Found 11 results
Filters: Author is Gillies, Christopher E [Clear All Filters]
APOL1-associated glomerular disease among African-American children: a collaboration of the Chronic Kidney Disease in Children (CKiD) and Nephrotic Syndrome Study Network (NEPTUNE) cohorts.. Nephrol Dial Transplant. 32(6):983-990.
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2017. 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. Evaluating Mendelian nephrotic syndrome genes for evidence for risk alleles or oligogenicity that explain heritability.. Pediatr Nephrol. 32(3):467-476.
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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. 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. An investigation of APOL1 risk genotypes and preterm birth in African American population cohorts.. Nephrol Dial Transplant.
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2016. A reference panel of 64,976 haplotypes for genotype imputation.. Nat Genet. 48(10):1279-83.
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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. GeneVetter: a web tool for quantitative monogenic assessment of rare diseases.. Bioinformatics. 31(22):3682-4.
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