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J

John A. Sayer

newcastle university

56H-index
1.2KPaper Count
1.2WCitation Count
Published Papers 128
Publication Date
Genetic Evaluation Practices in Living Kidney Donor Candidates
err2026-06-18
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errYasar Caliskan; Ozgur Akin Oto; Tarek Alhamad; Halil Yazici; Arzu Velioglu; Abdulmecit Yildiz; Danilo Radunovic; Neetika Garg; Andreas Kousios; Zeynep Ural; Christina Mejia; Ondrej Viklicky; John Sayer; Arksarapuk Jittirat; Mingyao Becky Ma; Mohit Madken; Sultan Ozkurt; Reem Daloul; Hernando Trujillo; Karim Soliman
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Primary hyperoxaluria type 1 – current practice in the siRNA era: an ERA Genes & Kidney Working Group survey
err2026-05-25
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errMalte P Bartram; Giovambattista Capasso; Emilie Cornec-Le Gall; Lisa J Deesker; Albertien M van Eerde; Lucile Figueres; Maria Vanessa Perez Gomez; Jaap Groothoff; Laila Oublam; Jan Halbritter; Ewout J Hoorn; Tom Nijenhuis; John A Sayer; Bodo B Beck; Roman-Ulrich Müller; the PH1 Survey Study Group
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#3174 Monoallelic IFT172 variants as a genetic contributor to the ADPKD spectrum
err2025-10-21
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errNikola Zagorec; Doaa Elbarougy; Marie-Pierre Audrezet; Hana Yang; Laurence Michel-Calemard; Pierre André Massard; John Sayer; Peter Harris; Emilie Cornec-Le Gall
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Mono-allelic pathogenic variants in JAG1 cause Autosomal Dominant Tubulo-interstitial Kidney Disease (ADTKD-JAG1)
err2025-10-06
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PREAI
errLucie Menguy; Laurent Hudier; Mohamad Zaidan; Bertrand Knebelmann; John A. Sayer; Juliana Arcila Galvis; Christelle Arondel; Aurélie Hummel; Guillaume Dorval; Vincent Morinière; Landrine Fula-Pitu; Chiara Guerrera; David Buob; Maud Rabeyrin; Pierre Marijon; Nolwen Jean-Marcais; Chloé Fournier; Jean-Paul Duong Van Huyen; Corinne Antignac; Sophie Saunier; Laurence Heidet
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Urinary renal epithelial cells can be used for NPHP1 phenotyping and a personalized therapeutic strategy
err2025-10-01
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PREAI
errSudhindar, Praveen Dhondurao; Olinger, Eric; Sentell, Zachary T.; Mabillard, Holly; Dicka, Barbora; Wood, Katrina; Rutland, Dominic; Collins, Catherine; Trevisan-Herraz, Marco; Sayer, John A.; Arcila-Galvis, Juliana E.
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PKD1 5’UTR variants are a rare cause of disease in ADPKD and suggest a new focus for therapeutic development
err2025-09-26
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errLaura Wedd; Yvonne Hort; Chirag Patel; John A. Sayer; Rocio Rius; Andrew J. Mallett; Denny L. Cottle; Ian M. Smyth; Timothy Furlong; John Shine; Amali Mallawaarachchi
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10 tips on how to take a proper family history in CKD patient care
err2025-09-01
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errCornec-Le Gall, Emilie; van Eerde, Albertien M.; Figueres, Lucile; Simons, Matias; Capasso, Giovambattista; Perez Gomez, Maria Vanessa; Nijenhuis, Tom; Sayer, John A.; Zagorec, Nikola; Mueller, Roman-Ulrich; Halbritter, Jan
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Using Large Genomic Biobanks to Generate Insights into Genetic Kidney Disease
err2025-07-11
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PREAI
errAlexander R. Chang; Janewit Wongboonsin; Andrew J. Mallett; Ana Morales; Kyle Retterer; Tooraj Mirshahi; John A. Sayer
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Genotype-phenotype correlations and clinical outcomes of genetic TRPC6 podocytopathies
err2025-06-01
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PREAI
errMcAnallen, Susan M.; Elhassan, Elhussein A. E.; Stoneman, Sinead; Vairo, Filippo Pinto e; Hogan, Marie C.; Hoefele, Julia; Clince, Michelle; Mekraksakit, Poemlarp; Titan, Silvia M.; Jorge, Sofia; Calado, Joaquim; Decramer, Stephane; Colliou, Eloise; Tellier, Stephanie; Francisco, Telma; Servais, Aude; Cornet, Josephine; de Fallois, Jonathan; Dossier, Claire; Fenoglio, Roberta; Renieri, Alessandra; Pinto, Anna Maria; Daga, Sergio; Loberti, Lorenzo; Fila, Marc; Quintana, Luis F.; Becherucci, Francesca; Godefroid, Nathalie; Dubrasquet, Astrid; Kalman, Tory; Dolan, Niamh; Alawi, Bushra Al; Sweeney, Clodagh; Riordan, Michael; Stack, Maria; Awan, Atif; Hui, Ng Kar; McCarthy, Hugh J.; Biros, Erik; Harris, Trudie; Kidd, Kendrah; Haeberle, Stefanie; Bleyer, Anthony J.; Mallett, Andrew J.; Sayer, John A.; Schafer, Franz; Benson, Katherine A.; McCann, Emma; Conlon, Peter J.
