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263 results for “Impact Factor”

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zenodo40/100

Spatially and taxonomically explicit characterisation factors for greenhouse gas emission impacts on biodiversity

<p>Gridded&nbsp;global potentially affected fraction of species (PAF) in 2050&nbsp;and 2100&nbsp;per kg GHG for 3 RCPs (2.6, 4.5,8.5)&nbsp;averaged over all species groups.&nbsp;</p> <p>Full method description is available in the article:&nbsp;<a href="https://www.sciencedirect.com/science/article/pii/S092134492300294X">Spatially and taxonomically explicit characterisation factors for greenhouse gas emission impacts on biodiversity - ScienceDirect</a></p>

opencc-by-4.0Dec 2022View details →
dryad40/100

The impact of stress and its influencing factors among dentists during the COVID-19 pandemic in Kingdom of Bahrain

Open the record for dataset details and reuse information.

publicJun 2022View details →
dryad40/100

Impacts of abiotic and biotic factors on terrestrial leeches in

Open the record for dataset details and reuse information.

publicJul 2022View details →
dryad40/100

Spatial distribution of benthic algae in the South China Sea: responses to gradually changing environmental factors and ecological impacts on coral communities

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publicMar 2021View details →
dryad36/100

Data from: A description of nesting behaviors, including factors impacting nest site selection, in black-and-white ruffed lemurs (Varecia variegata)

Nest site selection is at once fundamental to reproduction and a poorly understood component of many organisms' reproductive investment. This study investigates the nesting behaviors of black-and-white ruffed lemurs, Varecia variegata, a litter-bearing primate from the southeastern rainforests of Madagascar. Using a combination of behavioral, geospatial, and demographic data, I test the hypotheses that environmental and social cues influence nest site selection, and that these decisions ultimately impact maternal reproductive success. Gestating females built multiple large nests throughout their territories. Of these, females used only a fraction of the originally constructed nests, as well as several parking locations as infants aged. Nest construction was best predicted by environmental cues, including the size of the nesting tree and density of feeding trees within a 75 m radius of the nest, whereas nest use depended largely on the size and average distance to feeding trees within that same area. Microhabitat characteristics were unrelated to whether females built or used nests. Although unrelated to nest site selection, social cues, specifically the average distance to conspecifics' nest and park sites, were related to maternal reproductive success; mothers whose litters were parked in closer proximity to others' nests experienced higher infant survival than those whose nests were more isolated. This is likely because nesting proximity facilitated communal crèche use by neighboring females. Together, these results suggest a complex pattern of nesting behaviors that involves females strategically building nests in areas with high potential resource abundance, using nests in areas according to their realized productivity, and communally rearing infants within a network of nests distributed throughout the larger communal territory.

opencc-zeroDec 2018View details →
zenodo36/100

Global Regionalized Characterization Factors for Phosphorus and Nitrogen Impacts on Freshwater Fish Biodiversity

<p>Overview and guidance for using the data in "CFs_freshwater_eutrophication" related to the article "Global Regionalized Characterization Factors for Phosphorus and Nitrogen Impacts on Freshwater Fish Biodiversity"</p> <p>&nbsp;</p> <p>See the "readme_CFs_freshwater_eutrophication.pdf" file to find the details of the enclosed data.</p> <p>&nbsp;</p> <p>Units</p> <ul> <li>Phosphorus from direct emissions to freshwater or diffuse sources on the soil: PDF&middot;year/kgP</li> <li>Nitrogen from direct emissions to freshwater or diffuse sources on the soil: PDF&middot;year/kgN</li> <li>Erosion: PDF&middot;year/(m2&middot;year)</li> </ul> <p>Please excuse any typos in the units in the xlsx files.</p>

opencc-by-4.0Dec 2023View details →
dryad36/100

High-resolution environmental and host-related factors impacting questing Ixodes scapularis at their northern range edge

