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367 results for “finnish”
Figure 1 from: Hyvärinen M-T, Väinölä R, Väre H, Ståhls-Mäkelä G, Sihvonen P, Kuusijärvi A, Myllys L, Kröger B, Heikkinen M, Juslén A, Oinonen M, Schulman L (2020) General Collections Policy of the Finnish Museum of Natural History. Research Ideas and Outcomes 6: e58167. https://doi.org/10.3897/rio.6.e58167
Figure 1 The collection policies of the Finnish Museum of Natural History. * Not yet published
Data from: Genome-wide meta-analysis of sciatica in Finnish population
Sciatica or the sciatic syndrome is a common and often disabling low back disorder in the working-age population. It has a relatively high heritability but poorly understood molecular mechanisms. The Finnish population is a genetic isolate where small founder population and bottleneck events have led to enrichment of certain rare and low frequency variants. We performed here the first genome-wide association (GWAS) and meta-analysis of sciatica. The meta-analysis was conducted across two GWAS covering 291 Finnish sciatica cases and 3671 controls genotyped and imputed at 7.7 million autosomal variants. The most promising loci (p<1x10-6) were replicated in 776 Finnish sciatica patients and 18,489 controls. We identified five intragenic variants, with relatively low frequencies, at two novel loci associated with sciatica at genome-wide significance. These included chr9:14344410:I (rs71321981) at 9p22.3 (NFIB gene; p=1.30x10-8, MAF=0.08) and four variants at 15q21.2: rs145901849, rs80035109, rs190200374 and rs117458827 (MYO5A; p=1.34x10-8, MAF=0.06; p=2.32x10-8, MAF=0.07; p=3.85x10-8, MAF=0.06; p=4.78x10-8, MAF=0.07, respectively). The most significant association in the meta-analysis, a single base insertion rs71321981 within the regulatory region of the transcription factor NFIB, replicated in an independent Finnish population sample (p=0.04). Despite identifying 15q21.2 as a promising locus, we were not able to replicate it. It was differentiated; the lead variants within 15q21.2 were more frequent in Finland (6-7%) than in other European populations (1-2%). Imputation accuracies of the three significantly associated variants (chr9:14344410:I, rs190200374, and rs80035109) were validated by genotyping. In summary, our results suggest a novel locus, 9p22.3 (NFIB), which may be involved in susceptibility to sciatica. In addition, another locus, 15q21.2, emerged as a promising one, but failed to replicate.
Finnish inventory data of underwater marine biodiversity
<p>Dataset related to the article <em>Finnish inventory data of underwater marine biodiversity</em>. The data are described in detail in the article. The dataset contains underwater biodiversity observations from the Finnish marine area collected using multiple methods. We provide two datasets, one mainly containing vegetation mapping data and one focused on benthic fauna. In addition we provide a summary table and all custom code used to produce the data.</p>
Wild Berry image dataset collected in Finnish forests and peatlands using drones
<p>Berry picking has long-standing traditions in Finland, yet it is challenging and can potentially be dangerous. The integration of drones equipped with advanced imaging techniques represents a transformative leap forward, optimising harvests and promising sustainable practices. We propose WildBe, the first image dataset of wild berries captured in peatlands and under the canopy of Finnish forests using drones. Unlike previous and related datasets, WildBe includes new varieties of berries, such as bilberries, cloudberries, lingonberries, and crowberries, captured under severe light variations and in cluttered environments.</p>
The Finnish National Study to Facilitate Patient Access to Targeted Anti-cancer Drugs
ClinicalTrials.gov study NCT05159245. IPD Sharing: YES. Countries: 1. Publications: 0.
The Finnish Faecal Microbiota Transplantation Study (FINFMT)
ClinicalTrials.gov study NCT03732131. IPD Sharing: NO. Countries: 1. Publications: 0.
Finnish Genetic Study for Arrhythmic Events
ClinicalTrials.gov study NCT02075866. IPD Sharing: Not stated. Countries: 1. Publications: 0.
FINnish CardioVersion Study II
ClinicalTrials.gov study NCT02850679. IPD Sharing: UNDECIDED. Countries: 1. Publications: 0.
Reliability and Validity of the Finnish Version of the Prothesis Evaluation Questionnaire
ClinicalTrials.gov study NCT02436148. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Finnish Prehospital Whole Blood Study
ClinicalTrials.gov study NCT05744583. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Implementation of Finnish Prehospital Stroke Scale to Emergency Medical Services
ClinicalTrials.gov study NCT03520335. IPD Sharing: UNDECIDED. Countries: 1. Publications: 0.
First Line Treatment Trial in Multiple Myeloma, Finnish Myeloma Group- Multiple Myeloma 02
ClinicalTrials.gov study NCT01790737. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Hand Hygiene Intervention Study in Finnish Garrison
ClinicalTrials.gov study NCT01887730. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Finnish Patient-Reported Outcomes Initiative for Shoulder and Elbow
ClinicalTrials.gov study NCT05598541. IPD Sharing: NO. Countries: 1. Publications: 0.
Finnish Imaging of Shoulder Trauma
ClinicalTrials.gov study NCT05800184. IPD Sharing: NO. Countries: 1. Publications: 0.
Data from: Genome-wide meta-analysis of sciatica in Finnish population
Open the record for dataset details and reuse information.
Oxidative Stress and Inflammation-Related mRNAs Are Elevated in Serum of a Finnish Wet Age-Related Macular Degeneration Cohort
GEO Series GSE273435. Homo sapiens. 124 samples. Type: Expression profiling by high throughput sequencing.
RNA analysis in Finnish Schizophrenia Families
GEO Series GSE48072. Homo sapiens. 66 samples. Type: Expression profiling by array.
Comparative Genomics of Bordetella pertussis Reveals Progressive Gene Loss in Finnish Strains
GEO Series GSE8092. Bordetella pertussis. 26 samples. Type: Genome variation profiling by array.
Epigenetic differences in long non-coding RNA expression in Finnish and Russian Karelia teenagers with contrasting risk of allergy and asthma
GEO Series GSE200158. Homo sapiens. 144 samples. Type: Expression profiling by array; Non-coding RNA profiling by array.
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