Acute kidney injury: an increasing global concern von Lameire, Norbert H, Prof, Bagga, Arvind, Prof, Cruz, Dinna, MD, De Maeseneer, Jan, Prof, Endre, Zoltan, Prof, Kellum, John A, Prof, Liu, Kathleen D, MD, Mehta, Ravindra L, Prof, Pannu, Neesh, MD, Van Biesen, Wim, MD, Vanholder, Raymond, Prof

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Epidemiology, contributors to, and clinical trials of mortality risk in chronic kidney failure von Ortiz, Alberto, Prof, Covic, Adrian, MD, Fliser, Danilo, MD, Fouque, Denis, MD, Goldsmith, David, Prof, Kanbay, Mehmet, MD, Mallamaci, Francesca, MD, Massy, Ziad A, MD, Rossignol, Patrick, MD, Vanholder, Raymond, MD, Wiecek, Andrzej, MD, Zoccali, Carmine, MD, London, Gérard M, MD

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Renal replacement therapy: how can we contain the costs? von Vanholder, Raymond, Van Biesen, Wim, Lameire, Norbert

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Effects of Fractionated Plasma Separation and Adsorption on Survival in Patients With Acute-on-Chronic Liver Failure von Kribben, Andreas, Gerken, Guido, Haag, Sebastian, Herget–Rosenthal, Stefan, Treichel, Ulrich, Betz, Christoph, Sarrazin, Christoph, Hoste, Eric, Van Vlierberghe, Hans, Escorsell, Àngels, Hafer, Carsten, Schreiner, Oliver, Galle, Peter R, Mancini, Elena, Caraceni, Paolo, Karvellas, Constantine J, Salmhofer, Hermann, Knotek, Mladen, Ginès, Pere, Kozik–Jaromin, Justyna, Rifai, Kinan

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Renal medicine—a call for papers von Guo, Lin, Vanholder, Raymond

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Renal medicine—a call for papers von Guo, Lin, Vanholder, Raymond, Więcek, Andrzej

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Severe lactic acidosis in critically ill patients with acute kidney injury treated with renal replacement therapy von De Corte, Wouter, MD, Vuylsteke, S., MD, De Waele, Jan J., MD, PhD, Dhondt, Annemieke W., MD, PhD, Decruyenaere, Johan, MD, PhD, Vanholder, Raymond, MD, PhD, Hoste, Eric A.J., MD, PhD

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Noninvasive evaluation of large artery function and structure in dialysis patients: clinical applications von Verbeke, Francis, Van Biesen, Wim, Van Holder, Raymond, Van Bortel, Lucas

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Anamnestic dysmotility-like dyspepsia score (ADDS) in renal transplant patients: Influence of immunosuppression von Van Vlem, Bruno, Schoonjans, Renaat, Van Holder, Raymond, Mp De Vos, Martine, Vadamme, Wouter, Lameire, Norbert

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A Genetics-First Approach to Dissecting the Heterogeneity of Autism: Phenotypic Comparison of Autism Risk Copy Number Variants von Chawner, Samuel J.R.A, Doherty, Joanne L, Anney, Richard J. L, Antshel, Kevin M, Bearden, Carrie E, Bernier, Raphael, Chung, Wendy K, Clements, Caitlin C, Curran, Sarah R, Cuturilo, Goran, Fiksinski, Ania M, Gallagher, Louise, Goin-Kochel, Robin P, Gur, Raquel E, Hanson, Ellen, Jacquemont, Sebastien, Kates, Wendy R, Kushan, Leila, Maillard, Anne M, McDonald-McGinn, Donna M, Mihaljevic, Marina, Miller, Judith S, Moss, Hayley, Pejovic-Milovancevic, Milica, Schultz, Robert T, Green-Snyder, LeeAnne, Vorstman, Jacob A, Wenger, Tara L, Hall, Jeremy, Owen, Michael J, van den Bree, Marianne B.M

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Childhood intellectual disability and parents' mental health: integrating social, psychological and genetic influences von Baker, Kate, Devine, Rory T., Ng-Cordell, Elise, Raymond, F. Lucy, Hughes, Claire

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Mutations in REEP6 Cause Autosomal-Recessive Retinitis Pigmentosa von Arno, Gavin, Agrawal, Smriti A., Eblimit, Aiden, Bellingham, James, Xu, Mingchu, Wang, Feng, Chakarova, Christina, Parfitt, David A., Lane, Amelia, Burgoyne, Thomas, Hull, Sarah, Carss, Keren J., Fiorentino, Alessia, Hayes, Matthew J., Munro, Peter M., Nicols, Ralph, Pontikos, Nikolas, Holder, Graham E., Black, Graeme, Hall, Georgina, Ingram, Stuart, Gillespie, Rachel, Manson, Forbes, Sergouniotis, Panagiotis, Inglehearn, Chris, Toomes, Carmel, Ali, Manir, McKibbin, Martin, Poulter, James, Khan, Kamron, Lord, Emma, Nemeth, Andrea, Downes, Susan, Yu, Jing, Lise, Stefano, Arno, Gavin, Fiorentino, Alessia, Ponitkos, Nikos, Plagnol, Vincent, Michaelides, Michel, Hardcastle, Alison J., Cheetham, Michael E., Webster, Andrew R., van Heyningen, Veronica, Asomugha, Chinwe, Raymond, F. Lucy, Moore, Anthony T., Plagnol, Vincent, Michaelides, Michel, Hardcastle, Alison J., Li, Yumei, Cukras, Catherine, Webster, Andrew R., Cheetham, Michael E., Chen, Rui

