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Complement Mutations in Diacylglycerol Kinase-ε–Associated Atypical Hemolytic Uremic Syndrome
Daniel Sánchez Chinchilla, Sheila Pinto, Bernd Hoppe, Marta Adragna, Laura Lopez, Maria Luisa Justa Roldan, Antonia Peña, Margarita Lopez Trascasa, Pilar Sánchez-Corral and Santiago Rodríguez de Córdoba

CJASN September 2014, 9 (9) 1611-1619; DOI: https://doi.org/10.2215/CJN.01640214

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Coding Variants in Nephrin (NPHS1) and Susceptibility to Nephropathy in African Americans
Jason A. Bonomo, Maggie C.Y. Ng, Nicholette D. Palmer, Jacob M. Keaton, Chris P. Larsen, Pamela J. Hicks, The T2D-GENES Consortium, Carl D. Langefeld, Barry I. Freedman and Donald W. Bowden

CJASN August 2014, 9 (8) 1434-1440; DOI: https://doi.org/10.2215/CJN.00290114

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Rapid Detection of Monogenic Causes of Childhood-Onset Steroid-Resistant Nephrotic Syndrome
Svjetlana Lovric, Humphrey Fang, Virginia Vega-Warner, Carolin E. Sadowski, Heon Yung Gee, Jan Halbritter, Shazia Ashraf, Pawaree Saisawat, Neveen A. Soliman, Jameela A. Kari, Edgar A. Otto and Friedhelm Hildebrandt

CJASN June 2014, 9 (6) 1109-1116; DOI: https://doi.org/10.2215/CJN.09010813

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Association of Systemic Lupus Erythematosus Susceptibility Genes with IgA Nephropathy in a Chinese Cohort
Xu-Jie Zhou, Fa-Juan Cheng, Li Zhu, Ji-Cheng Lv, Yuan-Yuan Qi, Ping Hou and Hong Zhang

CJASN April 2014, 9 (4) 788-797; DOI: https://doi.org/10.2215/CJN.01860213

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Variable Clinical Presentation of an MUC1 Mutation Causing Medullary Cystic Kidney Disease Type 1
Anthony J. Bleyer, Stanislav Kmoch, Corinne Antignac, Vicki Robins, Kendrah Kidd, John R. Kelsoe, Gerald Hladik, Philip Klemmer, Stephen J. Knohl, Steven J. Scheinman, Nam Vo, Ann Santi, Alese Harris, Omar Canaday, Nelson Weller, Peter J. Hulick, Kristen Vogel, Frederick F. Rahbari-Oskoui, Jennifer Tuazon, Constantinos Deltas, Douglas Somers, Andre Megarbane, Paul L. Kimmel, C. John Sperati, Avi Orr-Urtreger, Shay Ben-Shachar, David A. Waugh, Stella McGinn, Anthony J. Bleyer, Kateřina Hodaňová, Petr Vylet'al, Martina Živná, Thomas C. Hart and P. Suzanne Hart

CJASN March 2014, 9 (3) 527-535; DOI: https://doi.org/10.2215/CJN.06380613

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HLA-DQA1 and PLA2R1 Polymorphisms and Risk of Idiopathic Membranous Nephropathy
Gemma Bullich, José Ballarín, Artur Oliver, Nadia Ayasreh, Irene Silva, Sheila Santín, Montserrat M. Díaz-Encarnación, Roser Torra and Elisabet Ars

CJASN February 2014, 9 (2) 335-343; DOI: https://doi.org/10.2215/CJN.05310513

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Generalization of Associations of Kidney-Related Genetic Loci to American Indians
Nora Franceschini, Karin Haack, Laura Almasy, Sandra Laston, Elisa T. Lee, Lyle G. Best, Richard R. Fabsitz, Jean W. MacCluer, Barbara V. Howard, Jason G. Umans and Shelley A. Cole

CJASN January 2014, 9 (1) 150-158; DOI: https://doi.org/10.2215/CJN.02300213

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Length Polymorphism in Heme Oxygenase-1 and Cardiovascular Events and Mortality in Hemodialysis Patients
Yu-Hsin Chen, Szu-Chun Hung and Der-Cherng Tarng

CJASN October 2013, 8 (10) 1756-1763; DOI: https://doi.org/10.2215/CJN.01110113

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Candidate Gene Analysis of Arteriovenous Fistula Failure in Hemodialysis Patients
Jeffrey J.W. Verschuren, Gurbey Ocak, Friedo W. Dekker, Ton J. Rabelink, J. Wouter Jukema and Joris I. Rotmans

CJASN August 2013, 8 (8) 1358-1366; DOI: https://doi.org/10.2215/CJN.11091012

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Association between Genotype and Phenotype in Uromodulin-Associated Kidney Disease
Jonathan L. Moskowitz, Sian E. Piret, Karl Lhotta, Thomas M. Kitzler, Adam P. Tashman, Erin Velez, Rajesh V. Thakker and Peter Kotanko

CJASN August 2013, 8 (8) 1349-1357; DOI: https://doi.org/10.2215/CJN.11151012

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