Robert Kleta

ORCID

Publication Activity (10 Years)

Years Active: 2016-2023
Publications (10 Years): 17

Top Venues

Journal of the American Society of Nephrology : JASN

BMC nephrology

Molecular genetics & genomic medicine

American journal of physiology. Renal physiology

This page only lists publications with an associated author ORCID identifier.

Publications

Carsten Alexander Wagner, Robert John Unwin, Sergio C Lopez-Garcia, Robert Kleta, Detlef Bockenhauer, Stephen Walsh
The pathophysiology of distal renal tubular acidosis. Nature reviews. Nephrology (2023)
Sumaya Islam, Mehmet Tekman, Sarah E. Flanagan, Lisa Guay-Woodford, Khalid Hussain, Sian Ellard, Robert Kleta, Detlef Bockenhauer, Horia Stanescu, Daniela Iancu
Founder mutation in the PMM2 promotor causes hyperinsulinemic hypoglycaemia/polycystic kidney disease (HIPKD). Molecular genetics & genomic medicine (2021)
Karl P Schlingmann, Aparna Renigunta, Ewout J Hoorn, Anna-Lena Forst, Vijay Renigunta, Velko Atanasov, Sinthura Mahendran, Tahsin Stefan Barakat, Valentine Gillion, Nathalie Godefroid, Alice S Brooks, Dorien Lugtenberg, Jennifer Lake, Huguette Debaix, Christoph Rudin, Bertrand Knebelmann, Stephanie Tellier, Caroline Rousset-Rouvière, Daan H H M Viering, Jeroen H F de Baaij, Stefanie Weber, Oleg Palygin, Alexander Staruschenko, Robert Kleta, Pascal Houillier, Detlef Bockenhauer, Olivier Devuyst, Rosa Vargas-Poussou, Richard Warth, Anselm A Zdebik, Martin Konrad
Defects in KCNJ16 Cause a Novel Tubulopathy with Hypokalemia, Salt Wasting, Disturbed Acid-Base Homeostasis, and Sensorineural Deafness. Journal of the American Society of Nephrology : JASN 32 (6) (2021)
Eszter Balogh, Jennifer C Chandler, Máté Varga, Mona Tahoun, Dóra K Menyhárd, Gusztáv Schay, Tomas Goncalves, Renáta Hamar, Regina Légrádi, Ákos Szekeres, Olivier Gribouval, Robert Kleta, Horia Stanescu, Detlef Bockenhauer, Andrea Kerti, Hywel Williams, Veronica Kinsler, Wei-Li Di, David Curtis, Maria Kolatsi-Joannou, Hafsa Hammid, Anna Szőcs, Kristóf Perczel, Erika Maka, Gergely Toldi, Florentina Sava, Christelle Arrondel, Magdolna Kardos, Attila Fintha, Ahmed Hossain, Felice D'Arco, Marios Kaliakatsos, Jutta Koeglmeier, William Mifsud, Mariya Moosajee, Ana Faro, Eszter Jávorszky, Gábor Rudas, Marwa H Saied, Salah Marzouk, Kata Kelen, Judit Götze, George S Reusz, Tivadar Tulassay, François Dragon, Geraldine Mollet, Susanne Motameny, Holger Thiele, Guillaume Dorval, Peter Nürnberg, András Perczel, Attila J Szabo, David A Long, Kazunori Tomita, Corinne Antignac, Aoife M Waters, Kálmán Tory
Pseudouridylation defect due to DKC1 and NOP10 mutations causes nephrotic syndrome with cataracts, hearing impairment, and enterocolitis. Proceedings of the National Academy of Sciences of the United States of America 117 (26) (2020)
