Dennis Dooijes

Armadillo Coactivates Transcription Driven by the Product of the Drosophila Segment Polarity Gene dTCF

Hans Clevers, Marc van de Wetering, Mark Peifer, 1997, Cell.

Frontotemporal dementia in The Netherlands: patient characteristics and prevalence estimates from a population-based study.

Philip Scheltens, Cornelia M van Duijn, Peter Heutink, 2003, Brain : a journal of neurology.

A mutation in CALM1 encoding calmodulin in familial idiopathic ventricular fibrillation in childhood and adolescence.

Marielle Alders, Abdelaziz Sefiani, A. Wilde, 2014, Journal of the American College of Cardiology.

Clinical Presentation, Long-Term Follow-Up, and Outcomes of 1001 Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Patients and Family Members

Stefan L. Zimmerman, Hugh Calkins, Crystal Tichnell, 2015, Circulation. Cardiovascular genetics.

A Mutation in the Fibroblast Growth Factor 14 Gene Is Associated with Autosomal Dominant Cerebral Ataxia

Elmar Krieger, Peter Heutink, Ben A. Oostra, 2003 .

Cloning of murine TCF-1, a T cell-specific trans cription factor interacting with functional motifs in the CD3ε and T cell receptor α enhancers.

H. Clevers, M. Wetering, A. Winoto, 1991 .

Cardiac beta-myosin heavy chain defects in two families with non-compaction cardiomyopathy: linking non-compaction to hypertrophic, restrictive, and dilated cardiomyopathies.

M. Simoons, F. T. ten Cate, K. Caliskan, 2007, European heart journal.

A mutation in the fibroblast growth factor 14 gene is associated with autosomal dominant cerebellar ataxia [corrected].

Elmar Krieger, Peter Heutink, E. Krieger, 2003, American journal of human genetics.

Evidence for an oligogenic basis of amyotrophic lateral sclerosis.

Leonard H van den Berg, P. D. de Bakker, L. H. van den Berg, 2012, Human molecular genetics.