V. Vega-Warner

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

Rapid detection of monogenic causes of childhood-onset steroid-resistant nephrotic syndrome.

F. Hildebrandt, S. Ashraf, V. Vega-Warner, 2014, Clinical journal of the American Society of Nephrology : CJASN.

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

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

A boy with proteinuria and focal global glomerulosclerosis: Answers

V. Vega-Warner, E. Otto, V. Kher, 2015, Pediatric Nephrology.

Steroid-resistant nephrotic syndrome: impact of genetic testing

V. Vega-Warner, D. Bockenhauer, J. Kari, 2013, Annals of Saudi medicine.

Precision nephrology identified tumor necrosis factor activation variability in minimal change disease and focal segmental glomerulosclerosis.

J. Lieske, W. Ju, V. Nair, 2022, Kidney international.

Mutation Analysis of NPHS1 in a Worldwide Cohort of Congenital Nephrotic Syndrome Patients

F. Hildebrandt, S. Ashraf, V. Vega-Warner, 2012, Nephron Clinical Practice.

Biallelic variants in the ciliary gene TMEM67 cause RHYNS syndrome

D. Taruscio, F. Brancati, A. Ferlini, 2018, European Journal of Human Genetics.

Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations.

D. Goldstein, S. Mane, G. Ardissino, 2017, American journal of human genetics.

Focal segmental glomerulosclerosis in association with neurofibromatosis type 1: a case report and proposed molecular pathways

V. Vega-Warner, P. Killen, F. Afshinnia, 2013, Clinical Kidney Journal.

A Familial Infantile Renal Failure

V. Vega-Warner, E. Otto, M. Sampson, 2016, Kidney international reports.

Focal segmental glomerulosclerosis in association with neurofibromatosis type 1: a case report and proposed molecular pathways

V. Vega-Warner, P. Killen, F. Afshinnia, 2013, Clinical kidney journal.

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

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

Genetic Drivers of Kidney Defects in the DiGeorge Syndrome

Craig S. Wong, E. Zackai, H. Hakonarson, 2017, The New England journal of medicine.

Evaluating Mendelian nephrotic syndrome genes for evidence of risk alleles or oligogenicity that explain heritability

Catherine C. Robertson, H. Kang, M. Kretzler, 2016, bioRxiv.

Using Population Genetics to Interrogate the Monogenic Nephrotic Syndrome Diagnosis in a Case Cohort.

Catherine C. Robertson, H. Kang, M. Kretzler, 2016, Journal of the American Society of Nephrology : JASN.

tarSVM: Improving the accuracy of variant calls derived from microfluidic PCR-based targeted next generation sequencing using a support vector machine

Catherine C. Robertson, H. Kang, C. Winkler, 2016, BMC Bioinformatics.

Whole Exome Sequencing Reveals Novel PHEX Splice Site Mutations in Patients with Hypophosphatemic Rickets

V. Vega-Warner, E. Otto, M. Sampson, 2015, PloS one.

FAT1 mutations cause a glomerulotubular nephropathy

T. Chan, R. Lifton, D. Milford, 2016, Nature Communications.

ARHGDIA mutations cause nephrotic syndrome via defective RHO GTPase signaling.

S. Levy, T. Hurd, O. Gribouval, 2013, The Journal of clinical investigation.

Integrative Genomics Identifies Novel Associations with APOL1 Risk Genotypes in Black NEPTUNE Subjects.

Catherine C. Robertson, V. Nair, M. Kretzler, 2016, Journal of the American Society of Nephrology : JASN.

Multidimensional Data Integration Identifies Tumor Necrosis Factor Activation in Nephrotic Syndrome: A Model for Precision Nephrology

D. Adu, J. Lieske, W. Ju, 2021, medRxiv.

Whole exome resequencing distinguishes cystic kidney diseases from phenocopies in renal ciliopathies

S. Levy, N. Katsanis, T. Hurd, 2013, Kidney international.

ADCK4 mutations promote steroid-resistant nephrotic syndrome through CoQ10 biosynthesis disruption.

A. Paterson, H. Prokisch, S. Levy, 2013, The Journal of clinical investigation.

Erratum to: Evaluating Mendelian nephrotic syndrome genes for evidence for risk alleles or oligogenicity that explain heritability

Catherine C. Robertson, M. Kretzler, V. Vega-Warner, 2017, Pediatric Nephrology.

Novel compound heterozygous mutations in AMN cause Imerslund-Gräsbeck syndrome in two half-sisters: a case report

J. Goodship, V. Vega-Warner, E. Otto, 2015, BMC Medical Genetics.

Denaturation and aggregation of myosin from two bovine muscle types.

V. Vega-Warner, D. Smith, 2001, Journal of agricultural and food chemistry.

Exome sequencing reveals cubilin mutation as a single-gene cause of proteinuria.

F. Hildebrandt, G. Chernin, S. Ashraf, 2011, Journal of the American Society of Nephrology : JASN.

Induction of antioxidant enzymes in murine podocytes precedes injury by puromycin aminonucleoside.

V. Vega-Warner, A. Vincent, F. Brosius, 2004, Kidney international.

NPHS2 V260E Is a Frequent Cause of Steroid-Resistant Nephrotic Syndrome in Black South African Children

C. Winkler, H. Coovadia, V. Vega-Warner, 2018, Kidney international reports.

A Rare Autosomal Dominant Variant in Regulator of Calcineurin Type 1 (RCAN1) Gene Confers Enhanced Calcineurin Activity and May Cause FSGS

G. Cavalleri, F. Hildebrandt, V. Vega-Warner, 2021, Journal of the American Society of Nephrology : JASN.

Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations.

D. Goldstein, S. Mane, G. Ardissino, 2017, American journal of human genetics.

Heat-induced gelation of chicken Pectoralis major myosin and beta-lactoglobulin.

V. Vega-Warner, J. Steffe, D. Smith, 2001, Journal of agricultural and food chemistry.

Respiratory-chain deficiency presenting as diffuse mesangial sclerosis with NPHS3 mutation

R. Horvath, F. Hildebrandt, V. Vega-Warner, 2011, Pediatric Nephrology.

Erratum : Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations (The American Journal of Human Genetics (2017) 101(5) (789–802) (S0002929717303877) (10.1016/j.ajhg.2017.09.018))

D. Goldstein, S. Mane, G. Ardissino, 2017 .

ADCK 4 mutations promote steroid-resistant nephrotic syndrome through CoQ 10 biosynthesis disruption

A. Paterson, H. Prokisch, S. Levy, 2018 .

An integrated organoid omics map extends modeling potential of kidney disease

Anja M. Billing, Markus M. Rinschen, Victor G. Puelles, 2023, Nature communications.

Integrin α3 mutations with kidney, lung, and skin disease.

Y. Anikster, F. Hildebrandt, V. Vega-Warner, 2012, The New England journal of medicine.

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

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

KANK deficiency leads to podocyte dysfunction and nephrotic syndrome.

Margaret Y. Nettleton, S. Levy, R. Lifton, 2015, The Journal of clinical investigation.