Jingyuan Xie, Lili Liu, Nikol Mladkova, Yifu Li, Hong Ren, Weiming Wang, Zhao Cui, Li Lin, Xiaofan Hu, Xialian Yu, Jing Xu, Gang Liu, Yasar Caliskan, Carlo Sidore, Olivia Balderes, Raphael J Rosen, Monica Bodria, Francesca Zanoni, Junying Zhang, Priya Krithivasan, Karla Mehl, Maddalena Marasà, Atlas Khan, Fatih Ozay, Pietro A Canetta, Andrew S Bomback, Gerald B Appel, Simone Sanna-Cherchi, Matthew G Sampson, Laura H Mariani, Agnieszka Perkowska-Ptasinska, Magdalena Durlik, Krzysztof Mucha, Barbara Moszczuk, Bartosz Foroncewicz, Leszek Pączek, Ireneusz Habura, Elisabet Ars, Jose Ballarin, Laila-Yasmin Mani, Bruno Vogt, Savas Ozturk, Abdülmecit Yildiz, Nurhan Seyahi, Hakki Arikan, Mehmet Koc, Taner Basturk, Gonca Karahan, Sebahat Usta Akgul, Mehmet Sukru Sever, Dan Zhang, Domenico Santoro, Mario Bonomini, Francesco Londrino, Loreto Gesualdo, Jana Reiterova, Vladimir Tesar, Claudia Izzi, Silvana Savoldi, Donatella Spotti, Carmelita Marcantoni, Piergiorgio Messa, Marco Galliani, Dario Roccatello, Simona Granata, Gianluigi Zaza, Francesca Lugani, GianMarco Ghiggeri, Isabella Pisani, Landino Allegri, Ben Sprangers, Jin Ho Park, BeLong Cho, Yon Su Kim, Dong Ki Kim, Hitoshi Suzuki, Antonio Amoroso, Daniel C Cattran, Fernando C Fervenza, Antonello Pani, Patrick Hamilton, Shelly Harris, Sanjana Gupta, Chris Cheshire, Stephanie Dufek-Kamperis, Naomi Issler, Ruth J Pepper, John Connolly, Stephen Powis, Detlef Bockenhauer, Horia C Stanescu, Neil Ashman, Ruth J F Loos, Eimear E Kenny, Matthias Wuttke, Kai-Uwe Eckardt, Anna Kottgen, Julia M Hofstra, Marieke J H Coenen, Lambertus A Kiemeney, Shreeram Akilesh, Matthias Kretzler, Lawrence H Beck, Benedicte Stengel, Hanna Debiec, Pierre Ronco, Jack F M Wetzels, Magdalena Zoledziewska, Francesco Cucca, Iuliana Ionita-Laza, Hajeong Lee, Elion Hoxha, Rolf A K Stahl, Paul Brenchley, Francesco Scolari, Ming-Hui Zhao, Ali G Gharavi, Robert Kleta, Nan Chen, Krzysztof Kiryluk
The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis. Nature communications 11 (1) (2020)
Stephanie Dufek, Chris Cheshire, Adam P Levine, Richard S Trompeter, Naomi Issler, Matthew Stubbs, Monika Mozere, Sanjana Gupta, Enriko Klootwijk, Vaksha Patel, Daljit Hothi, Aoife Waters, Hazel Webb, Kjell Tullus, Lucy Jenkins, Lighta Godinho, Elena Levtchenko, Jack Wetzels, Nine Knoers, Nynke Teeninga, Jeroen Nauta, Mohamed Shalaby, Sherif Eldesoky, Jameela A Kari, Shenal Thalgahagoda, Randula Ranawaka, Asiri Abeyagunawardena, Adebowale Adeyemo, Mark Kristiansen, Rasheed A Gbadegesin, Nicholas J Webb, Daniel P Gale, Horia C Stanescu, Robert Kleta, Detlef Bockenhauer
Genetic Identification of Two Novel Loci Associated with Steroid-Sensitive Nephrotic Syndrome. Journal of the American Society of Nephrology : JASN 30 (8) (2019)
Priya Outtandy, Claire Russell, Robert Kleta, Detlef Bockenhauer
Zebrafish as a model for kidney function and disease. Pediatric nephrology (Berlin, Germany) 34 (5) (2018)
Monika Mozere, Mehmet Tekman, Jameela Kari, Detlef Bockenhauer, Robert Kleta, Horia Stanescu
OVAS: an open-source variant analysis suite with inheritance modelling. BMC bioinformatics 19 (1) (2018)
Daniel P Gale, Robert Kleta
MUC1 Makes Me Miserable. Journal of the American Society of Nephrology : JASN 29 (9) (2018)
