Institution
Dublin City University
Education•Dublin, Ireland•
About: Dublin City University is a education organization based out in Dublin, Ireland. It is known for research contribution in the topics: Context (language use) & Machine translation. The organization has 5904 authors who have published 17178 publications receiving 389376 citations. The organization is also known as: National Institute for Higher Education, Dublin & DCU.
Topics: Context (language use), Machine translation, Laser, Irish, Population
Papers published on a yearly basis
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TL;DR: In this article, the integration of global mobility and global talent management can contribute to the success of the multinational enterprise's (MNEs) global workforce management systems, but the two areas of practice have largely been decoupled in research and practice.
205 citations
New York University1, University of Pennsylvania2, Katholieke Universiteit Leuven3, Karolinska Institutet4, Technical University of Berlin5, University of Eastern Finland6, Carlos III Health Institute7, King's College London8, University of Basel9, National and Kapodistrian University of Athens10, Dublin City University11
TL;DR: The translation approach described here may help researchers reduce threats to data validity and improve instrument reliability in multinational health services research studies involving comparisons across health systems and language translation.
205 citations
TL;DR: Analytical methods were optimised and validated for the quantification of pharmaceutical residues in wastewater effluent, receiving marine waters and marine mussels (Mytilus spp.) and an in situ study in which caged Mytilus Spp.
204 citations
National Institutes of Health1, University of California, Berkeley2, University of Alabama3, Memorial Sloan Kettering Cancer Center4, University of Utah5, University of Freiburg6, University of Southern California7, French Institute of Health and Medical Research8, City of Hope National Medical Center9, Imperial College London10, American Cancer Society11, University of British Columbia12, Simon Fraser University13, Harvard University14, University of Sydney15, University of Cagliari16, Yale University17, Cancer Council Victoria18, New York University19, Mayo Clinic20, Karolinska Institutet21, Statens Serum Institut22, Uppsala University23, Stanford University24, Exponent25, Veterans Health Administration26, University of Iowa27, University of California, San Francisco28, Ohio State University29, Fred Hutchinson Cancer Research Center30, German Cancer Research Center31, Icahn School of Medicine at Mount Sinai32, International Agency for Research on Cancer33, University of Burgundy34, Dublin City University35, University of Texas MD Anderson Cancer Center36, Duke University37, University of Minnesota38, Wayne State University39, Academy of Athens40, Utrecht University41, University of Oxford42, National Institute for Health and Welfare43, Macquarie University44, University of New South Wales45, University of Bari46, University of York47, Dongguk University48, University of North Carolina at Chapel Hill49, University of Sheffield50, University of Santiago de Compostela51, University of Oviedo52, University of Barcelona53
TL;DR: The largest meta-analysis for CLL thus far, including four GWAS with a total of 3,100 individuals with CLL (cases) and 7,667 controls, identified ten independent associated SNPs in nine new loci and found evidence for two additional promising loci below genome-wide significance.
Abstract: Genome-wide association studies (GWAS) have previously identified 13 loci associated with risk of chronic lymphocytic leukemia or small lymphocytic lymphoma (CLL). To identify additional CLL susceptibility loci, we conducted the largest meta-analysis for CLL thus far, including four GWAS with a total of 3,100 individuals with CLL (cases) and 7,667 controls. In the meta-analysis, we identified ten independent associated SNPs in nine new loci at 10q23.31 (ACTA2 or FAS (ACTA2/FAS), P=1.22×10(-14)), 18q21.33 (BCL2, P=7.76×10(-11)), 11p15.5 (C11orf21, P=2.15×10(-10)), 4q25 (LEF1, P=4.24×10(-10)), 2q33.1 (CASP10 or CASP8 (CASP10/CASP8), P=2.50×10(-9)), 9p21.3 (CDKN2B-AS1, P=1.27×10(-8)), 18q21.32 (PMAIP1, P=2.51×10(-8)), 15q15.1 (BMF, P=2.71×10(-10)) and 2p22.2 (QPCT, P=1.68×10(-8)), as well as an independent signal at an established locus (2q13, ACOXL, P=2.08×10(-18)). We also found evidence for two additional promising loci below genome-wide significance at 8q22.3 (ODF1, P=5.40×10(-8)) and 5p15.33 (TERT, P=1.92×10(-7)). Although further studies are required, the proximity of several of these loci to genes involved in apoptosis suggests a plausible underlying biological mechanism.
202 citations
TL;DR: The hypothesis that TNBC exosomes may be involved in cancer cell-to-cell communication, conferring phenotypic traits to secondary cells that reflect those of their cells of origin is supported.
202 citations
Authors
Showing all 6059 results
| Name | H-index | Papers | Citations |
|---|---|---|---|
| Joseph Wang | 158 | 1282 | 98799 |
| David Cameron | 154 | 1586 | 126067 |
| David Taylor | 131 | 2469 | 93220 |
| Gordon G. Wallace | 114 | 1267 | 69095 |
| David A. Morrow | 113 | 598 | 56776 |
| G. Hughes | 103 | 957 | 46632 |
| David Wilson | 102 | 757 | 49388 |
| Muhammad Imran | 94 | 3053 | 51728 |
| Haibo Zeng | 94 | 604 | 39226 |
| David Lloyd | 90 | 1017 | 37691 |
| Vikas Kumar | 89 | 859 | 39185 |
| Luke P. Lee | 84 | 413 | 22803 |
| James Chapman | 82 | 483 | 36468 |
| Muhammad Iqbal | 77 | 961 | 23821 |
| Michael C. Berndt | 76 | 228 | 16897 |