G. V. Ommen

Northern epilepsy syndrome: an inherited childhood onset epilepsy with associated mental deterioration.

J. J. Shepherd, D. Sillence, L. Mestroni, 1994, Journal of medical genetics.

The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion.

L. Kunkel, A. Covone, N. Archidiacono, 1989, American journal of human genetics.

Neonatal screening for muscular dystrophy Consensus recommendation of the 14th Workshop sponsored by the European Neuromuscular Center (ENMC)

G. V. Ommen, G. Scheuerbrandt, Garrit-Jan Boudewijn Van Ommen, 1993, Neuromuscular Disorders.

Probe 218EP6 (D16S246) detects RFLP's close to the locus affecting adult polycystic kidney disease (PKD1) on chromosome 16.

J. Saris, M. Breuning, F. Snijdewint, 1990, Nucleic acids research.

Muscle binding peptides found by phage display as delivery agent for antisense oligonucleotides

B. Aguilera, A. Aartsma-Rus, J. V. Deutekom, 2008 .

Normal and mutant HTT interact to affect clinical severity and progression in Huntington disease

T. Stijnen, R. Roos, G. van Ommen, 2009, Neurology.

Therapeutic Modulation of DMD Splicing by Blocking Exonic Splicing Enhancer Sites with Antisense Oligonucleotides

C. D. de Winter, G. van Ommen, A. Aartsma-Rus, 2006, Annals of the New York Academy of Sciences.