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Brunner, Edgar
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Brunner, Edgar
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Brunner, Edgar
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Brunner, E.
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2008Journal Article [["dc.bibliographiccitation.firstpage","416"],["dc.bibliographiccitation.issue","2"],["dc.bibliographiccitation.journal","Computational Statistics & Data Analysis"],["dc.bibliographiccitation.lastpage","427"],["dc.bibliographiccitation.volume","53"],["dc.contributor.author","Ahmad, Mohiuddin"],["dc.contributor.author","Werner, C."],["dc.contributor.author","Brunner, E."],["dc.date.accessioned","2018-11-07T11:07:56Z"],["dc.date.available","2018-11-07T11:07:56Z"],["dc.date.issued","2008"],["dc.description.abstract","A one sample statistic is derived for the analysis of repeated measures design when the data are multivariate normal and the dimension, d, can be large compared to the sample size, n, i.e. d > n. Quadratic and bilinear forms are used to define the statistic based on Box's approximation [Box, G.E.P., 1954. Some theorems on quadratic forms applied in the study of analysis of variance problems 1: Effect of inequality of variance in the one-way classification. Annals of Mathematical Statistics 25 (2), 290-302]. The statistic has an approximate x(f)(2) distribution, even for moderately large n. One of the main advantages of the statistic is that it can be used both for unstructured and factorially structured repeated measures designs. In the asymptotic derivations, it is assumed that IT -> infinity while d remains finite and fixed. However, it is demonstrated through simulations that for n as small as 10, the new statistic very closely approximates the target distribution, unaffected by even large values of d (d > n). The application is illustrated using a sleep lab example with n = 10, d = 18. (C) 2008 Elsevier B.V. All rights reserved."],["dc.identifier.doi","10.1016/j.csda.2008.08.013"],["dc.identifier.isi","000261670000015"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/6062"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/52683"],["dc.notes.intern","Merged from goescholar"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Elsevier Science Bv"],["dc.relation.issn","0167-9473"],["dc.rights","Goescholar"],["dc.rights.uri","https://goescholar.uni-goettingen.de/licenses"],["dc.title","Analysis of high-dimensional repeated measures designs: The one sample case"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]Details DOI WOS2013Journal Article [["dc.bibliographiccitation.firstpage","192"],["dc.bibliographiccitation.issue","1"],["dc.bibliographiccitation.journal","Diagnostics"],["dc.bibliographiccitation.lastpage","209"],["dc.bibliographiccitation.volume","3"],["dc.contributor.author","Lange, Katharina"],["dc.contributor.author","Brunner, Edgar"],["dc.date.accessioned","2019-07-09T11:54:17Z"],["dc.date.available","2019-07-09T11:54:17Z"],["dc.date.issued","2013"],["dc.description.abstract","The accuracy of diagnostic tests with binary end-points is most frequently measured by sensitivity and specificity. However, from the clinical perspective, the main purpose of a diagnostic agent is to assess the probability of a patient actually being diseased and hence predictive values are more suitable here. As predictive values depend on the pre-test probability of disease, we provide a method to take risk factors influencing the patient’s prior probability of disease into account, when calculating predictive values. Furthermore, approaches to assess confidence intervals and a methodology to compare predictive values by statistical tests are presented. Hereby the methods can be used to analyze predictive values of factorial diagnostic trials, such as multi-modality, multi-reader-trials. We further performed a simulation study assessing length and coverage probability for different types of confidence intervals, and we present the R-Package facROC that can be used to analyze predictive values in factorial diagnostic trials in particular. The methods are applied to a study evaluating CT-angiography as a noninvasive alternative to coronary angiography for diagnosing coronary artery disease. Hereby the patients’ symptoms are considered as risk factors influencing the respective predictive values."],["dc.identifier.doi","10.3390/diagnostics3010192"],["dc.identifier.fs","602016"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/8764"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/60613"],["dc.language.iso","en"],["dc.notes.intern","Merged from goescholar"],["dc.relation.issn","2075-4418"],["dc.rights","CC BY 3.0"],["dc.rights.uri","https://creativecommons.org/licenses/by/3.0"],["dc.title","Analysis of Predictive Values Based on Individual Risk Factors in Multi-Modality Trials"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]Details DOI2012-09Journal Article [["dc.bibliographiccitation.issue","12"],["dc.bibliographiccitation.journal","Journal of Statistical