| human | Q5 |
| P496 | ORCID iD | 0000-0002-6185-948X |
| P106 | occupation | researcher | Q1650915 |
| Q37259295 | A recessive gene for primary vesicoureteral reflux maps to chromosome 12p11-q13. |
| Q53938164 | Apolipoprotein E in idiopathic nephrotic syndrome and focal segmental glomerulosclerosis. |
| Q91997808 | Author Correction: The copy number variation landscape of congenital anomalies of the kidney and urinary tract |
| Q33220376 | Circulating anti-actin and anti-ATP synthase antibodies identify a sub-set of patients with idiopathic nephrotic syndrome. |
| Q40245141 | Cis and trans regulatory elements in NPHS2 promoter: implications in proteinuria and progression of renal diseases |
| Q36451480 | Copy-number disorders are a common cause of congenital kidney malformations |
| Q42639974 | Cyclosporine in patients with steroid-resistant nephrotic syndrome: an open-label, nonrandomized, retrospective study |
| Q34422205 | Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens |
| Q57980301 | Exome sequencing identified MYO1E and NEIL1 as candidate genes for human autosomal recessive steroid-resistant nephrotic syndrome |
| Q47073818 | Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations |
| Q50001526 | Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations. |
| Q37344693 | Familial forms of nephrotic syndrome. |
| Q42653487 | Familial vesicoureteral reflux: testing replication of linkage in seven new multigenerational kindreds |
| Q34680591 | Genetic Drivers of Kidney Defects in the DiGeorge Syndrome |
| Q36013624 | Genetic approaches to human renal agenesis/hypoplasia and dysplasia |
| Q57980353 | Genetic approaches to human renal agenesis/hypoplasia and dysplasia |
| Q58620325 | Glomerular clusterin is associated with PKC-α/β regulation and good outcome of membranous glomerulonephritis in humans |
| Q35677743 | Localization of a gene for nonsyndromic renal hypodysplasia to chromosome 1p32-33 |
| Q57980385 | Podocin mutations in sporadic focal-segmental glomerulosclerosis occurring in adulthood |
| Q36686723 | Podocin-related mechanisms in posttransplant [corrected] recurrence of focal segmental glomerulosclerosis [corrected] |
| Q55488762 | Rare functional variants of podocin (NPHS2) promoter in patients with nephrotic syndrome. |
| Q35140901 | Recurrence of focal segmental glomerulosclerosis after renal transplantation in patients with mutations of podocin |
| Q45964653 | Renal outcome in patients with congenital anomalies of the kidney and urinary tract. |
| Q125891160 | Risk of meningomyelocele mediated by the common 22q11.2 deletion |
| Q90712113 | The copy number variation landscape of congenital anomalies of the kidney and urinary tract |
| Q37578863 | The emerging role of genomics in the diagnosis and workup of congenital urinary tract defects: a novel deletion syndrome on chromosome 3q13.31-22.1. |
| Q90776289 | The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis |
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