Roland Heilig

A fine integrated map of the SPG4 locus excludes an expanded CAG repeat in chromosome 2p-linked autosomal dominant spastic paraplegia.

G. Gyapay, C. Fizames, D. Muselet, 1999, Genomics.

The NACP/synuclein gene: chromosomal assignment and screening for alterations in Alzheimer disease.

R. Heilig, D. Campion, D. Hannequin, 1995, Genomics.

Mutations of the presenilin I gene in families with early-onset Alzheimer's disease.

B. Dubois, D. Campion, D. Hannequin, 1995, Human molecular genetics.

Characterization of the NPHP1 locus: mutational mechanism involved in deletions in familial juvenile nephronophthisis.

J. Weissenbach, R. Heilig, F. Silbermann, 2000, American journal of human genetics.