Software"],["dc.bibliographiccitation.volume","50"],["dc.contributor.author","Noguchi, Kimihiro"],["dc.contributor.author","Gel, Yulia R."],["dc.contributor.author","Brunner, Edgar"],["dc.contributor.author","Konietschke, Frank"],["dc.date.accessioned","2019-07-10T08:14:06Z"],["dc.date.available","2019-07-10T08:14:06Z"],["dc.date.issued","2012-09"],["dc.description.abstract","Longitudinal data from factorial experiments frequently arise in various elds of study, ranging from medicine and biology to public policy and sociology. In most practical situations, the distribution of observed data is unknown and there may exist a number of atypical measurements and outliers. Hence, use of parametric and semiparametric procedures that impose restrictive distributional assumptions on observed longitudinal samples becomes questionable. This, in turn, has led to a substantial demand for statistical procedures that enable us to accurately and reliably analyze longitudinal measurements in factorial experiments with minimal conditions on available data, and robust nonparametric methodology o ering such a possibility becomes of particular practical importance. In this article, we introduce a new R package nparLD which provides statisticians and researchers from other disciplines an easy and user-friendly access to the most up-todate robust rank-based methods for the analysis of longitudinal data in factorial settings. We illustrate the implemented procedures by case studies from dentistry, biology, and medicine."],["dc.format.extent","23"],["dc.identifier.fs","592126"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/9492"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/61433"],["dc.language.iso","en"],["dc.notes.intern","Merged from goescholar"],["dc.relation.issn","1548-7660"],["dc.relation.orgunit","Universitätsmedizin Göttingen"],["dc.rights","CC BY 3.0"],["dc.rights.uri","http://creativecommons.org/licenses/by/3.0"],["dc.subject.ddc","610"],["dc.title","nparLD: An R Software Package for the Nonparametric Analysis of Longitudinal Data in Factorial Experiments"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]Details2020Journal Article [["dc.bibliographiccitation.journal","International Statistical Review"],["dc.contributor.affiliation","Konietschke, Frank; 2\r\nInstitute of Biometry and Clinical Epidemiology\r\nCharité\r\nBerlin Germany"],["dc.contributor.affiliation","Bathke, Arne C.; 3\r\nIntelligent Data Analytics (IDA) Lab\r\nSalzburg Austria"],["dc.contributor.affiliation","Pauly, Markus; 4\r\nFaculty of Statistics\r\nTU Dortmund University\r\nDortmund Germany"],["dc.contributor.author","Brunner, Edgar"],["dc.contributor.author","Konietschke, Frank"],["dc.contributor.author","Bathke, Arne C."],["dc.contributor.author","Pauly, Markus"],["dc.date.accessioned","2021-04-14T08:31:29Z"],["dc.date.available","2021-04-14T08:31:29Z"],["dc.date.issued","2020"],["dc.date.updated","2022-02-09T13:21:26Z"],["dc.description.abstract","Summary Rank‐based inference methods are applied in various disciplines, typically when procedures relying on standard normal theory are not justifiable. Various specific rank‐based methods have been developed for two and more samples and also for general factorial designs (e.g. Kruskal–Wallis test or Akritas–Arnold–Brunner test). It is the aim of the present paper (1) to demonstrate that traditional rank procedures for several samples or general factorial designs may lead to surprising results in case of unequal sample sizes as compared with equal sample sizes, (2) to explain why this is the case and (3) to provide a way to overcome these disadvantages. Theoretical investigations show that the surprising results can be explained by considering the non‐centralities of the test statistics, which may be non‐zero for the usual rank‐based procedures in case of unequal sample sizes, while they may be equal to 0 in case of equal sample sizes. A simple solution is to consider unweighted relative effects instead of weighted relative effects. The former effects are estimated by means of the so‐called pseudo‐ranks, while the usual ranks naturally lead to the latter effects. A real data example illustrates the practical meaning of the theoretical discussions."],["dc.description.sponsorship","Fonds zur Förderung der wissenschaftlichen Forschung http://dx.doi.org/10.13039/501100002428"],["dc.description.sponsorship","I 2697‐N31"],["dc.description.sponsorship","Deutsche Forschungsgemeinschaft http://dx.doi.org/10.13039/501100001659"],["dc.identifier.doi","10.1111/insr.12418"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/83611"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-399"],["dc.relation.eissn","1751-5823"],["dc.relation.issn","0306-7734"],["dc.rights","This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes."],["dc.title","Ranks and Pseudo‐ranks—Surprising Results of Certain Rank Tests in Unbalanced Designs"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]Details DOI2012Journal Article [["dc.bibliographiccitation.firstpage","3727"],["dc.bibliographiccitation.issue","1743"],["dc.bibliographiccitation.journal","Proceedings