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Duvvari, Maheswara R., Paun, Codrut C., Buitendijk, Gabrielle 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, Andre G., Klaver, Caroline C. W., Hoyng, Carel B., de Jong, Eiko K. and den Hollander, Anneke I. (2014). Analysis of Rare Variants in the C3 Gene in Patients with Age-Related Macular Degeneration. PLoS One, 9 (4). SAN FRANCISCO: PUBLIC LIBRARY SCIENCE. ISSN 1932-6203
Duvvari, Maheswara R., Saksens, Nicole T. M., van de Ven, Johannes P. H., de Jong-Hesse, Yvonne, Schick, Tina, Nillesen, Willy M., Fauser, Sascha, Hoefsloot, Lies H., Hoyng, Carel B., de Jong, Eiko K. and den Hollander, Anneke I. (2015). Analysis of rare variants in the CFH gene in patients with the cuticular drusen subtype of age-related macular degeneration. Mol. Vis., 21. S. 285 - 293. ATLANTA: MOLECULAR VISION. ISSN 1090-0535
Duvvari, Maheswara R., Saksens, Nicole T. M., van de Ven, Johannes P. H., de Jong-Hesse, Yvonne, Schick, Tina, Nillesen, Willy M., Fauser, Sascha, Hoefsloot, Lies H., Hoyng, Carel B., de Jong, Eiko K. and den Hollander, Anneke I. (2015). Analysis of rare variants in the CFH gene in patients with the cuticular drusen subtype of age-related macular degeneration. Mol. Vis., 21. S. 285 - 293. ATLANTA: MOLECULAR VISION. ISSN 1090-0535
Duvvari, Maheswara R., van de Ven, Johannes P. H., Geerlings, Maartje J., Saksens, Nicole T. M., Bakker, Bjorn, Henkes, Arjen, Neveling, Kornelia, del Rosario, Marisol, Westra, Dineke, van den Heuvel, Lambertus P. W. J., Schick, Tina, Fauser, Sascha, Boon, Camiel J. F., Hoyng, Carel B., de Jong, Eiko K. and den Hollander, Anneke I. (2016). Whole Exome Sequencing in Patients with the Cuticular Drusen Subtype of Age-Related Macular Degeneration. PLoS One, 11 (3). SAN FRANCISCO: PUBLIC LIBRARY SCIENCE. ISSN 1932-6203
Helgason, Hannes, Sulem, Patrick, Duvvari, Maheswara R., Luo, Hongrong, Thorleifsson, Gudmar, Stefansson, Hreinn 
ORCID: 0000-0002-9331-6666, Jonsdottir, Ingileif, Masson, Gisli, Gudbjartsson, Daniel F., Walters, G. Bragi ORCID: 0000-0002-5415-6487, Magnusson, Olafur Th, Kong, Augustine ORCID: 0000-0001-8193-5438, Rafnar, Thorunn, Kiemeney, Lambertus A. ORCID: 0000-0002-2368-1326, Schoenmaker-Koller, Frederieke E., Zhao, Ling, Boon, Camiel J. F., Song, Yaojun, Fauser, Sascha, Pei, Michelle, Ristau, Tina, Patel, Shirrina, Liakopoulos, Sandra, van de Ven, Johannes P. H., Hoyng, Carel B., Ferreyra, Henry, Duan, Yaou, Bernstein, Paul S., Geirsdottir, Asbjorg, Helgadottir, Gudleif, Stefansson, Einar, den Hollander, Anneke I., Zhang, Kang ORCID: 0000-0002-4549-1697, Jonasson, Fridbert, Sigurdsson, Haraldur, Thorsteinsdottir, Unnur and Stefansson, Kari
(2013).
A rare nonsynonymous sequence variant in C3 is associated with high risk of age-related macular degeneration.
Nature Genet., 45 (11).
S. 1371 - 1377.
NEW YORK:
NATURE PUBLISHING GROUP.
ISSN 1546-1718