Zoekresultaten
Finance
School of Business and Economics
t.post@maastrichtuniversity.nl
Finance
School of Business and Economics
k.godker@maastrichtuniversity.nl
Finance
School of Business and Economics
t.post@maastrichtuniversity.nl
Finance
School of Business and Economics
k.godker@maastrichtuniversity.nl
Finance
School of Business and Economics
21
jan
15:00
- 17:00
… The most striking observation of this pathway was that observed phenotypes can be caused or influenced not by one but multiple genes in this region, although TBX1 was thought to be mainly responsible for heart defects. Woosub Shin PhD candidate Department of Bioinformatics - BiGCaT, NUTRIM Title : Applying pathway interaction method to hypothesize molecular signature of neuropsychiatric diseases caused by 22q11.2 deletion syndrome. Abstract : In this study, we explore the Pathway … effects on brain structure across pathogenic copy number variants. Abstract : Recent findings have revealed convergent effects of multiple CNVs on different chromosomes, on core sensory, cognitive, and motor domains. Furthermore, recent evidence showed that the penetrance of a CNV for schizophrenia and developmental delay – reflecting the probability of manifesting the given phenotype – was associated with changes in medial white matter structures. These results suggest that different … (extracted from T1-weighted MRI data) and penetrance scores for schizophrenia and development delay, previously calculated for each CNV. Emma von Scheibler PhD candidate Department of Psychiatry and Neuropsychology, MHeNs Title : Ocular findings in 142 individuals with 22q11.2 deletion syndrome Abstract : 22q11.2 deletion syndrome (22q11.2DS) is a multi-system disorder caused by heterozygous microdeletions on chromosome 22q11.2, with an incidence of 1:3000 live births. Characteristics include …