Jean-Marie Naeyaert

Loss-of-function mutations in LEMD3 result in osteopoikilosis, Buschke-Ollendorff syndrome and melorheostosis

Philippe Debeer, Frank Speleman, Jan Hellemans, 2004, Nature Genetics.

Inter‐observer variation in the histopathological diagnosis of clinically suspicious pigmented skin lesions

J. Naeyaert, G. Piérard, L. Brochez, 2002, The Journal of pathology.

The Quest for the Mechanism of Melanin Transfer

Jo Lambert, J. Lambert, J. Naeyaert, 2006, Traffic.

Acanthosis nigricans in a child with mild osteochondrodysplasia and K650Q mutation in the FGFR3 gene

Jo Lambert, Lieve Nuytinck, G. Mortier, 2007, American journal of medical genetics. Part A.

Homozygosity for a missense mutation in fibulin-5 (FBLN5) results in a severe form of cutis laxa.

Paul Coucke, Bart Loeys, Geert Mortier, 2002, Human molecular genetics.