Thermodynamic description of peptide adsorption on mixed-mode resins von Chilamkurthi, Sreekanth, Sevillano, David Méndez, Albers, Leonoor H.G., Sahoo, Manas Ranjan, Verheijen, Peter J.T., van der Wielen, Luuk A.M., Hollander, Jeroen L. den, Ottens, Marcel

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Discrete Countercurrent Contacting:  An Experimental Method for Developing Continuous Countercurrent Reactors von den Hollander, Jeroen L, Aversente, Antonio, Diender, Marjon B, Straathof, Adrie J. J, van der Wielen, Luuk A. M

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Performance of fractionating reactors in the absence of rate limitations von den Hollander, Jeroen L, Straathof, Adrie JJ, van der Wielen, Luuk AM

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Non-separating effects in a centrifugal partition chromatographic reactor for the enzymatic production of L-amino acids von den Hollander, Jeroen L., Wai Wong, Yiu, Ch.A.M. Luyben, Karel, van der Wielen, Luuk A.M.

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Effects of potent neutralizing antibodies from convalescent plasma in patients hospitalized for severe SARS-CoV-2 infection von Gharbharan, Arvind, Jordans, Carlijn C. E., GeurtsvanKessel, Corine, den Hollander, Jan G., Karim, Faiz, Mollema, Femke P. N., Stalenhoef – Schukken, Janneke E., Dofferhoff, Anthonius, Ludwig, Inge, Koster, Adrianus, Hassing, Robert-Jan, Bos, Jeannet C., van Pottelberge, Geert R., Vlasveld, Imro N., Ammerlaan, Heidi S. M., van Leeuwen – Segarceanu, Elena M., Miedema, Jelle, van der Eerden, Menno, Schrama, Thijs J., Papageorgiou, Grigorios, te Boekhorst, Peter, Swaneveld, Francis H., Mueller, Yvonne M., Schreurs, Marco W. J., van Kampen, Jeroen J. A., Rockx, Barry, Okba, Nisreen M. A., Katsikis, Peter D., Koopmans, Marion P. G., Haagmans, Bart L., Rokx, Casper, Rijnders, Bart J. A.

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Identification of a 2 Mb Human Ortholog of Drosophila eyes shut/spacemaker that Is Mutated in Patients with Retinitis Pigmentosa von Collin, Rob W.J., Littink, Karin W., Klevering, B. Jeroen, van den Born, L. Ingeborgh, Koenekoop, Robert K., Zonneveld, Marijke N., Blokland, Ellen A.W., Strom, Tim M., Hoyng, Carel B., den Hollander, Anneke I., Cremers, Frans P.M.

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Exome Sequencing and cis-Regulatory Mapping Identify Mutations in MAK, a Gene Encoding a Regulator of Ciliary Length, as a Cause of Retinitis Pigmentosa von Özgül, Rıza Köksal, Siemiatkowska, Anna M., Yücel, Didem, Myers, Connie A., Collin, Rob W.J., Zonneveld, Marijke N., Beryozkin, Avigail, Banin, Eyal, Hoyng, Carel B., van den Born, L. Ingeborgh, Bose, Ron, Shen, Wei, Sharon, Dror, Cremers, Frans P.M., Klevering, B. Jeroen, den Hollander, Anneke I., Corbo, Joseph C.

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Next-generation genetic testing for retinitis pigmentosa von Neveling, Kornelia, Collin, Rob W.J., Gilissen, Christian, van Huet, Ramon A.C., Visser, Linda, Kwint, Michael P., Gijsen, Sabine J., Zonneveld, Marijke N., Wieskamp, Nienke, de Ligt, Joep, Siemiatkowska, Anna M., Hoefsloot, Lies H., Buckley, Michael F., Kellner, Ulrich, Branham, Kari E., den Hollander, Anneke I., Hoischen, Alexander, Hoyng, Carel, Klevering, B. Jeroen, van den Born, L. Ingeborgh, Veltman, Joris A., Cremers, Frans P.M., Scheffer, Hans

