Large-Scale Whole-Genome Sequencing Reveals the Genetic Architecture of Primary Membranoproliferative GN and C3 Glomerulopathy von Levine, Adam P., Chan, Melanie M. Y., Sadeghi-Alavijeh, Omid, Wong, Edwin K. S., Cook, H. Terence, Ashford, Sofie, Carss, Keren, Christian, Martin T., Hall, Matthew, Harris, Claire Louise, McAlinden, Paul, Marchbank, Kevin J., Marks, Stephen D., Maxwell, Heather, Megy, Karyn, Penkett, Christopher J., Mozere, Monika, Stirrups, Kathleen E., Tuna, Salih, Wessels, Julie, Whitehorn, Deborah, Johnson, Sally A., Gale, Daniel P.

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Daily low-dose prednisolone to prevent relapse of steroid-sensitive nephrotic syndrome in children with an upper respiratory tract infection: PREDNOS2 RCT von Christian, Martin T, Webb, Nicholas Ja, Woolley, Rebecca L, Afentou, Nafsika, Mehta, Samir, Frew, Emma, Brettell, Elizabeth A, Khan, Adam R, Milford, David V, Bockenhauer, Detlef, Saleem, Moin A, Hall, Angela S, Koziell, Ania, Maxwell, Heather, Hegde, Shivaram, Finlay, Eric R, Gilbert, Rodney D, Jones, Caroline, McKeever, Karl, Cook, Wendy, Ives, Natalie

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Optimizing the corticosteroid dose in steroid-sensitive nephrotic syndrome von Christian, Martin T., Maxted, Andrew P.

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Correction to: Optimizing the corticosteroid dose in steroid-sensitive nephrotic syndrome von Christian, Martin T., Maxted, Andrew P.

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Low-dose rituximab is no less effective for nephrotic syndrome measured by 12-month outcome von Maxted, Andrew P., Dalrymple, Rebecca A., Chisholm, Denise, McColl, John, Tse, Yincent, Christian, Martin T., Reynolds, Ben C.

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Renal tubular disorders von Broodbank, David, Christian, Martin T

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Renal tubular disorders von Christian, Martin T

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Renal tubular disorders von Broodbank, David, Christian, Martin T.

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Modeling 13C Breath Curves to Determine Site and Extent of Starch Digestion and Fermentation in Infants von Christian, Martin T, Amarri, Sergio, Franchini, Fabio, Preston, Tom, Morrison, Douglas J, Dodson, Brian, Edwards, Christine A, Weaver, Lawrence T

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Whole-genome sequencing of patients with rare diseases in a national health system von Turro, Ernest, Astle, William J., Megy, Karyn, Gräf, Stefan, Greene, Daniel, Shamardina, Olga, Allen, Hana Lango, Sanchis-Juan, Alba, Frontini, Mattia, Thys, Chantal, Stephens, Jonathan, Mapeta, Rutendo, Burren, Oliver S., Downes, Kate, Haimel, Matthias, Tuna, Salih, Deevi, Sri V. V., Aitman, Timothy J., Bennett, David L., Calleja, Paul, Carss, Keren, Caulfield, Mark J., Chinnery, Patrick F., Dixon, Peter H., Gale, Daniel P., James, Roger, Koziell, Ania, Laffan, Michael A., Levine, Adam P., Maher, Eamonn R., Markus, Hugh S., Morales, Joannella, Morrell, Nicholas W., Mumford, Andrew D., Ormondroyd, Elizabeth, Rankin, Stuart, Rendon, Augusto, Richardson, Sylvia, Roberts, Irene, Roy, Noemi B. A., Saleem, Moin A., Smith, Kenneth G. C., Stark, Hannah, Tan, Rhea Y. Y., Themistocleous, Andreas C., Thrasher, Adrian J., Watkins, Hugh, Webster, Andrew R., Wilkins, Martin R., Williamson, Catherine, Whitworth, James, Humphray, Sean, Bentley, David R., Kingston, Nathalie, Walker, Neil, Bradley, John R., Ashford, Sofie, Penkett, Christopher J., Freson, Kathleen, Stirrups, Kathleen E., Raymond, F. Lucy, Ouwehand, Willem H.