Markus Reichold, Enriko D Klootwijk, Joerg Reinders, Edgar A Otto, Mario Milani, Carsten Broeker, Chris Laing, Julia Wiesner, Sulochana Devi, Weibin Zhou, Roland Schmitt, Ines Tegtmeier, Christina Sterner, Hannes Doellerer, Kathrin Renner, Peter J Oefner, Katja Dettmer, Johann M Simbuerger, Ralph Witzgall, Horia C Stanescu, Simona Dumitriu, Daniela Iancu, Vaksha Patel, Monika Mozere, Mehmet Tekman, Graciana Jaureguiberry, Naomi Issler, Anne Kesselheim, Stephen B Walsh, Daniel P Gale, Alexander J Howie, Joana R Martins, Andrew M Hall, Michael Kasgharian, Kevin O'Brien, Carlos R Ferreira, Paldeep S Atwal, Mahim Jain, Alexander Hammers, Geoffrey Charles-Edwards, Chi-Un Choe, Dirk Isbrandt, Alberto Cebrian-Serrano, Benjamin Davies, Richard N Sandford, Christopher Pugh, David S Konecki, Sue Povey, Detlef Bockenhauer, Uta Lichter-Konecki, William A Gahl, Robert J Unwin, Richard Warth, Robert Kleta
Glycine Amidinotransferase (GATM), Renal Fanconi Syndrome, and Kidney Failure. Journal of the American Society of Nephrology : JASN 29 (7) (2018)
Naomi Issler, Stephanie Dufek, Robert Kleta, Detlef Bockenhauer, Naima Smeulders, William Van't Hoff
Epidemiology of paediatric renal stone disease: a 22-year single centre experience in the UK. BMC nephrology 18 (1) (2017)
Robert Kleta, Detlef Bockenhauer
Salt-Losing Tubulopathies in Children: What's New, What's Controversial? Journal of the American Society of Nephrology : JASN 29 (3) (2017)
Sven Enerbäck, Daniel Nilsson, Noel Edwards, Mikael Heglind, Sumaya Alkanderi, Emma Ashton, Asma Deeb, Feras E B Kokash, Abdul R A Bakhsh, William Van't Hoff, Stephen B Walsh, Felice D'Arco, Arezoo Daryadel, Soline Bourgeois, Carsten Alexander Wagner, Robert Kleta, Detlef Bockenhauer, John Andrew Sayer
Acidosis and Deafness in Patients with Recessive Mutations in FOXI1. Journal of the American Society of Nephrology : JASN 29 (3) (2017)
Stephen Benedict Walsh, Robert Unwin, Robert Kleta, William Van't Hoff, Paul Bass, Khalid Hussain, Sian Ellard, Detlef Bockenhauer
Fainting Fanconi syndrome clarified by proxy: a case report. BMC nephrology 18 (1) (2017)
Sanjana Gupta, John Connolly, Ruth J Pepper, Stephen B Walsh, Magdi M Yaqoob, Robert Kleta, Neil Ashman
Membranous nephropathy: a retrospective observational study of membranous nephropathy in north east and central London. BMC nephrology 18 (1) (2017)
Ariane S I Standing, Dessislava Malinova, Ying Hong, Julien Record, Dale A Moulding, Michael P Blundell, Karolin Nowak, Hannah Jones, Ebun Omoyinmi, Kimberley C Gilmour, Alan Medlar, Horia Stanescu, Robert Kleta, Glenn Anderson, Sira Nanthapisal, Sonia Melo Gomes, Nigel Klein, Despina Eleftheriou, Adrian J Thrasher, Paul A Brogan
Autoinflammatory periodic fever, immunodeficiency, and thrombocytopenia (PFIT) caused by mutation in actin-regulatory gene WDR1. The Journal of experimental medicine 214 (1) (2016)
Ben Oliveira, Robert Kleta, Detlef Bockenhauer, Stephen B Walsh
Genetic, pathophysiological, and clinical aspects of nephrocalcinosis. American journal of physiology. Renal physiology 311 (6) (2016)

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Publication Activity (10 Years)

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Robert Kleta