Institution
Poznan University of Medical Sciences
Education•Poznań, Poland•
About: Poznan University of Medical Sciences is a education organization based out in Poznań, Poland. It is known for research contribution in the topics: Population & Medicine. The organization has 5021 authors who have published 10098 publications receiving 145607 citations.
Topics: Population, Medicine, Cancer, Diabetes mellitus, Pregnancy
Papers published on a yearly basis
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University of Limerick1, University College Cork2, University of Plymouth3, French Institute of Health and Medical Research4, Centre national de la recherche scientifique5, École Normale Supérieure6, Poznan University of Medical Sciences7, University of Ulm8, Leibniz Association9, Wageningen University and Research Centre10, University of Auckland11, Institut national de la recherche agronomique12, Medical University of Vienna13, University of Erlangen-Nuremberg14, Public Health Research Institute15
TL;DR: There are multiple potentially modifiable determinants of malnutrition however strong robust evidence is lacking for the majority of determinants.
120 citations
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Heidelberg University1, University of Bonn2, Aarhus University3, Poznan University of Medical Sciences4, Ludwig Maximilian University of Munich5, Utrecht University6, Aarhus University Hospital7, University of Duisburg-Essen8, University of Kiel9, Erasmus University Rotterdam10, Erasmus University Medical Center11, Max Planck Society12, University of California, Los Angeles13, Charité14, University of Göttingen15, Forschungszentrum Jülich16, Medical Research Council17
TL;DR: In this article, the authors performed a genome-wide association study (GWAS) of 1169 clinically well characterized and ethnically homogeneous SCZ patients from a confined area of Western Europe (464 from Germany, 705 from The Netherlands) and 3714 ethnically matched controls (1272 and 2442, respectively).
Abstract: Recent molecular studies have implicated common alleles of small to moderate effect and rare alleles with larger effect sizes in the genetic architecture of schizophrenia (SCZ). It is expected that the reliable detection of risk variants with very small effect sizes can only be achieved through the recruitment of very large samples of patients and controls (that is tens of thousands), or large, potentially more homogeneous samples that have been recruited from confined geographical areas using identical diagnostic criteria. Applying the latter strategy, we performed a genome-wide association study (GWAS) of 1169 clinically well characterized and ethnically homogeneous SCZ patients from a confined area of Western Europe (464 from Germany, 705 from The Netherlands) and 3714 ethnically matched controls (1272 and 2442, respectively). In a subsequent follow-up study of our top GWAS results, we included an additional 2569 SCZ patients and 4088 controls (from Germany, The Netherlands and Denmark). Genetic variation in a region on chromosome 11 that contains the candidate genes AMBRA1, DGKZ, CHRM4 and MDK was significantly associated with SCZ in the combined sample (n=11 540; P=3.89 × 10−9, odds ratio (OR)=1.25). This finding was replicated in 23 206 independent samples of European ancestry (P=0.0029, OR=1.11). In a subsequent imaging genetics study, healthy carriers of the risk allele exhibited altered activation in the cingulate cortex during a cognitive control task. The area of interest is a critical interface between emotion regulation and cognition that is structurally and functionally abnormal in SCZ and bipolar disorder.
120 citations
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King's College London1, Geneva College2, University of Geneva3, Hoffmann-La Roche4, GlaxoSmithKline5, University of Bristol6, Pfizer7, Poznan University of Medical Sciences8, University of Zagreb9, Jožef Stefan Institute10, University of Bonn11, Aarhus University Hospital12, Cardiff University13, Université libre de Bruxelles14, University of Alberta15, Lundbeck16, Dalhousie University17
TL;DR: Testing whether genetic information could inform the selection of the best drug for patients with depression, Rudolf Uher and colleagues searched for genetic variants that could predict clinically meaningful responses to two major groups of antidepressants.
Abstract: Background
It has been suggested that outcomes of antidepressant treatment for major depressive disorder could be significantly improved if treatment choice is informed by genetic data. This study aims to test the hypothesis that common genetic variants can predict response to antidepressants in a clinically meaningful way.
