Steven S. Scherer

Harmonizing Clinical Sequencing and Interpretation for the eMERGE III Network.

Robert C. Green, Keith Marsolo, Casey Overby Taylor, 2019, American journal of human genetics.

Genetic test utilization and diagnostic yield in adult patients with neurological disorders

Steven S. Scherer, Ingo Helbig, I. Helbig, 2018, neurogenetics.

Molecular KCNQ 2 Is a Nodal K Channel

Steven S. Scherer, Edward C. Cooper, S. Scherer, 2004 .

Nectin-like proteins mediate axon–Schwann cell interactions along the internode and are essential for myelination

Steven S. Scherer, David H. Gutmann, D. Gutmann, 2007, The Journal of cell biology.

Dominant Cx26 mutants associated with hearing loss have dominant-negative effects on wild type Cx26

Steven S. Scherer, S. Scherer, S. Yum, 2011, Molecular and Cellular Neuroscience.

Dominant connexin26 mutants associated with human hearing loss have trans-dominant effects on connexin30

Steven S. Scherer, S. Scherer, S. Yum, 2010, Neurobiology of Disease.