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Kidney International|March 14, 2009
Specific podocin mutations determine age of onset of nephrotic syndrome all the way into adult lifeFriedhelm Hildebrandt, Saskia F HeeringaClinical & Developmental Immunology|December 11, 2012
Kidney diseases caused by complement dysregulation: acquired, inherited, and still more to comeSaskia F Heeringa, Clemens D CohenPediatric Nephrology (Berlin, Germany)|October 15, 2008
Complete remission of nephrotic syndrome in an infant with focal segmental glomerulosclerosis: is it renin-angiotensin blockade?Neveen A Soliman, Magdi Francis, Saskia F Heeringa, et al.Pediatric Nephrology (Berlin, Germany)|February 12, 2009
Membranoproliferative glomerulonephritis associated with a mutation in Wilms' tumour suppressor gene 1Detlef Bockenhauer, William van't Hoff, Gil Chernin, et al.Pediatric Nephrology (Berlin, Germany)|October 31, 2009
Adequate use of allele frequencies in Hispanics--a problem elucidated in nephrotic syndromeGil Chernin, Saskia F Heeringa, Virginia Vega-Warner, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|April 20, 2007
Focal segmental glomerulosclerosis is not a sufficient predictor of renal outcome in patients with membranous nephropathySaskia F Heeringa, Amanda J W Branten, Jeroen K J Deegens, et al.Pediatric Nephrology (Berlin, Germany)|June 11, 2008
Low prevalence of NPHS2 mutations in African American children with steroid-resistant nephrotic syndromeGil Chernin, Saskia F Heeringa, Rasheed Gbadegesin, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|May 27, 2008
Thirteen novel NPHS1 mutations in a large cohort of children with congenital nephrotic syndromeSaskia F Heeringa, Christopher N Vlangos, Gil Chernin, et al.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.Plos One|November 26, 2009
A novel TRPC6 mutation that causes childhood FSGSSaskia F Heeringa, Clemens C Möller, Jianyang Du, et al.Pageof 2