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Clinical Journal of the American Society of Nephrology : CJASN|July 3, 2010
Genotype/phenotype correlation in nephrotic syndrome caused by WT1 mutationsGil Chernin, Virginia Vega-Warner, Dominik S Schoeb, et al.Journal of the American Society of Nephrology : JASN|November 5, 2015
Using Population Genetics to Interrogate the Monogenic Nephrotic Syndrome Diagnosis in a Case CohortMatthew G Sampson, Christopher E Gillies, Catherine C Robertson, et al.BMC Medical Genetics|June 5, 2015
Novel compound heterozygous mutations in AMN cause Imerslund-Gräsbeck syndrome in two half-sisters: a case reportEmma Montgomery, John A Sayer, Laura A Baines, et al.Kidney International|September 9, 2011
Identification of two novel CAKUT-causing genes by massively parallel exon resequencing of candidate genes in patients with unilateral renal agenesisPawaree Saisawat, Velibor Tasic, Virginia Vega-Warner, et al.European Journal of Human Genetics : EJHG|June 13, 2018
Biallelic variants in the ciliary gene TMEM67 cause RHYNS syndromeFrancesco Brancati, Letizia Camerota, Emma Colao, et al.Journal of the American Society of Nephrology : JASN|September 10, 2011
Exome sequencing reveals cubilin mutation as a single-gene cause of proteinuriaBugsu Ovunc, Edgar A Otto, Virginia Vega-Warner, et al.BMC Bioinformatics|June 12, 2016
tarSVM: Improving the accuracy of variant calls derived from microfluidic PCR-based targeted next generation sequencing using a support vector machineChristopher E Gillies, Edgar A Otto, Virginia Vega-Warner, et al.Clinical Journal of the American Society of Nephrology : CJASN|April 19, 2014
Rapid detection of monogenic causes of childhood-onset steroid-resistant nephrotic syndromeSvjetlana Lovric, Humphrey Fang, Virginia Vega-Warner, et al.Pediatric Nephrology (Berlin, Germany)|December 18, 2012
NPHS2 p.V290M mutation in late-onset steroid-resistant nephrotic syndromeAndrea Kerti, Rózsa Csohány, Attila Szabó, et al.Kidney International Reports|November 20, 2018
NPHS2 V260E Is a Frequent Cause of Steroid-Resistant Nephrotic Syndrome in Black South African ChildrenKareshma Asharam, Rajendra Bhimma, Victor A David, et al.Pageof 5