Joris Veltman

Identification of tumor-specific molecular signatures in intracranial ependymoma and association with clinical characteristics.

Flavio Giordano, James F Reid, Lorenzo Genitori, 2006, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Gene identification in the congenital disorders of glycosylation type I by whole-exome sequencing.

Christian Gilissen, Alexander Hoischen, Ron A Wevers, 2012, Human molecular genetics.

Disruption of the neurexin 1 gene is associated with schizophrenia.

Elvira Bramon, Chiara Sabatti, Kari Stefansson, 2009, Human molecular genetics.

Identification of recurrent chromosomal aberrations in germ cell tumors of neonates and infants using genomewide array‐based comparative genomic hybridization

Christina Hulsbergen-van de Kaa, Ulrich Göbel, J. Veltman, 2005, Genes, chromosomes & cancer.