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A clinical and molecular characterisation of CRB1-associated maculopathy von Khan, Kamron N, Robson, Anthony, Mahroo, Omar A R, Arno, Gavin, Inglehearn, Chris F, Armengol, Monica, Waseem, Naushin, Holder, Graham E, Carss, Keren J, Raymond, Lucy F, Webster, Andrew R, Moore, Anthony T, McKibbin, Martin, van Genderen, Maria M, Poulter, James A, Michaelides, Michel

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A global scientific strategy to cure hepatitis B von Revill, Peter A, Chisari, Francis V, Block, Joan M, Dandri, Maura, Gehring, Adam J, Guo, Haitao, Hu, Jianming, Kramvis, Anna, Lampertico, Pietro, Janssen, Harry L A, Levrero, Massimo, Li, Wenhui, Liang, T Jake, Lim, Seng-Gee, Lu, Fengmin, Penicaud, M Capucine, Tavis, John E, Thimme, Robert, Arbuthnot, Patrick, Boonstra, Andre, Chang, Kyong-Mi, Chen, Per-Jei, Glebe, Dieter, Guidotti, Luca G., Fellay, Jacques, Ferrari, Carlo, Jansen, Louis, Lau, Daryl T Y, Lok, Anna S, Maini, Mala K, Mason, William, Matthews, Gail, Paraskevis, Dimitrios, Petersen, Jörg, Rehermann, Barbara, Shin, Eui-Cheol, Thompson, Alex, van Bömmel, Florian, Wang, Fu-Sheng, Watashi, Koichi, Yang, Hung-Chih, Yuan, Zhenghong, Yuen, Man-Fung, Block, Timothy, Miller, Veronica, Protzer, Ulrike, Bréchot, Christian, Locarnini, Stephen, Peters, Marion G, Schinazi, Raymond F, Zoulim, Fabien

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Reevaluation of the Retinal Dystrophy Due to Recessive Alleles of RGR With the Discovery of a Cis-Acting Mutation in CDHR1 von Arno, Gavin, Hull, Sarah, Carss, Keren, Dev-Borman, Arundhati, Chakarova, Christina, Bujakowska, Kinga, van den Born, L Ingeborgh, Robson, Anthony G, Holder, Graham E, Michaelides, Michel, Cremers, Frans P M, Pierce, Eric, Raymond, F Lucy, Moore, Anthony T, Webster, Andrew R

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Neuropsychiatric risk in children with intellectual disability of genetic origin: IMAGINE, a UK national cohort study von Wolstencroft, Jeanne, Wicks, Francesca, Srinivasan, Ramya, Wynn, Sarah, Ford, Tamsin, Baker, Kate, Chawner, Samuel J R A, Hall, Jeremy, van den Bree, Marianne B M, Owen, Michael J, Wolstencroft, Jeanne, Wicks, Francesca, Srinivasan, Ramya, Erwood, Marie, Lafont, Amy, Timur, Husne, Ye, Zheng, Walker, Susan, Printzlau, Frida, Juj, Manoj, Davies, Sarah, Denyer, Hayley, Watkins, Alice, Kerry, Eleanor, Coscini, Nadia, Fatih, Nasrtullah, Lucock, Anna, Denaxas, Spiros, Mandy, William, Walker, Neil, Wallwork, Sarah, Dewhurst, Eleanor, Cuthbert, Andrew, Challenger, Aimee, Andrews, Sophie, Holmans, Peter, Bowen, Samantha, Bradley, Karen, Birch, Philippa, Tong, Molly, Lewis, Nicola, Ray, Sinead, Sopp, Matthew, Moss, Hayley, Wynn, Sarah, Searle, Beverley, Robertson, Lisa, Berg, Jonathan, Lampe, Anne, Joss, Shelagh, Brennan, Paul, Kraus, Alison, Lahiri, Nayana, Weber, Astrid, Rawson, Myfanwy, Johnson, Diana, Vasudevan, Pradeep, Harrison, Rachel, Williams, Denise, Maher, Eamonn, Kini, Usha, Van Dijk, Fleur, Clowes, Virginia, Gurasashvilli, Jana, Mansour, Sahar, Holder-Espinasse, Muriel, Watford, Amy, Rankin, Julia, Baralle, Diana, Procter, Annie, Ford, Tamsin, Baker, Kate, Chawner, Samuel, Hall, Jeremy, Van den Bree, Marianne B M, Owen, Michael J, Skuse, David, Raymond, F Lucy, Skuse, David, Raymond, F Lucy

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‘We have been in lockdown since he was born’: a mixed methods exploration of the experiences of families caring for children with intellectual disability during the COVID-19 pandem... von Wolstencroft, Jeanne, Hull, Laura, Warner, Lauren, Akhtar, Tooba Nadeem, Mandy, William, Skuse, David, Baker, Kate, Dewhurst, Eleanor, Lafont, Amy, Lucy Raymond, F, Shirley, Terry, Tilley, Hayley, Timur, Husne, Titterton, Catherine, Walker, Neil, Wallwork, Sarah, Wicks, Francesca, Ye, Zheng, Erwood, Marie, Andrews, Sophie, Birch, Philippa, Bowen, Samantha, Bradley, Karen, Challenger, Aimee, Chawner, Samuel, Cuthbert, Andrew, Hall, Jeremy, Holmans, Peter, Law, Sarah, Lewis, Nicola, Morrison, Sinead, Moss, Hayley, Owen, Michael, Ray, Sinead, Sopp, Matthew, Tong, Molly, Bree, Marianne van den, Coscini, Nadia, Davies, Sarah, Denaxas, Spiros, Denyer, Hayley, Fatih, Nasrtullah, Juj, Manoj, Kerry, Ellie, Lucock, Anna, Printzlau, Frida, Srinivasan, Ramya, Walker, Susan, Watkins, Alice, Searle, Beverly, Pelling, Anna, Dean, John, Robertson, Lisa, Alan, Denise Williams, Lucy, Donaldson, Procter, Annie, Berg, Jonathan, Lampe, Anne, Rankin, Julia, Joss, Shelagh, Chitty, Lyn, Flinter, Frances, Holder, Muriel, Kraus, Alison, Barwell, Julian, Vasudevan, Pradeep, Weber, Astrid, Newman, William, Splitt, Miranda, Clowes, Virginia, Dijk, Fleur van, Harrison, Rachel, Kini, Usha, Quarrell, Oliver, Baralle, Diana, Mansour, Sahar, Crow, Yanick

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Mutation analysis of 18 nephronophthisis associated ciliopathy disease genes using a DNA pooling and next generation sequencing strategy von Otto, Edgar A, Ramaswami, Gokul, Janssen, Sabine, Chaki, Moumita, Allen, Susan J, Zhou, Weibin, Airik, Rannar, Hurd, Toby W, Ghosh, Amiya K, Wolf, Matthias T, Hoppe, Bernd, Neuhaus, Thomas J, Bockenhauer, Detlef, Milford, David V, Soliman, Neveen A, Antignac, Corinne, Saunier, Sophie, Johnson, Colin A, Hildebrandt, Friedhelm

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Neurodevelopmental dimensional assessment of young children at high genomic risk of neuropsychiatric conditions von Chawner, Samuel J. R. A., Paine, Amy L., Dunn, Matt J., Walsh, Alice, Sloane, Poppy, Thomas, Megan, Evans, Alexandra, Hopkins‐Jones, Lucinda, Struik, Siske, Hall, Jeremy, Erichsen, Jonathan T., Leekam, Susan R., Owen, Michael J., Hay, Dale, Bree, Marianne B. M., Raymond, F. Lucy, Dewhurst, Eleanor, Lafont, Amy, Timur, Husniye, Wicks, Francesca, Ye, Zheng, Baker, Kate, Walker, Neil, Wallwork, Sarah, Skuse, David, Denaxas, Spiros, Mandy, William, Wolstencroft, Jeanne, Davies, Sarah, Erwood, Marie, Juj, Manoj, Kerry, Eleanor, Lucock, Anna, Printzlau, Frida, Srinivasan, Ramya, Walker, Susan, Coscini, Nadia, Fatih, Nasrtullah, Denyer, Hayley, Andrews, Sophie, Chawner, Samuel, Cuthbert, Andrew, Challenger, Aimee, Hall, Jeremy, Lewis, Nicola, Owen, Michael, Ray, Sinead, Sopp, Matthew, Moss, Hayley, Bree, Marianne, Holmans, Peter, Bowen, Samantha, Bradley, Karen, Birch, Philippa, Tong, Molly, Ford, Tasmin, Searle, Beverly, Wynn, Sarah, Robertson, Lisa, Berg, Jonathan, Lampe, Anne, Joss, Shelagh, Brennan, Paul, Kraus, Alison, Weber, Astrid, Rawson, Myfanwy, Quarrell, Oliver, Vasudevan, Pradeep, Harrison, Rachel, Williams, Denise, Maher, Eamonn, Kini, Usha, Clowes, Virginia, Van Dijk, Fleur, Gurasashvilli, Jana, Mansour, Sahar, Holder‐Espinasse, Muriel, Watford, Amy, Rankin, Julia, Baralle, Diana, Procter, Annie

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A clinical and molecular characterisation of CRB1-associated maculopathy von Khan, Kamron N, Robson, Anthony, Mahroo, Omar AR, Arno, Gavin, Inglehearn, Chris F, Armengol, Monica, Waseem, Naushin, Holder, Graham E, Carss, Keren J, Raymond, Lucy F, Webster, Andrew R, Moore, Anthony T, McKibbin, Martin, van Genderen, Maria M, Poulter, James A, Michaelides, Michel, UK Inherited Retinal Disease Consortium

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