ESHG: Session Overview

Session Overview

Plenary Sessions

Opening - Welcome Adresses	Saturday, June 8 16.00 - 16.30 hrs
P1. Opening Plenary Session	Saturday, June 8 16.30 - 18.00 hrs
P2. What's New?	Saturday, June 8 18.00 - 20.00 hrs
P3. Large Scale Cohorts Studies to Identify Novel Highly Penetrant Genetic Disease Causing Variants	Tuesday, June 11 9.00 - 10.30 hrs
P4. Mendel Lecture	Tuesday, June 11 13.30 - 14.15 hrs
P5. ESHG Award Lecture, ESHG Education Award, EJHG Nature Awards, Young Investigator & Poster Awards, Closing	Tuesday, June 11 14.15 - 15.45 hrs

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Concurrent Symposia

S01. Chromatin organisation and gene expression	Sunday, June 9 8.30 - 10.00 hrs
S02. From genes to treatment in multifactorial diseases	Sunday, June 9 8.30 - 10.00 hrs
S03. Gene regulation in cancer	Sunday, June 9 8.30 - 10.00 hrs
S04. Emerging topics in neurobiology	Sunday, June 9 8.30 - 10.00 hrs
S05. Interpreting NGS data	Sunday, June 9 17.15 - 18.45 hrs
S06. Cancer genetics	Sunday, June 9 17.15 - 18.45 hrs
S07. Genetics of skin diseases and new therapies	Sunday, June 9 17.15 - 18.45 hrs
S08. Evolution of organs	Sunday, June 9 17.15 - 18.45 hrs
S09. New therapeutic highlights in rare diseases	Monday, June 10 8.30 - 10.00 hrs
S10. Reproductive genetics and newborn screening	Monday, June 10 8.30 - 10.00 hrs
S11. Animal Models for Human Diseases	Monday, June 10 8.30 - 10.00 hrs
S12. Judging our genes	Monday, June 10 8.30 - 10.00 hrs
S13. Stem cells and IPS cells in genetic diseases	Monday, June 10 17.15 - 18.45 hrs
S14. The interrelated world of drugs and genes	Monday, June 10 17.15 - 18.45 hrs
S15. The expanding world of the primary cilia	Monday, June 10 17.15 - 18.45 hrs
S16. Chromosomal (in)stability	Monday, June 10 17.15 - 18.45 hrs

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Concurrent Sessions

C01. Structural variation and de novo mutations	Sunday, June 9 13.15 - 14.45 hrs
C02. Genotype phenotype correlation	Sunday, June 9 13.15 - 14.45 hrs
C03. Prenatal diagnosis	Sunday, June 9 13.15 - 14.45 hrs
C04. Cancer predisposition	Sunday, June 9 13.15 - 14.45 hrs
C05. Functional Genomics	Sunday, June 9 13.15 - 14.45 hrs
C06. Neuromuscular disorders: From genes and modifiers to function and therapy	Sunday, June 9 13.15 - 14.45 hrs
C07. Metabolic and mitochondrial disorders	Sunday, June 9 13.15 - 14.45 hrs
C08. Intellectual disability: Gene discovery and dysfunction	Monday, June 10 13.15 - 14.45 hrs
C09. Population-based sequencing	Monday, June 10 13.15 - 14.45 hrs
C10. Genetic Counselling, Education and Public Services	Monday, June 10 13.15 - 14.45 hrs
C11. Molecular mechanisms in tumorigenesis	Monday, June 10 13.15 - 14.45 hrs
C12. Connective tissue disorders: Gene identification	Monday, June 10 13.15 - 14.45 hrs
C13. Neurodegenerative disorders: From gene discovery to therapy	Monday, June 10 11.00 - 12.30 hrs
C14. Sensory disorders and Immunological disorders	Monday, June 10 11.00 - 12.30 hrs
C15. NGS-based diagnostics	Tuesday, June 11 11.00 - 12.30 hrs
C16. Developmental syndromes	Tuesday, June 11 11.00 - 12.30 hrs
C17. Basic mechanisms in cytogenetics and molecular genetics	Tuesday, June 11 11.00 - 12.30 hrs
C18. Big GWAS	Tuesday, June 11 11.00 - 12.30 hrs
C19. Internal organs and endocrinology: Gene identification and function	Tuesday, June 11 11.00 - 12.30 hrs
C20. Neurodevelopmental and neuropsychiatric disorders	Tuesday, June 11 11.00 - 12.30 hrs

