A new method to graft titania using Grignard reagents von Van Heetvelde, P, Beyers, E, Wyns, K, Adriaensens, P, Maes, B U W, Mullens, S, Buekenhoudt, A, Meynen, V

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A new method to graft titania using Grignard reagentsElectronic supplementary information (ESI) available. See DOI: 10.1039/c3cc43695k von Van Heetvelde, P, Beyers, E, Wyns, K, Adriaensens, P, Maes, B. U. W, Mullens, S, Buekenhoudt, A, Meynen, V

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2023 Focused Update of the 2021 ESC Guidelines for the diagnosis and treatment of acute and chronic heart failure von McDonagh, Theresa A., Adamo, Marianna, Butler, Javed, Chioncel, Ovidiu, Crespo‐Leiro, Maria Generosa, Farmakis, Dimitrios, Gilard, Martine, Heymans, Stephane, Hoes, Arno W., Jaarsma, Tiny, Jankowska, Ewa A., Lainscak, Mitja, Lam, Carolyn S.P., Lyon, Alexander R., Mebazaa, Alexandre, Mindham, Richard, Muneretto, Claudio, Francesco Piepoli, Massimo, Price, Susanna, Ruschitzka, Frank, Skibelund, Anne Kathrine, Boer, Rudolf A., Bartunek, Jozef, Bauersachs, Johann, Borger, Michael A., Cerbai, Elisabetta, Donal, Erwan, Edelmann, Frank, Färber, Gloria, Heidecker, Bettina, Køber, Lars, McEvoy, John William, Mentz, Robert, Neubeck, Lis, Prescott, Eva, Rakisheva, Amina, Rocca, Bianca, Rossello, Xavier, Sade, Leyla Elif, Schaubroeck, Hannah, Tessitore, Elena, Tokmakova, Mariya, Van Gelder, Isabelle C., Van Heetvelde, Mattias, Wilhelm, Matthias, Witkowski, Adam, Shuka, Naltin, Hayrapetyan, Hamlet, Pavo, Noemi, Islamli, Aysel, Kusljugic, Zumreta, Tokmakova, Mariya, Christodoulides, Theodoros, Køber, Lars, Põder, Pentti, Lassus, Johan, Roubille, François, Frantz, Stefan, Stavrati, Alexia, Kosztin, Annamaria, Ingimarsdóttir, Inga Jóna, Campbell, Patricia, Oliva, Fabrizio, Aidargaliyeva, Nazipa, Bajraktari, Gani, Mirrakhimov, Erkin, Zaliaduonyte, Diana, Moore, Alice, Vataman, Eleonora, Boskovic, Aneta, Alami, Mohamed, Manintveld, Olivier, Nessler, Jadwiga, Popescu, Bogdan A., Foscoli, Marina, Milosavljevic, Anastazija Stojsic, Gonzalez‐Costello, Jose, Paul, Matthias, Oudeh, Abdulnasser, Zakhama, Lilia, Celik, Ahmet, Clark, Andrew, James, Stefan, Arbelo, Elena, Baigent, Colin, Borger, Michael A., Buccheri, Sergio, Ibanez, Borja, Køber, Lars, Koskinas, Konstantinos C., McEvoy, John William, Mihaylova, Borislava, Neubeck, Lis, Nielsen, Jens Cosedis, Rakisheva, Amina, Rocca, Bianca, Rossello, Xavier, Vaartjes, Ilonca, Vrints, Christiaan, Witkowski, Adam

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Combining a prioritization strategy and functional studies nominates 5'UTR variants underlying inherited retinal disease von Dueñas Rey, Alfredo, Del Pozo Valero, Marta, Bouckaert, Manon, Wood, Katherine A, Van den Broeck, Filip, Daich Varela, Malena, Thomas, Huw B, Van Heetvelde, Mattias, De Bruyne, Marieke, Van de Sompele, Stijn, Bauwens, Miriam, Lenaerts, Hanne, Mahieu, Quinten, Josifova, Dragana, Rivolta, Carlo, O'Keefe, Raymond T, Ellingford, Jamie, Webster, Andrew R, Arno, Gavin, Ayuso, Carmen, De Zaeytijd, Julie, Leroy, Bart P, De Baere, Elfride, Coppieters, Frauke

