Integration of cryocooled superconducting analog-to-digital converter and SiGe output amplifier von Gupta, D., Kadin, A.M., Webber, R.J., Rochwarger, I., Bryce, D., Hollander, W.J., Young Uk Yim, Channakeshav, Kraft, R.P., Jin-Woo Kim, McDonald, J.F.

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Expression of Plet1 controls interstitial migration of murine small intestinal dendritic cells von Karrich, Julien J., Romera‐Hernández, Mónica, Papazian, Natalie, Veenbergen, Sharon, Cornelissen, Ferry, Aparicio‐Domingo, Patricia, Stenhouse, Frances H., Peddie, C. Diana, Hoogenboezem, Remco M., den Hollander, Chelsea W. J., Gaskell, Terri, Medley, Tanya, Boon, Louis, Blackburn, C. Clare, Withers, David R., Samsom, Janneke N., Cupedo, Tom

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A social perspective on sport-related trends and careers von Burnett, C., Hollander, W.J.

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Non-syndromic retinitis pigmentosa von Verbakel, Sanne K., van Huet, Ramon A.C., Boon, Camiel J.F., den Hollander, Anneke I., Collin, Rob W.J., Klaver, Caroline C.W., Hoyng, Carel B., Roepman, Ronald, Klevering, B. Jeroen

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Mutations in IFT172 cause isolated retinal degeneration and Bardet-Biedl syndrome von Bujakowska, Kinga M, Zhang, Qi, Siemiatkowska, Anna M, Liu, Qin, Place, Emily, Falk, Marni J, Consugar, Mark, Lancelot, Marie-Elise, Antonio, Aline, Lonjou, Christine, Carpentier, Wassila, Mohand-Saïd, Saddek, den Hollander, Anneke I, Cremers, Frans P M, Leroy, Bart P, Gai, Xiaowu, Sahel, José-Alain, van den Born, L Ingeborgh, Collin, Rob W J, Zeitz, Christina, Audo, Isabelle, Pierce, Eric A

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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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Mutations in the Mevalonate Kinase ( MVK ) Gene Cause Nonsyndromic Retinitis Pigmentosa von Siemiatkowska, Anna M., PhD, van den Born, L. Ingeborgh, MD, PhD, van Hagen, P. Martin, MD, PhD, Stoffels, Monique, MSc, Neveling, Kornelia, PhD, Henkes, Arjen, BSc, Kipping-Geertsema, Mieke, BSc, Hoefsloot, Lies H., PhD, Hoyng, Carel B., MD, PhD, Simon, Anna, MD, PhD, den Hollander, Anneke I., PhD, Cremers, Frans P.M., PhD, Collin, Rob W.J., PhD

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PRPH2 mutation update: In silico assessment of 245 reported and 7 novel variants in patients with retinal disease von Peeters, Manon H. C. A, Khan, Mubeen, Rooijakkers, Anoek A. M. B, Mulders, Timo, Haer‐Wigman, Lonneke, Boon, Camiel J. F., Klaver, Caroline C. W., Born, L. Ingeborgh, Hoyng, Carel B., Cremers, Frans P. M., Hollander, Anneke I., Dhaenens, Claire‐Marie, Collin, Rob W. J.

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Intravitreal antisense oligonucleotide sepofarsen in Leber congenital amaurosis type 10: a phase 1b/2 trial von Russell, Stephen R., Drack, Arlene V., Cideciyan, Artur V., Jacobson, Samuel G., Leroy, Bart P., Van Cauwenbergh, Caroline, Ho, Allen C., Dumitrescu, Alina V., Han, Ian C., Martin, Mitchell, Pfeifer, Wanda L., Sohn, Elliott H., Walshire, Jean, Garafalo, Alexandra V., Krishnan, Arun K., Powers, Christian A., Sumaroka, Alexander, Roman, Alejandro J., Vanhonsebrouck, Eva, Jones, Eltanara, Nerinckx, Fanny, De Zaeytijd, Julie, Collin, Rob W. J., Hoyng, Carel, Adamson, Peter, Cheetham, Michael E., Schwartz, Michael R., den Hollander, Wilhelmina, Asmus, Friedrich, Platenburg, Gerard, Rodman, David, Girach, Aniz

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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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Mutations in C8orf37, Encoding a Ciliary Protein, are Associated with Autosomal-Recessive Retinal Dystrophies with Early Macular Involvement von Estrada-Cuzcano, Alejandro, Neveling, Kornelia, Kohl, Susanne, Banin, Eyal, Rotenstreich, Ygal, Sharon, Dror, Falik-Zaccai, Tzipora C., Hipp, Stephanie, Roepman, Ronald, Wissinger, Bernd, Letteboer, Stef J.F., Mans, Dorus A., Blokland, Ellen A.W., Kwint, Michael P., Gijsen, Sabine J., van Huet, Ramon A.C., Collin, Rob W.J., Scheffer, H., Veltman, Joris A., Zrenner, Eberhart, den Hollander, Anneke I., Klevering, B. Jeroen, Cremers, Frans P.M.