of The Royal Society B Biological Sciences"],["dc.bibliographiccitation.lastpage","3735"],["dc.bibliographiccitation.volume","279"],["dc.contributor.author","Benhaiem, Sarah"],["dc.contributor.author","Hofer, Heribert"],["dc.contributor.author","Kramer-Schadt, Stephanie"],["dc.contributor.author","Brunner, Edgar"],["dc.contributor.author","East, Marion L."],["dc.date.accessioned","2018-11-07T09:05:46Z"],["dc.date.available","2018-11-07T09:05:46Z"],["dc.date.issued","2012"],["dc.description.abstract","Within-brood or -litter dominance provides fitness-related benefits if dominant siblings selfishly skew access to food provided by parents in their favour. Models of facultative siblicide assume that dominants exert complete control over their subordinate sibling's access to food and that control is maintained, irrespective of the subordinate's hunger level. By contrast, a recent functional hypothesis suggests that subordinates should contest access to food when the cost of not doing so is high. Here, we show that within spotted hyena (Crocuta crocuta) twin litters, dominants most effectively skew access to maternal milk in their favour when their aggression prompts a highly submissive response. When hungry, subordinates were less submissive in response to aggression, thereby decreasing lost suckling time and increasing suckling time lost by dominants. In a species where adult females socially dominate adult males, juvenile females were more often dominant than males in mixed-sex litters, and subordinate sisters used more effective counter-tactics against dominant brothers than subordinate brothers against dominant sisters. Our results provide, to our knowledge, the first evidence in a mammal that dominant offspring in twin litters do not exert complete control over their sibling's access to resources (milk), and that sibling dominance relationships are influenced by sibling sex and training effects."],["dc.description.sponsorship","TAWIRI; IZW"],["dc.identifier.doi","10.1098/rspb.2012.0925"],["dc.identifier.isi","000307780400013"],["dc.identifier.pmid","22719032"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/10619"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/25403"],["dc.notes.intern","Merged from goescholar"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Royal Soc"],["dc.relation.issn","0962-8452"],["dc.rights","Goescholar"],["dc.rights.uri","https://goescholar.uni-goettingen.de/licenses"],["dc.title","Sibling rivalry: training effects, emergence of dominance and incomplete control"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]Details DOI PMID PMC WOS2002Journal Article [["dc.bibliographiccitation.firstpage","367"],["dc.bibliographiccitation.issue","3"],["dc.bibliographiccitation.journal","Sociological Methods & Research"],["dc.bibliographiccitation.lastpage","393"],["dc.bibliographiccitation.volume","30"],["dc.contributor.author","Domhof, S."],["dc.contributor.author","Brunner, E."],["dc.contributor.author","Osgood, D. W."],["dc.date.accessioned","2018-11-07T10:32:25Z"],["dc.date.available","2018-11-07T10:32:25Z"],["dc.date.issued","2002"],["dc.description.abstract","This article presents a nonparametric approach to analyzing research designs that include repeated observations on the same set of individuals or units, such as longitudinal panel studies. The data collected from different individuals are generally assumed to be independent, while several observations from the same individual or unit may, be dependent. The approach suggested in this study is nonparametric in the sense that only the distribution functions are used to define the treatment effects, and suggested procedures are extensions of well-established rank order methods. Missing observations are especially common in studies with repeated measures, and three strategies Jar addressing this problem are compared: complete case analysis, last observation carried forward, and complete set analysis. The authors demonstrate these methods with an analysis of age trends and sex differences in alcohol consumption in a sample of U.S. adolescents who completed questionnaires four times in the 7th through 10th grades."],["dc.identifier.doi","10.1177/0049124102030003004"],["dc.identifier.isi","000173298800004"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/12991"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/44343"],["dc.notes.intern","Merged from goescholar"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Sage Publications Inc"],["dc.relation.issn","0049-1241"],["dc.title","Rank procedures for repeated measures with missing values"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]Details DOI WOS2006Journal Article [["dc.bibliographiccitation.firstpage","2534"],["dc.bibliographiccitation.issue","7"],["dc.bibliographiccitation.journal","Biophysical Journal"],["dc.bibliographiccitation.lastpage","2547"],["dc.bibliographiccitation.volume","90"],["dc.contributor.author","Chen, T. W."],["dc.contributor.author","Lin, B. J."],["dc.contributor.author","Brunner, E."],["dc.contributor.author","Schild, Detlev"],["dc.date.accessioned","2018-11-07T10:00:35Z"],["dc.date.available","2018-11-07T10:00:35Z"],["dc.date.issued","2006"],["dc.description.abstract","Fluorescence