Hilde Van Esch

Network Analysis of Differential Expression for the Identification of Disease-Causing Genes

Yves Moreau, Lieven Thorrez, Léon-Charles Tranchevent, 2009, PloS one.

Submicroscopic duplications of the hydroxysteroid dehydrogenase HSD17B10 and the E3 ubiquitin ligase HUWE1 are associated with mental retardation.

Peter Marynen, Rodney Scott, Patrick S Tarpey, 2008, American journal of human genetics.

Mutation screening of ASMT, the last enzyme of the melatonin pathway, in a large sample of patients with Intellectual Disability

Thomas Bourgeron, Richard Delorme, Marion Leboyer, 2011, BMC Medical Genetics.

Towards a 21st-century roadmap for biomedical research and drug discovery: consensus report and recommendations.

Martin Hofmann-Apitius, Brigitte Landesmann, Christoph Giese, 2017, Drug discovery today.

Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling.

Michael J Parker, Katrina Tatton-Brown, Christian Gilissen, 2015, American journal of human genetics.

Positron Emission Tomography (PET) Quantification of GABAA Receptors in the Brain of Fragile X Patients

Koen Van Laere, Wim Van Paesschen, Michel Koole, 2015, PloS one.

Mutations in NOTCH2 in families with Hajdu‐Cheney syndrome

Kym M Boycott, Jacek Majewski, Mark E Samuels, 2011, Human mutation.