Diverse molecular causes of unsolved autosomal dominant tubulointerstitial kidney diseases von Wopperer, Florian J., Knaup, Karl X., Stanzick, Kira J., Schneider, Karen, Jobst-Schwan, Tilman, Ekici, Arif B., Uebe, Steffen, Wenzel, Andrea, Schliep, Stefan, Schürfeld, Carsten, Seitz, Randolf, Bernhardt, Wanja, Gödel, Markus, Wiesener, Antje, Popp, Bernt, Stark, Klaus J., Gröne, Hermann-Josef, Friedrich, Björn, Weiß, Martin, Basic-Jukic, Nikolina, Schiffer, Mario, Schröppel, Bernd, Huettel, Bruno, Beck, Bodo B., Sayer, John A., Ziegler, Christine, Büttner-Herold, Maike, Amann, Kerstin, Heid, Iris M., Reis, André, Pasutto, Francesca, Wiesener, Michael S.

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Characteristics of p.Gln368Ter Myocilin Variant and Influence of Polygenic Risk on Glaucoma Penetrance in the UK Biobank von Zebardast, Nazlee, Sekimitsu, Sayuri, Wang, Jiali, Elze, Tobias, Gharahkhani, Puya, Cole, Brian S., Lin, Michael M., Segrè, Ayellet V., Wiggs, Janey L., Aung, Tin, Craig, Jamie E., Cheng, Ching-Yu, Cooke Bailey, Jessica N., Cree, Angela J., Foster, Paul J., Gharahkhani, Puya, Hammond, Christopher J., Hewitt, Alex W., Höhn, René, Hysi, Pirro G., Iglesias, Adriana I., Jonas, Jost B., Klaver, Caroline C.W., Khawaja, Anthony P., Khor, Chiea Chuen, Lotery, Andrew J., MacGregor, Stuart, Mackey, David A., Ong, Jue Sheng, Mitchell, Paul, Pasquale, Louis R., Pang, ChiPui, Pasutto, Francesca, Pfeiffer, Norbert, Segre, Ayellet V., van Duijn, Cornelia M., Viswanathan, Ananth C., Vitart, Veronique, Vithana, Eranga N., Wiggs, Janey L., Wojciechowski, Robert, Young, Terri L., Wong, Tien Yin, Yazar, Seyhan

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Integrating genetic regulation and single-cell expression with GWAS prioritizes causal genes and cell types for glaucoma von Hamel, Andrew R., Yan, Wenjun, Rouhana, John M., Monovarfeshani, Aboozar, Jiang, Xinyi, Mehta, Puja A., Advani, Jayshree, Luo, Yuyang, Liang, Qingnan, Rajasundaram, Skanda, Shrivastava, Arushi, Duchinski, Katherine, Mantena, Sreekar, Wang, Jiali, van Zyl, Tavé, Pasquale, Louis R., Swaroop, Anand, Gharahkhani, Puya, Khawaja, Anthony P., MacGregor, Stuart, Chen, Rui, Vitart, Veronique, Sanes, Joshua R., Wiggs, Janey L., Segrè, Ayellet V.

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Systems genetics identifies a role for Cacna2d1 regulation in elevated intraocular pressure and glaucoma susceptibility von Chintalapudi, Sumana R., Maria, Doaa, Di Wang, Xiang, Bailey, Jessica N. Cooke, Hysi, Pirro G., Wiggs, Janey L., Williams, Robert W., Jablonski, Monica M.

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Multi-trait genome-wide association study identifies new loci associated with optic disc parameters von Bonnemaijer, Pieter W. M., Leeuwen, Elisabeth M. van, Iglesias, Adriana I., Gharahkhani, Puya, Vitart, Veronique, Khawaja, Anthony P., Simcoe, Mark, Höhn, René, Cree, Angela J., Igo, Rob P., Gerhold-Ay, Aslihan, Nickels, Stefan, Wilson, James F., Hayward, Caroline, Boutin, Thibaud S., Polašek, Ozren, Aung, Tin, Khor, Chiea Chuen, Amin, Najaf, Lotery, Andrew J., Wiggs, Janey L., Cheng, Ching-Yu, Hysi, Pirro G., Hammond, Christopher J., Thiadens, Alberta A. H. J., MacGregor, Stuart, Klaver, Caroline C. W., Duijn, Cornelia M. van

