Search Abstract DatabasePreliminary Programme
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| 14.00 | Educational Sessions | ||
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Session I:
Genetic predisposition of cancer D. Stoppa-Lyonnet, T. Frebourg, H. Vasen |
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Session II: Syndromology G. Gillesen-Kaesbach, E. Semanova |
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Session III:
Mutation or polymorphism? L. Messiaen |
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Session IV:
Design of studies of complex diseases C. van Duijn |
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| 15:45 | Opening
Ceremony Chair: L. Peltonen, M. Macek Presentation of the ESHG education award to Professor Giovanni Romeo |
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| 16.30 -
18.00 |
Opening
Plenary Session P1: Medical
and Molecular Genetics Research in the Czech Republic: overview of projects
with a high impact Chair: L. Peltonen, M. Macek |
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| 16.30 | Garrod´s inborn
errors of metabolism: Lessons from defective heme pathways Pavel Martasek |
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| 16.50 |
Garrod´s inborn errors of metabolism: Lessons from homocystinuria Victor Kozich |
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| 17.10 | TEL/AML1
fusion gene in childhood acute lymphoblastic leukaemia Jan Trka |
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| 17.30 |
New Mouse Model of Human Aneuploidy syndrome Jiri Forejt |
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| 18.00 | Coffee Break | ||
| 18.30
- 20.00 |
Plenary
P2: Pharmacogenetics and prevention Chair: H. Brunner, S. Aymé |
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| 18.30 |
Pharmacogenetics of drug metabolising enzymes. Implications for a safer and
more efficient drug therapy. Magnus Ingelman-Sundberg |
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| 19.00 | The future
of pharmacogenetics A. Roses |
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| 19.30 |
Advances in human genetics : what benefits for the patients ? A. Munnich |
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| 20:00 | Welcome Reception at the PCC | ||
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| 08.45 - 10.15 |
Plenary
P3 Auto-Immune disease Chair: J. Kere, A. Reis |
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| 8.45 | Asthma Juha Kere |
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| 9.15 |
Genes and mechanisms in type 1 diabetes John Todd |
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| 9.45 |
Genetics of Crohn disease, an archetypal inflammatory barrier disease Stefan Schreiber |
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| 10.15 | Coffee Break, Poster viewing, Exhibition | ||
| 10.45 |
Special Session The success of the oppositions against the BRCA1 patents: how did it occur and what will be the impact on genetic testing? G. Matthijs1, D. Halley2, G. Lenoir3, D. Stoppa-Lyonnet4 1Center for Human Genetics, University of Leuven, Belgium; 2Dept of Clinical Genetics, Erasmus MC, Rotterdam, the Netherlands; 3Institut Gustave-Roussy, Villejuif, France; 4Institut Curie, Paris, France. |
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| 11.15 | Poster discussion with presenters (odd poster numbers) | ||
| 12.45 | Lunch, Poster Viewing, Exhibition | ||
| 13.15 |
Workshops W1 Cytogenetics W2 Syndrome identification 1 - Submit an abstract W3 Community Genetics W4 The lessons of CF W5 Common diseases |
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| 15.00 - 16.30 |
Concurrent Sessions - Click here for detailed
programme C01 Cytogenetics C02 Molecular Genetics I C03 Complex Genetics I C04 Signalling and therapy in genetic disease C05 Clinical Genetics I |
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| 16.30 | Coffee Break, Poster viewing, Exhibition | ||
| 17.00 -
18.30 |
Concurrent Symposia | ||
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Symposium S1 Systems biology Chair: GJ van Ommen, L. Foretova |
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| 17.00 | Systems
biology in cardiovascular disease F. Cambien |
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| 17.30 |
Bioinformatics of signalling pathways R. Eils |
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| 18.00 |
Integral Membrane Proteins and Visual Defects J. Findlay |
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Symposium S2 Kidney disease Chair: H. Kääriäinen, R. Lukovska |
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| 17.00 |
Lessons from rare disorders: The Bardet-Biedl syndrome P. Beales |
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| 17.30 |
Nephronophthisis C. Antignac |
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| 18.00 | Molecular
basis of congenital nephrotic syndrome M. Zenker |
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Symposium S3 Mitochondria Chair: P. Gasparinin, V. Kucinskas |
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| 17.00 |
Mitochondrial dysfunction in neurodegeneration Anu Suomalainen-Wartiovaara |
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| 17.30 |
The assembly of OXPHOS complexes in health and disease L. Nijtmans |
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| 18.00 |
Immunohistochemical tests for mitochondrial dysfunction Rod Capaldi |
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| 18.30- 20.30 |
