Gene expression and functional annotation of human choroid plexus epithelium failure in Alzheimer’s disease

por Bergen, Arthur A., Kaing, Sovann, ten Brink, Jacoline B., Gorgels, Theo G., Janssen, Sarah F.
Publicado 2015

Comparative gene expression study and pathway analysis of the human iris- and the retinal pigment epithelium

por Bennis, Anna, ten Brink, Jacoline B., Moerland, Perry D., Heine, Vivi M., Bergen, Arthur A.
Publicado 2017

Genome-wide CNV investigation suggests a role for cadherin, Wnt, and p53 pathways in primary open-angle glaucoma

por Lo Faro, Valeria, ten Brink, Jacoline B., Snieder, Harold, Jansonius, Nomdo M., Bergen, Arthur A.
Publicado 2021

Gene expression-based comparison of the human secretory neuroepithelia of the brain choroid plexus and the ocular ciliary body: potential implications for glaucoma

por Janssen, Sarah F, Gorgels, Theo GMF, ten Brink, Jacoline B, Jansonius, Nomdo M, Bergen, Arthur AB
Publicado 2014

Mitochondrial Genome Study Identifies Association Between Primary Open-Angle Glaucoma and Variants in MT-CYB, MT-ND4 Genes and Haplogroups

por Lo Faro, Valeria, Nolte, Ilja M., Ten Brink, Jacoline B., Snieder, Harold, Jansonius, Nomdo M., Bergen, Arthur A.
Publicado 2021

An alternative approach to produce versatile retinal organoids with accelerated ganglion cell development

por Wagstaff, Ellie L., ten Asbroek, Anneloor L. M. A., ten Brink, Jacoline B., Jansonius, Nomdo M., Bergen, Arthur A. B.
Publicado 2021

Sodium-Iodate Injection Can Replicate Retinal Degenerative Disease Stages in Pigmented Mice and Rats: Non-Invasive Follow-Up Using OCT and ERG

por Koster, Céline, van den Hurk, Koen T., ten Brink, Jacoline B., Lewallen, Colby F., Stanzel, Boris V., Bharti, Kapil, Bergen, Arthur A.
Publicado 2022

The Lrat(−/−) Rat: CRISPR/Cas9 Construction and Phenotyping of a New Animal Model for Retinitis Pigmentosa

por Koster, Céline, van den Hurk, Koen T., Lewallen, Colby F., Talib, Mays, ten Brink, Jacoline B., Boon, Camiel J. F., Bergen, Arthur A.
Publicado 2021

Dietary magnesium, not calcium, prevents vascular calcification in a mouse model for pseudoxanthoma elasticum

por Gorgels, Theo G. M. F., Waarsing, Jan H., de Wolf, Anneke, ten Brink, Jacoline B., Loves, Willem J. P., Bergen, Arthur A. B.
Publicado 2010

Comparison of Mouse and Human Retinal Pigment Epithelium Gene Expression Profiles: Potential Implications for Age-Related Macular Degeneration

por Bennis, Anna, Gorgels, Theo G. M. F., ten Brink, Jacoline B., van der Spek, Peter J., Bossers, Koen, Heine, Vivi M., Bergen, Arthur A.
Publicado 2015

A New Strategy to Identify and Annotate Human RPE-Specific Gene Expression

por Booij, Judith C., ten Brink, Jacoline B., Swagemakers, Sigrid M. A., Verkerk, Annemieke J. M. H., Essing, Anke H. W., van der Spek, Peter J., Bergen, Arthur A. B.
Publicado 2010

Gene Expression and Functional Annotation of the Human Ciliary Body Epithelia

por Janssen, Sarah F., Gorgels, Theo G. M. F., Bossers, Koen, ten Brink, Jacoline B., Essing, Anke H. W., Nagtegaal, Martijn, van der Spek, Peter J., Jansonius, Nomdo M., Bergen, Arthur A. B.
Publicado 2012

Gene Expression and Functional Annotation of the Human and Mouse Choroid Plexus Epithelium

por Janssen, Sarah F., van der Spek, Sophie J. F., ten Brink, Jacoline B., Essing, Anke H. W., Gorgels, Theo G. M. F., van der Spek, Peter J., Jansonius, Nomdo M., Bergen, Arthur A. B.
Publicado 2013

Long-Term Follow-Up of Retinal Degenerations Associated With LRAT Mutations and Their Comparability to Phenotypes Associated With RPE65 Mutations

por Talib, Mays, van Schooneveld, Mary J, van Duuren, Roos J. G., Van Cauwenbergh, Caroline, ten Brink, Jacoline B., De Baere, Elfride, Florijn, Ralph J., Schalij-Delfos, Nicoline E., Leroy, Bart P., Bergen, Arthur A., Boon, Camiel J. F.
Publicado 2019

The ERCC6 Gene and Age-Related Macular Degeneration

por Baas, Dominique C., Despriet, Dominiek D., Gorgels, Theo G. M. F., Bergeron-Sawitzke, Julie, Uitterlinden, André G., Hofman, Albert, van Duijn, Cornelia M., Merriam, Joanna E., Smith, R. Theodore, Barile, Gaetano R., ten Brink, Jacoline B., Vingerling, Johannes R., Klaver, Caroline C. W., Allikmets, Rando, Dean, Michael, Bergen, Arthur A. B.
Publicado 2010