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Forest damage inventory after the "Vaia" storm in Italy von Chirici G, Giannetti F, Travaglini D, Nocentini S, Francini S, D’Amico G, Calvo E, Fasolini D, Broll M, Maistrelli F, Tonner J, Pietrogiovanna M, Oberlechner K, Andriolo A, Comino R, Faidiga A, Pasutto I, Carraro G, Zen S, Contarin F, Alfonsi L, Wolynski A, Zanin M, Gagliano C, Tonolli S, Zoanetti R, Tonetti R, Cavalli R, Lingua E, Pirotti F, Grigolato S, Bellingeri D, Zini E, Gianelle D, Dalponte M, Pompei E, Stefani A, Motta R, Morresi D, Garbarino M, Alberti G, Valdevit F, Tomelleri E, Torresani M, Tonon G, Marchi M, Corona P, Marchetti M

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Multi-trait genome-wide association study identifies new loci associated with optic disc parameters von Bonnemaijer, Pieter W M, Leeuwen, Elisabeth M van, Iglesias, Adriana I, Gharahkhani, Puya, Vitart, Veronique, Khawaja, Anthony P, Simcoe, Mark, Höhn, René, Cree, Angela J, Igo, Rob P, Gerhold-Ay, Aslihan, Nickels, Stefan, Wilson, James F, Hayward, Caroline, Boutin, Thibaud S, Polašek, Ozren, Aung, Tin, Khor, Chiea Chuen, Amin, Najaf, Lotery, Andrew J, Wiggs, Janey L, Cheng, Ching-Yu, Hysi, Pirro G, Hammond, Christopher J, Thiadens, Alberta A H J, MacGregor, Stuart, Klaver, Caroline C W, Duijn, Cornelia M van

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Forest damage inventory after the "Vaia" storm in Italy von Chirici, G, Giannetti, F, Travaglini, D, Nocentini, S, Francini, S, D’Amico, G, Calvo, E, Fasolini, D, Broll, M, Maistrelli, F, Tonner, J, Pietrogiovanna, M, Oberlechner, K, Andriolo, A, Comino, R, Faidiga, A, Pasutto, I, Carraro, G, Zen, S, Contarin, F, Alfonsi, L, Wolynski, A, Zanin, M, Gagliano, C, Tonolli, S, Zoanetti, R, Tonetti, R, Cavalli, R, Lingua, E, Pirotti, F, Grigolato, S, Bellingeri, D, Zini, E, Gianelle, D, Dalponte, M, Pompei, E, Stefani, A, Motta, R, Morresi, D, Garbarino, M, Alberti, G, Valdevit, F, Tomelleri, E, Torresani, M, Tonon, G, Marchi, M, Corona, P, Marchetti, M

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Genetic variants and cellular stressors associated with exfoliation syndrome modulate promoter activity of a lncRNA within the LOXL1 locus von Hauser, Michael A

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Variants in RUNX3 contribute to susceptibility to psoriatic arthritis exhibiting further common ground with ankylosing spondylitis

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Advanced in early‐ and adult‐onset glaucoma genetics von Pasutto, Francesca

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Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progression von Craig, Jamie E., Han, Xikun, Qassim, Ayub, Hassall, Mark, Cooke Bailey, Jessica N., Kinzy, Tyler G., Khawaja, Anthony P., An, Jiyuan, Marshall, Henry, Gharahkhani, Puya, Igo, Robert P., Graham, Stuart L., Healey, Paul R., Ong, Jue-Sheng, Zhou, Tiger, Siggs, Owen, Law, Matthew H., Souzeau, Emmanuelle, Ridge, Bronwyn, Hysi, Pirro G., Burdon, Kathryn P., Mills, Richard A., Landers, John, Ruddle, Jonathan B., Agar, Ashish, Galanopoulos, Anna, White, Andrew J. R., Willoughby, Colin E., Andrew, Nicholas H., Best, Stephen, Vincent, Andrea L., Goldberg, Ivan, Radford-Smith, Graham, Martin, Nicholas G., Montgomery, Grant W., Vitart, Veronique, Hoehn, Rene, Wojciechowski, Robert, Jonas, Jost B., Aung, Tin, Pasquale, Louis R., Cree, Angela Jane, Sivaprasad, Sobha, Vallabh, Neeru A., Viswanathan, Ananth C., Pasutto, Francesca, Haines, Jonathan L., Klaver, Caroline C. W., van Duijn, Cornelia M., Casson, Robert J., Foster, Paul J., Khaw, Peng Tee, Hammond, Christopher J., Mackey, David A., Mitchell, Paul, Lotery, Andrew J., Wiggs, Janey L., Hewitt, Alex W., MacGregor, Stuart

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Broad Genetic Analysis Reveals Diverse Molecular Causes of Autosomal Dominant Tubulointerstitial Kidney Disease-Not Otherwise Specified (ADTKD-NOS): PO1349 von Wopperer, Florian, Pasutto, Francesca, Wiesener, Michael S.

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Automating relative and absolute environmental sustainability assessments of bio-based products von Meramo, Samir, Pasutto, Eleonora, Sukumara, Sumesh

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Perifoveal Cone- and Rod-Mediated Temporal Contrast Sensitivities in Stargardt Disease/Fundus Flavimaculatus von Fars, Julien, Pasutto, Francesca, Kremers, Jan, Huchzermeyer, Cord

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Chemoenzymatic indican for light-driven denim dyeing von Bidart, Gonzalo Nahuel, Teze, David, Jansen, Charlotte Uldahl, Pasutto, Eleonora, Putkaradze, Natalia, Sesay, Anna-Mamusu, Fredslund, Folmer, Lo Leggio, Leila, Ögmundarson, Olafur, Sukumara, Sumesh, Qvortrup, Katrine, Welner, Ditte Hededam

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Angiopoietin-1 is required for Schlemm's canal development in mice and humans von Thomson, Benjamin R, Souma, Tomokazu, Tompson, Stuart W, Onay, Tuncer, Kizhatil, Krishnakumar, Siggs, Owen M, Feng, Liang, Whisenhunt, Kristina N, Yanovitch, Tammy L, Kalaydjieva, Luba, Azmanov, Dimitar N, Finzi, Simone, Tanna, Christine E, Hewitt, Alex W, Mackey, David A, Bradfield, Yasmin S, Souzeau, Emmanuelle, Javadiyan, Shari, Wiggs, Janey L, Pasutto, Francesca, Liu, Xiaorong, John, Simon Wm, Craig, Jamie E, Jin, Jing, Young, Terri L, Quaggin, Susan E

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Pseudoexfoliation syndrome-associated genetic variants affect transcription factor binding and alternative splicing of LOXL1 von Pasutto, Francesca, Zenkel, Matthias, Hoja, Ursula, Berner, Daniel, Uebe, Steffen, Ferrazzi, Fulvia, Schödel, Johannes, Liravi, Panah, Ozaki, Mineo, Paoli, Daniela, Frezzotti, Paolo, Mizoguchi, Takanori, Nakano, Satoko, Kubota, Toshiaki, Manabe, Shinichi, Salvi, Erika, Manunta, Paolo, Cusi, Daniele, Gieger, Christian, Wichmann, Heinz-Erich, Aung, Tin, Khor, Chiea Chuen, Kruse, Friedrich E., Reis, André, Schlötzer-Schrehardt, Ursula

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3639 WHEN WHOLE EXOME SEQUENCING IS NOT GOOD ENOUGH: BACK TO THE ROOTS OR FORWARD TO THE FUTURE von Ekici, Arif, Knaup, Karl, Schneider, Karen, Wopperer, Florian, Wiesener, Antje, Dieterle, Anne, Schiffer, Mario, Reis, Andre, Pasutto, Francesca, Wiesener, Michael

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3166 RECOGNITION OF RENAL TUBULAR DYSGENESIS IN ADOLESCENT CKD BY BIALLELIC AGT VARIANTS REQUIRED BROAD GENETIC ANALYSIS von Wopperer, Florian, Olinger, Eric, Knaup, Karl, Wiesener, Antje, Broeker, Katharina, Schiffer, Mario, Hilgers, Karl, Pasutto, Francesca, Sayer, John, Wiesener, Michael

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