Effective CRISPR/Cas9-based nucleotide editing in zebrafish to model human genetic cardiovascular disorders von Tessadori, Federico, Roessler, Helen I, Savelberg, Sanne M C, Chocron, Sonja, Kamel, Sarah M, Duran, Karen J, van Haelst, Mieke M, van Haaften, Gijs, Bakkers, Jeroen

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ABCC9-related Intellectual disability Myopathy Syndrome is a KATP channelopathy with loss-of-function mutations in ABCC9 von Smeland, Marie F., McClenaghan, Conor, Roessler, Helen I., Savelberg, Sanne, Hansen, Geir Åsmund Myge, Hjellnes, Helene, Arntzen, Kjell Arne, Müller, Kai Ivar, Dybesland, Andreas Rosenberger, Harter, Theresa, Sala-Rabanal, Monica, Emfinger, Chris H., Huang, Yan, Singareddy, Soma S., Gunn, Jamie, Wozniak, David F., Kovacs, Attila, Massink, Maarten, Tessadori, Federico, Kamel, Sarah M., Bakkers, Jeroen, Remedi, Maria S., Van Ghelue, Marijke, Nichols, Colin G., van Haaften, Gijs

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Drug Repurposing for Rare Diseases von Roessler, Helen I., Knoers, Nine V.A.M., van Haelst, Mieke M., van Haaften, Gijs

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ATP‐sensitive potassium channels in zebrafish cardiac and vascular smooth muscle von Singareddy, Soma S., Roessler, Helen I., McClenaghan, Conor, Ikle, Jennifer M., Tryon, Robert C., Haaften, Gijs, Nichols, Colin G.

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Isolation of Cardiac and Vascular Smooth Muscle Cells from Adult, Juvenile, Larval and Embryonic Zebrafish for Electrophysiological Studies von Singareddy, Soma S, McClenaghan, Conor, Roessler, Helen I, Tryon, Robert, Nichols, Colin G

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Behavioral and cognitive functioning in individuals with Cantú syndrome von Roessler, Helen I., Heuvel, Lieke M., Shields, Kathleen, Guilliams, Kristin P., Knoers, Nine V. A. M., Haaften, Gijs, Grange, Dorothy K., Haelst, Mieke M.

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Young adult with Cantú syndrome: dealing with a rare genetic skin disorder von Roessler, Helen I, van Haaften, Gijs, van Haelst, Mieke M

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Cantu syndrome–associated SUR2 (ABCC9) mutations in distinct structural domains result in KATP channel gain-of-function by differential mechanisms von McClenaghan, Conor, Hanson, Alex, Sala-Rabanal, Monica, Roessler, Helen I., Josifova, Dragana, Grange, Dorothy K., van Haaften, Gijs, Nichols, Colin G.

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Three‐dimensional facial morphology in Cantú syndrome von Roessler, Helen I., Shields, Kathleen, Grange, Dorothy K., Knoers, Nine V.A.M., Haaften, Gijs, Hammond, Peter, Haelst, Mieke M.

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Cantu syndrome-associated SUR2 (ABCC9) mutations in distinct structural domains result in K ATP channel gain-of-function by differential mechanisms von McClenaghan, Conor, Hanson, Alex, Sala-Rabanal, Monica, Roessler, Helen I, Josifova, Dragana, Grange, Dorothy K, van Haaften, Gijs, Nichols, Colin G

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KATP Channels in Zebrafish Cardiovascular System: A Model to Study Cantú Syndrome von Singareddy, Soma S., Roessler, Helen I., McClenaghan, Conor, Tryon, Rob C., van Haaften, Gijs, Nichols, Colin G.

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Isolation of Cardiac and Vascular Smooth Muscle Cells from Adult, Juvenile, Larval and Embryonic Zebrafish for Electrophysiological Studies von Singareddy, Soma S., McClenaghan, Conor, Roessler, Helen I., Tryon, Robert, Nichols, Colin G.

