Publications by authors named "Saskia Heeringa"

Claim this Profile
S
Standardized multilevel transition program: Does it affect renal transplant outcome?
Marcus Weitz, Saskia Heeringa, Thomas J Neuhaus, Thomas Fehr, Guido F Laube

Pediatr Transplant· November 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
K
Kidney diseases caused by complement dysregulation: acquired, inherited, and still more to come.
Saskia F Heeringa, Clemens D Cohen

Clin Dev Immunol· August 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness.
Saskia F Heeringa, Gil Chernin, Moumita Chaki, Weibin Zhou, Alexis J Sloan

J Clin Invest· May 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
Nineteen novel NPHS1 mutations in a worldwide cohort of patients with congenital nephrotic syndrome (CNS).
Dominik S Schoeb, Gil Chernin, Saskia F Heeringa, Verena Matejas, Susanne Held

Nephrol Dial Transplant· September 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genotype/phenotype correlation in nephrotic syndrome caused by WT1 mutations.
Gil Chernin, Virginia Vega-Warner, Dominik S Schoeb, Saskia F Heeringa, Bugsu Ovunc

Clin J Am Soc Nephrol· September 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Individuals with mutations in XPNPEP3, which encodes a mitochondrial protein, develop a nephronophthisis-like nephropathy.
John F O'Toole, Yangjian Liu, Erica E Davis, Christopher J Westlake, Massimo Attanasio, Saskia Heeringa

J Clin Invest· March 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Adequate use of allele frequencies in Hispanics--a problem elucidated in nephrotic syndrome.
Gil Chernin, Saskia F Heeringa, Virginia Vega-Warner, Dominik S Schoeb, Peter Nürnberg

Pediatr Nephrol· February 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A novel TRPC6 mutation that causes childhood FSGS.
Saskia F Heeringa, Clemens C Möller, Jianyang Du, Lixia Yue, Bernward Hinkes

PLoS One· November 2009

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Membranoproliferative glomerulonephritis associated with a mutation in Wilms' tumour suppressor gene 1.
Detlef Bockenhauer, William van't Hoff, Gil Chernin, Saskia F Heeringa, Neil J Sebire

Pediatr Nephrol· July 2009

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
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, Gil Chernin

Pediatr Nephrol· May 2009

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Specific podocin mutations determine age of onset of nephrotic syndrome all the way into adult life.
Friedhelm Hildebrandt, Saskia F Heeringa

Kidney Int· April 2009

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A systematic approach to mapping recessive disease genes in individuals from outbred populations.
Friedhelm Hildebrandt, Saskia F Heeringa, Franz Rüschendorf, Massimo Attanasio, Gudrun Nürnberg

PLoS Genet· January 2009

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
Thirteen novel NPHS1 mutations in a large cohort of children with congenital nephrotic syndrome.
Saskia F Heeringa, Christopher N Vlangos, Gil Chernin, Bernward Hinkes, Rasheed Gbadegesin

Nephrol Dial Transplant· November 2008

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
L
Low prevalence of NPHS2 mutations in African American children with steroid-resistant nephrotic syndrome.
Gil Chernin, Saskia F Heeringa, Rasheed Gbadegesin, Jinhong Liu, Bernward G Hinkes

Pediatr Nephrol· September 2008

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Mutations in PLCE1 are a major cause of isolated diffuse mesangial sclerosis (IDMS).
Rasheed Gbadegesin, Bernward G Hinkes, Bethan E Hoskins, Christopher N Vlangos, Saskia F Heeringa

Nephrol Dial Transplant· April 2008

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Eye involvement in children with primary focal segmental glomerulosclerosis.
Fatih Ozaltin, Saskia Heeringa, Ceren Erdogan Poyraz, Yelda Bilginer, Sibel Kadayifcilar

Pediatr Nephrol· March 2008

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Specific podocin mutations correlate with age of onset in steroid-resistant nephrotic syndrome.
Bernward Hinkes, Christopher Vlangos, Saskia Heeringa, Bettina Mucha, Rasheed Gbadegesin

J Am Soc Nephrol· February 2008

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
Focal segmental glomerulosclerosis is not a sufficient predictor of renal outcome in patients with membranous nephropathy.
Saskia F Heeringa, Amanda J W Branten, Jeroen K J Deegens, Eric Steenbergen, Jack F M Wetzels

Nephrol Dial Transplant· August 2007

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis