Donna M Michel
Overview
Explore the profile of Donna M Michel including associated specialties, affiliations and a list of published articles.
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5
Citations
907
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Recent Articles
1.
Kopp J, Nelson G, Sampath K, Johnson R, Genovese G, An P, et al.
J Am Soc Nephrol
. 2011 Oct;
22(11):2129-37.
PMID: 21997394
Trypanolytic variants in APOL1, which encodes apolipoprotein L1, associate with kidney disease in African Americans, but whether APOL1-associated glomerular disease has a distinct clinical phenotype is unknown. Here we determined...
2.
Kopp J, Smith M, Nelson G, Johnson R, Freedman B, Bowden D, et al.
Nat Genet
. 2008 Sep;
40(10):1175-84.
PMID: 18794856
The increased burden of chronic kidney and end-stage kidney diseases (ESKD) in populations of African ancestry has been largely unexplained. To identify genetic variants predisposing to idiopathic and HIV-1-associated focal...
3.
McKenzie L, Hendrickson S, Briggs W, Dart R, Korbet S, Mokrzycki M, et al.
J Am Soc Nephrol
. 2007 Oct;
18(11):2987-95.
PMID: 17942957
Mutations in NPHS2, the gene that encodes podocin, are well-established causes of both familial and sporadic steroid-resistant focal segmental glomerulosclerosis (FSGS) in the pediatric population, but have not been well-characterized...
4.
Michel D, Moss A
Adv Chronic Kidney Dis
. 2005 Apr;
12(2):196-201.
PMID: 15822055
Recent guidelines recommend shared decision making between patients and nephrologists as the model for dialysis decision making. A key component of this shared decision making is obtaining informed consent. As...
5.
Orloff M, Iyengar S, Winkler C, Goddard K, Dart R, Ahuja T, et al.
Physiol Genomics
. 2005 Feb;
21(2):212-21.
PMID: 15687485
Wilms' tumor gene (WT1) is important for nephrogenesis and gonadal growth. WT1 mutations cause Denys-Drash and Frasier syndromes, which are characterized by glomerular scarring. To test whether genetic variations in...