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Behavioral and cognitive functioning in individuals with Cantú syndrome von Roessler, Helen I, van Der Heuvel, Lieke M, Shields, Kathleen, Guilliams, Kristin P, Knoers, Nine V. A. M, van Haaften, Gijs, Grange, Dorothy K, van Haelst, Mieke M

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Three-dimensional facial morphology in Cantu syndrome von Roessler, Helen I, Shields, Kathleen, Grange, Dorothy K, Knoers, Nine V.A.M, van Haaften, Gijs, Hammond, Peter, van Haelst, Mieke M

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Cantu syndrome-Associated SUR2 (ABCC9) mutations in distinct structural domains result in KATP channel gain-offunction by differential mechanisms von McClenaghan, Conor, Hanson, Alex, Sala-Rabanal, Monica, Roessler, Helen I, Josifova, Dragana, Grange, Dorothy K, Van Haaften, Gijs, Nichols, Colin G

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ABCC9-related Intellectual disability Myopathy Syndrome is a KATP channelopathy with loss-of-function mutations in ABCC9 von Smeland, Marie F, McClenaghan, Conor, Roessler, Helen I, Savelberg, Sanne, Hansen, Geir Åsmund Myge, Hjellnes, Helene, Arntzen, Kjell Arne, Müller, Kai Ivar, Dybesland, Andreas Rosenberger, Harter, Theresa, Sala-Rabanal, Monica, Emfinger, Chris H, Huang, Yan, Singareddy, Soma S, Gunn, Jamie, Wozniak, David F, Kovacs, Attila, Massink, Maarten, Tessadori, Federico, Kamel, Sarah M, Bakkers, Jeroen, Remedi, Maria S, Van Ghelue, Marijke, Nichols, Colin G, van Haaften, Gijs

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Effective CRISPR/Cas9-based nucleotide editing in zebrafish to model human genetic cardiovascular disorders von Tessadori, Federico, Roessler, Helen I, Savelberg, Sanne M.C, Chocron, Sonja, Kamel, Sarah M, Duran, Karen J, Van Haelst, Mieke M, Van Haaften, Gijs, Bakkers, Jeroen

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ABCC9-related Intellectual disability Myopathy Syndrome is a K ATP channelopathy with loss-of-function mutations in ABCC9 von Smeland, Marie F, McClenaghan, Conor, Roessler, Helen I, Savelberg, Sanne, Hansen, Geir Åsmund Myge, Hjellnes, Helene, Arntzen, Kjell Arne, Müller, Kai Ivar, Dybesland, Andreas Rosenberger, Harter, Theresa, Sala-Rabanal, Monica, Emfinger, Chris H, Huang, Yan, Singareddy, Soma S, Gunn, Jamie, Wozniak, David F, Kovacs, Attila, Massink, Maarten, Tessadori, Federico, Kamel, Sarah M, Bakkers, Jeroen, Remedi, Maria S, Van Ghelue, Marijke, Nichols, Colin G, van Haaften, Gijs

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Technology, autonomy, and manipulation von Susser, Daniel, Roessler, Beate, Nissenbaum, Helen

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Timing of referral to evaluate for epilepsy surgery: Expert Consensus Recommendations from the Surgical Therapies Commission of the International League Against Epilepsy von Jehi, Lara, Jette, Nathalie, Kwon, Churl‐Su, Josephson, Colin B., Burneo, Jorge G., Cendes, Fernando, Sperling, Michael R., Baxendale, Sallie, Busch, Robyn M., Triki, Chahnez Charfi, Cross, J. Helen, Ekstein, Dana, Englot, Dario J., Luan, Guoming, Palmini, Andre, Rios, Loreto, Wang, Xiongfei, Roessler, Karl, Rydenhag, Bertil, Ramantani, Georgia, Schuele, Stephan, Wilmshurst, Jo M., Wilson, Sarah, Wiebe, Samuel

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