The European Society
of Human Genetics

Tuesday, June 11

Tuesday, June 11, 2013

09.00 - 10.30

Plenary Session PL3: Large Scale Cohorts Studies to Identify Novel Highly Penetrant Genetic Disease Causing Variants


PL3.1 Deciphering Developmental Disorders Project, Matt Hurles, United Kingdom

PL3.2 Duke Fetal and Neonatal Cohort Study, Nicholas Katsanis, United States

PL3.3 Ethical implications of Whole Genome Sequencing in medicine, Jane Kaye, United Kingdom 

10.30 - 11.00

Coffee Break, Free Poster Viewing, Exhibition


11.00 - 12.30

Concurrent Sessions C15 - C20

C15. NGS-based diagnostics

C16. Developmental syndromes

C17. Basic mechanisms in cytogenetics and molecular genetics

C18. Big GWAS

C19. Internal organs and endocrinology: Gene identification and function

C20. Neurodevelopmental and neuropsychiatric disorders

View details of concurrent sessions

12.30 - 13.30Lunch, Exhibition, Poster Removal


13.30 - 14.15

Plenary Session PL4


PL4.1 Mendel Lecture: Rett syndrome and MECP2 Disorders: From the Clinic to Genes and Neurobiology, Huda Zoghbi, United States

14.15 - 15.45

Plenary Session PL5

PL5.1 ESHG Award Lecture, Felix Mitelman, Sweden

ESHG Education Award

EJHG Nature Awards

Young Investigator & Poster Awards


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