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2022
de Jong, Sarah 
ORCID: 0000-0002-3705-3371, de Breuk, Anita, Volokhina, Elena B., Bakker, Bjorn, Garanto, Alejandro ORCID: 0000-0001-5721-1560, Fauser, Sascha, Katti, Suresh, Hoyng, Carel B., Lechanteur, Yara T. E., van den Heuvel, Lambert P. and den Hollander, Anneke, I
(2022).
Systemic complement levels in patients with age-related macular degeneration carrying rare or low-frequency variants in the CFH gene.
Hum. Mol. Genet., 31 (3).
S. 455 - 471.
OXFORD:
OXFORD UNIV PRESS.
ISSN 1460-2083
2021
de Breuk, Anita ORCID: 0000-0001-7072-1928, Acar, Ilhan E., Kersten, Eveline, Schijvenaars, Mascha M. V. A. P., Colijn, Johanna M., Haer-Wigman, Lonneke, Bakker, Bjorn, de Jong, Sarah ORCID: 0000-0002-3705-3371, Meester-Smoor, Magda A., Verzijden, Timo, Missotten, Tom O. A. R., Mones, Jordi, Biarnes, Marc, Pauleikhoff, Daniel, Hense, Hans W., Silva, Rufino ORCID: 0000-0001-8676-0833, Nunes, Sandrina, Melo, Joana B., Fauser, Sascha, Hoyng, Carel B., Ueffing, Marius, Coenen, Marieke J. H., Klaver, Caroline C. W. and den Hollander, Anneke, I
(2021).
Development of a Genotype Assay for Age-Related Macular Degeneration The EYE-RISK Consortium.
Ophthalmology, 128 (11).
S. 1604 - 1618.
NEW YORK:
ELSEVIER SCIENCE INC.
ISSN 1549-4713
2018
Kremlitzka, Mariann, Geerlings, Maartje J., de Jong, Sarah, Bakker, Bjorn, Nilsson, Sara C., Fauser, Sascha, Hoyng, Carel B., de Jong, Eiko K., den Hollander, Anneke I. and Blom, Anna M. (2018). Functional analyses of rare genetic variants in complement component C9 identified in patients with age-related macular degeneration. Hum. Mol. Genet., 27 (15). S. 2678 - 2689. OXFORD: OXFORD UNIV PRESS. ISSN 1460-2083
2017
Kremlitzka, Mariann, de Jong, Sarah, Geerlings, Maartje ORCID: 0000-0003-1164-3573, Bakker, Bjorn, Nilsson, Sara C., Fauser, Sascha, Hoyng, Carel B., de Jong, Eiko K., den Hollander, Anneke I. and Blom, Anna M.
(2017).
Functional analysis of AMD-associated rare genetic variants in C9.
Mol. Immunol., 89.
S. 150 - 151.
OXFORD:
PERGAMON-ELSEVIER SCIENCE LTD.
ISSN 0161-5890