A novel locus for autosomal recessive nonsyndromic hearing impairment, DFNB63, maps to chromosome 11q13.2-q13.4 von KALAY, E, CAYLAN, R, KREMER, H, KIROGLU, A. F, YASAR, T, COLLIN, R. W. J, HEISTER, J. G. A. M, OOSTRIK, J, CREMERS, C. W. R. J, BRUNNER, H. G, KARAGUZEL, A

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Clinical aspects of an autosomal dominantly inherited hearing impairment linked to the DFNA60 locus on chromosome 2q23.1–2q23.3 von van Beelen, E., Schraders, M., Huygen, P.L.M., Oostrik, J., Plantinga, R.F., van Drunen, W., Collin, R.W.J., Kooper, D.P., Pennings, R.J.E., Cremers, C.W.R.J., Kremer, H., Kunst, H.P.M.

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Homozygosity mapping identifies genetic defects in four consanguineous families with retinal dystrophy from Pakistan von Khan, MI, Ajmal, M, Micheal, S, Azam, M, Hussain, A, Shahzad, A, Venselaar, H, Bokhari, H, de Wijs, IJ, Hoefsloot, LH, Waheed, NK, Collin, RWJ, den Hollander, AI, Qamar, R, Cremers, FPM

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A Nonsense Mutation in PDE6H Causes Autosomal-Recessive Incomplete Achromatopsia von Kohl, Susanne, Coppieters, Frauke, Meire, Françoise, Schaich, Simone, Roosing, Susanne, Brennenstuhl, Christina, Bolz, Sylvia, van Genderen, Maria M., Riemslag, Frans C.C., Lukowski, Robert, den Hollander, Anneke I., Cremers, Frans P.M., De Baere, Elfride, Hoyng, Carel B., Wissinger, Bernd

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Flat Threshold and Mid-Frequency Hearing Impairment in a Dutch DFNA8/12 Family with a Novel Mutation in TECTA : Some Evidence for Protection of the Inner Ear von DE HEER, A. R, PAUW, R. J, HUYGEN, P. L. M, COLLIN, R. W. J, KREMER, H, CREMERS, C. W. R. J

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Flat Threshold and Mid-Frequency Hearing Impairment in a Dutch DFNA8/12 Family with a Novel Mutation in TECTA von de Heer, A.R., Pauw, R.J., Huygen, P.L.M., Collin, R.W.J., Kremer, H., Cremers, C.W.R.J.

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Genomic approaches for the discovery of genes mutated in inherited retinal degeneration von Siemiatkowska, Anna M, Collin, Rob W J, den Hollander, Anneke I, Cremers, Frans P M

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Homozygosity mapping identifies genetic defects in four consanguineous families with retinal dystrophy from Pakistan von Khan, M I, Ajmal, M, Micheal, S, Azam, M, Hussain, A, Shahzad, A, Venselaar, H, Bokhari, H, de Wijs, I J, Hoefsloot, L H, Waheed, N K, Collin, R W J, den Hollander, A I, Qamar, R, Cremers, F P M

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A DNA vaccine for Crimean-Congo hemorrhagic fever protects against disease and death in two lethal mouse models von Garrison, Aura R, Shoemaker, Charles J, Golden, Joseph W, Fitzpatrick, Collin J, Suschak, John J, Richards, Michelle J, Badger, Catherine V, Six, Carolyn M, Martin, Jacqueline D, Hannaman, Drew, Zivcec, Marko, Bergeron, Eric, Koehler, Jeffrey W, Schmaljohn, Connie S

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GRAECUM LEXICON MANUALE von Benjamin Hederich, nlk20010102893

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Delivery of oligonucleotide‐based therapeutics: challenges and opportunities von Hammond, Suzan M, Aartsma‐Rus, Annemieke, Alves, Sandra, Borgos, Sven E, Buijsen, Ronald A M, Collin, Rob W J, Covello, Giuseppina, Denti, Michela A, Desviat, Lourdes R, Echevarría, Lucía, Foged, Camilla, Gaina, Gisela, Garanto, Alejandro, Goyenvalle, Aurelie T, Guzowska, Magdalena, Holodnuka, Irina, Jones, David R, Krause, Sabine, Lehto, Taavi, Montolio, Marisol, Van Roon‐Mom, Willeke, Arechavala‐Gomeza, Virginia

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Assembly and Function of a Bioengineered Human Liver for Transplantation Generated Solely from Induced Pluripotent Stem Cells von Takeishi, Kazuki, Collin de l’Hortet, Alexandra, Wang, Yang, Handa, Kan, Guzman-Lepe, Jorge, Matsubara, Kentaro, Morita, Kazutoyo, Jang, Sae, Haep, Nils, Florentino, Rodrigo M., Yuan, Fangchao, Fukumitsu, Ken, Tobita, Kimimasa, Sun, Wendell, Franks, Jonathan, Delgado, Evan R., Shapiro, Erik M., Fraunhoffer, Nicolas A., Duncan, Andrew W., Yagi, Hiroshi, Mashimo, Tomoji, Fox, Ira J., Soto-Gutierrez, Alejandro