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Mutations in the EYS Gene Account for Approximately 5% of Autosomal Recessive Retinitis Pigmentosa and Cause a Fairly Homogeneous Phenotype von Littink, Karin W., MD, van den Born, L. Ingeborgh, MD, PhD, Koenekoop, Robert K., MD, PhD, Collin, Rob W.J., PhD, Zonneveld, Marijke N., BSc, Blokland, Ellen A.W., BSc, Khan, Hayat, MD, Theelen, Thomas, MD, PhD, Hoyng, Carel B., MD, PhD, Cremers, Frans P.M., PhD, den Hollander, Anneke I., PhD, Klevering, B. Jeroen, MD, PhD

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Heterozygous Deep-Intronic Variants and Deletions in ABCA4 in Persons with Retinal Dystrophies and One Exonic ABCA4 Variant von Bax, Nathalie M., Sangermano, Riccardo, Roosing, Susanne, Thiadens, Alberta A.H.J., Hoefsloot, Lies H., van den Born, L. Ingeborgh, Phan, Milan, Klevering, B. Jeroen, Westeneng-van Haaften, Carla, Braun, Terry A., Zonneveld-Vrieling, Marijke N., de Wijs, Ilse, Mutlu, Merve, Stone, Edwin M., den Hollander, Anneke I., Klaver, Caroline C.W., Hoyng, Carel B., Cremers, Frans P.M.

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Macular Dystrophy and Cone-Rod Dystrophy Caused by Mutations in the RP1 Gene: Extending the RP1 Disease Spectrum von Verbakel, Sanne K, van Huet, Ramon A C, den Hollander, Anneke I, Geerlings, Maartje J, Kersten, Eveline, Klevering, B Jeroen, Klaver, Caroline C W, Plomp, Astrid S, Wesseling, Nieneke L, Bergen, Arthur A B, Nikopoulos, Konstantinos, Rivolta, Carlo, Ikeda, Yasuhiro, Sonoda, Koh-Hei, Wada, Yuko, Boon, Camiel J F, Nakazawa, Toru, Hoyng, Carel B, Nishiguchi, Koji M

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Disruption of the Basal Body Protein POC1B Results in Autosomal-Recessive Cone-Rod Dystrophy von Roosing, Susanne, Lamers, Ideke J.C., de Vrieze, Erik, van den Born, L. Ingeborgh, Lambertus, Stanley, Arts, Heleen H., Boldt, Karsten, de Baere, Elfride, Klaver, Caroline C.W., Coppieters, Frauke, Koolen, David A., Lugtenberg, Dorien, Neveling, Kornelia, van Reeuwijk, Jeroen, Ueffing, Marius, van Beersum, Sylvia E.C., Zonneveld-Vrieling, Marijke N., Peters, Theo A., Hoyng, Carel B., Kremer, Hannie, Hetterschijt, Lisette, Letteboer, Stef J.F., van Wijk, Erwin, Roepman, Ronald, den Hollander, Anneke I., Cremers, Frans P.M.

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Disruption of intraflagellar protein transport in photoreceptor cilia causes Leber congenital amaurosis in humans and mice von Boldt, Karsten, Mans, Dorus A, Won, Jungyeon, van Reeuwijk, Jeroen, Vogt, Andreas, Kinkl, Norbert, Letteboer, Stef J F, Hicks, Wanda L, Hurd, Ron E, Naggert, Jürgen K, Texier, Yves, den Hollander, Anneke I, Koenekoop, Robert K, Bennett, Jean, Cremers, Frans P M, Gloeckner, Christian J, Nishina, Patsy M, Roepman, Ronald, Ueffing, Marius

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IMPG2-associated retinitis pigmentosa displays relatively early macular involvement von van Huet, Ramon A C, Collin, Rob W J, Siemiatkowska, Anna M, Klaver, Caroline C W, Hoyng, Carel B, Simonelli, Francesca, Khan, Muhammad I, Qamar, Raheel, Banin, Eyal, Cremers, Frans P M, Theelen, Thomas, den Hollander, Anneke I, van den Born, L Ingeborgh, Klevering, B Jeroen

