More articles from Genetics

  • Preimplantation Genetic Testing for Monogenic Kidney Disease
    Open Access
    Preimplantation Genetic Testing for Monogenic Kidney Disease
    Rozemarijn Snoek, Marijn F. Stokman, Klaske D. Lichtenbelt, Theodora C. van Tilborg, Cindy E. Simcox, Aimée D.C. Paulussen, Jos C.M.F. Dreesen, Franka van Reekum, A. Titia Lely, Nine V.A.M. Knoers, Christine E.M. de Die-Smulders and Albertien M. van Eerde
    CJASN September 2020, 15 (9) 1279-1286; DOI: https://doi.org/10.2215/CJN.03550320
  • Pilot Study of Return of Genetic Results to Patients in Adult Nephrology
    Pilot Study of Return of Genetic Results to Patients in Adult Nephrology
    Jordan G. Nestor, Maddalena Marasa, Hila Milo-Rasouly, Emily E. Groopman, S. Ali Husain, Sumit Mohan, Hilda Fernandez, Vimla S. Aggarwal, Dina F. Ahram, Natalie Vena, Kelsie Bogyo, Andrew S. Bomback, Jai Radhakrishnan, Gerald B. Appel, Wooin Ahn, David J. Cohen, Pietro A. Canetta, Geoffrey K. Dube, Maya K. Rao, Heather K. Morris, Russell J. Crew, Simone Sanna-Cherchi, Krzysztof Kiryluk and Ali G. Gharavi
    CJASN May 2020, 15 (5) 651-664; DOI: https://doi.org/10.2215/CJN.12481019
  • Reverse Phenotyping after Whole-Exome Sequencing in Steroid-Resistant Nephrotic Syndrome
    Open Access
    Reverse Phenotyping after Whole-Exome Sequencing in Steroid-Resistant Nephrotic Syndrome
    Samuela Landini, Benedetta Mazzinghi, Francesca Becherucci, Marco Allinovi, Aldesia Provenzano, Viviana Palazzo, Fiammetta Ravaglia, Rosangela Artuso, Emanuele Bosi, Stefano Stagi, Giulia Sansavini, Francesco Guzzi, Luigi Cirillo, Augusto Vaglio, Luisa Murer, Licia Peruzzi, Andrea Pasini, Marco Materassi, Rosa Maria Roperto, Hans-Joachim Anders, Mario Rotondi, Sabrina Rita Giglio and Paola Romagnani
    CJASN January 2020, 15 (1) 89-100; DOI: https://doi.org/10.2215/CJN.06060519
  • <em>APOL1</em> Nephropathy Risk Alleles and Risk of Sepsis in Blacks
    APOL1 Nephropathy Risk Alleles and Risk of Sepsis in Blacks
    Ninad S. Chaudhary, Justin X. Moore, Neil A. Zakai, Suzanne E. Judd, Rakhi P. Naik, Sophie Limou, Mary Cushman, Leslie A. Lange, Henry E. Wang, Cheryl A. Winkler, Marguerite R. Irvin, Jeffrey B. Kopp and Orlando M. Gutiérrez
    CJASN December 2019, 14 (12) 1733-1740; DOI: https://doi.org/10.2215/CJN.04490419
  • Genetic and Environmental Influences on the Correlations between Traits of Metabolic Syndrome and CKD
    Genetic and Environmental Influences on the Correlations between Traits of Metabolic Syndrome and CKD
    Xu Chen, Istiak Bhuiyan, Ralf Kuja-Halkola, Patrik K. E. Magnusson and Per Svensson
    CJASN November 2019, 14 (11) 1590-1596; DOI: https://doi.org/10.2215/CJN.11971018
  • Integration of Genetic Testing and Pathology for the Diagnosis of Adults with FSGS
    Integration of Genetic Testing and Pathology for the Diagnosis of Adults with FSGS