<p>The geographic range of tick populations has expanded in Canada due to climate warming and the associated poleward range shifts of their vertebrate hosts. Abiotic factors, such as temperature, precipitation, and snow, are known to directly affect tick abundance. Yet, biotic factors, such as the abundance and diversity of mammal hosts, may also alter tick abundance and consequent tick-borne disease risk. Here, we incorporated host surveillance data with high-resolution environmental data to evaluate the combined impact of abiotic and biotic factors on questing <em>Ixodes scapularis </em>abundance in Ontario and Quebec, Canada. High-resolution abiotic factors were derived from remote sensing satellites and meteorological towers, while biotic factors related to mammal hosts were derived from active surveillance data that we collected in the field. Generalized additive models were used to determine the relative importance of abiotic and biotic factors on questing <em>I. scapularis</em> abundance. Combinations of abiotic and biotic factors were identified as important drivers of abundances of questing <em>I. scapularis</em>. Positive and negative linear relationships were found for questing <em>I. scapularis </em>abundance with precipitation and accumulated snow, but no effect was found for the relative abundance of white-footed mice. Positive relationships were also identified between questing <em>I. scapularis </em>abundance with monthly mean precipitation and mammal species richness. Therefore, future studies that assess <em>I. scapularis </em>should incorporate host surveillance data with high-resolution environmental factors to determine the key drivers impacting the<em> </em>abundance and geographic spread of tick populations and tick-borne pathogens.</p>

opencc-zeroJan 2024View details →
zenodo36/100

Pleiotropic Expression Quantitative Trait Loci Are Enriched in Enhancers and Transcription Factor Binding Sites and Impact More Genes

<p>This dataset comprises two files that accompany the article (link to be added upon publication).</p> <h2>1. gwas2eqtl_colocalization_full.tar.gz</h2> <p>This file contains the complete colocalization dataset generated using the code from the following GitHub repository: gwas2eqtl. This dataset is used as input for the pleiotropic eQTL analysis available at gwas2eqtl_pleiotropy, which produces the figures in the article.</p> <p><strong>File structure:</strong></p> <blockquote> <p>.<br>└── gwas417<br>&nbsp; &nbsp; └── coloc<br>&nbsp; &nbsp; &nbsp; &nbsp; ├── ebi-a-GCST000998<br>&nbsp; &nbsp; &nbsp; &nbsp; │ &nbsp; └── pval_5e-08<br>&nbsp; &nbsp; &nbsp; &nbsp; │ &nbsp; &nbsp; &nbsp; └── r2_0.1<br>&nbsp; &nbsp; &nbsp; &nbsp; │ &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; └── kb_1000<br>&nbsp; &nbsp; &nbsp; &nbsp; │ &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; └── window_1000000<br>&nbsp; &nbsp; &nbsp; &nbsp; │ &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; ├── Alasoo_2018_ge_macrophage_IFNg+Salmonella.tsv<br>&nbsp; &nbsp; &nbsp; &nbsp; │ &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; ├── Alasoo_2018_ge_macrophage_IFNg.tsv<br>...</p> </blockquote> <p>Each TSV file contains the following columns:</p> <blockquote> <p>chrom &nbsp; &nbsp;pos &nbsp; &nbsp;rsid &nbsp; &nbsp;ref &nbsp; &nbsp;alt &nbsp; &nbsp;eqtl_gene_id &nbsp; &nbsp;gwas_beta &nbsp; &nbsp;gwas_pval &nbsp; &nbsp;gwas_id &nbsp; &nbsp;eqtl_beta &nbsp; &nbsp;eqtl_pval &nbsp; &nbsp;eqtl_id &nbsp; &nbsp;PP.H4.abf &nbsp; &nbsp;SNP.PP.H4 &nbsp; &nbsp;nsnps &nbsp; &nbsp;PP.H3.abf &nbsp; &nbsp;PP.H2.abf &nbsp; &nbsp;PP.H1.abf &nbsp; &nbsp;PP.H0.abf &nbsp; &nbsp;coloc_variant_id &nbsp; &nbsp;coloc_region<br>1 &nbsp; &nbsp;109272258 &nbsp; &nbsp;rs4970834 &nbsp; &nbsp;C &nbsp; &nbsp;T &nbsp; &nbsp;ENSG00000168765 &nbsp; &nbsp;-0.12874.25001047052626e-09 &nbsp; &nbsp;ebi-a-GCST000998 &nbsp; &nbsp;-0.250697 &nbsp; &nbsp;0.0893351 &nbsp; &nbsp;Alasoo_2018_ge_macrophage_IFNg+Salmonella &nbsp; &nbsp;0.108283426725895 &nbsp; &nbsp;0.0520205502224409 &nbsp; &nbsp;6 &nbsp; &nbsp;0.000552728832012655 &nbsp; &nbsp;2.09397277427793e-07 &nbsp; &nbsp;0.890881419183881 &nbsp; &nbsp;0.000282215860934432 &nbsp; &nbsp;1_109279544_G_A &nbsp; &nbsp;1:108779544-109779543<br>1 &nbsp; &nbsp;109274968 &nbsp; &nbsp;rs12740374 &nbsp; &nbsp;G &nbsp; &nbsp;T &nbsp; &nbsp;ENSG00000168765 &nbsp; &nbsp;-0.103341 &nbsp; &nbsp;1.63998546891446e-09 &nbsp; &nbsp;ebi-a-GCST000998 &nbsp; &nbsp;-0.197397 &nbsp; &nbsp;0.172673Alasoo_2018_ge_macrophage_IFNg+Salmonella &nbsp; &nbsp;0.108283426725895 &nbsp; &nbsp;0.0857585178966856 &nbsp; &nbsp;6 &nbsp; &nbsp;0.000552728832012655 &nbsp; &nbsp;2.09397277427793e-07 &nbsp; &nbsp;0.890881419183881 &nbsp; &nbsp;0.000282215860934432 &nbsp; &nbsp;1_109279544_G_A &nbsp; &nbsp;1:108779544-109779543<br>1 &nbsp; &nbsp;109275216 &nbsp; &nbsp;rs660240 &nbsp; &nbsp;T &nbsp; &nbsp;C &nbsp; &nbsp;ENSG00000168765 &nbsp; &nbsp;0.1044492.78997299740827e-09 &nbsp; &nbsp;ebi-a-GCST000998 &nbsp; &nbsp;0.214165 &nbsp; &nbsp;0.139318 &nbsp; &nbsp;Alasoo_2018_ge_macrophage_IFNg+Salmonella &nbsp; &nbsp;0.108283426725895 &nbsp; &nbsp;0.0557749486050279 &nbsp; &nbsp;6 &nbsp; &nbsp;0.000552728832012655 &nbsp; &nbsp;2.09397277427793e-07 &nbsp; &nbsp;0.890881419183881 &nbsp; &nbsp;0.000282215860934432 &nbsp; &nbsp;1_109279544_G_A &nbsp; &nbsp;1:108779544-109779543<br>1 &nbsp; &nbsp;109275684 &nbsp; &nbsp;rs629301 &nbsp; &nbsp;G &nbsp; &nbsp;T &nbsp; &nbsp;ENSG00000168765 &nbsp; &nbsp;0.1054716.129993302249e-10 &nbsp; &nbsp;ebi-a-GCST000998 &nbsp; &nbsp;0.197397 &nbsp; &nbsp;0.172673 &nbsp; &nbsp;Alasoo_2018_ge_macrophage_IFNg+Salmonella &nbsp; &nbsp;0.108283426725895 &nbsp; &nbsp;0.22229240584331 &nbsp; &nbsp;6 &nbsp; &nbsp;0.000552728832012655 &nbsp; &nbsp;2.09397277427793e-07 &nbsp; &nbsp;0.890881419183881 &nbsp; &nbsp;0.000282215860934432 &nbsp; &nbsp;1_109279544_G_A &nbsp; &nbsp;1:108779544-109779543<br>1 &nbsp; &nbsp;109278889 &nbsp; &nbsp;rs602633 &nbsp; &nbsp;T &nbsp; &nbsp;G &nbsp; &nbsp;ENSG00000168765 &nbsp; &nbsp;0.1034352.15998134341707e-09 &nbsp; &nbsp;ebi-a-GCST000998 &nbsp; &nbsp;0.226329 &nbsp; &nbsp;0.102673 &nbsp; &nbsp;Alasoo_2018_ge_macrophage_IFNg+Salmonella &nbsp; &nbsp;0.108283426725895 &nbsp; &nbsp;0.0782482718431504 &nbsp; &nbsp;6 &nbsp; &nbsp;0.000552728832012655 &nbsp; &nbsp;2.09397277427793e-07 &nbsp; &nbsp;0.890881419183881 &nbsp; &nbsp;0.000282215860934432 &nbsp; &nbsp;1_109279544_G_A &nbsp; &nbsp;1:108779544-109779543<br>...