A meta-analysis of genome-wide data from five European isolates reveals an association of COL22A1, SYT1, and GABRR2with serum creatinine level

Genome-wide Association Study of Anthropometric Traits in Korčula Island, Croatia

(2009) Ozren Polašek et al.   CROATIAN MEDICAL JOURNAL

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

(2009) Cristian Pattaro et al.   KIDNEY INTERNATIONAL

Polymorphisms in the non-muscle myosin heavy chain 9 gene (MYH9) are strongly associated with end-stage renal disease historically attributed to hypertension in African Americans

(2009) Barry I. Freedman et al.   KIDNEY INTERNATIONAL

Multiple loci associated with indices of renal function and chronic kidney disease

(2009) Anna Köttgen et al.   NATURE GENETICS

Failure to Replicate a Genetic Association May Provide Important Clues About Genetic Architecture

(2009) