scispace - formally typeset
Search or ask a question
Institution

University of Turku

EducationTurku, Finland
About: University of Turku is a education organization based out in Turku, Finland. It is known for research contribution in the topics: Population & Galaxy. The organization has 16296 authors who have published 45124 publications receiving 1505428 citations. The organization is also known as: Turun yliopisto & Åbo universitet.


Papers
More filters
Journal ArticleDOI
TL;DR: The results present rhinoviruses as important inducers of wheezing even in infancy and call for reevaluation of the role of rhinOViruses in the development of asthma.
Abstract: Background: Although known as common causes of upper respiratory infections, rhinoviruses, enteroviruses, and corona-viruses are poorly studied as inducers of wheezing in infants, and their possible role in the development of childhood asthma has not been investigated. Objective: The purposes of this study were to assess the occurrence of RV, enterovirus, and coronavirus infections in wheezing infants and to evaluate the association of these viral findings with early school-age asthma. Methods: In 1999, outcome in relation to asthma was studied in 82 of 100 initially recruited children who had been hospitalized for wheezing in infancy during the period 1992-1993. In 2000, etiologic viral studies regarding the index episode of wheezing were supplemented by rhinovirus, enterovirus, and coronavirus detection by RT-PCR from frozen nasopharyngeal aspirates in 81 of the children for whom adequate samples were available. Of these children, 66 had participated in the follow-up in 1999. Results: Rhinoviruses were identified in 27 (33%) of the 81 children, enteroviruses in 10 (12%), and coronaviruses in none. Rhinoviruses were present as single viral findings in 22 (81%) of the 27 rhinovirus-positive cases, and rhinovirus infections were associated with the presence of atopic dermatitis in infancy. Enteroviruses were commonly encountered in mixed infections and had no association with atopy. As single viral findings, rhinoviruses were associated with the development of asthma ( P = .047; odds ratio, 4.14; 95% CI, 1.02-16.77 versus rhinovirus-negative cases [by logistic regression adjusted for age, sex, and atopic dermatitis on entry)]. Conclusion: Our results present rhinoviruses as important inducers of wheezing even in infancy. The association with atopy and subsequent asthma calls for reevaluation of the role of rhinoviruses in the development of asthma. (J Allergy Clin Immunol 2003;111:66-71.)

406 citations

Journal ArticleDOI
TL;DR: The development and testing of the Nurse Competence Scale is described, an instrument with which the level of nurse competence can be assessed in different hospital work environments and the results provide strong evidence of the reliability and validity of the nurse competence Scale.
Abstract: Background. Self-assessment assists nurses to maintain and improve their practice by identifying their strengths and areas that may need to be further developed. Professional competence profiles encourage them to take an active part in the learning process of continuing education. Although competence recognition offers a way to motivate practising nurses to produce quality care, few measuring tools are available for this purpose. Aim. This paper describes the development and testing of the Nurse Competence Scale, an instrument with which the level of nurse competence can be assessed in different hospital work environments. Methods. The categories of the Nurse Competence Scale were derived from Benner's From Novice to Expert competency framework. A seven-step approach, including literature review and six expert groups, was used to identify and validate the indicators of nurse competence. After a pilot test, psychometric testing of the Nurse Competence Scale (content, construct and concurrent validity, and internal consistency) was undertaken with 498 nurses. The 73-item scale consists of seven categories, with responses on a visual analogy scale format. The frequency of using competencies was additionally tested with a four-point scale. Results. Self-assessed overall scores indicated a high level of competence across categories. The Nurse Competence Scale data were normally distributed. The higher the frequency of using competencies, the higher was the self-assessed level of competence. Age and length of work experience had a positive but not very strong correlation with level of competence. According to the item analysis, the categories of the Nurse Competence Scale showed good internal consistency. Conclusion. The results provide strong evidence of the reliability and validity of the Nurse Competence Scale.