Molecular Inversion Probe-Based Sequencing of USH2A Exons and Splice Sites as a Cost-Effective Screening Tool in USH2 and arRP Cases

por Reurink, Janine, Dockery, Adrian, Oziębło, Dominika, Farrar, G. Jane, Ołdak, Monika, ten Brink, Jacoline B., Bergen, Arthur A., Rinne, Tuula, Yntema, Helger G., Pennings, Ronald J. E., van den Born, L. Ingeborgh, Aben, Marco, Oostrik, Jaap, Venselaar, Hanka, Plomp, Astrid S., Khan, M. Imran, van Wijk, Erwin, Cremers, Frans P. M., Roosing, Susanne, Kremer, Hannie
Publicado 2021

Defining inclusion criteria and endpoints for clinical trials: a prospective cross‐sectional study in CRB1‐associated retinal dystrophies

por Talib, Mays, van Schooneveld, Mary J., Wijnholds, Jan, van Genderen, Maria M., Schalij‐Delfos, Nicoline E., Talsma, Herman E., Florijn, Ralph J., ten Brink, Jacoline B., Cremers, Frans P.M., Thiadens, Alberta A.H.J., van den Born, L. Ingeborgh, Hoyng, Carel B., Meester‐Smoor, Magda A., Bergen, Arthur A., Boon, Camiel J.F.
Publicado 2021

Multicenter cohort association study of SLC2A1 single nucleotide polymorphisms and age-related macular degeneration

por Baas, Dominique C., Ho, Lintje, Tanck, Michael W.T., Fritsche, Lars G., Merriam, Joanna E., van het Slot, Ruben, Koeleman, Bobby P.C., Gorgels, Theo G.M.F., van Duijn, Cornelia M., Uitterlinden, André G., de Jong, Paulus T.V.M., Hofman, Albert, ten Brink, Jacoline B., Vingerling, Johannes R., Klaver, Caroline C.W., Dean, Michael, Weber, Bernhard H. F., Allikmets, Rando, Hageman, Gregory S., Bergen, Arthur A.B.
Publicado 2012

Common Genetic Determinants of Intraocular Pressure and Primary Open-Angle Glaucoma

por van Koolwijk, Leonieke M. E., Ramdas, Wishal D., Ikram, M. Kamran, Jansonius, Nomdo M., Pasutto, Francesca, Hysi, Pirro G., Macgregor, Stuart, Janssen, Sarah F., Hewitt, Alex W., Viswanathan, Ananth C., ten Brink, Jacoline B., Hosseini, S. Mohsen, Amin, Najaf, Despriet, Dominiek D. G., Willemse-Assink, Jacqueline J. M., Kramer, Rogier, Rivadeneira, Fernando, Struchalin, Maksim, Aulchenko, Yurii S., Weisschuh, Nicole, Zenkel, Matthias, Mardin, Christian Y., Gramer, Eugen, Welge-Lüssen, Ulrich, Montgomery, Grant W., Carbonaro, Francis, Young, Terri L., Bellenguez, Céline, McGuffin, Peter, Foster, Paul J., Topouzis, Fotis, Mitchell, Paul, Wang, Jie Jin, Wong, Tien Y., Czudowska, Monika A., Hofman, Albert, Uitterlinden, Andre G., Wolfs, Roger C. W., de Jong, Paulus T. V. M., Oostra, Ben A., Paterson, Andrew D., Mackey, David A., Bergen, Arthur A. B., Reis, André, Hammond, Christopher J., Vingerling, Johannes R., Lemij, Hans G., Klaver, Caroline C. W., van Duijn, Cornelia M.
Publicado 2012

Whole genome sequencing for USH2A-associated disease reveals several pathogenic deep-intronic variants that are amenable to splice correction

por Reurink, Janine, Weisschuh, Nicole, Garanto, Alejandro, Dockery, Adrian, van den Born, L. Ingeborgh, Fajardy, Isabelle, Haer-Wigman, Lonneke, Kohl, Susanne, Wissinger, Bernd, Farrar, G. Jane, Ben-Yosef, Tamar, Pfiffner, Fatma Kivrak, Berger, Wolfgang, Weener, Marianna E., Dudakova, Lubica, Liskova, Petra, Sharon, Dror, Salameh, Manar, Offenheim, Ashley, Heon, Elise, Girotto, Giorgia, Gasparini, Paolo, Morgan, Anna, Bergen, Arthur A., ten Brink, Jacoline B., Klaver, Caroline C.W., Tranebjærg, Lisbeth, Rendtorff, Nanna D., Vermeer, Sascha, Smits, Jeroen J., Pennings, Ronald J.E., Aben, Marco, Oostrik, Jaap, Astuti, Galuh D.N., Corominas Galbany, Jordi, Kroes, Hester Y., Phan, Milan, van Zelst-Stams, Wendy A.G., Thiadens, Alberta A.H.J., Verheij, Joke B.G.M., van Schooneveld, Mary J., de Bruijn, Suzanne E., Li, Catherina H.Z., Hoyng, Carel B., Gilissen, Christian, Vissers, Lisenka E.L.M., Cremers, Frans P.M., Kremer, Hannie, van Wijk, Erwin, Roosing, Susanne
Publicado 2023