Insights into the Genetic Architecture of Diabetic Nephropathy

Association of APOL1 variants with mild kidney disease in the first-degree relatives of African American patients with non-diabetic end-stage renal disease

(2012) Barry I. Freedman et al.   KIDNEY INTERNATIONAL

DNA methylation profiling identifies epigenetic differences between diabetes patients with ESRD and diabetes patients without nephropathy

(2011) Carmen Sapienza et al.   Epigenetics

The MYH9/APOL1 region and chronic kidney disease in European-Americans

(2011) Conall M. O'Seaghdha et al.   HUMAN MOLECULAR GENETICS

APOL1 Genetic Variants in Focal Segmental Glomerulosclerosis and HIV-Associated Nephropathy

(2011) J. B. Kopp et al.   JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY

Population-Based Risk Assessment of APOL1 on Renal Disease

(2011) D. J. Friedman et al.   JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY

Meta-analysis of genome-wide linkage scans for renal function traits

(2011) Madhumathi Rao et al.   NEPHROLOGY DIALYSIS TRANSPLANTATION

Polymorphisms in MYH9 are associated with diabetic nephropathy in European Americans

(2011) J. N. Cooke et al.   NEPHROLOGY DIALYSIS TRANSPLANTATION

Differential Effects of MYH9 and APOL1 Risk Variants on FRMD3 Association with Diabetic ESRD in African Americans

(2011) Barry I. Freedman et al.   PLoS Genetics

Genetic Heterogeneity in Human Disease

(2010) Jon McClellan et al.   CELL

Missense mutations in the APOL1 gene are highly associated with end stage kidney disease risk previously attributed to the MYH9 gene

(2010) Shay Tzur et al.   HUMAN GENETICS

Genetic Variants of the Protein Kinase C-β 1 Gene and Development of End-Stage Renal Disease in Patients With Type 2 Diabetes

(2010) Ronald C. W. Ma   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

The Apolipoprotein L1 (APOL1) Gene and Nondiabetic Nephropathy in African Americans

(2010) B. I. Freedman et al.   JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY

A genome-wide association study for diabetic nephropathy genes in African Americans

(2010) Caitrin W. McDonough et al.   KIDNEY INTERNATIONAL

Beyond genetics: epigenetic code in chronic kidney disease

(2010) Rama S. Dwivedi et al.   KIDNEY INTERNATIONAL

The acetyl-coenzyme A carboxylase beta (ACACB) gene is associated with nephropathy in Chinese patients with type 2 diabetes

(2010) S. C. W. Tang et al.   NEPHROLOGY DIALYSIS TRANSPLANTATION

A Single Nucleotide Polymorphism within the Acetyl-Coenzyme A Carboxylase Beta Gene Is Associated with Proteinuria in Patients with Type 2 Diabetes

(2010) Shiro Maeda et al.   PLoS Genetics

Variants in Intron 13 of theELMO1Gene are Associated with Diabetic Nephropathy in African Americans

(2009) T. S. Leak et al.   ANNALS OF HUMAN GENETICS

The HapMap and Genome-Wide Association Studies in Diagnosis and Therapy

(2009) Teri A. Manolio et al.   Annual Review of Medicine

Confirmation of Genetic Associations at ELMO1 in the GoKinD Collection Supports Its Role as a Susceptibility Gene in Diabetic Nephropathy

(2009) M. G. Pezzolesi et al.   DIABETES

Genome-Wide Association Scan for Diabetic Nephropathy Susceptibility Genes in Type 1 Diabetes

(2009) M. G. Pezzolesi et al.   DIABETES

Genome-wide linkage analysis of serum creatinine in three isolated European populations

(2009) Cristian Pattaro et al.   KIDNEY INTERNATIONAL

In patients with type 1 diabetes and new-onset microalbuminuria the development of advanced chronic kidney disease may not require progression to proteinuria

(2009) Bruce A. Perkins et al.   KIDNEY INTERNATIONAL

Finding the missing heritability of complex diseases

(2009) Teri A. Manolio et al.   NATURE

A Flexible and Accurate Genotype Imputation Method for the Next Generation of Genome-Wide Association Studies

(2009) Bryan N. Howie et al.   PLoS Genetics

Association of Genetic Variants at 3q22 with Nephropathy in Patients with Type 1 Diabetes Mellitus

(2008) Bing He et al.   AMERICAN JOURNAL OF HUMAN GENETICS

A HapMap harvest of insights into the genetics of common disease

(2008) Teri A. Manolio et al.   JOURNAL OF CLINICAL INVESTIGATION

MYH9 is associated with nondiabetic end-stage renal disease in African Americans

(2008) W H Linda Kao et al.   NATURE GENETICS

MYH9 is a major-effect risk gene for focal segmental glomerulosclerosis

(2008) Jeffrey B Kopp et al.   NATURE GENETICS

Promoter polymorphism of the erythropoietin gene in severe diabetic eye and kidney complications

(2008) Z. Tong et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA