Found 19 results
Filters: Author is Sampson, Matthew G  [Clear All Filters]
2017
Ng DK, Robertson CC, Woroniecki RP, Limou S, Gillies CE, Reidy KJ, Winkler CA, Hingorani S, Gibson KL, Hjorten R et al..  2017.  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.
Crawford BD, Gillies CE, Robertson CC, Kretzler M, Otto EA, Vega-Warner V, Sampson MG.  2017.  Erratum to: Evaluating Mendelian nephrotic syndrome genes for evidence for risk alleles or oligogenicity that explain heritability.. Pediatr Nephrol. 32(7):1285.
Crawford BD, Gillies CE, Robertson CC, Kretzler M, Otto E, Vega-Wagner V, Sampson MG.  2017.  Evaluating Mendelian nephrotic syndrome genes for evidence for risk alleles or oligogenicity that explain heritability.. Pediatr Nephrol. 32(3):467-476.
Lopez-Rivera E, Liu YP, Verbitsky M, Anderson BR, Capone VP, Otto EA, Yan Z, Mitrotti A, Martino J, Steers NJ et al..  2017.  Genetic Drivers of Kidney Defects in the DiGeorge Syndrome.. N Engl J Med. 376(8):742-754.
Skorecki KL, Lee JH, Langefeld CD, Rosset S, Tzur S, Wasser WG, Shemer R, Hawkins GA, Divers J, Parekh RS et al..  2017.  A null variant in the apolipoprotein L3 gene is associated with non-diabetic nephropathy.. Nephrol Dial Transplant.
2016
Gipson DS, Troost JP, Lafayette RA, Hladunewich MA, Trachtman H, Gadegbeku CA, Sedor JR, Holzman LB, Moxey-Mims MM, Perumal K et al..  2016.  Complete Remission in the Nephrotic Syndrome Study Network.. Clin J Am Soc Nephrol. 11(1):81-9.
Sampson MG, Robertson CC, Martini S, Mariani LH, Lemley KV, Gillies CE, Otto EA, Kopp JB, Randolph A, Vega-Warner V et al..  2016.  Integrative Genomics Identifies Novel Associations with APOL1 Risk Genotypes in Black NEPTUNE Subjects.. J Am Soc Nephrol. 27(3):814-23.
Robertson CC, Gillies CE, Putler RKB, Ng D, Reidy KJ, Crawford B, Sampson MG.  2016.  An investigation of APOL1 risk genotypes and preterm birth in African American population cohorts.. Nephrol Dial Transplant.
McCarthy S, Das S, Kretzschmar W, Delaneau O, Wood AR, Teumer A, Kang HMin, Fuchsberger C, Danecek P, Sharp K et al..  2016.  A reference panel of 64,976 haplotypes for genotype imputation.. Nat Genet. 48(10):1279-83.
Yu H, Artomov M, Brähler S, M Stander C, Shamsan G, Sampson MG, J White M, Kretzler M, Miner JH, Jain S et al..  2016.  A role for genetic susceptibility in sporadic focal segmental glomerulosclerosis.. J Clin Invest. 126(4):1603.
Yu H, Artomov M, Brähler S, M Stander C, Shamsan G, Sampson MG, J White M, Kretzler M, Miner JH, Jain S et al..  2016.  A role for genetic susceptibility in sporadic focal segmental glomerulosclerosis.. J Clin Invest. 126(3):1067-78.
Gillies CE, Otto EA, Vega-Warner V, Robertson CC, Sanna-Cherchi S, Gharavi A, Crawford B, Bhimma R, Winkler C, Kang HMin et al..  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.
Sampson MG, Gillies CE, Robertson CC, Crawford B, Vega-Warner V, Otto EA, Kretzler M, Kang HMin.  2016.  Using Population Genetics to Interrogate the Monogenic Nephrotic Syndrome Diagnosis in a Case Cohort.. J Am Soc Nephrol. 27(7):1970-83.
2015
Sampson MG, Hodgin JB, Kretzler M.  2015.  Defining nephrotic syndrome from an integrative genomics perspective.. Pediatr Nephrol. 30(1):51-63;quiz59.
Gillies CE, Robertson CC, Sampson MG, Kang HMin.  2015.  GeneVetter: a web tool for quantitative monogenic assessment of rare diseases.. Bioinformatics. 31(22):3682-4.
Ju W, Nair V, Smith S, Zhu L, Shedden K, Song PXK, Mariani LH, Eichinger FH, Berthier CC, Randolph A et al..  2015.  Tissue transcriptome-driven identification of epidermal growth factor as a chronic kidney disease biomarker.. Sci Transl Med. 7(316):316ra193.
2013
Gadegbeku CA, Gipson DS, Holzman LB, Ojo AO, Song PXK, Barisoni L, Sampson MG, Kopp JB, Lemley KV, Nelson PJ et al..  2013.  Design of the Nephrotic Syndrome Study Network (NEPTUNE) to evaluate primary glomerular nephropathy by a multidisciplinary approach.. Kidney Int. 83(4):749-56.
Sampson MG, Gillies CE, Ju W, Kretzler M, Kang HMin.  2013.  Gene-level integrated metric of negative selection (GIMS) prioritizes candidate genes for nephrotic syndrome.. PLoS One. 8(11):e81062.
Sampson MG, Jüppner H.  2013.  Genes, Exomes, Genomes, Copy Number: What is Their Future in Pediatric Renal Disease.. Curr Pediatr Rep. 1(1):52-59.