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Workshops

WS01. Next Generation sequencing in clinical practice - Filtering and reporting	Sunday, June 9 11.40 - 13.10 hrs
WS02. Debate: Preimplantation genetic screening	Sunday, June 9 11.40 - 13.10 hrs
WS3. USCS Genome Browser 1	Sunday, June 9 11.40 - 13.10 hrs
WS04. Dysmorphology Workshop 1	Sunday, June 9 15.15 - 16.45 hrs
WS05. Analysis, interpretation and reporting of array data	Sunday, June 9 15.15 - 16.45 hrs
WS06. Quality assurance	Sunday, June 9 15.15 - 16.45 hrs
WS07. Inequality in Genetic Services	Sunday, June 9 15.15 - 16.45 hrs
WS08. GALAXY	Sunday, June 9 15.15 - 16.45 hrs
WS09. Clinical Cancer Genetics Club	Sunday, June 9 15.15 - 16.45 hrs
WS10. Dysmorphology 2	Monday, June 10 15.15 - 16.45 hrs
WS11. Prenatal Diagnostic	Monday, June 10 15.15 - 16.45 hrs
WS12. DNA Dysmorphology	Monday, June 10 15.15 - 16.45 hrs
WS13. Community genetics	Monday, June 10 15.15 - 16.45 hrs
WS14. USCS Genome Browser 2	Monday, June 10 15.15 - 16.45 hrs

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Educational Sessions

ES1. Performance and future of next generation sequencing (what's next?)	Saturday, June 8 14.00 - 15.30 hrs
ES2. Prenatal and Preimplantation Genetic Screening	Saturday, June 8 14.00 - 15.30 hrs
ES3. Understanding Genomics. Trends in Science Communication	Sunday, June 9 8.30 - 10.00 hrs
ES4. Cancer risk in developmental syndromes	Sunday, June 9 11.40 - 13.10 hrs
ES5. Epilepsies	Sunday, June 9 17.15 - 18.45 hrs
ES6. Retinal dystrophies: news and views	Monday, June 10 8.30 - 10.00 hrs
ES7. NGS in the clinic	Monday, June 10 11.40 - 13.10 hrs
ES8. How to get published in the European Journal of Human Genetics (EJHG)	Monday, June 10 11.40 - 13.10 hrs
ES9. Where do we come from?	Monday, June 10 17.15 - 18.45 hrs

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The European Society
of Human Genetics

Session Overview

Session Overview

Opening - Welcome Adresses

P1. Opening Plenary Session

P2. What's New?

P3. Large Scale Cohorts Studies to Identify Novel Highly Penetrant Genetic Disease Causing Variants

P4. Mendel Lecture

P5. ESHG Award Lecture,
ESHG Education Award, EJHG Nature Awards, Young Investigator & Poster Awards, Closing

S01. Chromatin organisation and gene expression

S02. From genes to treatment in multifactorial diseases

S03. Gene regulation in cancer

S04. Emerging topics in neurobiology

S05. Interpreting NGS data

S06. Cancer genetics

S07. Genetics of skin diseases and new therapies

S08. Evolution of organs

S09. New therapeutic highlights in rare diseases

S10. Reproductive genetics and newborn screening

S11. Animal Models for Human Diseases

S12. Judging our genes

S13. Stem cells and IPS cells in genetic diseases

S14. The interrelated world of drugs and genes

S15. The expanding world of the primary cilia

S16. Chromosomal (in)stability

ES1. Performance and future of next generation sequencing (what's next?)

ES2. Prenatal and Preimplantation Genetic Screening

ES3. Understanding Genomics. Trends in Science Communication

ES4. Cancer risk in developmental syndromes

ES5. Epilepsies

ES6. Retinal dystrophies: news and views

ES7. NGS in the clinic

ES8. How to get published in the European Journal of Human Genetics (EJHG)

ES9. Where do we come from?

ESHG 2013