</p> </blockquote> <p>&nbsp;</p> <p>The dataset provides colocalization statistics for GWAS-eQTL pairs, including posterior probabilities and variant annotations.</p> <h2>2. gwas2eqtl0.1.3.tsv.gz</h2> <p>This file is a filtered version of the colocalization dataset, refined based on cutoffs of PP.H4.abf &ge; 0.75 and SNP.PP.H4 &ge; 0. This subset is utilized in the gwas2eqtl web application for data visualization.</p> <p>Sample Columns:</p> <blockquote> <p>chrom &nbsp; pos19 &nbsp; pos38 &nbsp; cytoband &nbsp; &nbsp; &nbsp; &nbsp;rsid &nbsp; &nbsp;ref &nbsp; &nbsp; alt &nbsp; &nbsp; gwas_trait &nbsp; &nbsp; &nbsp;gwas_class &nbsp; &nbsp; &nbsp;gwas_beta &nbsp; &nbsp; &nbsp; eqtl_gene_symbol &nbsp; &nbsp; &nbsp; &nbsp;eqtl_beta &nbsp; &nbsp; &nbsp; eqtl_id eqtl_gene_id &nbsp; &nbsp;gwas_id gwas_pval &nbsp; &nbsp; &nbsp; eqtl_pval &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;pp_h4_abf &nbsp; &nbsp; &nbsp; snp_pp_h4 &nbsp; &nbsp; &nbsp; tophits_variant_id &nbsp; &nbsp; &nbsp;nsnps<br>1 &nbsp; &nbsp; &nbsp; 1163804 1228424 1p36.33 rs7515488 &nbsp; &nbsp; &nbsp; C &nbsp; &nbsp; &nbsp; T &nbsp; &nbsp; &nbsp; Inflammatory bowel disease &nbsp; &nbsp; &nbsp;Autoimmune dis. 0.0874308 &nbsp; &nbsp; &nbsp; ANKRD65 -0.175816 &nbsp; &nbsp; &nbsp; BrainSeq_ge_brain &nbsp; &nbsp; &nbsp; ENSG00000235098 ebi-a-GCST003043 &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; 2.85292266979231e-10 &nbsp; &nbsp;0.000841046 &nbsp; &nbsp; 0.978425254116226 &nbsp; &nbsp; &nbsp; 6.18454060493069e-12 &nbsp; &nbsp;1_1312114_T_C &nbsp; 3<br>1 &nbsp; &nbsp; &nbsp; 1163804 1228424 1p36.33 rs7515488 &nbsp; &nbsp; &nbsp; C &nbsp; &nbsp; &nbsp; T &nbsp; &nbsp; &nbsp; Inflammatory bowel disease &nbsp; &nbsp; &nbsp;Autoimmune dis. 0.0874308 &nbsp; &nbsp; &nbsp; ANKRD65 -0.175816 &nbsp; &nbsp; &nbsp; BrainSeq_ge_brain &nbsp; &nbsp; &nbsp; ENSG00000235098 ieu-a-294 &nbsp; &nbsp; &nbsp; 2.85292266979231e-10 &nbsp; &nbsp; &nbsp; 0.000841046 &nbsp; &nbsp; 0.974019788384412 &nbsp; &nbsp; &nbsp; 7.52286530905187e-12 &nbsp; &nbsp;1_1312114_T_C &nbsp; 4<br>1 &nbsp; &nbsp; &nbsp; 1163804 1228424 1p36.33 rs7515488 &nbsp; &nbsp; &nbsp; C &nbsp; &nbsp; &nbsp; T &nbsp; &nbsp; &nbsp; Inflammatory bowel disease &nbsp; &nbsp; &nbsp;Autoimmune dis. 0.0874308 &nbsp; &nbsp; &nbsp; ANKRD65 -0.293529 &nbsp; &nbsp; &nbsp; CommonMind_ge_DLPFC_naive &nbsp; &nbsp; &nbsp; ENSG00000235098 ebi-a-GCST003043 &nbsp; 2.85292266979231e-10 &nbsp; &nbsp;2.30452e-06 &nbsp; &nbsp; 0.953333690803618 &nbsp; &nbsp; &nbsp; 6.9758581004380506e-15 &nbsp;1_1312114_T_C &nbsp; 6<br>1 &nbsp; &nbsp; &nbsp; 1163804 1228424 1p36.33 rs7515488 &nbsp; &nbsp; &nbsp; C &nbsp; &nbsp; &nbsp; T &nbsp; &nbsp; &nbsp; Inflammatory bowel disease &nbsp; &nbsp; &nbsp;Autoimmune dis. 0.0874308 &nbsp; &nbsp; &nbsp; ANKRD65 -0.293529 &nbsp; &nbsp; &nbsp; CommonMind_ge_DLPFC_naive &nbsp; &nbsp; &nbsp; ENSG00000235098 ieu-a-294 &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;2.85292266979231e-10 &nbsp; &nbsp;2.30452e-06 &nbsp; &nbsp; 0.951092499048109 &nbsp; &nbsp; &nbsp; 7.0876793540547e-15 &nbsp; &nbsp; 1_1312114_T_C &nbsp; 7<br>1 &nbsp; &nbsp; &nbsp; 1163804 1228424 1p36.33 rs7515488 &nbsp; &nbsp; &nbsp; C &nbsp; &nbsp; &nbsp; T &nbsp; &nbsp; &nbsp; Inflammatory bowel disease &nbsp; &nbsp; &nbsp;Autoimmune dis. 0.0874308 &nbsp; &nbsp; &nbsp; ANKRD65 -0.510549 &nbsp; &nbsp; &nbsp; FUSION_ge_adipose_naive ENSG00000235098 ebi-a-GCST003043 &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; 2.85292266979231e-10 &nbsp; &nbsp;1.2212e-06 &nbsp; &nbsp; &nbsp;0.974412793352836 &nbsp; &nbsp; &nbsp; 1.70246427912903e-11 &nbsp; &nbsp;1_1312114_T_C &nbsp; 6</p> </blockquote> <p>&nbsp;</p> <p>This filtered dataset focuses on high-confidence colocalization events for functional exploration of genetic associations and regulatory mechanisms.</p>

