Research lines

The Department of Genetics is working on the following research lines. Click on the project links or names of the principal investigators (PI) for more information.

Congenital diseases	Project leader
Dystrophic epidermolysis bullosa (DEB)	Peter van de Akker
L1CAM	Yvonne Vos
Hirschsprung	Robert Hofstra
CHARGE syndrome	Conny van Ravenswaaij
Epidemiological surveillance of congenital anomalies	Marian Bakker
Oncogenetics
Lynch syndrome and DNA mismatch repair	Rolf Sijmons Helga Westers
Renal Cell Cancer	Eva van den Berg
FaCD (Familial Cancer Database)	Rolf Sijmons
Testicular Cancer	Rolf Sijmons
Neurogenetics
C. elegans models for neurodegenerative diseases	Ellen Nollen
SpinoCerebellar Ataxia (SCA)	Dineke Verbeek
Multifactorial diseases
Genetics of complex immune-related diseases	Cisca Wijmenga
Cardiogenetics
Chronic heart failure	Peter van Tintelen
Cardiac fibrosis	Peter van Tintelen
CHF subforms	Peter van Tintelen
LVOTO (Left ventricular outflow tract obstructions)	Mieke Kerstjens
ARCV (Arrhythmogenic right ventricular cardiomyopathy)	Jan Jongbloed
DIDCARE (Dutch idiopathic dilated cardiomyopathy registry)	Jan Jongbloed
Statistical Genetics/Bioinformatics
Integration of high-throughput expression and sequence data into the Oncology workstation (CTMM project) Factor analytic modeling of expression data and EQTL mapping	Gerard te Meerman Lude Franke

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Last modified:

May 11, 2012 16:44

Research lines

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