Sunday, June 24, 2012 | ||
08.30 - 10.00 | Concurrent Symposia S01 - S04 | |
S01. Statistical analysis of sequence data in complex diseaseS01.1 Combined tests for rare variants, Ben Neale, USA S01.2 Statistical analysis of rare variants in genome-wide association studies of complex traits, Andrew Morris, UK S01.3 Homing in on causative genes in GWAS-identified risk loci using eQTL information, Yukihide Momozawa, Belgium S02. Mechanisms and consequences of chromosomal/genetic mosaicismS02.1 Copy number variation and selection during reprogramming, Andras Nagy, Canada S02.2 Single cell sequencing to reveal chromosomal copy number variations, Nicholas Navin, USA S02.3 Genomic instability in early stages of cancer development, Batsheva Kerem, Israel S03. EpigeneticsS03.1 Epigenetic regulation of the circadian clock, Paolo Sassone Corsi, USA S03.2 Epigenetics in diabetes, Assam El-Osta, Australia S03.3 Epigenetics of the impact of early trauma on behavior across generations, Johannes Bohacek, Switzerland S04. The molecular basis of facial malformationsS04.1 Integrating clinical and genomic approaches to identify causative genetic loci for orofacial clefting, Elisabeth Mangold, Germany S04.2 Facial Dysostoses in Mouse, Mike Dixon, UK S04.3 Human Facial Dysostoses, Dagmar Wieczorek, Germany | ||
08.30 - 10.00 | Educational Session 4 | |
ES4. Applying family dynamics/therapy in genetic counselling (joint with EMPAG)ES4.1 The Family's Experience of a Genetic Disorder, Suzan McDaniel, USA ES4.1 Using systemic ideas in Genetic Counsellors' group supervision, Tom O'Neill, UK | ||
10.00 - 10.30 | Coffee Break, Free Poster Viewing, Exhibition | |
10.30 - 11.30 | Poster Viewing with Authors (Odd poster numbers) | |
11.30 - 13.15 | Free Poster Viewing, Exhibition, Lunch as of 12.15 hrs | |
11.40 - 13.10 | Workshops WS02-WS03 | |
WS02. Array CGH (Ros Hastings & Nicole de Leeuw)WS03. USCS Genome Browser I (Robert Kuhn) | ||
11.40 - 13.10 | Corporate Satellites | |
AffymetrixLife Technologies | ||
13.15 - 14.45 | Concurrent Sessions C01 - C06 | |
C01. New Genes and New Therapies in Clinical Genetics | ||
14.45 - 15.15 | Fitness Break, Free Poster Viewing, Exhibition | |
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15.15 - 16.45 | Workshops W04 - W10 | |
WS04. Dysmorphology 1 (Dian Donnai & Jill Clayton-Smith) | ||
15.15 - 16.45 | Corporate Satellites | |
| CartageniaRoche Applied Science | |
16.45 - 17.15 | Coffee Break, Free Poster Viewing, Exhibition | |
17.15 - 18.45 | Concurrent Symposia S05 - S08 | |
S05. Advances in Neuropsychiatric DisordersS05.1 Alzheimer's disease, Denise Harold, UK S05.2 Schizophrenia, Mick O'Donovan, UK S05.3 Bipolar affective disorder, Sven Cichon, Germany S06. Prenatal diagnosisS06.1 Tailoring and implementing aCGH for prenatal diagnosis: experience from Hong Kong, Richard KW Choy, Hong Kong S06.2 Prenatal diagnosis: Challenges in the interpretation of high resolution genetic screening tests, Koen Devriendt, Belgium S06.3 Get ready for the flood of fetal gene screening, Henry T. (Hank) Greely, USA S07. Genomics and drug responseS07.1 Pharmacogenomics biomarkers, Wolfgang Sadee, USA S07.2 Clinical pharmagenomics: perspectives and limitations, Matthias Schwab, Germany S07.3 Pharmacogenomics - Is it a hype really?, Henk Jan Guchelaar, The Netherlands S08. 25 Years Psychosocial research in Clinical Genetics: Making up the balance (joint with EMPAG)S08.1 Past, present and future of psychological research in genetics: a personal view and a focus on the impact of predictive testing, Gerry Evers-Kiebooms, Belgium S08.2 Translation of psychosocial research findings into an evidence base for genetic counselling practice and training , Lauren Kerzin-Storrar, United Kingdom S08.3 Psychosocial issues in cancer genetics, Eveline Bleiker, The Netherlands | ||
17.15 - 18.45 | Educational Session 5 | |
ES5. Array CGH and Next generation sequencingES5.1 Array CGH and applications, Lars Feuk, Sweden ES5.2 Next generation sequencing and applications, Ivo Gut, Spain | ||
18.45 - 20.15 | Corporate Satellites | |
| Bio-RadIlumina | |
19.00 - 20.00 | ESHG Membership Meeting |