Genomic Disorders Nijmegen
Projects
| Genomic copy number variation; unravelling its etiology and role in human disease |
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| In-depth molecular characterization of breakpoint-flanking sequences of human CNVs causing mental retardation and congenital malformations in conjunction with in-depth bioinformatic analyses for known and novel genomic architectural features |
| Lisenka Vissers; NWO VENI 2007 |
| Human genome disorders and genomic architecture |
| Identification and characterization of novel genomic disorders |
| Joris Veltman; NWO VIDI 2005 |
| Genomic profiling in mental retardation |
| Identification and characterization of novel candidate genes for mental retardation |
| Bert de Vries; NWO VIDI 2007 |
| Identifying dosage sensitive genes causing mental retardation |
| Development of in-depth bioinformatic approaches to identify and classify novel dosage sensitive genes underlying mental retardation |
| Jayne Hehir-Kwa; UMCN young researchers grant 2007 |
| High-throughput medical resequencing of candidate disease genes and genomic regions |
| Application of novel 'whole genome' resequencing technology to the study of monogenic diseases with locus heterogeneity |
| Alexander Hoischen; NWO Groot |
| TECHGENE |
| Technological innovation of high throughput molecular diagnostics of clinically and molecularly heterogeneous genetic disorders |
| Kornelia Neveling; FP7-HEALTH-2007 |
| Aneuploidy |
| Understanding the importance of gene dosage imbalance in human health using genetics, functional genomic and systems biology |
| Alexander Hoischen; FP6-LIFESCIHEALTH-2005 |
| GEUVADIS |
| Harmonising genomic medical research in Europe, set up standards in medical sequencing and review the current diagnostic standards according to the new insights gained from genomic and phenotypic data integration. |
| Terry Vrijenhoek |
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