opencc-by-4.0Nov 2024View details →
zenodo36/100

Fig. 1 in Waterbird Distribution Patterns And Environmentally Impacted Factors In Reclaimed Coastal Wetlands Of The Eastern End Of Nanhui County, Shanghai, China

Fig. 1. LocationofstudysitesinNanhuiCounty, Shanghai.

opencc-by-4.0May 2013View details →
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Fig. 2 in A Review Of Major Impact Factors Of Hostilities Influencing Biodiversity In The Eastern Ukraine (Modeled On Selected Animal Species)

Fig. 2. Temporal distribution of numbers of ignitions in ATO zone in 2010–2014.

opencc-by-4.0Mar 2015View details →
zenodo36/100

Infection of mice by the enteroaggregative E. coli strain 042 and two mutant derivatives overexpressing virulence factors: impact on disease markers, gut microbiota and concentration of SCFAs in feces

<p>This dataset contains raw sequencing data from the microbiota analysis conducted in the enteroaggregative E. coli strain 042 study. The data includes FASTQ files generated from Illumina sequencing, along with metadata describing the sample collection and processing methods.</p>

opencc-by-4.0Jun 2024View details →
zenodo36/100

Fig. 4 in The correlations between certain features of the journal Neotropical Ichthyology and its impact factor: a comparative analysis at the thematic and national levels

Fig. 4. Uncitedness rate of articles published in the Brazilian journals in Sample 2.

opencc-by-4.0Mar 2013View details →
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Fig. 1 in The correlations between certain features of the journal Neotropical Ichthyology and its impact factor: a comparative analysis at the thematic and national levels

Fig. 1. Brazilian journals and their corresponding self-cited rates between 2006 and 2011.

opencc-by-4.0Mar 2013View details →
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Fig. 2 in The correlations between certain features of the journal Neotropical Ichthyology and its impact factor: a comparative analysis at the thematic and national levels

Fig. 2. Brazilian journals and their corresponding self-citing rates between 2006 and 2011.

opencc-by-4.0Mar 2013View details →
zenodo36/100

Figure 1 in Impacts of environmental factors on zooplankton taxonomic diversity in coastal lagoons in Turkey

Figure 1. The location of the Dalyan and Arapçiftliği lagoons.

opencc-by-4.0Sep 2017View details →
zenodo36/100

Novel Endpoint Characterization Factors for Life Cycle Impact Assessment of Terrestrial Acidification