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Persistent Crimean-Congo hemorrhagic fever virus infection in the testes and within granulomas of non-human primates with latent tuberculosis von Smith, Darci R, Shoemaker, Charles J, Zeng, Xiankun, Garrison, Aura R, Golden, Joseph W, Schellhase, Christopher W, Pratt, William, Rossi, Franco, Fitzpatrick, Collin J, Shamblin, Joshua, Kimmel, Adrienne, Zelko, Justine, Flusin, Olivier, Koehler, Jeffrey W, Liu, Jun, Coffin, Kayla M, Ricks, Keersten M, Voorhees, Matt A, Schoepp, Randal J, Schmaljohn, Connie S

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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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Deep-intronic ABCA4 variants explain missing heritability in Stargardt disease and allow correction of splice defects by antisense oligonucleotides von Sangermano, Riccardo, Garanto, Alejandro, Khan, Mubeen, Runhart, Esmee H., Bauwens, Miriam, Bax, Nathalie M., van den Born, L. Ingeborgh, Khan, Muhammad Imran, Cornelis, Stéphanie S., Verheij, Joke B. G. M., Pott, Jan-Willem R., Thiadens, Alberta A. H. J., Klaver, Caroline C. W., Puech, Bernard, Meunier, Isabelle, Naessens, Sarah, Arno, Gavin, Fakin, Ana, Carss, Keren J., Raymond, F. Lucy, Webster, Andrew R., Dhaenens, Claire-Marie, Stöhr, Heidi, Grassmann, Felix, Weber, Bernhard H. F., Hoyng, Carel B., De Baere, Elfride, Albert, Silvia, Collin, Rob W. J., Cremers, Frans P. M.

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A gut bacterial amyloid promotes α-synuclein aggregation and motor impairment in mice von Sampson, Timothy R, Challis, Collin, Jain, Neha, Moiseyenko, Anastasiya, Ladinsky, Mark S, Shastri, Gauri G, Thron, Taren, Needham, Brittany D, Horvath, Istvan, Debelius, Justine W, Janssen, Stefan, Knight, Rob, Wittung-Stafshede, Pernilla, Gradinaru, Viviana, Chapman, Matthew, Mazmanian, Sarkis K

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The host inflammatory response contributes to disease severity in Crimean-Congo hemorrhagic fever virus infected mice von Golden, Joseph W, Zeng, Xiankun, Cline, Curtis R, Smith, Jeffrey M, Daye, Sharon P, Carey, Brian D, Blancett, Candace D, Shoemaker, Charles J, Liu, Jun, Fitzpatrick, Collin J, Stefan, Christopher P, Garrison, Aura R

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Initiation of Antiretroviral Therapy in Early Asymptomatic HIV Infection von Lundgren, Jens D, Babiker, Abdel G, Gordin, Fred, Emery, Sean, Grund, Birgit, Sharma, Shweta, Avihingsanon, Anchalee, Cooper, David A, Fätkenheuer, Gerd, Llibre, Josep M, Molina, Jean-Michel, Munderi, Paula, Schechter, Mauro, Wood, Robin, Klingman, Karin L, Collins, Simon, Lane, H Clifford, Phillips, Andrew N, Neaton, James D

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An aged immune system drives senescence and ageing of solid organs von Yousefzadeh, Matthew J., Flores, Rafael R., Zhu, Yi, Schmiechen, Zoe C., Brooks, Robert W., Trussoni, Christy E., Cui, Yuxiang, Angelini, Luise, Lee, Kyoo-A, McGowan, Sara J., Burrack, Adam L., Wang, Dong, Dong, Qing, Lu, Aiping, Sano, Tokio, O’Kelly, Ryan D., McGuckian, Collin A., Kato, Jonathan I., Bank, Michael P., Wade, Erin A., Pillai, Smitha P. S., Klug, Jenna, Ladiges, Warren C., Burd, Christin E., Lewis, Sara E., LaRusso, Nicholas F., Vo, Nam V., Wang, Yinsheng, Kelley, Eric E., Huard, Johnny, Stromnes, Ingunn M., Robbins, Paul D., Niedernhofer, Laura J.

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ABCA4-associated disease as a model for missing heritability in autosomal recessive disorders: novel noncoding splice, cis-regulatory, structural, and recurrent hypomorphic variant... von Bauwens, Miriam, Garanto, Alejandro, Sangermano, Riccardo, Naessens, Sarah, Weisschuh, Nicole, De Zaeytijd, Julie, Khan, Mubeen, Sadler, Françoise, Balikova, Irina, Van Cauwenbergh, Caroline, Rosseel, Toon, Bauwens, Jim, De Leeneer, Kim, De Jaegere, Sarah, Van Laethem, Thalia, De Vries, Meindert, Carss, Keren, Arno, Gavin, Fakin, Ana, Webster, Andrew R., de Ravel de l’Argentière, Thomy J. L., Sznajer, Yves, Vuylsteke, Marnik, Kohl, Susanne, Wissinger, Bernd, Cherry, Timothy, Collin, Rob W. J., Cremers, Frans P. M., Leroy, Bart P., De Baere, Elfride

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