Free Poster Viewing | ||
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| 8.45 | Plenary
P4 Aging Chair: J.L. Mandel |
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| 8.45 |
Identifying the genes encoding longevity Rudy Westendorp |
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| 9.15 | IGF
signalling and aging Martin Holzenberger |
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| 9.45 | Genetics
of early and accelerated ageing syndromes Nicolas Levy |
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| 10.15 | Coffee Break, Poster viewing, Exhibition | ||
| 11.15 | Poster Discussion with Authors (Even Poster Numbers) | ||
| 12.45 | Lunch, Poster viewing, Exhibition | ||
| 13.15 |
Workshops W6 Quality Control W7 Syndrome identification 2 - Submit an abstract. W8 Prenatal Diagnosis W9 Counselling issues in cancer genetic clinics W10 Genetic education |
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| 15.00- 16.30 |
Concurrent Sessions - Click here for detailed
programme C06 Genomics and bioinformatics C07 Complex Genetics II C08 Clinical Genetics II C09 Genetic counselling and genetic services |
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| 16.30 | Coffee Break, Poster viewing, Exhibition | ||
| 17.00 -
18.30 |
Concurrent Symposia | ||
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Symposium S4 Cancer mechanisms Chair: P. Lichter, P. Goetz |
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| 17.00 |
Genetic and Epigenetic Changes in Early Carcinogenesis T. Tlsty |
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| 17.30 |
Cell Cycle Control: How to Preserve Genome Integrity during Cell Division? E. Nigg |
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| 18.00 |
Functional genomics of the Wnt signaling pathway in tumorigenesis J. Behrens |
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Symposium S5 Neurogenetics Chair: S. Lyonnet, G. Rappold |
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| 17.00 |
VEGF in amyotrophic lateral sclerosis Peter Carmeliet |
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| 17.30 | Leukoencephalopathies: from MRI pattern to basic defect M. van der Knaap |
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| 18.00 |
BDNF
signalling in anorexia Bulimia X. Estivill |
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Symposium S6 New molecular techniques Chair: A. Metspalu, L. Kadasi |
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| 17.00 | Digital
karyotyping M. Speicher |
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| 17.30 |
Canceromics: Molecular, cellular and clinical biochip technologies for
cancer genetics O. Kallioniemi |
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| 18.00 |
Single-molecule detection in situ using padlock and proximity probes U. Landegren |
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| 20.00 | Congress Party at 'U.Fleku' | ||
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| 8.45 - 10.15 |
Concurrent Symposia | ||
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Symposium S7 Function of non-coding DNA Chair: K.H. Grzeschik |
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| 8.45 | CNGs
conserved noncoding E. Dermitzakis |
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| 9.15 |
Activation of Non-coding RNAs by Epigenetic Therapy P. Jones |
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| 9.45 |
Ultraconserved elements in the human genome D. Haussler |
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Symposium S8 Reproductive genetics Chair: N. Tommerup, L. Gianaroli |
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| 8.45 | Overview
of preimplantation diagnosis Luca Gianaroli |
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| 9.15 |
Circulating fetal cells and cell free fetal DNA: what is the current status? Sinoue Hahn |
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| 9.45 | Practice
of preimplantation genetic diagnosis I. Liebaers |
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Symposium S9 Haplotypes Chair: C. van Duijn, A. Reis |
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| 8.45 | LD in
genetic isolated populations Cornelia van Duijn |
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| 9.15 |
Selecting the right SNPs for genetic mapping studies in European populations Thomas Meitinger |
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| 9.45 |
Influence of LD on high-density SNP genome linkage scans Bertram Müller-Myhsok |
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| 10.15 | Coffee Break, Poster viewing, Exhibition | ||
| 10.45 - 12.15 |
Concurrent Sessions - Click here for detailed
programme C10 Molecular Genetics II C11 Prenatal diagnosis and fetal pathology C12 Cancer Genetics C13 Normal variation, population genetics, genetic epidemiology |
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| 12.15 | Lunch, Poster removal, Exhibition | ||
| 13.15 - 14.00 |
Plenary
P5 Chair: H. Brunner, A. Read |
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| 13.15 | Late Breaking Research | ||
| 14.00 | Young Investigator Awards | ||
| 14.30 | ESHG Award | ||
| 14.45 | ESHG
Award Lecture Stylianos Antonarakis |
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| 15.30 | Closing Ceremony | ||
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Quick Jump to: Saturday - Sunday
- Monday - Tuesday |
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