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Multi-omics approach dissects cis-regulatory mechanisms underlying North Carolina macular dystrophy, a retinal enhanceropathy von Van de Sompele, Stijn, Small, Kent W., Cicekdal, Munevver Burcu, Soriano, Víctor López, D’haene, Eva, Shaya, Fadi S., Agemy, Steven, Van der Snickt, Thijs, Rey, Alfredo Dueñas, Rosseel, Toon, Van Heetvelde, Mattias, Vergult, Sarah, Balikova, Irina, Bergen, Arthur A., Boon, Camiel J.F., De Zaeytijd, Julie, Inglehearn, Chris F., Kousal, Bohdan, Leroy, Bart P., Rivolta, Carlo, Vaclavik, Veronika, van den Ende, Jenneke, van Schooneveld, Mary J., Gómez-Skarmeta, José Luis, Tena, Juan J., Martinez-Morales, Juan R., Liskova, Petra, Vleminckx, Kris, De Baere, Elfride

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Mutations in SAMD7 cause autosomal-recessive macular dystrophy with or without cone dysfunction von Bauwens, Miriam, Celik, Elifnaz, Zur, Dinah, Lin, Siying, Quinodoz, Mathieu, Michaelides, Michel, Webster, Andrew R., Van Den Broeck, Filip, Leroy, Bart P., Rizel, Leah, Moye, Abigail R., Meunier, Audrey, Tran, Hoai Viet, Moulin, Alexandre P., Mahieu, Quinten, Van Heetvelde, Mattias, Arno, Gavin, Rivolta, Carlo, De Baere, Elfride, Ben-Yosef, Tamar

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Correction: Mapping the genomic landscape of inherited retinal disease genes prioritizes genes prone to coding and noncoding copy-number variations von Van Schil, Kristof, Naessens, Sarah, Van de Sompele, Stijn, Carron, Marjolein, Aslanidis, Alexander, Van Cauwenbergh, Caroline, Mayer, Anja K., Van Heetvelde, Mattias, Bauwens, Miriam, Verdin, Hannah, Coppieters, Frauke, Greenberg, Michael E., Yang, Marty G., Karlstetter, Marcus, Langmann, Thomas, De Preter, Katleen, Kohl, Susanne, Cherry, Timothy J., Leroy, Bart P., De Baere, Elfride

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Mapping the genomic landscape of inherited retinal disease genes prioritizes genes prone to coding and noncoding copy-number variations von Van Schil, Kristof, Naessens, Sarah, Van de Sompele, Stijn, Carron, Marjolein, Aslanidis, Alexander, Van Cauwenbergh, Caroline, Mayer, Anja K, Van Heetvelde, Mattias, Bauwens, Miriam, Verdin, Hannah, Coppieters, Frauke, Greenberg, Michael E, Yang, Marty G, Karlstetter, Marcus, Langmann, Thomas, De Preter, Katleen, Kohl, Susanne, Cherry, Timothy J, Leroy, Bart P, De Baere, Elfride

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2023 Focused Update of the 2021 ESC Guidelines for the diagnosis and treatment of acute and chronic heart failure von McDonagh, Theresa A, Metra, Marco, Adamo, Marianna, Gardner, Roy S, Baumbach, Andreas, Böhm, Michael, Burri, Haran, Butler, Javed, Čelutkienė, Jelena, Chioncel, Ovidiu, Cleland, John G F, Crespo-Leiro, Maria Generosa, Farmakis, Dimitrios, Gilard, Martine, Heymans, Stephane, Hoes, Arno W, Jaarsma, Tiny, Jankowska, Ewa A, Lainscak, Mitja, Lam, Carolyn S P, Lyon, Alexander R, McMurray, John J V, Mebazaa, Alexandre, Mindham, Richard, Muneretto, Claudio, Francesco Piepoli, Massimo, Price, Susanna, Rosano, Giuseppe M C, Ruschitzka, Frank, Skibelund, Anne Kathrine

