Structural Variants Create New Topological-Associated Domains and Ectopic Retinal Enhancer-Gene Contact in Dominant Retinitis Pigmentosa von de Bruijn, Suzanne E., Fiorentino, Alessia, Ottaviani, Daniele, Fanucchi, Stephanie, Melo, Uirá S., Corral-Serrano, Julio C., Mulders, Timo, Georgiou, Michalis, Rivolta, Carlo, Pontikos, Nikolas, Arno, Gavin, Roberts, Lisa, Greenberg, Jacquie, Albert, Silvia, Gilissen, Christian, Aben, Marco, Rebello, George, Mead, Simon, Raymond, F. Lucy, Corominas, Jordi, Smith, Claire E.L., Kremer, Hannie, Downes, Susan, Black, Graeme C., Webster, Andrew R., Inglehearn, Chris F., van den Born, L. Ingeborgh, Koenekoop, Robert K., Michaelides, Michel, Ramesar, Raj S., Hoyng, Carel B., Mundlos, Stefan, Mhlanga, Musa M., Cremers, Frans P.M., Cheetham, Michael E., Roosing, Susanne, Hardcastle, Alison J.

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Optical genome mapping and revisiting short-read genome sequencing data reveal previously overlooked structural variants disrupting retinal disease−associated genes von de Bruijn, Suzanne E., Rodenburg, Kim, Corominas, Jordi, Ben-Yosef, Tamar, Reurink, Janine, Kremer, Hannie, Whelan, Laura, Plomp, Astrid S., Berger, Wolfgang, Farrar, G. Jane, Ferenc Kovács, Árpád, Fajardy, Isabelle, Hitti-Malin, Rebekkah J., Weisschuh, Nicole, Weener, Marianna E., Sharon, Dror, Pennings, Ronald J.E., Haer-Wigman, Lonneke, Hoyng, Carel B., Nelen, Marcel R., Vissers, Lisenka E.L.M., van den Born, L. Ingeborgh, Gilissen, Christian, Cremers, Frans P.M., Hoischen, Alexander, Neveling, Kornelia, Roosing, Susanne

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The Impact of Modern Technologies on Molecular Diagnostic Success Rates, with a Focus on Inherited Retinal Dystrophy and Hearing Loss von de Bruijn, Suzanne E., Fadaie, Zeinab, Cremers, Frans P. M., Kremer, Hannie, Roosing, Susanne

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Efficient Generation of Knock-In Zebrafish Models for Inherited Disorders Using CRISPR-Cas9 Ribonucleoprotein Complexes von de Vrieze, Erik, de Bruijn, Suzanne E., Reurink, Janine, Broekman, Sanne, van de Riet, Vince, Aben, Marco, Kremer, Hannie, van Wijk, Erwin

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A proteogenomic atlas of the human neural retina von Riepe, Tabea V, Stemerdink, Merel, Salz, Renee, Rey, Alfredo Dueñas, de Bruijn, Suzanne E, Boonen, Erica, Tomkiewicz, Tomasz Z, Kwint, Michael, Gloerich, Jolein, Wessels, Hans J C T, Delanote, Emma, De Baere, Elfride, van Nieuwerburgh, Filip, De Keulenaer, Sarah, Ferrari, Barbara, Ferrari, Stefano, Coppieters, Frauke, Cremers, Frans P M, van Wyk, Erwin, Roosing, Susanne, de Vrieze, Erik, 't Hoen, Peter A C

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Correction to: Exploring the missing heritability in subjects with hearing loss, enlarged vestibular aqueducts, and a single or no pathogenic SLC26A4 variant von Smits, Jeroen J., de Bruijn, Suzanne E., Lanting, Cornelis P., Oostrik, Jaap, O’Gorman, Luke, Mantere, Tuomo, Cremers, Frans P. M., Roosing, Susanne, Yntema, Helger G., de Vrieze, Erik, Derks, Ronny, Hoischen, Alexander, Pegge, Sjoert A. H., Neveling, Kornelia, Pennings, Ronald J. E., Kremer, Hannie

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ABCA4 c.6480-35A>G, a novel branchpoint variant associated with Stargardt disease von Rodríguez-Hidalgo, María, de Bruijn, Suzanne E., Corradi, Zelia, Rodenburg, Kim, Lara-López, Araceli, Valverde-Megías, Alicia, Ávila-Fernández, Almudena, Fernandez-Caballero, Lidia, Del Pozo-Valero, Marta, Corominas, Jordi, Gilissen, Christian, Irigoyen, Cristina, Cremers, Frans P. M., Ayuso, Carmen, Ruiz-Ederra, Javier, Roosing, Susanne

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Identification of novel 3D-genome altering and complex structural variants underlying retinitis pigmentosa type 17 through a multistep and high-throughput approach von de Bruijn, Suzanne E., Panneman, Daan M., Weisschuh, Nicole, Cadena, Elizabeth L., Boonen, Erica G. M., Holtes, Lara K., Astuti, Galuh D. N., Cremers, Frans P. M., Leijsten, Nico, Corominas, Jordi, Gilissen, Christian, Skowronska, Anna, Woodley, Jessica, Beggs, Andrew D., Toulis, Vasileios, Chen, Di, Cheetham, Michael E., Hardcastle, Alison J., McLaren, Terri L., Lamey, Tina M., Thompson, Jennifer A., Chen, Fred K., de Roach, John N., Urwin, Isabella R., Sullivan, Lori S., Roosing, Susanne