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Whole-genome sequencing of a sporadic primary immunodeficiency cohort von Thaventhiran, James E. D., Lango Allen, Hana, Burren, Oliver S., Rae, William, Greene, Daniel, Staples, Emily, Zhang, Zinan, Farmery, James H. R., Simeoni, Ilenia, Rivers, Elizabeth, Maimaris, Jesmeen, Penkett, Christopher J., Stephens, Jonathan, Deevi, Sri V. V., Sanchis-Juan, Alba, Gleadall, Nicholas S., Thomas, Moira J., Sargur, Ravishankar B., Gordins, Pavels, Baxendale, Helen E., Brown, Matthew, Tuijnenburg, Paul, Worth, Austen, Hanson, Steven, Linger, Rachel J., Buckland, Matthew S., Rayner-Matthews, Paula J., Gilmour, Kimberly C., Samarghitean, Crina, Seneviratne, Suranjith L., Sansom, David M., Lynch, Andy G., Megy, Karyn, Ellinghaus, Eva, Ellinghaus, David, Jorgensen, Silje F., Karlsen, Tom H., Stirrups, Kathleen E., Cutler, Antony J., Kumararatne, Dinakantha S., Chandra, Anita, Edgar, J. David M., Herwadkar, Archana, Cooper, Nichola, Grigoriadou, Sofia, Huissoon, Aarnoud P., Goddard, Sarah, Jolles, Stephen, Schuetz, Catharina, Boschann, Felix, Lyons, Paul A., Hurles, Matthew E., Savic, Sinisa, Burns, Siobhan O., Kuijpers, Taco W., Turro, Ernest, Ouwehand, Willem H., Thrasher, Adrian J., Smith, Kenneth G. C.

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Effects of rare kidney diseases on kidney failure: a longitudinal analysis of the UK National Registry of Rare Kidney Diseases (RaDaR) cohort von Braddon, Fiona, Downward, Lewis, Coward, Richard J, Griffin, Sian, Hall, Matt, Karet Frankl, Fiona, Kerecuk, Larissa, Pinney, Jenny, Sayer, John A, Waters, Aoife, Bockenhauer, Detlef, Gale, Daniel P, Agbonmwandolor, Joy, Ahmad, Zubaidah, Asgari, Ellie, Ayers, Amanda, Barratt, Alison, Barratt, Jonathan, Benyon, Sarah, Bhandari, Sunil, Bond, Sally, Bramham, Kate, Branson, Angela, Byrne, Conor, Campbell, Gary, Capell, Alys, Cathcart, Tracy, Cheung, Chee Kay, Chick, Katy-Jane, Chrysochou, Tina, Clayton, Christopher, Cook, Wendy, Coward, Richard J, Drayson, Mark, Evans, Dawn, Flinter, Frances, Gale, Daniel P, Gallagher, Hugh, Game, David, Gavrila, Madita, Gilchrist, Mark, Goldsmith, Christopher, Gray, Barry, Griffith, Megan, Gupta, Sanjana, Hillman, Kate, Htet, Zay, Huish, Sharon, Hull, Richard, Hunter, Karl, Inston, Nick, Jayne, David, Jenkins, Alison, Kamesh, Lavanya, Kanigicherla, Durga, Karet Frankl, Fiona, Kaur, Amrit, King, Garry, King, Grant, Kislowska, Ewa, Kokocinska, Maria, Lawless, Laura, Mabillard, Holly, Mahdi, Khalid, Masoud, Sherry, Mayfair, Jake, Meyrick, Simon, Moochhala, Shabbir, Morgan, Ann, Muhammad, Fawad, Murray, Shona, Osmaston, Kate, Padmanabhan, Neal, Pattison, James, Persu, Alexandre, Petchey, William G, Post, Frank, Sandford, Richard, Sarween, Nadia, Sayer, John A, Sebire, Neil, Selvaskandan, Haresh, Sharma, Asheesh, Sheerin, Neil, Shetty, Harish, Simms, Roslyn, Smith, Kerry, Swift, Pauline, Szklarzewicz, Justyna, Tam, Fred, Tan, Kay, Tischkowitz, Marc, Tse, Yincent, Tyerman, Kay, Usher, Miranda, Wechalekar, Ashutosh, Welsh, Gavin I, West, Nicol, Williams, Angharad, Wilson, Patricia D

