Intelligent Systems'2014
Proceedings of the 7th IEEE International Conference Intelligent Systems IS’2014, September 24‐26, 2014, Warsaw, Poland, Volume 2: Tools, Architectures, Systems, Applications
Article
Over the course of COVID-19 pandemic, evidence has accumulated that SARS-CoV-2 infections may affect multiple organs and have serious clinical sequelae, but on-site clinical examinations with non-hospitalized ...
Article
Fatty liver disease (FLD) is an important intermediate trait along the cardiometabolic disease spectrum and strongly associates with type 2 diabetes. Knowledge of biological pathways implicated in FLD is limit...
Article
There are limited data available concerning endofistular therapies for fistula-in-ano, with our group reporting the first preliminary outcomes of the use of the radial fibre Fistula laser Closing (FiLaC ™) de...
Book and Conference Proceedings
Proceedings of the 7th IEEE International Conference Intelligent Systems IS’2014, September 24‐26, 2014, Warsaw, Poland, Volume 2: Tools, Architectures, Systems, Applications
Article
Next Generation Sequencing (NGS) erlaubt die Untersuchung des kompletten Exoms oder Genoms eines Patienten mit vertretbarem zeitlichem und finanziellem Aufwand. Dieser diagnostische Quantensprung hat neben rec...
Article
Angesichts der zunehmenden Datenflut in der Genomforschung wird ein effizientes Forschungsdatenmanagement, verbunden mit einer sicheren und nachhaltigen Archivierung, auch in diesem Wissenschaftsbereich immer ...
Article
Die Entwicklung der DNA-Sequenzierungstechnologien stellt die humane Genomforschung vor große datenschutzrechtliche und ethische Herausforderungen. Der heute bereits mögliche tiefe Einblick in die genetische A...
Article
Die Biobank PopGen wurde 2003 zur Erforschung genetischer Risikofaktoren für komplexe Humanerkrankungen etabliert. Neben Daten betroffener Patienten umfasst sie auch solche zufällig ausgewählter Personen aus d...
Article
With the advent of technologies that allow simultaneous genoty** of thousands of single-nucleotide polymorphisms (SNPs) across the genome, the genetic contributions to complex diseases can be explored at an ...
Chapter
The used generalized net will give us a possibility for parallel optimization of a feed-forward neural network based on assigned training pairs with variable learning rate backpropagation algorithm with time l...
Chapter
In a series of research papers, the authors study some of the most important processes of functioning of universities and construct their Generalized Net (GN) models. The main focus in this paper is to analyse...
Chapter and Conference Paper
Gallstone disease is a common disorder with a prevalence of approximately 20 % in industrialized countries. We performed a genome-wide disease association scan of over 500,000 single nucleotide polymorphisms (...
Article
In both human immunodeficiency virus-infected humans and simian immunodeficiency virus (SIV)-infected macaques, genes encoded in the major histocompatibility complex (MHC) class I region are important determin...
Article
Im Gegensatz zu monogenen Erkrankungen kann bei multifaktoriellen genetisch bedingten Krankheiten aufgrund der Vielzahl genetischer und nichtgenetischer Faktoren keine klare Genotyp-Phänotyp-Beziehung erwartet...
Article
The phenotypic heterogeneity of metabolic syndrome (MSX) suggests heterogeneity of the underlying genotype. The aim of the present study was to examine the common genetic background that contributes to the clu...
Article
Nat. Genet. 37, 357–364 (2005). In the version of Supplementary Table 3 initially published online, the nomenclature of DQB and DPB alleles was partly incorrect. The errors have now been corrected and Suppleme...
Article
In forensic science, X-chromosomal short tandem repeats (ChrX STRs) bear the potential to efficiently complement the analysis of other genetic markers (autosomal, Y-chromosomal or mitochondrial). We review the...
Article
Linkage disequilibrium (LD) map** was used to follow up reports of linkage between reading disability (RD) and an 18 cM region of chromosome 6p21.3–22. Using a two-stage approach, we tested for association b...
Article
We examined whether variation within six genes from the VCFS critical region at 22q11 (DGSC, Stk22A1, DGSI, Gscl, Slc25A1 and Znf74) confers susceptibility to schizophrenia. We screened the exons and flanking int...
Article
Infliximab (anti-TNF-α monoclonal antibody) induces remission in 30–40% of Crohn's disease patients. Treatment response is a stable trait. Two cohorts from independent, prospective clinical trials of inflixima...