406 citations

Journal ArticleDOI
TL;DR: A web application is implemented that uses key functions of R‐package SynergyFinder, and provides not only the flexibility of using multiple synergy scoring models, but also a user‐friendly interface for visualizing the drug combination landscapes in an interactive manner.
Abstract: Summary Rational design of drug combinations has become a promising strategy to tackle the drug sensitivity and resistance problem in cancer treatment. To systematically evaluate the pre-clinical significance of pairwise drug combinations, functional screening assays that probe combination effects in a dose-response matrix assay are commonly used. To facilitate the analysis of such drug combination experiments, we implemented a web application that uses key functions of R-package SynergyFinder, and provides not only the flexibility of using multiple synergy scoring models, but also a user-friendly interface for visualizing the drug combination landscapes in an interactive manner. Availability and implementation The SynergyFinder web application is freely accessible at https://synergyfinder.fimm.fi ; The R-package and its source-code are freely available at http://bioconductor.org/packages/release/bioc/html/synergyfinder.html . Contact jing.tang@helsinki.fi.

405 citations

Journal ArticleDOI
TL;DR: These findings provide new regions for investigation into the pathogenesis of prostate cancer and demonstrate the usefulness of combining ancestrally diverse populations to discover risk loci for disease.
Abstract: Genome-wide association studies (GWAS) have identified 76 variants associated with prostate cancer risk predominantly in populations of European ancestry. To identify additional susceptibility loci for this common cancer, we conducted a meta-analysis of > 10 million SNPs in 43,303 prostate cancer cases and 43,737 controls from studies in populations of European, African, Japanese and Latino ancestry. Twenty-three new susceptibility loci were identified at association P < 5 × 10(-8); 15 variants were identified among men of European ancestry, 7 were identified in multi-ancestry analyses and 1 was associated with early-onset prostate cancer. These 23 variants, in combination with known prostate cancer risk variants, explain 33% of the familial risk for this disease in European-ancestry populations. These findings provide new regions for investigation into the pathogenesis of prostate cancer and demonstrate the usefulness of combining ancestrally diverse populations to discover risk loci for disease.