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GWAS meta-analysis of intrahepatic cholestasis of pregnancy implicates multiple hepatic genes and regulatory elements von Dixon, Peter H., Levine, Adam P., Cebola, Inês, Chan, Melanie M. Y., Amin, Aliya S., Aich, Anshul, Mozere, Monika, Maude, Hannah, Mitchell, Alice L., Zhang, Jun, Chambers, Jenny, Syngelaki, Argyro, Donnelly, Jennifer, Cooley, Sharon, Geary, Michael, Nicolaides, Kypros, Thorsell, Malin, Hague, William M., Estiu, Maria Cecilia, Marschall, Hanns-Ulrich, Gale, Daniel P., Williamson, Catherine

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C3 Glomerulopathy and Related Disorders in Children: Etiology-Phenotype Correlation and Outcomes von Wong, Edwin K. S., Marchbank, Kevin J., Lomax-Browne, Hannah, Pappworth, Isabel Y., Denton, Harriet, Cooke, Katie, Ward, Sophie, Mcloughlin, Amy-Claire, Richardson, Grant, Wilson, Valerie, Harris, Claire L., Morgan, B. Paul, Hakobyan, Svetlana, McAlinden, Paul, Gale, Daniel P., Maxwell, Heather, Christian, Martin, Malcomson, Roger, Goodship, Timothy H. J., Marks, Stephen D., Pickering, Matthew C., Kavanagh, David, Cook, H. Terence, Johnson, Sally A.

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Economic Evaluation of Using Daily Prednisolone versus Placebo at the Time of an Upper Respiratory Tract Infection for the Management of Children with Steroid-Sensitive Nephrotic S... von Afentou, Nafsika, Frew, Emma, Mehta, Samir, Ives, Natalie J, Woolley, Rebecca L, Brettell, Elizabeth A, Khan, Adam R, Milford, David V, Bockenhauer, Detlef, Saleem, Moin A, Hall, Angela S, Koziell, Ania, Maxwell, Heather, Hegde, Shivaram, Finlay, Eric, Gilbert, Rodney D, Jones, Caroline, McKeever, Karl, Cook, Wendy, Webb, Nicholas JA, Christian, Martin T, PREDNOS Collaborative Group, NIHR Medicines for Children Researc

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Daily low-dose prednisolone to prevent relapse of steroid-sensitive nephrotic syndrome in children with an upper respiratory tract infection: PREDNOS2 RCT von Christian, Martin T, Webb, Nicholas Ja, Woolley, Rebecca L, Afentou, Nafsika, Mehta, Samir, Frew, Emma, Brettell, Elizabeth A, Khan, Adam R, Milford, David V, Bockenhauer, Detlef, Saleem, Moin A, Hall, Angela S, Koziell, Ania, Maxwell, Heather, Hegde, Shivaram, Finlay, Eric R, Gilbert, Rodney D, Jones, Caroline, McKeever, Karl, Cook, Wendy, Ives, Natalie

