Karen E. Wain

Identification of single gene deletions at 15q13.3: further evidence that CHRNA7 causes the 15q13.3 microdeletion syndrome phenotype

K. Wain, Jennelle C Hodge, N. Hoppman-Chaney, 2013, Clinical genetics.

Living at Risk: The Sibling’s Perspective of Early-Onset Alzheimer’s Disease

J. Roberts, J. Heidebrink, W. Uhlmann, 2009, Journal of Genetic Counseling.