404 citations

Journal ArticleDOI
Virginie J. M. Verhoeven1, Pirro G. Hysi2, Robert Wojciechowski3, Robert Wojciechowski4, Qiao Fan5, Jeremy A. Guggenheim6, René Höhn7, Stuart MacGregor8, Alex W. Hewitt9, Alex W. Hewitt10, Abhishek Nag2, Ching-Yu Cheng11, Ching-Yu Cheng5, Ekaterina Yonova-Doing2, Xin Zhou5, M. Kamran Ikram5, M. Kamran Ikram11, Gabriëlle H.S. Buitendijk1, George McMahon12, John P. Kemp12, Beate St Pourcain12, Claire L. Simpson4, Kari-Matti Mäkelä13, Terho Lehtimäki13, Mika Kähönen13, Andrew D. Paterson14, S. Mohsen Hosseini14, Hoi Suen Wong14, Liang Xu15, Jost B. Jonas16, Olavi Pärssinen17, Juho Wedenoja18, Shea Ping Yip6, Daniel W.H. Ho19, Daniel W.H. Ho6, Chi Pui Pang19, Li Jia Chen19, Kathryn P. Burdon20, Jamie E Craig20, Barbara E.K. Klein21, Ronald Klein21, Toomas Haller22, Andres Metspalu22, Chiea Chuen Khor5, Chiea Chuen Khor23, E-Shyong Tai5, Tin Aung11, Tin Aung5, Eranga N. Vithana11, Wan Ting Tay11, Veluchamy A. Barathi5, Veluchamy A. Barathi11, Myopia (Cream), Peng Chen5, Ruoying Li5, Jiemin Liao5, Yingfeng Zheng11, Rick Twee-Hee Ong5, Angela Döring, Complications Trial24, Complications (Dcct)25, David M. Evans12, Nicholas J. Timpson12, Annemieke J.M.H. Verkerk1, Thomas Meitinger24, Olli T. Raitakari26, Felicia Hawthorne25, Tim D. Spector2, Lennart C. Karssen1, Mario Pirastu27, Federico Murgia27, Wei Ang10, Aniket Mishra8, Grant W. Montgomery8, Craig E. Pennell10, Phillippa M. Cumberland28, Ioana Cotlarciuc29, Paul Mitchell30, Jie Jin Wang9, Jie Jin Wang30, Maria Schache9, Sarayut Janmahasatian31, Robert P. Igo31, Jonathan H. Lass31, Emily Y. Chew4, Sudha K. Iyengar31, Theo G. M. F. Gorgels32, Igor Rudan33, Caroline Hayward33, Alan F. Wright33, Ozren Polasek34, Zoran Vatavuk35, James F. Wilson33, Brian W Fleck36, Tanja Zeller, Alireza Mirshahi7, Christian P. Müller, André G. Uitterlinden1, Fernando Rivadeneira1, Johannes R. Vingerling1, Albert Hofman1, Ben A. Oostra1, Najaf Amin1, Arthur A.B. Bergen, Yik Ying Teo5, Jugnoo S Rahi28, Jugnoo S Rahi37, Jugnoo S Rahi8, Veronique Vitart33, Cathy Williams12, Paul N. Baird9, Tien Yin Wong5, Tien Yin Wong11, Konrad Oexle24, Norbert Pfeiffer7, David A. Mackey10, David A. Mackey9, Terri L. Young25, Cornelia M. van Duijn1, Seang-Mei Saw5, Seang-Mei Saw38, Seang-Mei Saw11, Joan E. Bailey-Wilson4, Joan E. Bailey-Wilson38, Dwight Stambolian38, Caroline C W Klaver38, Caroline C W Klaver1, Christopher J Hammond38, Christopher J Hammond2 
TL;DR: The CREAM consortium conducted genome-wide meta-analyses, which identified 16 new loci for refractive error in individuals of European ancestry and 8 were shared with Asians, and identified 8 additional associated loci.
Abstract: Refractive error is the most common eye disorder worldwide and is a prominent cause of blindness Myopia affects over 30% of Western populations and up to 80% of Asians The CREAM consortium conducted genome-wide meta-analyses, including 37,382 individuals from 27 studies of European ancestry and 8,376 from 5 Asian cohorts We identified 16 new loci for refractive error in individuals of European ancestry, of which 8 were shared with Asians Combined analysis identified 8 additional associated loci The new loci include candidate genes with functions in neurotransmission (GRIA4), ion transport (KCNQ5), retinoic acid metabolism (RDH5), extracellular matrix remodeling (LAMA2 and BMP2) and eye development (SIX6 and PRSS56) We also confirmed previously reported associations with GJD2 and RASGRF1 Risk score analysis using associated SNPs showed a tenfold increased risk of myopia for individuals carrying the highest genetic load Our results, based on a large meta-analysis across independent multiancestry studies, considerably advance understanding of the mechanisms involved in refractive error and myopia

404 citations


Authors

Showing all 16461 results

NameH-indexPapersCitations
Kari Alitalo174817114231
Mika Kivimäki1661515141468
Jaakko Kaprio1631532126320
Veikko Salomaa162843135046
Markus W. Büchler148154593574
Eugene C. Butcher14644672849
Steven Williams144137586712
Terho Lehtimäki1421304106981
Olli T. Raitakari1421232103487
Pim Cuijpers13698269370
Jeroen J. Bax132130674992
Sten Orrenius13044757445
Aarno Palotie12971189975
Stefan W. Hell12757765937
Carlos López-Otín12649483933
Network Information
Related Institutions (5)
University of Helsinki
113.1K papers, 4.6M citations

97% related

Lund University
124.6K papers, 5M citations

96% related

University of Copenhagen
149.7K papers, 5.9M citations

96% related

University of Amsterdam
140.8K papers, 5.9M citations

94% related

University of Manchester
168K papers, 6.4M citations

92% related

Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
2023102
2022290
20212,673
20202,688
20192,407
20182,189