imaging of bulk-stained tissue is a popular technique for monitoring the activities in a large population of cells. However, a precise quanti. cation of such experiments is often compromised by an ambiguity of background estimation. Although, in single-cell-staining experiments, background can be measured from a neighboring nonstained region, such a region often does not exist in bulk-stained tissue. Here we describe a novel method that overcomes this problem. In contrast to previous methods, we determined the background of a given region of interest (ROI) using the information contained in the temporal dynamics of its individual pixels. Since no information outside the ROI is needed, the method can be used regardless of the staining pro. le in the surrounding tissue. Moreover, we extend the method to deal with background inhomogeneities within a single ROI, a problem not yet solved by any of the currently available tools. We performed computer simulations to demonstrate the accuracy of our method and give example applications in ratiometric calcium imaging of bulk-stained olfactory bulb slices. Converting the fluorescence signals into [Ca2+] gives resting values consistent with earlier single-cell staining results, and odorant-induced [Ca2+] transients can be quantitatively compared in different cells. Using these examples we show that inaccurate background subtraction introduces large errors ( easily in the range of 100%) in the assessment of both resting [Ca2+] and [Ca2+] dynamics. The proposed method allows us to avoid such errors."],["dc.identifier.doi","10.1529/biophysj.105.070854"],["dc.identifier.isi","000235972100027"],["dc.identifier.pmid","16387783"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/7746"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/37835"],["dc.notes.intern","Merged from goescholar"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Biophysical Society"],["dc.relation.issn","0006-3495"],["dc.rights","Goescholar"],["dc.rights.uri","https://goescholar.uni-goettingen.de/licenses"],["dc.title","In situ background estimation in quantitative fluorescence imaging"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]Details DOI PMID PMC WOS2009Journal Article [["dc.bibliographiccitation.firstpage","2355"],["dc.bibliographiccitation.issue","18"],["dc.bibliographiccitation.journal","Bioinformatics"],["dc.bibliographiccitation.lastpage","2361"],["dc.bibliographiccitation.volume","25"],["dc.contributor.author","Latif, A. H. M. Mahbub"],["dc.contributor.author","Bretz, Frank"],["dc.contributor.author","Brunner, Edgar"],["dc.date.accessioned","2018-11-07T11:24:15Z"],["dc.date.available","2018-11-07T11:24:15Z"],["dc.date.issued","2009"],["dc.description.abstract","The main goal of microarray experiments is to select a small subset of genes that are differentially expressed among competing mRNA samples. For a given set of such mRNA samples, it is possible to consider a number of two-color cDNA microarray designs with a fixed number of arrays. Appropriate criteria can be used to select an efficient design from such a set of alternative experimental designs. In practice, however, microarray expression data often contain missing observations and the most efficient design ( with complete observations) for a specific setup may not be efficient in the presence of missing observations. In this article, we propose two criteria to address the robustness of microarray designs against missing observations. We demonstrate the simultaneous use of efficiency and robustness criteria to select good microarray designs for both one-factor and multi-factor experiments."],["dc.identifier.doi","10.1093/bioinformatics/btp407"],["dc.identifier.isi","000269607700010"],["dc.identifier.pmid","19570802"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/6061"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/56362"],["dc.notes.intern","Merged from goescholar"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Oxford Univ Press"],["dc.relation.issn","1367-4803"],["dc.rights","Goescholar"],["dc.rights.uri","https://goescholar.uni-goettingen.de/licenses"],["dc.title","Robustness considerations in selecting efficient two-color microarray designs"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]Details DOI PMID PMC WOS2009Journal Article [["dc.bibliographiccitation.firstpage","313"],["dc.bibliographiccitation.issue","3"],["dc.bibliographiccitation.journal","Lasers in Medical Science"],["dc.bibliographiccitation.lastpage","320"],["dc.bibliographiccitation.volume","24"],["dc.contributor.author","Sennhenn-Kirchner, Sabine"],["dc.contributor.author","Schwarz, Peter"],["dc.contributor.author","Schliephake, Henning"],["dc.contributor.author","Konietschke, Frank"],["dc.contributor.author","Brunner, Edgar"],["dc.contributor.author","Borg-von