Carrier Frequency of CYP1B1 Mutations in the United States (An American Ophthalmological Society Thesis)

Por Wiggs, Janey L., Langgurth, Anne M., Allen, Keri F.
Publicado no Trans Am Ophthalmol Soc (2014)

Genetics of Primary Inherited Disorders of the Optic Nerve: Clinical Applications

Por Allen, Keri F., Gaier, Eric D., Wiggs, Janey L.
Publicado no Cold Spring Harb Perspect Med (2015)

Diagnostic genetic testing for patients with bilateral optic neuropathy and comparison of clinical features according to OPA1 mutation status

Por Gaier, Eric D., Boudreault, Katherine, Nakata, Isao, Janessian, Maria, Skidd, Philip, DelBono, Elizabeth, Allen, Keri F., Pasquale, Louis R., Place, Emily, Cestari, Dean M., Stacy, Rebecca C., Rizzo, Joseph F., Wiggs, Janey L.
Publicado no Mol Vis (2017)

Angiopoietin receptor TEK mutations underlie primary congenital glaucoma with variable expressivity

Por Souma, Tomokazu, Tompson, Stuart W., Thomson, Benjamin R., Siggs, Owen M., Kizhatil, Krishnakumar, Yamaguchi, Shinji, Feng, Liang, Limviphuvadh, Vachiranee, Whisenhunt, Kristina N., Maurer-Stroh, Sebastian, Yanovitch, Tammy L., Kalaydjieva, Luba, Azmanov, Dimitar N., Finzi, Simone, Mauri, Lucia, Javadiyan, Shahrbanou, Souzeau, Emmanuelle, Zhou, Tiger, Hewitt, Alex W., Kloss, Bethany, Burdon, Kathryn P., Mackey, David A., Allen, Keri F., Ruddle, Jonathan B., Lim, Sing-Hui, Rozen, Steve, Tran-Viet, Khanh-Nhat, Liu, Xiaorong, John, Simon, Wiggs, Janey L., Pasutto, Francesca, Craig, Jamie E., Jin, Jing, Quaggin, Susan E., Young, Terri L.
Publicado no J Clin Invest (2016)