Found 8 results
Filters: Author is Otto, Edgar A [Clear All Filters]
Erratum to: Evaluating Mendelian nephrotic syndrome genes for evidence for risk alleles or oligogenicity that explain heritability.. Pediatr Nephrol. 32(7):1285.
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2017. Genetic Drivers of Kidney Defects in the DiGeorge Syndrome.. N Engl J Med. 376(8):742-754.
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2017. .
2017. Integrative Genomics Identifies Novel Associations with APOL1 Risk Genotypes in Black NEPTUNE Subjects.. J Am Soc Nephrol. 27(3):814-23.
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2016. tarSVM: Improving the accuracy of variant calls derived from microfluidic PCR-based targeted next generation sequencing using a support vector machine.. BMC Bioinformatics. 17(1):233.
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2016. Using Population Genetics to Interrogate the Monogenic Nephrotic Syndrome Diagnosis in a Case Cohort.. J Am Soc Nephrol. 27(7):1970-83.
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2016. ADCK4 mutations promote steroid-resistant nephrotic syndrome through CoQ10 biosynthesis disruption.. J Clin Invest. 123(12):5179-89.
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2013. ARHGDIA mutations cause nephrotic syndrome via defective RHO GTPase signaling.. J Clin Invest. 123(8):3243-53.
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2013.