<p>This repository contains Excel files with the characterization factorsand the soil response factors for the publication entitled "Novel Endpoint Characterization Factors for Life Cycle Impact Assessment of Terrestrial Acidification", published in the "Journal of Ecological Indicators" .<br><br></p> <p>Content:</p> <p><strong>Datasets.zip</strong>&nbsp;is an folder containing the following Excel files:&nbsp;</p> <ul> <li><strong>CF_Terrestrial_Acidification_2024-08-01.xlsx</strong> with the following sheets <ul> <li><em>Dataframe</em> gathering terrestrial acidification marginal endpoint CF [PDF.yr/kg_emitted] values at country level (with the world average value), for 3 acidifying substances (NOx, NHx, SOx) at global and regional impact scales (with and without the inclusion of the Global Extinction Probability - GEP - respectively)</li> <li><em>Calc Info</em> summing up calculation informations</li> <li><em>Calc Table</em> registering input parameters used to run the calculations leading to the <em>Dataframe</em> sheet (substance used, original and adapted resolutions for emission and deposition compartments, resolutions for each CF components&nbsp; and spatial transformations, GEP normalization method)</li> </ul> </li> <li><strong>RF_NO3_2024-03-27.xlsx</strong> with the following sheet:<br> <ul> <li><em>RFs</em> containing the soil response values [(molH+ / L).(yr / kg_dep)] at ecoregion level (referred to as "idTarget") for a marginal increase of 10% in NO3 deposition rate. It also gathers the intermediate results leading the final RFs (sustances' deposition rates, reference and post-deposition increase pHs)&nbsp;</li> </ul> </li> <li><strong>RF_NH4_2024-03-25.xlsx</strong> with the following sheet:<br> <ul> <li><em>RFs</em> containing the soil response values [(molH+ / L).(yr / kg_dep)] at ecoregion level (referred to as "idTarget") for a marginal increase of 10% in NH4 deposition rate. It also gathers the intermediate results leading the final RFs (sustances' deposition rates, reference and post-deposition increase pHs)</li> </ul> </li> <li><strong>RF_SO4_2024-03-25.xlsx</strong> with the following sheet:<br> <ul> <li><em>RFs</em> containing the soil response values [(molH+ / L).(yr / kg_dep)] at ecoregion level (referred to as "idTarget") for a marginal increase of 10% in SO4 deposition rate. It also gathers the intermediate results leading the final RFs (sustances' deposition rates, reference and post-deposition increase pHs)</li> </ul> </li> </ul>

opencc-by-4.0Sep 2024View details →
zenodo36/100

Raw Data for the article: Continuous Renal Replacement Therapy after Liver Transplantation: Peri-Operative Associated Factors and Impact on Survival

<p>Continuous renal replacement therapy (CRRT) following orthotopic liver transplantation (OLT) is usually started for multifactorial reasons, with variable incidence among series. This paper presents a single-center retrospective observational study on the early use (within one week) of CRRT after consecutive cadaveric OLT from January 2008 to December 2016. Preoperative patient characteristics and intraoperative data were collected, and patients were divided into two groups (CRRT and no CRRT) to explore the factors associated with the use of CRRT. Repeated measurements of postoperative creatinine were analyzed with generalized estimating equation (GEE) models. Among 528 OLT patients, 75 (14.2%) were treated with CRRT at least once in the first week. Patients treated with CRRT showed lower survival in a Kaplan-Meier curve (log-rank&nbsp;<em>p</em>&nbsp;value &amp;lt; 0.01). Patients treated with CRRT had a more severe preoperative profile, with a significantly higher age, MELD, BUN, creatinine, and total bilirubin, as well as a longer surgery time and a higher number of transfusions of red blood cells, plasma, and platelets (all&nbsp;<em>p</em>&nbsp;values &amp;lt; 0.05). In a stepwise multiple analysis, the following characteristics remained independently associated with the use of CRRT: the MELD score OR 1.12 (95% CL: 1.07-1.16),&nbsp;<em>p</em>&nbsp;value &amp;lt; 0.001, and the preoperative value for blood urea nitrogen OR 1.016 (95% CL: 1.010-1.023),&nbsp;<em>p</em>&nbsp;value &amp;lt; 0.001. The early use of CRRT after OLT occurred at a low rate in this large cohort; however, it was associated with worse outcomes. Apart from the preoperative severity, repeated intraoperative hypotension episodes, which were likely modifiable or preventable, were associated with the increased use of CRRT and higher postoperative creatinine.</p>

opencc-by-4.0Feb 2023View details →
dryad36/100

Seed limitation interacts with biotic and abiotic factors to constrain novel species' impact on community biomass and richness

