Jeffrey W. Walter

Evidence for loss of heterozygosity of 5q in sporadic haemangiomas: are somatic mutations involved in haemangioma formation?

M. Waner, M. Porteous, D. Marchuk, 2001, Journal of clinical pathology.

Genetic mapping of a novel familial form of infantile hemangioma.

S. Orlow, D. Marchuk, F. Blei, 1999, American journal of medical genetics.

Somatic mutation of vascular endothelial growth factor receptors in juvenile hemangioma

M. Waner, D. Marchuk, F. Blei, 2002, Genes, chromosomes & cancer.

Distribution of Optineurin Sequence Variations in an Ethnically Diverse Population of Low-tension Glaucoma Patients From the United States

J. Haines, M. Pericak-Vance, M. Hauser, 2006, Journal of glaucoma.

Serial analysis of gene expression (SAGE) in normal human trabecular meshwork

M. Hauser, C. B. Rickman, Yutao Liu, 2011, Molecular vision.

Genomic convergence to identify candidate genes for Parkinson disease: SAGE analysis of the substantia nigra

F. Dietrich, J. M. van der Walt, Yi-Ju Li, 2005, Movement disorders : official journal of the Movement Disorder Society.

Familial segregation of hemangiomas and vascular malformations as an autosomal dominant trait.

S. Orlow, D. Marchuk, F. Blei, 1998, Archives of dermatology.