better specification of these correlates of prejudice. And the blatant-subtle distinction also aids in more precise specification of the effects of prejudice on attitudes toward immigrants. The paper closes with a normative interpretation of Subtle Prejudice.

1,676 citations

Journal ArticleDOI
TL;DR: It is proposed that stemness of colon cancer cells is in part orchestrated by the microenvironment and is a much more dynamic quality than previously expected that can be defined by high Wnt activity.
Abstract: Despite the presence of mutations in APC or beta-catenin, which are believed to activate the Wnt signalling cascade constitutively, most colorectal cancers show cellular heterogeneity when beta-catenin localization is analysed, indicating a more complex regulation of Wnt signalling. We explored this heterogeneity with a Wnt reporter construct and observed that high Wnt activity functionally designates the colon cancer stem cell (CSC) population. In adenocarcinomas, high activity of the Wnt pathway is observed preferentially in tumour cells located close to stromal myofibroblasts, indicating that Wnt activity and cancer stemness may be regulated by extrinsic cues. In agreement with this notion, myofibroblast-secreted factors, specifically hepatocyte growth factor, activate beta-catenin-dependent transcription and subsequently CSC clonogenicity. More significantly, myofibroblast-secreted factors also restore the CSC phenotype in more differentiated tumour cells both in vitro and in vivo. We therefore propose that stemness of colon cancer cells is in part orchestrated by the microenvironment and is a much more dynamic quality than previously expected that can be defined by high Wnt activity.

1,674 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
2022699
20219,646
20208,532
20197,821
20186,407