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SOX9-dependent fibrosis drives renal function in nephronophthisis
err2025-04-10
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errPatel, Maulin Mukeshchandra; Gerakopoulos, Vasileios; Lettenmaier, Bryan; Petsouki, Eleni; Zimmerman, Kurt A.; Sayer, John A.; Tsiokas, Leonidas
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Global access to management of primary hyperoxaluria: a survey on behalf of OxalEurope, G&K Working Group of the ERA and ESPN
err2025-02-21
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PREAI
errLisa J Deesker; Laila Oubram; Reham Almardini; Michelle A Baum; M Bonilla-Felix; Lucile Figueres; Sander F Garrelfs; Jaap W Groothoff; Pépé M Ekulu; Roman-Ulrich Müller; Michiel J S Oosterveld; Shen Qian; John A Sayer; Neveen Soliman; Shabbir H Moochhala; Justine Bacchetta
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SGLT2-Inhibition in Patients With Alport Syndrome
err2024-12-01
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errBoeckhaus, Jan; Gale, Daniel P.; Simon, James; Ding, Jie; Zhang, Yanqin; Bergmann, Carsten; Turner, A. Neil; Hall, Matthew; Sayer, John A.; Srivastava, Shalabh; Kang, Hee Gyung; Cerkauskaite-Kerpauskiene, Agne; Gillion, Valentine; Claes, Kathleen J.; Krueger, Bastian; de Fallois, Jonathan; Walden, Ulrike; Choi, Mira; Schueler, Markus; Mueller, Roman-Ulrich; Todorova, Polina; Hohenstein, Bernd; Zeisberg, Michael; Friede, Tim; Knebelmann, Bertrand; Halbritter, Jan; Gross, Oliver
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Clinical Spectrum and Prognosis of Atypical Autosomal Dominant Polycystic Kidney Disease Caused by Monoallelic Pathogenic Variants of IFT140
err2024-12-01
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PREAI
errZagorec, N; Calamel, A; Delaporte, M; Olinger, E; Orr, S; Sayer, JA; Pillay, VG; Denommé-Pichon, AS; Mau-Them, FT; Nambot, S; Faivre, L; Ars, E; Torra, R; Ong, ACM; Devuyst, O; Perico, N; Després, AM; Lemoine, H; de Fallois, J; Brousse, R; Hummel, A; Knebelmann, B; Maisonneuve, N; Halbritter, J; Le Meur, Y; Audrézet, MP; Cornec-Le Gall, E
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UMOD Genotype and Determinants of Urinary Uromodulin in African Populations
err2024-12-01
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errStrauss-Kruger, Michel; Olinger, Eric; Hofmann, Patrick; Wilson, Ian J.; Mels, Carina; Kruger, Ruan; Gafane-Matemane, Lebo F.; Sayer, John A.; Ricci, Cristian; Schutte, Aletta E.; Devuyst, Olivier
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Progressive Kidney Failure by Angiotensinogen Inactivation in the Germline
err2024-09-01
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PREAI
errWopperer, Florian J.; Olinger, Eric; Wiesener, Antje; Broeker, Katharina A. E.; Knaup, Karl X.; Schaefer, Jan T.; Galiano, Matthias; Schneider, Karen; Schiffer, Mario; Buettner-Herold, Maike; Reis, Andre; Schmieder, Roland; Pasutto, Francesca; Hilgers, Karl F.; Poglitsch, Marko; Ziegler, Christine; Shoemaker, Robin; Sayer, John A.; Wiesener, Michael S.
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Description and Cross-Sectional Analyses of 25,880 Adults and Children in the UK National Registry of Rare Kidney Diseases Cohort
err2024-07-01
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errOAAI
errWong, Katie; Pitcher, David; Braddon, Fiona; Downward, Lewis; Steenkamp, Retha; Masoud, Sherry; Annear, Nicholas; Barratt, Jonathan; Bingham, Coralie; Coward, Richard J.; Chrysochou, Tina; Game, David; Griffin, Sian; Hall, Matt; Johnson, Sally; Kanigicherla, Durga; Frankl, Fiona Karet; Kavanagh, David; Kerecuk, Larissa; Maher, Eamonn R.; Moochhala, Shabbir; Pinney, Jenny; Sayer, John A.; Simms, Roslyn; Sinha, Smeeta; Srivastava, Shalabh; Tam, Frederick W. K.; Thomas, Kay; Turner, A. Neil; Walsh, Stephen B.; Waters, Aoife; Wilson, Patricia; Wong, Edwin; Sy, Karla Therese L.; Huang, Kui; Ye, Jamie; Nitsch, Dorothea; Saleem, Moin; Bockenhauer, Detlef; Bramham, Kate; Gale, Daniel P.
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A Randomized Controlled Clinical Trial Testing Effects of Lademirsen on Kidney Function Decline in Adults with Alport Syndrome
err2024-06-03
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errGale, Daniel P.; Gross, Oliver; Wang, Fang; Esteban de la Rosa, Rafael Jose; Hall, Matthew; Sayer, John A.; Appel, Gerald; Hariri, Ali; Liu, Shiguang; Maski, Manish; Shen, Yuqian; Zhang, Qi; Iqbal, Sajida; Kowthalam, Madhurima Uppara; Lin, Julie; Ding, Jie
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