Association of known common genetic variants with primary open angle, primary angle closure, and pseudoexfoliation glaucoma in Pakistani cohorts

Por Micheal, Shazia, Ayub, Humaira, Khan, Muhammad Imran, Bakker, Bjorn, Schoenmaker-Koller, Frederieke E., Ali, Mahmood, Akhtar, Farah, Khan, Wajid Ali, Qamar, Raheel, den Hollander, Anneke I.
Publicado no Mol Vis (2014)

Association of a Polymorphism in the BIRC6 Gene with Pseudoexfoliative Glaucoma

Por Ayub, Humaira, Micheal, Shazia, Akhtar, Farah, Khan, Muhammad Imran, Bashir, Shaheena, Waheed, Nadia K., Ali, Mahmood, Schoenmaker-Koller, Frederieke E., Shafique, Sobia, Qamar, Raheel, den Hollander, Anneke I.
Publicado em 2014

Analysis of Rare Variants in the C3 Gene in Patients with Age-Related Macular Degeneration

Por Duvvari, Maheswara R., Paun, Codrut C., Buitendijk, Gabriëlle H. S., Saksens, Nicole T. M., Volokhina, Elena B., Ristau, Tina, Schoenmaker-Koller, Frederieke E., van de Ven, Johannes P. H., Groenewoud, Joannes M. M., van den Heuvel, Lambertus P. W. J., Hofman, Albert, Fauser, Sascha, Uitterlinden, André G., Klaver, Caroline C. W., Hoyng, Carel B., de Jong, Eiko K., den Hollander, Anneke I.
Publicado em 2014

Mutations in CTNNA1 cause butterfly-shaped pigment dystrophy and perturbed retinal pigment epithelium integrity

Por Saksens, Nicole T.M., Krebs, Mark P., Schoenmaker-Koller, Frederieke E., Hicks, Wanda, Yu, Minzhong, Shi, Lanying, Rowe, Lucy, Collin, Gayle B., Charette, Jeremy R., Letteboer, Stef J., Neveling, Kornelia, van Moorsel, Tamara W., Abu-Ltaif, Sleiman, De Baere, Elfride, Walraedt, Sophie, Banfi, Sandro, Simonelli, Francesca, Cremers, Frans P.M., Boon, Camiel J.F., Roepman, Ronald, Leroy, Bart P., Peachey, Neal S., Hoyng, Carel B., Nishina, Patsy M., den Hollander, Anneke I.
Publicado no Nat Genet (2015)