S. Heeringa

发表

A Systematic Approach to Mapping Recessive Disease Genes in Individuals from Outbred Populations

Peter Nürnberg, Dominik Seelow, Shazia Ashraf, 2009, PLoS genetics.

Mutations in PLCE1 are a major cause of isolated diffuse mesangial sclerosis (IDMS).

Bethan E. Hoskins, C. Antignac, F. Hildebrandt, 2007, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Complete remission of nephrotic syndrome in an infant with focal segmental glomerulosclerosis: is it renin–angiotensin blockade?

S. Heeringa, G. Chernin, N. Soliman, 2009, Pediatric Nephrology.

Genotype/phenotype correlation in nephrotic syndrome caused by WT1 mutations.

F. Hildebrandt, S. Heeringa, G. Chernin, 2010, Clinical journal of the American Society of Nephrology : CJASN.

A Novel TRPC6 Mutation That Causes Childhood FSGS

F. Hildebrandt, S. Heeringa, G. Chernin, 2009, PloS one.

Nineteen novel NPHS1 mutations in a worldwide cohort of patients with congenital nephrotic syndrome (CNS).

F. Hildebrandt, S. Heeringa, G. Chernin, 2010, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Specific podocin mutations determine age of onset of nephrotic syndrome all the way into adult life.

F. Hildebrandt, S. Heeringa, 2009, Kidney international.

Low prevalence of NPHS2 mutations in African American children with steroid-resistant nephrotic syndrome

F. Hildebrandt, S. Heeringa, G. Chernin, 2008, Pediatric Nephrology.

Eye involvement in children with primary focal segmental glomerulosclerosis

A. Bakkaloğlu, F. Hildebrandt, S. Heeringa, 2008, Pediatric Nephrology.

Thirteen novel NPHS1 mutations in a large cohort of children with congenital nephrotic syndrome.

F. Hildebrandt, S. Heeringa, G. Chernin, 2008, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Specific podocin mutations correlate with age of onset in steroid-resistant nephrotic syndrome.

F. Hildebrandt, S. Heeringa, C. Vlangos, 2008, Journal of the American Society of Nephrology : JASN.

Focal segmental glomerulosclerosis is not a sufficient predictor of renal outcome in patients with membranous nephropathy.

J. Deegens, J. Wetzels, S. Heeringa, 2007, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Standardized multilevel transition program: Does it affect renal transplant outcome?

T. Fehr, S. Heeringa, M. Weitz, 2015, Pediatric transplantation.

COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness.

V. Pertegato, Y. Raphael, H. Prokisch, 2011, The Journal of clinical investigation.

Kidney Diseases Caused by Complement Dysregulation: Acquired, Inherited, and Still More to Come

C. Cohen, S. Heeringa, 2012, Clinical & developmental immunology.

Individuals with mutations in XPNPEP3, which encodes a mitochondrial protein, develop a nephronophthisis-like nephropathy.

Bethan E. Hoskins, D. Seelow, H. Prokisch, 2010, The Journal of clinical investigation.

Individuals with mutations in XPNPEP3, which encodes a mitochondrial protein, develop a nephronophthisis-like nephropathy (Journal of Clinical Investigation (2010) 120, 3 (791-802) DOI: 10.1172/JCI40076)

Bethan E. Hoskins, D. Seelow, H. Prokisch, 2010 .

Adequate use of allele frequencies in Hispanics—a problem elucidated in nephrotic syndrome

F. Hildebrandt, S. Heeringa, G. Chernin, 2010, Pediatric Nephrology.