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2023 Focused Update of the 2021 ESC Guidelines for the diagnosis and treatment of acute and chronic heart failure von McDonagh, Theresa A, Metra, Marco, Adamo, Marianna, Gardner, Roy S, Baumbach, Andreas, Boehm, Michael, Burri, Haran, Butler, Javed, Celutkiene, Jelena, Chioncel, Ovidiu, Cleland, John G.F, Crespo-Leiro, Maria Generosa, Farmakis, Dimitrios, Gilard, Martine, Heymans, Stephane, Hoes, Arno W, Jaarsma, Tiny, Jankowska, Ewa A, Lainscak, Mitja, Lam, Carolyn S.P, Lyon, Alexander R, McMurray, John J.V, Mebazaa, Alexandre, Mindham, Richard, Muneretto, Claudio, Francesco Piepoli, Massimo, Price, Susanna, Rosano, Giuseppe M.C, Ruschitzka, Frank, Skibelund, Anne Kathrine, de Boer, Rudolf A, Schulze, P. Christian, Arbelo, Elena, Bartunek, Jozef, Bauersachs, Johann, Borger, Michael A, Buccheri, Sergio, Cerbai, Elisabetta, Donal, Erwan, Edelmann, Frank, Faerber, Gloria, Heidecker, Bettina, Ibanez, Borja, James, Stefan, Kober, Lars, Koskinas, Konstantinos C, Masip, Josep, McEvoy, John William, Mentz, Robert, Mihaylova, Borislava, Moller, Jacob Eifer, Mullens, Wilfried, Neubeck, Lis, Nielsen, Jens Cosedis, Pasquet, Agnes A, Ponikowski, Piotr, Prescott, Eva, Rakisheva, Amina, Rocca, Bianca, Rossello, Xavier, Sade, Leyla Elif, Schaubroeck, Hannah, Tessitore, Elena, Tokmakova, Mariya, van der Meer, Peter, Van Gelder, Isabelle C, Van Heetvelde, Mattias, Vrints, Christiaan, Wilhelm, Matthias, Witkowski, Adam, Zeppenfeld, Katja

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Mutations in SAMD7 cause autosomal-recessive macular dystrophy with or without cone dysfunction von Bauwens, Miriam, Celik, Elifnaz, Zur, Dinah, Lin, Siying, Quinodoz, Mathieu, Michaelides, Michel, Webster, Andrew R, Van Den Broeck, Filip, Leroy, Bart P, Rizel, Leah, Moye, Abigail R, Meunier, Audrey, Tran, Hoai Viet, Moulin, Alexandre P, Mahieu, Quinten, Van Heetvelde, Mattias, Arno, Gavin, Rivolta, Carlo, De Baere, Elfride, Ben-Yosef, Tamar

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Combining a prioritization strategy and functional studies nominates 5’UTR variants underlying inherited retinal disease von Dueñas Rey, A, del Pozo Valero, M, Bouckaert, M, Wood, KA, Van den Broeck, F, Varela, MD, Thomas, HB, Van Heetvelde, M, De Bruyne, M, Van de Sompele, S, Bauwens, M, Lenaerts, H, Mahieu, Q, Josifova, D, Rivolta, C, O’Keefe, RT, Ellingford, J, Webster, AR, Arno, G, Ayuso, C, De Zaeytijd, J, Leroy, BP, De Baere, E, Coppieters, F

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Multi-omics approach dissects cis-regulatory mechanisms underlying North Carolina macular dystrophy: a retinal enhanceropathy von Sompele, S. van de, Small, K.W., Cicekdal, M.B., Soriano, V.L., D'haene, E., Shaya, F.S., Agemy, S., Snickt, T. van der, Rey, A.D., Rosseel, T., Heetvelde, M. van, Vergult, S., Balikova, I., Bergen, A.A., Boon, C.J.F., Zaeytijd, J. de, Inglehearn, C.F., Kousal, B., Leroy, B.P., Rivolta, C., Vaclavik, V., Ende, J. van den, Schooneveld, M.J. van, Gómez-Skarmeta, J.L., Tena, J.J., Martinez-Morales, J.R., Liskova, P., Vleminckx, K., Baere, E. de

