E. Korvatska

Kerato-epithelin mutations in four 5q31-linked corneal dystrophies.

D. Schorderet, F. Munier, L. Zografos, 1997 .

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

Thomas Bourgeron, Alberto Segre, Alberto Maria Segre, 2007, Nature Genetics.

Erratum: Genetic and immunologic considerations in autism (Neurobiology of Disease (2002) 9:2 (107-125))

M. Gershwin, T. Anders, E. Korvatska, 2002 .

Mutation hot spots in 5q31-linked corneal dystrophies.

W. Culbertson, D. Schorderet, S. Uffer, 1998, American journal of human genetics.

Kerato-epithelin mutations in four 5q31-linked corneal dystrophies

D. Paslier, D. Schorderet, G. Pescia, 1997, Nature Genetics.

Amyloid and Non-amyloid Forms of 5q31-linked Corneal Dystrophy Resulting from Kerato-epithelin Mutations at Arg-124 Are Associated with Abnormal Turnover of the Protein*

D. Schorderet, H. Henry, F. Munier, 2000, The Journal of Biological Chemistry.

On the role of kerato-epithelin in the pathogenesis of 5q31-linked corneal dystrophies.

D. Schorderet, S. Uffer, F. Munier, 1999, Investigative ophthalmology & visual science.

Delineation of a 1-cM Region on Distal 5q Containing the Locus for Corneal Dystrophies Groenouw Type I and Lattice Type I and Exclusion of the Candidate Genes SPARC and LOX

D. Schorderet, G. Pescia, S. Uffer, 1996, European journal of human genetics : EJHG.

Impaired dopaminergic neurotransmission and microtubule-associated protein tau alterations in human LRRK2 transgenic mice

David I. Bass, G. Schellenberg, M. Farrer, 2010, Neurobiology of Disease.

Heterogeneous association between engrailed‐2 and autism in the CPEA network

Geraldine Dawson, Kristina Allen-Brady, Bernie Devlin, 2008, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Genetic and Immunologic Considerations in Autism

M. Eric Gershwin, M. Gershwin, T. Anders, 2002, Neurobiology of Disease.

Tau isoform regulation is region‐ and cell‐specific in mouse brain

G. Schellenberg, P. Poorkaj, J. Leverenz, 2008, The Journal of comparative neurology.

The human TAX1 gene encoding the axon-associated cell adhesion molecule TAG-1/axonin-1: genomic structure and basic promoter.

P. Sonderegger, D. Schorderet, R. Giger, 1995, Genomics.

Haplotype analysis of Japanese families with a superficial variant of granular corneal dystrophy: evidence for multiple origins of R124L mutation of kerato-epithelin

D. Schorderet, F. Munier, E. Korvatska, 2000 .