    Tony Yao, Khalil Udwan, Rohan John, Akanchaya Rana, Amirreza Haghighi, Lizhen Xu, Saidah Hack, Heather N. Reich, Michelle Adrienne Hladunewich, Daniel C. Cattran, Andrew D. Paterson, York Pei and Moumita Barua
    CJASN February 2019, 14 (2) 213-223; DOI: https://doi.org/10.2215/CJN.08750718
  • IgA Nephropathy Susceptibility Loci and Disease Progression
    IgA Nephropathy Susceptibility Loci and Disease Progression
    Manman Shi, Yan Ouyang, Mingxin Yang, Meng Yang, Xiaoyan Zhang, Wei Huang, Weiming Wang, Zhaohui Wang, Wen Zhang, Xiaonong Chen, Xiaoxia Pan, Hong Ren, Nan Chen and Jingyuan Xie
    CJASN September 2018, 13 (9) 1330-1338; DOI: https://doi.org/10.2215/CJN.13701217
  • Prevalence of Novel <em>MAGED2</em> Mutations in Antenatal Bartter Syndrome
    Prevalence of Novel MAGED2 Mutations in Antenatal Bartter Syndrome
    Anne Legrand, Cyrielle Treard, Isabelle Roncelin, Sophie Dreux, Aurélia Bertholet-Thomas, Françoise Broux, Daniele Bruno, Stéphane Decramer, Georges Deschenes, Djamal Djeddi, Vincent Guigonis, Nadine Jay, Tackwa Khalifeh, Brigitte Llanas, Denis Morin, Gilles Morin, François Nobili, Christine Pietrement, Amélie Ryckewaert, Rémi Salomon, Isabelle Vrillon, Anne Blanchard and Rosa Vargas-Poussou
    CJASN February 2018, 13 (2) 242-250; DOI: https://doi.org/10.2215/CJN.05670517
  • Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome
    Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome
    Jillian K. Warejko, Weizhen Tan, Ankana Daga, David Schapiro, Jennifer A. Lawson, Shirlee Shril, Svjetlana Lovric, Shazia Ashraf, Jia Rao, Tobias Hermle, Tilman Jobst-Schwan, Eugen Widmeier, Amar J. Majmundar, Ronen Schneider, Heon Yung Gee, J. Magdalena Schmidt, Asaf Vivante, Amelie T. van der Ven, Hadas Ityel, Jing Chen, Carolin E. Sadowski, Stefan Kohl, Werner L. Pabst, Makiko Nakayama, Michael J.G. Somers, Nancy M. Rodig, Ghaleb Daouk, Michelle Baum, Deborah R. Stein, Michael A. Ferguson, Avram Z. Traum, Neveen A. Soliman, Jameela A. Kari, Sherif El Desoky, Hanan Fathy, Martin Zenker, Sevcan A. Bakkaloglu, Dominik Müller, Aytul Noyan, Fatih Ozaltin, Melissa A. Cadnapaphornchai, Seema Hashmi, Jeffrey Hopcian, Jeffrey B. Kopp, Nadine Benador, Detlef Bockenhauer, Radovan Bogdanovic, Nataša Stajić, Gil Chernin, Robert Ettenger, Henry Fehrenbach, Markus Kemper, Reyner Loza Munarriz, Ludmila Podracka, Rainer Büscher, Erkin Serdaroglu, Velibor Tasic, Shrikant Mane, Richard P. Lifton, Daniela A. Braun and Friedhelm Hildebrandt
    CJASN January 2018, 13 (1) 53-62; DOI: https://doi.org/10.2215/CJN.04120417
  • Long-Term Dose-Dependent Agalsidase Effects on Kidney Histology in Fabry Disease
    Rannveig Skrunes, Camilla Tøndel, Sabine Leh, Kristin Kampevold Larsen, Gunnar Houge, Einar Skulstad Davidsen, Carla Hollak, André B.P. van Kuilenburg, Frédéric M. Vaz and Einar Svarstad
    CJASN September 2017, 12 (9) 1470-1479; DOI: https://doi.org/10.2215/CJN.01820217

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