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Multi-omics approach dissects cis-regulatory mechanisms underlying North Carolina macular dystrophy, a retinal enhanceropathy von Van de Sompele, S, Small, KW, Cicekdal, MB, Soriano, VL, D'haene, E, Shaya, FS, Agemy, S, Van der Snickt, T, Rey, AD, Rosseel, T, Van Heetvelde, M, Vergult, S, Balikova, I, Bergen, AA, Boon, CJF, De Zaeytijd, J, Inglehearn, CF, Kousal, B, Leroy, BP, Rivolta, C, Vaclavik, V, van den Ende, J, van Schooneveld, MJ, Gómez-Skarmeta, JL, Tena, JJ, Martinez-Morales, JR, Liskova, P, Vleminckx, K, De Baere, E

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Long-Read Sequencing to Unravel Complex Structural Variants of CEP78 Leading to Cone-Rod Dystrophy and Hearing Loss von Ascari, G, Rendtorff, ND, De Bruyne, M, De Zaeytijd, J, Van Lint, M, Bauwens, M, Van Heetvelde, M, Arno, G, Jacob, J, Creytens, D, Van Dorpe, J, Van Laethem, T, Rosseel, T, De Pooter, T, De Rijk, P, De Coster, W, Menten, B, Rey, AD, Strazisar, M, Bertelsen, M, Tranebjaerg, L, De Baere, E

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Additional file 3 of Combining a prioritization strategy and functional studies nominates 5’UTR variants underlying inherited retinal disease von Dueñas Rey, Alfredo, del Pozo Valero, Marta, Bouckaert, Manon, Wood, Katherine A, Van den Broeck, Filip, Daich Varela, Malena, Thomas, Huw B, Van Heetvelde, Mattias, De Bruyne, Marieke, Van de Sompele, Stijn, Bauwens, Miriam, Lenaerts, Hanne, Mahieu, Quinten, Josifova, Dragana, Rivolta, Carlo, O’Keefe, Raymond T, Ellingford, Jamie, Webster, Andrew R, Arno, Gavin, Ayuso, Carmen, De Zaeytijd, Julie, Leroy, Bart P, De Baere, Elfride, Coppieters, Frauke

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Additional file 1 of Combining a prioritization strategy and functional studies nominates 5’UTR variants underlying inherited retinal disease von Dueñas Rey, Alfredo, del Pozo Valero, Marta, Bouckaert, Manon, Wood, Katherine A, Van den Broeck, Filip, Daich Varela, Malena, Thomas, Huw B, Van Heetvelde, Mattias, De Bruyne, Marieke, Van de Sompele, Stijn, Bauwens, Miriam, Lenaerts, Hanne, Mahieu, Quinten, Josifova, Dragana, Rivolta, Carlo, O’Keefe, Raymond T, Ellingford, Jamie, Webster, Andrew R, Arno, Gavin, Ayuso, Carmen, De Zaeytijd, Julie, Leroy, Bart P, De Baere, Elfride, Coppieters, Frauke

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Mapping the genomic landscape of inherited retinal disease genes prioritizes genes prone to coding and noncoding copy-number variations von Van Schil, Kristof, Naessens, Sarah, Van de Sompele, Stijn, Carron, Marjolein, Aslanidis, Alexander, Van Cauwenbergh, Caroline, Kathrin Mayer, Anja, Van Heetvelde, Mattias, Bauwens, Miriam, Verdin, Hannah, Coppieters, Frauke, Greenberg, Michael E, Yang, Marty G, Karlstetter, Marcus, Langmann, Thomas, De Preter, Katleen, Kohl, Susanne, Cherry, Timothy J, Leroy, Bart P, Lupski, James R, Carvalho, Claudia, van Min, Max, Klous, Petra, De Jaegere, Sarah, Hooghe, Sally, De Baere, Elfride

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