Monday, May 30, 2011
08.30 - 10.00 | Concurrent Symposia S09 - S12 | |
S09. No Genome for Old (Wo)MenS09.1 Old men and selfish spermatogonia: how much do they contribute to the mutation burden? S09.2 Telomeres, aging and stem cells S09.3 DNA damage and its implications for the aging epigenome | ||
S10. Complex diseaseS10.1 Using custom arrays to improve the understanding of metabolic disorder S10.2 Ankylosing Spondylitis S10.3 Genetic Analysis of Autoimmune Disease in the Wellcome Trust Case-Control Consortium 2 | ||
S11. Model organisms for diseaseS11.1 Dog: how comparative genetics inform human diseases S11.2 Drosophila: Parkinson's disease S11.3 Modeling Parkinson's disease in zebrafish | ||
S12. Prenatal DiagnosisS12.1 PGD - 21 years on S12.2 Use of aCGH in Prenatal Diagnosis S12.3 Non-invasive prenatal diagnosis using circulating fetal DNA: state of the art | ||
Educational Session ES6. Marfan and EDSES6.1 Marfan syndrome: evolving nosology, evolving pathophysiology and evolving treatment with improved survival ES6.2 The Ehlers-Danlos syndrome, a disorder with many faces | ||
10.00 - 10.30 | Coffee Break, Free Poster Viewing, Exhibition | |
10.30 - 11.30 | Poster Viewing with Authors (Even poster numbers) | |
11.30 - 13.15 | Free Poster Viewing, Exhibition, Lunch | |
Educational Session ES7. Noonan Syndrome and NeurofibromatosisES7.1 Noonan Syndrome ES7.2 Neurofibromatosis | ||
11.40 - 13.10 | Educational Session ES8. European Journal of Human Genetics - How to get your paper publishedIntroduction Panel discussion with three Section Editors: Presentation on publishing matters | |
11.40 - 13.10 | Corporate Satellites | |
Application of PCR Tools for the Analysis of FMR1 Expanded AllelesAbbott Molecular Satellite | ||
Targeted resequencing and novel tools for human genetics researchAgilent Technologies | ||
13.15 - 14.45 | Concurrent Sessions C07 - C12 from submitted abstractsC07 Prenatal Diagnosis and Reproduction | |
14.45 - 15.15 | Fitness Break, Free Poster Viewing, Exhibition | |
| ||
15.15 - 16.45 | Workshops W08 - W14WS8. Dysmorphology Workshop 2 (D. Donnai, J. Clayton-Smith) | |
15.15 - 16.45 | Corporate Satellites | |
New qPCR techniques for translating discoveries into medical realitiesLife Technologies | ||
Discover the Roche NimbleGen Difference: Using Sequence Capture and CGH to discover mechanisms of diseaseRoche-NimbleGen | ||
16.45 - 17.15 | Coffee Break | |
17.15 - 18.45 | Concurrent Symposia S13 - S16 | |
S13. Epigenetics and imprintingS13.1 Genomic imprinting: an epigenetic gene regulatory model S13.2 How epigenetics disconnects the ability to learn with increasing age S13.3 Towards epigenome-wide association studies (EWAS) | ||
S14. Cardiovascular GeneticsS14.1 Venous anomalies: From identification of causes towards mouse models S14.2 CCM protein interactions, double KO mouse models S14.3 Genomics of blood pressure and hypertension | ||
S15. Population GeneticsS15.1 Jewish population structure S15.2 A fine-scale map of recombination rates and hotpots in the chimpanzee reveals conservation and turnover in factors localising cross-overs S15.3 Genome diversity in Asia | ||
S16. EthicsS16.1 International data sharing in genomics S16.2 Return of results to participants in genetics and genomics research S16.3 Ethics, genetics and the family | ||
Educational Session ES9. Copy Number Variation and arrays in practiceES9.1 Array in practice ES9.2 Deciphering Developmental Disorders | ||
19.00 | ESHG Congress Party |