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Diagnostic and therapeutic management of vesico‐ureteral reflux in pediatric kidney transplantation—Results of an online survey on behalf of the European Society for Paediatric Nep... von Zirngibl, Matthias, Buder, Kathrin, Luithle, Tobias, Tönshoff, Burkhard, Weitz, Marcus, Alonso‐Melgar, Ángel, Ariceta, Gema, Awan, Atif, Bakkaloglu, Sevcan A., Baskin, Esra, Bekassy, Zivile, Bhimma, Rajendra, Bitzan, Martin, Bjerre, Anna Kristina, Bootsma‐Robroeks, Charlotte M., Bouts, Antonia, Büscher, Anja, Bulum, Burcu, Christian, Martin, Cicek, Neslihan, Clothier, Joanna, Cornelissen, Marlies, Dehoux, Laurène, Kılıç, Beltinge Demircioğlu, Dinçel, Nida Temizkan, Esfandiar, Nasrin, Espinosa‐Román, Laura, Fila, Marc, Galiano, Matthias, Gander, Romy, Gessner, Michaela, Grenda, Ryszard, Henne, Thomas, Herthelius, Maria, Goñi, Maria Herrero, Higueras, Walter, Hooman, Nakisa, Jahnukainen, Timo, Jankauskiene, Augustina, Jong, Huib, Knops, Noël, Konrad, Martin, Levtchenko, Elena, Madrid‐Aris, Alvaro, Marks, Stephen D., Mattoo, Tej K., Maxted, Andrew, Melgosa‐Hijosa, Marta, Mincham, Christine Marie, Mitsioni, Andromachi, Montini, Giovanni, Morgan, Henry, Müller‐Sacherer, Thomas, Murer, Luisa, Özçakar, Z Birsin, Pape, Lars, Parvex, Paloma, Printza, Nikoleta, Prytula, Agnieszka, Reynolds, Ben, Roussinov, Dimitar, Rubik, Jacek, Rumyantsev, Alexander, Rus, Rina, Seeman, Tomas, Shenoy, Mohan, Silva, Ana Cristina Simões E., Sinha, Rajiv, Stabouli, Stella, Taşdemir, Mehmet, Tasic, Velibor, Teixeira, Ana, Thumfart, Julia, Topaloğlu, Rezan, Torres, Diletta, Trnka, Peter, Tschumi, Sibylle, Tse, Yincent, Aki, Fazil Tuncay, Verrina, Enrico Eugenio, Vidal, Enrico, Weber, Lutz T., Yalçınkaya, Fatma Fatoş, Yap, Yok‐Chin, Yıldız, Nurdan, Yüksel, Selçuk, Zieg, Jakub

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Publisher Correction: Whole-genome sequencing of a sporadic primary immunodeficiency cohort von Thaventhiran, James E. D., Lango Allen, Hana, Burren, Oliver S., Rae, William, Greene, Daniel, Staples, Emily, Zhang, Zinan, Farmery, James H. R., Simeoni, Ilenia, Rivers, Elizabeth, Maimaris, Jesmeen, Penkett, Christopher J., Stephens, Jonathan, Deevi, Sri V. V., Sanchis-Juan, Alba, Gleadall, Nicholas S., Thomas, Moira J., Sargur, Ravishankar B., Gordins, Pavels, Baxendale, Helen E., Brown, Matthew, Tuijnenburg, Paul, Worth, Austen, Hanson, Steven, Linger, Rachel J., Buckland, Matthew S., Rayner-Matthews, Paula J., Gilmour, Kimberly C., Samarghitean, Crina, Seneviratne, Suranjith L., Sansom, David M., Lynch, Andy G., Megy, Karyn, Ellinghaus, Eva, Ellinghaus, David, Jorgensen, Silje F., Karlsen, Tom H., Stirrups, Kathleen E., Cutler, Antony J., Kumararatne, Dinakantha S., Chandra, Anita, Edgar, J. David M., Herwadkar, Archana, Cooper, Nichola, Grigoriadou, Sofia, Huissoon, Aarnoud P., Goddard, Sarah, Jolles, Stephen, Schuetz, Catharina, Boschann, Felix, Lyons, Paul A., Hurles, Matthew E., Savic, Sinisa, Burns, Siobhan O., Kuijpers, Taco W., Turro, Ernest, Ouwehand, Willem H., Thrasher, Adrian J., Smith, Kenneth G. C.

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Modeling 13C Breath Curves to Determine Site and Extent of Starch Digestion and Fermentation in Infants von Christian, Martin T., Amarri, Sergio, Franchini, Fabio, Preston, Tom, Morrison, Douglas J., Dodson, Brian, Edwards, Christine A., Weaver, Lawrence T.

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Modeling 13 C Breath Curves to Determine Site and Extent of Starch Digestion and Fermentation in Infants von Christian, Martin T., Amarri, Sergio, Franchini, Fabio, Preston, Tom, Morrison, Douglas J., Dodson, Brian, Edwards, Christine A., Weaver, Lawrence T.

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