Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome
Jillian K. Warejko(United Nations), Robert B. Ettenger(University of California, Los Angeles), Tilman Jobst‐Schwan(Harvard University), Svjetlana Lovric(Boston Children's Hospital), Jameela A. Kari(King Abdulaziz University), Amar J. Majmundar(Boston Children's Hospital), Neveen A. Soliman(Cairo University), Avram Z. Traum, Detlef Böckenhauer(KU Leuven), Johanna Magdalena Schmidt, Fatih Özaltın(University of Michigan), Ghaleb H. Daouk, Weizhen Tan(Boston Children's Hospital), Gil Chernin(Hebrew University of Jerusalem), Tobias Hermle(University Medical Center Freiburg), Eugen Widmeier, Shazia Ashraf(Riphah International University), Jeffrey B. Kopp(National Institute of Diabetes and Digestive and Kidney Diseases), Jeffrey Hopcian, Sherif El Desoky(King Abdulaziz University), Stefan Kohl(Boston Children's Hospital), Radovan Bogdanović(Institute of Public Health of Serbia), Nataša Stajić, Hanan Fathy(Alexandria University), Ronen Schneider(MACOM (United States)), Heon Yung Gee(Yonsei University), Jia Rao(Shanghai Jiao Tong University), Ankana Daga, Asaf Vivante(Edmond and Lily Safra Children's Hospital), Shirlee Shril(MACOM (United States)), Deborah R. Stein, Michael A. Ferguson(Augusta University), Aytül Noyan, Michelle A. Baum(Boston Children's Hospital), Nadine Benador, Hadas Ityel, Sevcan A. Bakkaloğlu, Dominik Müller(Spitalzentrum Centre hospitalier Biel- Bienne), Michael J.G. Somers(Boston Children's Hospital), Amelie T. van der Ven, Makiko Nakayama, Werner L. Pabst(Boston Children's Hospital), Carolin E. Sadowski(Boston Children's Hospital), David Schapiro, Jennifer A. Lawson(Eugene Research Institute), Seema Hashmi, Melissa A. Cadnapaphornchai, Martin Zenker(Friedrich-Alexander-Universität Erlangen-Nürnberg), Jing Chen(Kunming University of Science and Technology), Nancy Rodig(Unknown)
Cited by 237
Related Papers
APOL1 Genetic Variants in Focal Segmental Glomerulosclerosis and HIV-Associated Nephropathy
|Journal of the American Society of Nephrology|2011|856
Nomenclature for kidney function and disease: report of a Kidney Disease: Improving Global Outcomes (KDIGO) Consensus Conference
|Kidney International|2020|708
MYH9 is a major-effect risk gene for focal segmental glomerulosclerosis
|Nature Genetics|2008|706
Fluid Overload and Mortality in Children Receiving Continuous Renal Replacement Therapy: The Prospective Pediatric Continuous Renal Replacement Therapy Registry
|American Journal of Kidney Diseases|2009|690
A Single-Gene Cause in 29.5% of Cases of Steroid-Resistant Nephrotic Syndrome
|Journal of the American Society of Nephrology|2014|660