Methods and Findings
The NEWMEDS consortium, an academia–industry partnership, assembled a database of over 2,000 European-ancestry individuals with major depressive disorder, prospectively measured treatment outcomes with serotonin reuptake inhibiting or noradrenaline reuptake inhibiting antidepressants and available genetic samples from five studies (three randomized controlled trials, one part-randomized controlled trial, and one treatment cohort study). After quality control, a dataset of 1,790 individuals with high-quality genome-wide genotyping provided adequate power to test the hypotheses that antidepressant response or a clinically significant differential response to the two classes of antidepressants could be predicted from a single common genetic polymorphism. None of the more than half million genetic markers significantly predicted response to antidepressants overall, serotonin reuptake inhibitors, or noradrenaline reuptake inhibitors, or differential response to the two types of antidepressants (genome-wide significance p<5×10−8). No biological pathways were significantly overrepresented in the results. No significant associations (genome-wide significance p<5×10−8) were detected in a meta-analysis of NEWMEDS and another large sample (STAR*D), with 2,897 individuals in total. Polygenic scoring found no convergence among multiple associations in NEWMEDS and STAR*D.
Conclusions
No single common genetic variant was associated with antidepressant response at a clinically relevant level in a European-ancestry cohort. Effects specific to particular antidepressant drugs could not be investigated in the current study.
120 citations
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Stanford University1, Harvard University2, Herlev Hospital3, University of Calgary4, Ludwig Maximilian University of Munich5, University of Hamburg6, European Institute of Oncology7, Katholieke Universiteit Leuven8, University College London9, University of British Columbia10, Free University of Berlin11, Poznan University of Medical Sciences12, Medical University of Vienna13, Copenhagen University Hospital14
TL;DR: The analysis presented suggests that patients with baseline body weight of <77 kg or baseline platelets of<150 000/µl may benefit from a starting dose of 200 mg/day, which was the most commonly administered dose in the ENGOT-OV16/NOVA trial.
120 citations
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TL;DR: A panel of expert dermatologists and paediatricians from across Europe aimed to provide a consensus on infant bathing and cleansing and found that guidelines for skin care in newborns are limited.
Abstract: Background Development of the skin barrier continues up to 12 months after birth; therefore, care must be taken when cleansing and bathing infants’ skin. Available guidelines for skin care in newborns are, however, limited. In 2007, the 1st European Round Table meeting on ‘Best Practice for Infant Cleansing’ was held, at which a panel of expert dermatologists and paediatricians from across Europe aimed to provide a consensus on infant bathing and cleansing.
Outcomes Based on discussions at the meeting and a comprehensive literature review, the panel developed a series of recommendations relating to several aspects of infant skin care, including initial and routine bathing, safety while bathing, and post-bathing procedures. The panel also focused on the use of liquid cleansers in bathing, particularly relating to the benefits of liquid cleansers over water alone, and the criteria that should be used when choosing an appropriate liquid cleanser for infants. Alkaline soaps have numerous disadvantages compared with liquid cleansers, with effects on skin pH and lipid content, as well as causing skin drying and irritation. Liquid cleansers used in newborns should have documented evidence of their mildness on skin and eyes, and those containing an emollient may have further benefits. Finally, the panel discussed seasonal differences in skin care, and issues relating to infants at high risk of atopic dermatitis. The panel further discussed the need of clinical studies to investigate the impact of liquid cleansers on skin physiology parameters on newborns’ and infants’ skin.
Conclusions Bathing is generally superior to washing, provided basic safety procedures are followed, and has psychological benefits for the infant and parents. When bathing infants with a liquid cleanser, a mild one not altering the normal pH of the skin surface or causing irritation to skin or eyes should be chosen.
Conflicts of interest
M.J. Cork and F. Vanaclocha are advisors to Johnson and Johnson. U. Blume-Peytavi is a member of the advisory board of the ‘Penaten Beirat’, Johnson & Johnson, Germany. J. Faergemann, C. Gelmetti, J. Szczapa declared to have no conflict of interest.
119 citations
Authors
Showing all 5055 results
Name | H-index | Papers | Citations |
---|---|---|---|
Thorkild I. A. Sørensen | 114 | 747 | 60060 |
Ingrid E. Scheffer | 113 | 585 | 53463 |
Kim A. Papp | 82 | 361 | 28368 |
Carle Paul | 72 | 437 | 21426 |
Sirkka Keinänen-Kiukaanniemi | 69 | 372 | 29268 |
George R. Blumenschein | 64 | 358 | 21605 |
Janusz K. Rybakowski | 59 | 485 | 14097 |
Marie-Claude Morice | 58 | 279 | 22264 |
Joerg Lahann | 56 | 262 | 13872 |
Roman Kaliszan | 54 | 282 | 9089 |
Karl-Heinz Herzig | 54 | 321 | 12623 |
Matti Uusitupa | 54 | 123 | 34387 |
Joanna Hauser | 53 | 196 | 9860 |
Maria Siemionow | 47 | 350 | 8055 |
Sakari Reitamo | 46 | 148 | 7381 |