Forward genetic screens have been instrumental in defining molecular components of visual function.

Our results show that the expression signatures defining molecular subtypes of NIBC are also present in IBC.

As a result, we present a phenotype-centered gene association network, defining molecular systems that correspond temporally to hemodynamic and electrical remodeling processes.

Defining molecular markers which reflect the metastatic potential of a tumor has also proved elusive.

Summary background data: Defining molecular abnormalities in breast cancer is an important strategy for early detection, assessment of prognosis, and treatment selection.