<p>Seed limitation can narrow down the number of coexisting plant species, limit plant community productivity, and can also constrain community responses to changing environmental and biotic conditions. In a 10-year full-factorial experiment of seed addition, fertilisation, warming, and herbivore exclusion, we tested how seed addition alters community richness and biomass, and how its effects depend on seed origin and biotic and abiotic context. We found that seed addition increased species richness in all treatments, and increased plant community biomass depending on nutrient addition and warming. Novel species, originally absent from the communities, increased biomass the most, especially in fertilised plots and in the absence of herbivores, while adding seeds of local species did not affect biomass. Our results show that seed limitation constrains both community richness and biomass, and highlight the importance of considering trophic interactions and soil nutrients when assessing novel species immigrations and their effects on community biomass.</p>

opencc-zeroMar 2023View details →
dryad36/100

Data for: The impact of wildlife and environmental factors on hantavirus infection in host and its translation into human risk

<p><span>Identifying factors that drive infection dynamics in reservoir host populations is essential in understanding human risk from wildlife-originated zoonoses. We studied zoonotic <em>Puumala</em> <em>orthohantavirus</em> (PUUV) in the host, the bank vole (<em>Myodes</em> <em>glareolus</em>), populations in relation to the host population, rodent and predator community and environment-related factors and whether these processes are translated into human infection incidence. We used 5-year rodent trapping and bank vole PUUV serology data collected from 30 sites located in 24 municipalities in Finland. We found that PUUV seroprevalence was negatively associated with the abundance of red foxes, but this process did not translate into human disease incidence, which showed no association with PUUV seroprevalence. The abundance of weasels, the proportion of juvenile bank voles in the host populations and rodent species diversity were negatively associated with the abundance index of PUUV-positive bank voles, which, in turn, showed a positive association with human disease incidence. Our results suggest certain predators, high proportion of young bank vole individuals and a diverse rodent community, may reduce PUUV risk for humans through their negative impacts on the abundance of infected bank voles.</span></p>

opencc-zeroApr 2023View details →
zenodo36/100

Journal metrics as predictors of Research Excellence Framework 2021 results: Comparison of impact factor quartiles and Finnish expert-ratings - dataset

<p>This dataset accompanies the conference submission &#39;Journal metrics as predictors of Research Excellence Framework 2021 results: Comparison of impact factor quartiles and Finnish expert-ratings&#39;. It contains the data in CSV format, one file per unit of analysis (Units of Assessment, Higher Education Institutions, and Subject Areas).</p> <p>The format of the UoA file is as follows (the other two files are analogous):</p> <ul> <li> <p>institution_name: name of higher education institution (e.g. university)</p> </li> <li> <p>unit_of_assessment_name: UoA name in REF (https://www.ref.ac.uk/panels/units-of-assessment/)</p> </li> <li> <p>main_panel: main panel in REF</p> </li> <li> <p>multiple_submission_letter: blank unless submitted to multiple panels.Exceptionally HEIs may have requested permission to make <a href="https://ref.ac.uk/publications-and-reports/invitation-to-make-requests-for-multiple-submissions-exception-from-submission-for-small-units-and-for-impact-case-studies-requiring-security-clearance/">two submissions from the same UoA to different panels</a>.</p> </li> <li> <p>multiple_submission_name: blank unless submitted to multiple panels</p> </li> <li> <p>non_english: number of articles in language other than English</p> </li> <li> <p>jufo_score_uoa: JUFO score (see paper for calculation details) of UoA</p> </li> <li> <p>jif_score_uoa: JIF score (see paper for calculation details) of UoA</p> </li> <li> <p>ref_score_uoa: REF score (see paper for calculation details) of UoA</p> </li> </ul>

opencc-by-4.0Apr 2023View details →

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Allen Brain Atlas

Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

Annotated Behaviour and Observability Dataset (ABODe)

ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

DANDI Archive for NWB datasets

DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

International Brain Laboratory public data

The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

OpenNeuro

OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record

ScienceDex for faculty

Your academic CV and NIH biosketch

Make your CV in your school's format and your NIH biosketch from it, then download both as Word files.