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Homozygosity mapping and targeted sanger sequencing reveal genetic defects underlying inherited retinal disease in families from pakistan von Maria, Maleeha, Ajmal, Muhammad, Azam, Maleeha, Waheed, Nadia Khalida, Siddiqui, Sorath Noorani, Mustafa, Bilal, Ayub, Humaira, Ali, Liaqat, Ahmad, Shakeel, Micheal, Shazia, Hussain, Alamdar, Shah, Syed Tahir Abbas, Ali, Syeda Hafiza Benish, Ahmed, Waqas, Khan, Yar Muhammad, den Hollander, Anneke I, Haer-Wigman, Lonneke, Collin, Rob W J, Khan, Muhammad Imran, Qamar, Raheel, Cremers, Frans P M

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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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Position-dependent alternative splicing activity revealed by global profiling of alternative splicing events regulated by PTB von Smith, Christopher W J, Llorian, Miriam, Schwartz, Schraga, Clark, Tyson A, Hollander, Dror, Tan, Lit-Yeen, Spellman, Rachel, Gordon, Adele, Schweitzer, Anthony C, de la Grange, Pierre, Ast, Gil

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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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Mutations in IMPG2, Encoding Interphotoreceptor Matrix Proteoglycan 2, Cause Autosomal-Recessive Retinitis Pigmentosa von Bandah-Rozenfeld, Dikla, Collin, Rob W.J., Banin, Eyal, Ingeborgh van den Born, L., Coene, Karlien L.M., Siemiatkowska, Anna M., Zelinger, Lina, Khan, Muhammad I., Lefeber, Dirk J., Erdinest, Inbar, Testa, Francesco, Simonelli, Francesca, Voesenek, Krysta, Blokland, Ellen A.W., Strom, Tim M., Klaver, Caroline C.W., Qamar, Raheel, Banfi, Sandro, Cremers, Frans P.M., Sharon, Dror, den Hollander, Anneke I.

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Mutations in C2ORF71 Cause Autosomal-Recessive Retinitis Pigmentosa von Collin, Rob W.J., Safieh, Christine, Littink, Karin W., Shalev, Stavit A., Garzozi, Hanna J., Rizel, Leah, Abbasi, Anan H., Cremers, Frans P.M., den Hollander, Anneke I., Klevering, B. Jeroen, Ben-Yosef, Tamar

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Homozygosity Mapping Reveals PDE6C Mutations in Patients with Early-Onset Cone Photoreceptor Disorders von Thiadens, Alberta A.H.J., den Hollander, Anneke I., Roosing, Susanne, Nabuurs, Sander B., Zekveld-Vroon, Renate C., Collin, Rob W.J., De Baere, Elfride, Koenekoop, Robert K., van Schooneveld, Mary J., Strom, Tim M., van Lith-Verhoeven, Janneke J.C., Lotery, Andrew J., van Moll-Ramirez, Norka, Leroy, Bart P., van den Born, L. Ingeborgh, Hoyng, Carel B., Cremers, Frans P.M., Klaver, Caroline C.W.

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Comprehensive Analysis of the Achromatopsia Genes CNGA3 and CNGB3 in Progressive Cone Dystrophy von Thiadens, Alberta A.H.J., MD, Roosing, Susanne, Collin, Rob W.J., PhD, van Moll-Ramirez, Norka, MD, van Lith-Verhoeven, Janneke J.C., MD, PhD, van Schooneveld, Mary J., MD, PhD, den Hollander, Anneke I., PhD, van den Born, L. Ingeborgh, MD, PhD, Hoyng, Carel B., MD, PhD, Cremers, Frans P.M., PhD, Klaver, Caroline C.W., MD, PhD

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CLRN1 Mutations Cause Nonsyndromic Retinitis Pigmentosa von Khan, Muhammad Imran, MSc, MS, Kersten, Ferry F.J., BSc, Azam, Maleeha, PhD, Collin, Rob W.J., PhD, Hussain, Alamdar, MSc, Shah, Syed Tahir-A., MSc, Keunen, Jan E.E., MD, PhD, Kremer, Hannie, PhD, Cremers, Frans P.M., PhD, Qamar, Raheel, PhD, den Hollander, Anneke I., PhD

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