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10.1016/j.semnephrol.2015.04.002 http://scihub22266oqcxt.onion/10.1016/j.semnephrol.2015.04.002 C4745990!4745990!26215859     free     free     free Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Semin+Nephrol 2015 ; 35 (3): 212-21 Nephropedia Template TP {{tp|p=26215859|t=2015. Opportunities and challenges of genotyping of patients with nephrotic syndrome in the genomic era |pdf=|usr=}}{{26215859}} gab.com Text Opportunities and challenges of genotyping of patients with nephrotic syndrome in the genomic era JO: Semin Nephrol http://www.kidney.de/pget.php?&tw=1&pmid=26215859 #FOAvip Both targeted and genome-wide linkage and association studies have identified a number of genes and genetic variants associated with nephrotic syndrome (NS). Genotype-phenotype studies of subjects with these variants have identified correlations of clear clinical significance. This, combined with improved genomic technologies, has resulted in increasing, and justifiable, enthusiasm for incorporating our patients? genomic information into our clinical management decisions. Here, we will summarize our understanding of NS associated genetic factors, namely rare causal mutations or common risk alleles in apolipoprotein L1. We then discuss the complexities inherent in trying to ascribe risk or causality to these variants, particularly as we seek to extend genetic testing to a broader group of patients, including many with sporadic disease. Overall, the thoughtful application and interpretation of these genetic tests will maximize the benefits to our patients with NS in the form of more precise clinical care. Twit Text FOAVip Opportunities and challenges of genotyping of patients with nephrotic syndrome in the genomic era ????Semin Nephrol http://www.kidney.de/pget.php?&tw=1&pmid=26215859 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=26215859 #FOAvip English Wikipedia <ref>{{Cite pmid|26215859}}</ref> Opportunities and challenges of genotyping of patients with nephrotic syndrome in the genomic era #MMPMID26215859 Sampson MG; Pollak MR Semin Nephrol 2015[May]; 35 (3): 212-21 PMID26215859show ga Both targeted and genome-wide linkage and association studies have identified a number of genes and genetic variants associated with nephrotic syndrome (NS). Genotype-phenotype studies of subjects with these variants have identified correlations of clear clinical significance. This, combined with improved genomic technologies, has resulted in increasing, and justifiable, enthusiasm for incorporating our patients? genomic information into our clinical management decisions. Here, we will summarize our understanding of NS associated genetic factors, namely rare causal mutations or common risk alleles in apolipoprotein L1. We then discuss the complexities inherent in trying to ascribe risk or causality to these variants, particularly as we seek to extend genetic testing to a broader group of patients, including many with sporadic disease. Overall, the thoughtful application and interpretation of these genetic tests will maximize the benefits to our patients with NS in the form of more precise clinical care. äOpportunities and challenges of genotyping of patients with nephrotic (epmc).pdf DeepDyve Pubget Overpricing