Program
The program has been finalised and is available HERE.
Invited Speakers
Lars Bertram, Germany
Online encyclopedias and field synopses of genetic association studies in Alzheimer's and Parkinson's disease
Abstract
Richard G.H. Cotton, Australia
The Human Variome Project - introduction
Abstract
Diane W. Cox, Canada
Wilson disease Database: an Aid to DNA Diagnosis
Abstract
Marc Cruts, Belgium
The Alzheimer Disease & Frontotemporal Dementia Mutation Database
Abstract
Matthew Farrer, USA
Who appropriated the PARK loci, and where were the geneticists?
Abstract
John K. Fink, USA
Hereditary motor neuron disorders: genetic heterogeneity, genetic pleiotropy, and clinical overlap
Abstract
Antonio Salas, Spain
Guidelines towards a MITOvariome project
Abstract
Birgitt Schuele, USA
Update of the Parkinson’s Disease Mutation Database
Abstract
María-Jesús Sobrido, Spain
LSDBs for Neurological Disorders: Is there a rationale for a Neurogenetics Database Consortium?
Abstract
Michael Woods, Canada
Insights into InSiGHT and the HVP experience
Abstract
Accepted abstracts
Sherifa Hamed, Egypt
Genetic Disorders among Egyptian Population: Experience from Epidemiologic & Molecular Data
Abstract | Presentation
Andrea Haworth, UK
Everyday problems for a diagnostic Neurogenetics Laboratory
Abstract
Non-attendee abstracts
Paola Carrera, Italy and Sara Benedetti, Italy
Set up of a clinical-molecular database for the definition of a diagnostic flow chart in hereditary spastic paraplegia
Abstract
Ming Qi, China
CINCH Genetic Database of Neuromuscular Channelopathies
Abstract
Ivo Fokkema, Jacopo Celli, et al
Locus-Specific Mutation Database Solutions for Neurogenetics
Abstract
Xinjing Wang, USA, et al
eyeGene - National Ophthalmic Disease Genotyping and Phenotyping Network
Abstract
Company Lectures
If you are a company and are interested in presenting a lecture, please see the Sponsors page link above.