Institution
University of Latvia
Education•Riga, Latvia•
About: University of Latvia is a education organization based out in Riga, Latvia. It is known for research contribution in the topics: Luminescence & Population. The organization has 4865 authors who have published 9320 publications receiving 136986 citations. The organization is also known as: Latvijas Universitāte.
Topics: Luminescence, Population, Dielectric, Photoluminescence, Magnetic field
Papers published on a yearly basis
Papers
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TL;DR: In this article, the authors used a Bayesian hierarchical model to estimate trends in diabetes prevalence, defined as fasting plasma glucose of 7.0 mmol/L or higher, or history of diagnosis with diabetes, or use of insulin or oral hypoglycaemic drugs in 200 countries and territories in 21 regions, by sex and from 1980 to 2014.
2,782 citations
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Technische Universität München1, Central Institution for Meteorology and Geodynamics2, University of Tartu3, Swedish Museum of Natural History4, University of Latvia5, Humboldt University of Berlin6, University of Ljubljana7, MeteoSwiss8, Trinity College, Dublin9, Autonomous University of Barcelona10, Norwegian University of Life Sciences11, Norwegian Meteorological Institute12, Finnish Meteorological Institute13, Czech Hydrometeorological Institute14, Environment Agency15, Wageningen University and Research Centre16, University of Oslo17
TL;DR: In this article, the authors used an enormous systematic phenological network data set of more than 125 000 observational series of 542 plant and 19 animal species in 21 European countries (1971-2000) and concluded that previously published results of phenological changes were not biased by reporting or publication predisposition.
Abstract: Global climate change impacts can already be tracked in many physical and biological systems; in particular, terrestrial ecosystems provide a consistent picture of observed changes. One of the preferred indicators is phenology, the science of natural recurring events, as their recorded dates provide a high-temporal resolution of ongoing changes. Thus, numerous analyses have demonstrated an earlier onset of spring events for mid and higher latitudes and a lengthening of the growing season. However, published single-site or single-species studies are particularly open to suspicion of being biased towards predominantly reporting climate change-induced impacts. No comprehensive study or meta-analysis has so far examined the possible lack of evidence for changes or shifts at sites where no temperature change is observed. We used an enormous systematic phenological network data set of more than 125 000 observational series of 542 plant and 19 animal species in 21 European countries (1971–2000). Our results showed that 78% of all leafing, flowering and fruiting records advanced (30% significantly) and only 3% were significantly delayed, whereas the signal of leaf colouring/fall is ambiguous. We conclude that previously published results of phenological changes were not biased by reporting or publication predisposition: the average advance of spring/summer was 2.5 days decade � 1 in Europe. Our analysis of 254 mean national time series undoubtedly demonstrates that species’ phenology is responsive to temperature of the preceding
2,457 citations
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15 Apr 2010
TL;DR: Systematic studies of more than 25,000 cancer genomes will reveal the repertoire of oncogenic mutations, uncover traces of the mutagenic influences, define clinically relevant subtypes for prognosis and therapeutic management, and enable the development of new cancer therapies.
Abstract: The International Cancer Genome Consortium (ICGC) was launched to coordinate large-scale cancer genome studies in tumours from 50 different cancer types and/or subtypes that are of clinical and societal importance across the globe. Systematic studies of more than 25,000 cancer genomes at the genomic, epigenomic and transcriptomic levels will reveal the repertoire of oncogenic mutations, uncover traces of the mutagenic influences, define clinically relevant subtypes for prognosis and therapeutic management, and enable the development of new cancer therapies.
2,041 citations
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TL;DR: The flagship paper of the ICGC/TCGA Pan-Cancer Analysis of Whole Genomes Consortium describes the generation of the integrative analyses of 2,658 whole-cancer genomes and their matching normal tissues across 38 tumour types, the structures for international data sharing and standardized analyses, and the main scientific findings from across the consortium studies.
Abstract: Cancer is driven by genetic change, and the advent of massively parallel sequencing has enabled systematic documentation of this variation at the whole-genome scale1,2,3. Here we report the integrative analysis of 2,658 whole-cancer genomes and their matching normal tissues across 38 tumour types from the Pan-Cancer Analysis of Whole Genomes (PCAWG) Consortium of the International Cancer Genome Consortium (ICGC) and The Cancer Genome Atlas (TCGA). We describe the generation of the PCAWG resource, facilitated by international data sharing using compute clouds. On average, cancer genomes contained 4–5 driver mutations when combining coding and non-coding genomic elements; however, in around 5% of cases no drivers were identified, suggesting that cancer driver discovery is not yet complete. Chromothripsis, in which many clustered structural variants arise in a single catastrophic event, is frequently an early event in tumour evolution; in acral melanoma, for example, these events precede most somatic point mutations and affect several cancer-associated genes simultaneously. Cancers with abnormal telomere maintenance often originate from tissues with low replicative activity and show several mechanisms of preventing telomere attrition to critical levels. Common and rare germline variants affect patterns of somatic mutation, including point mutations, structural variants and somatic retrotransposition. A collection of papers from the PCAWG Consortium describes non-coding mutations that drive cancer beyond those in the TERT promoter4; identifies new signatures of mutational processes that cause base substitutions, small insertions and deletions and structural variation5,6; analyses timings and patterns of tumour evolution7; describes the diverse transcriptional consequences of somatic mutation on splicing, expression levels, fusion genes and promoter activity8,9; and evaluates a range of more-specialized features of cancer genomes8,10,11,12,13,14,15,16,17,18.
1,600 citations
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TL;DR: The global estimate of viraemic HCV infections is lower than previous estimates, largely due to more recent prevalence estimates in Africa, and increased mortality due to liver-related causes and an ageing population may have contributed to a reduction in infections.
1,578 citations
Authors
Showing all 4946 results
Name | H-index | Papers | Citations |
---|---|---|---|
Ralf Hertenberger | 128 | 1128 | 78115 |
Paul A. Janmey | 109 | 473 | 48858 |
Bengt Nordén | 81 | 514 | 24613 |
Andreas Winter | 71 | 407 | 21729 |
Alvis Brazma | 69 | 214 | 37252 |
Hans-Ulrich Kauczor | 61 | 378 | 13255 |
Javier Jiménez | 61 | 277 | 18061 |
Sune Svanberg | 60 | 678 | 16382 |
Alexander L. Shluger | 58 | 402 | 14857 |
David Moore | 56 | 399 | 11760 |
Andris Ambainis | 54 | 297 | 12836 |
Arunas Ramanavicius | 52 | 287 | 9624 |
Keita Ito | 51 | 279 | 11074 |
Eugene A. Kotomin | 50 | 480 | 9756 |
Sampath Kannan | 47 | 185 | 9643 |