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Whole genome sequencing identifies elusive variants in genetically unsolved Italian inherited retinal disease patients von Zeuli, Roberta, Karali, Marianthi, de Bruijn, Suzanne E., Rodenburg, Kim, Scarpato, Margherita, Capasso, Dalila, Astuti, Galuh D.N., Gilissen, Christian, Rodríguez-Hidalgo, María, Ruiz-Ederra, Javier, Testa, Francesco, Simonelli, Francesca, Cremers, Frans P.M., Banfi, Sandro, Roosing, Susanne

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Dual inheritance patterns: A spectrum of non-syndromic inherited retinal disease phenotypes with varying molecular mechanisms von Holtes, Lara K., de Bruijn, Suzanne E., Cremers, Frans P.M., Roosing, Susanne

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Altered neural responsivity to food cues in relation to food preferences, but not appetite-related hormone concentrations after RYGB-surgery von Zoon, Harriët F.A., de Bruijn, Suzanne E.M., Smeets, Paul A.M., de Graaf, Cees, Janssen, Ignace M.C., Schijns, Wendy, Aarts, Edo O., Jager, Gerry, Boesveldt, Sanne

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Next-generation sequencing to genetically diagnose a diverse range of inherited eye disorders in 15 consanguineous families from Pakistan von Basharat, Rabia, de Bruijn, Suzanne E., Zahid, Muhammad, Rodenburg, Kim, Hitti-Malin, Rebekkah J., Rodríguez-Hidalgo, María, Boonen, Erica G.M., Jarral, Afeefa, Mahmood, Arif, Corominas, Jordi, Khalil, Sharqa, Zai, Jawaid Ahmed, Ali, Ghazanfar, Ruiz-Ederra, Javier, Gilissen, Christian, Cremers, Frans P.M., Ansar, Muhammad, Panneman, Daan M., Roosing, Susanne

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Combined Single Gene Testing and Genome Sequencing as an Effective Diagnostic Approach for Anophthalmia and Microphthalmia Patients von Basharat, Rabia, Rodenburg, Kim, Rodríguez-Hidalgo, María, Jarral, Afeefa, Ullah, Ehsan, Corominas, Jordi, Gilissen, Christian, Zehra, Syeda Tatheer, Hameed, Usman, Ansar, Muhammad, de Bruijn, Suzanne E

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Walking through Apertures: Do You Know What You are Doing during Body-Scaled Action? von Keizer, Anouk, De Bruijn, Suzanne E M, Smeets, Monique A M, Dijkerman, H Chris, Postma, Albert

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

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The reliability and validity of the Macronutrient and Taste Preference Ranking Task: A new method to measure food preferences von de Bruijn, Suzanne E.M., de Vries, Yfke C., de Graaf, Cees, Boesveldt, Sanne, Jager, Gerry

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Diverging metabolic effects of 2 energy-restricted diets differing in nutrient quality: a 12-week randomized controlled trial in subjects with abdominal obesity von Schutte, Sophie, Esser, Diederik, Siebelink, Els, Michielsen, Charlotte JR, Daanje, Monique, Matualatupauw, Juri C, Boshuizen, Hendriek C, Mensink, Marco, Afman, Lydia A

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Optical genome mapping and revisiting short-read genome sequencing data reveal previously overlooked structural variants disrupting retinal disease-associated genes von de Bruijn, Suzanne E, Rodenburg, Kim, Corominas, Jordi, Ben-Yosef, Tamar, Reurink, Janine, Kremer, Hannie, Whelan, Laura, Plomp, Astrid S, Berger, Wolfgang

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A proteogenomic atlas of the human neural retina von Riepe, Tabea V, Stemerdink, Merel, Salz, Renee, Dueñas Rey, Alfredo, de Bruijn, Suzanne E, Boonen, Erica, Tomkiewicz, Tomasz Z, Kwint, Michael, Gloerich, Jolein, Wessels, Hans J. C. T, Delanote, Emma, De Baere, Elfride, Van Nieuwerburgh, Filip, De Keulenaer, Sarah, Ferrari, Barbara, Ferrari, Stefano, Coppieters, Frauke, Cremers, Frans P. M, van Wyk, Erwin, Roosing, Susanne, de Vrieze, Erik, t Hoen, Peter A. C

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MPZL2, Encoding the Epithelial Junctional Protein Myelin Protein Zero-like 2, Is Essential for Hearing in Man and Mouse von Wesdorp, Mieke, Murillo-Cuesta, Silvia, Peters, Theo, Celaya, Adelaida M., Oonk, Anne, Schraders, Margit, Oostrik, Jaap, Gomez-Rosas, Elena, Beynon, Andy J., Hartel, Bas P., Okkersen, Kees, Koenen, Hans J.P.M., Weeda, Jack, Lelieveld, Stefan, Voermans, Nicol C., Joosten, Irma, Hoyng, Carel B., Lichtner, Peter, Kunst, Henricus P.M., Feenstra, Ilse, de Bruijn, Suzanne E., van Dooren, M.F., de Gier, H.H.W., Hoefsloot, E.H., van der Schroeff, M.P., Kant, S.G., Rotteveel, L.J.C., Frints, S.G.M., Hof, J.R., Stokroos, R.J., Vanhoutte, E.K., Admiraal, R.J.C., Feenstra, I., Kremer, H., Kunst, H.P.M., Pennings, R.J.E., Yntema, H.G., van Essen, A.J., Free, R.H., Klein-Wassink, J.S., Admiraal, Ronald J.C., Yntema, Helger G., van Wijk, Erwin, del Castillo, Ignacio, Serra, Pau, Varela-Nieto, Isabel, Pennings, Ronald J.E., Kremer, Hannie

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