Zepelin, Margarete"],["dc.date.accessioned","2018-06-25T07:08:41Z"],["dc.date.available","2018-06-25T07:08:41Z"],["dc.date.issued","2009"],["dc.description.abstract","The different forms of superficial and systemic candidiasis are often associated with biofilm formation on surfaces of host tissues or medical devices. The biofilm formation of Candida spp., in general, necessitates significantly increased amounts of antifungal agents for therapy. Often the therapeutic effect is doubtful. A 5-day biofilm model with oral Candida isolates was established according to Chandra et al. (J Dent Res 80:903-908, 2001) on glass and titanium surfaces and was modified by Sennhenn-Kirchner et al. (Z Zahnärztl Implantol 3:45-51, 2007) to investigate different aspects unanswered in the field of dentistry. In this model, the efficacy of erbium:yttrium-aluminium-garnet (Er:YAG) light (2940 nm, 100 mJ, 10 Hz, 300 micros pulsed mode applied for 80 s) and diode laser light (810 nm, 1 W, continuous wave mode applied for 20 s with four repetitions after 30 s pauses each) was evaluated and compared to untreated controls. The photometric evaluation of the samples was completed by observations on morphological changes of yeast cells grown in the biofilm. Compared to the untreated controls Candida cells grown in mature in vitro biofilms were significantly reduced by both wavelengths investigated. Comparison between the different methods of laser treatment additionally revealed a significantly greater effect of the Er:YAG over the diode laser. Scanning electron microscopy findings proved that the diode laser light was effective in direct contact mode. In contrast, in the areas without direct contact, the fungal cells were left almost unchanged. The Er:YAG laser damaged the fungal cells to a great extent wherever it was applied."],["dc.identifier.doi","10.1007/s10103-008-0561-3"],["dc.identifier.pmid","18458992"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?goescholar/3106"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/15129"],["dc.language.iso","en"],["dc.notes.intern","Merged from goescholar"],["dc.notes.status","final"],["dc.relation.eissn","1435-604X"],["dc.rights","Goescholar"],["dc.rights.uri","https://goescholar.uni-goettingen.de/licenses"],["dc.title","Decontamination efficacy of erbium:yttrium–aluminium–garnet and diode laser light on oral Candida albicans isolates of a 5-day in vitro biofilm model"],["dc.type","journal_article"],["dc.type.internalPublication","unknown"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]Details DOI PMID PMC2008Journal Article [["dc.bibliographiccitation.firstpage","941"],["dc.bibliographiccitation.issue","10"],["dc.bibliographiccitation.journal","Oral Oncology"],["dc.bibliographiccitation.lastpage","948"],["dc.bibliographiccitation.volume","44"],["dc.contributor.author","Fialka, Florian"],["dc.contributor.author","Gruber, Rudolf Matthias"],["dc.contributor.author","Hitt, Reiner"],["dc.contributor.author","Pitz, Lennart"],["dc.contributor.author","Brunner, Edgar"],["dc.contributor.author","Schliephake, Henning"],["dc.contributor.author","Kramer, Franz-Josef"],["dc.date.accessioned","2018-11-07T11:10:46Z"],["dc.date.available","2018-11-07T11:10:46Z"],["dc.date.issued","2008"],["dc.description.abstract","To identify novel genes that could be involved in oncogenesis of oral squamous cell carcinoma a microarray-based gene-expression analysis was performed using tumour samples from patients with low-stage (n = 4) and high-stage (n = 4) disease in a pilot study. Genes (601) were found to be significantly regulated in cancer tissue compared to adjacent intraindividual mucosa controls. Genes (25) were identified with differences in their regulation comparing samples from early-stage cancer with those from advanced disease. The gene expression pattern of 5 of 7 genes examined by real-time-PCR verified the results received from the microarray-experiment. Among these, FMO2, CPA6, TNC and SIAT1 were significantly upregulated in early disease stages. LGI1 gene expression was significantly enhanced in normal adjacent mucosa of patients with early-stage disease without showing a differential expression in carcinoma biopsies. With this pilot study several novel genes were identified, which could be related to early and late stage disease. Hypotheses from these findings are discussed and have to be confirmed in a larger study sample. (C) 2007 Elsevier Ltd. All rights reserved."],["dc.identifier.doi","10.1016/j.oraloncology.2007.10.011"],["dc.identifier.isi","000261081800006"],["dc.identifier.pmid","18234543"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/6201"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/53279"],["dc.notes.intern","Merged from goescholar"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Elsevier Science Bv"],["dc.relation.issn","1368-8375"],["dc.rights","Goescholar"],["dc.rights.uri","https://goescholar.uni-goettingen.de/licenses"],["dc.title","CPA6, FMO2. LGI1, SIAT1 and TNC are differentially expressed in early- and late-stage oral squamous cell carcinoma - A pilot study"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]Details DOI PMID PMC WOS