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High-resolution homozygosity mapping is a powerful tool to detect novel mutations causative of autosomal recessive RP in the Dutch population von Collin, Rob W J, van den Born, L Ingeborgh, Klevering, B Jeroen, de Castro-Miró, Marta, Littink, Karin W, Arimadyo, Kentar, Azam, Maleeha, Yazar, Volkan, Zonneveld, Marijke N, Paun, Codrut C, Siemiatkowska, Anna M, Strom, Tim M, Hehir-Kwa, Jayne Y, Kroes, Hester Y, de Faber, Jan-Tjeerd H N, van Schooneveld, Mary J, Heckenlively, John R, Hoyng, Carel B, den Hollander, Anneke I, Cremers, Frans P M

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A new gene associated with a β-thalassemia phenotype: the observation of variants in SUPT5H von Achour, Ahlem, Koopmann, Tamara, Castel, Rob, Santen, Gijs W.E., den Hollander, Nicolette, Knijnenburg, Jeroen, Ruivenkamp, Claudia A.L., Arkesteijn, Sandra G.J., ter Huurne, Jeanet, Bisoen, Sharda, Verschuren, Maaike, Vijfhuizen, Linda, Schaap, Rianne, Grimbergen, Anneliese, Slomp, Jennichjen, Traeger-Synodinos, Joanne, Vrettou, Christina, Pissard, Serge, Galacteros, Frederic, Baas, Frank, Harteveld, Cornelis L.

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Retinitis pigmentosa caused by mutations in the ciliary MAK gene is relatively mild and is not associated with apparent extra‐ocular features von Huet, Ramon A. C., Siemiatkowska, Anna M., Özgül, Riza K., Yücel, Didem, Hoyng, Carel B., Banin, Eyal, Blumenfeld, Anat, Rotenstreich, Ygal, Riemslag, Frans C. C., Hollander, Anneke I., Theelen, Thomas, Collin, Rob W. J., Born, L. Ingeborgh, Klevering, B. Jeroen

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A Nonsense Mutation in FAM161A Is a Recurrent Founder Allele in Dutch and Belgian Individuals With Autosomal Recessive Retinitis Pigmentosa von Van Schil, Kristof, Klevering, B Jeroen, Leroy, Bart P, Pott, Jan Willem R, Bandah-Rozenfeld, Dikla, Zonneveld-Vrieling, Marijke N, Sharon, Dror, den Hollander, Anneke I, Cremers, Frans P M, De Baere, Elfride, Collin, Rob W J, van den Born, L Ingeborgh

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Association of Smoking and CFH and ARMS2 Risk Variants With Younger Age at Onset of Neovascular Age-Related Macular Degeneration von Lechanteur, Yara T. E, van de Camp, Patrick L, Smailhodzic, Dzenita, van de Ven, Johannes P. H, Buitendijk, Gabriëlle H. S, Klaver, Caroline C. W, Groenewoud, Joannes M. M, den Hollander, Anneke I, Hoyng, Carel B, Klevering, B. Jeroen

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Screening of a Large Cohort of Leber Congenital Amaurosis and Retinitis Pigmentosa Patients Identifies Novel LCA5 Mutations and New Genotype-Phenotype Correlations von Mackay, Donna S., Borman, Arundhati Dev, Sui, Ruifang, van den Born, L. Ingeborgh, Berson, Eliot L., Ocaka, Louise A., Davidson, Alice E., Heckenlively, John R., Branham, Kari, Ren, Huanan, Lopez, Irma, Maria, Maleeha, Azam, Maleeha, Henkes, Arjen, Blokland, Ellen, Andreasson, Sten, de Baere, Elfride, Bennett, Jean, Chader, Gerald J., Berger, Wolfgang, Golovleva, Irina, Greenberg, Jacquie, den Hollander, Anneke I., Klaver, Caroline C.W., Klevering, B. Jeroen, Lorenz, Birgit, Preising, Markus N., Ramesar, Raj, Roberts, Lisa, Roepman, Ronald, Rohrschneider, Klaus, Wissinger], Bernd, Qamar, Raheel, Webster, Andrew R., Cremers, Frans P.M., Moore, Anthony T., Koenekoop, Robert K.

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