PubRank

Krzysztof Kiryluk

Author PubWeight™ 23.44‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Genome-wide association study identifies susceptibility loci for IgA nephropathy. Nat Genet 2011 3.15
2 The pathophysiology of IgA nephropathy. J Am Soc Nephrol 2011 2.27
3 APOL1 variants increase risk for FSGS and HIVAN but not IgA nephropathy. J Am Soc Nephrol 2011 1.67
4 Copy-number disorders are a common cause of congenital kidney malformations. Am J Hum Genet 2012 1.63
5 Genomic imbalances in pediatric patients with chronic kidney disease. J Clin Invest 2015 1.56
6 Susceptibility loci for murine HIV-associated nephropathy encode trans-regulators of podocyte gene expression. J Clin Invest 2009 1.49
7 The level of galactose-deficient IgA1 in the sera of patients with IgA nephropathy is associated with disease progression. Kidney Int 2012 1.31
8 Predicting progression of IgA nephropathy: new clinical progression risk score. PLoS One 2012 1.30
9 The genetics and immunobiology of IgA nephropathy. J Clin Invest 2014 1.22
10 Coiled versus straight peritoneal dialysis catheters: a randomized controlled trial and meta-analysis. Am J Kidney Dis 2011 1.02
11 The association between kidney disease and cardiovascular risk in a multiethnic cohort: findings from the Northern Manhattan Study (NOMAS). Stroke 2008 0.99
12 The molecular pathogenesis of HIV-1 associated nephropathy: recent advances. J Mol Med (Berl) 2011 0.90
13 Risk alleles in idiopathic membranous nephropathy. N Engl J Med 2011 0.84
14 IgA nephropathy--the case for a genetic basis becomes stronger. Nephrol Dial Transplant 2009 0.81
15 Identification of a potential susceptibility locus for macular telangiectasia type 2. PLoS One 2012 0.80
16 Peritoneal dialysis outflow failure from omental wrapping diagnosed by catheterography. Am J Kidney Dis 2010 0.80
17 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. Pediatr Nephrol 2013 0.78
18 Glomerular diseases: emerging tests and therapies for IgA nephropathy. Clin J Am Soc Nephrol 2013 0.78
19 The genetics of albuminuria: from haplotype association mapping in mice to genetic causation in humans. Kidney Int 2010 0.77
20 Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations. Am J Hum Genet 2017 0.75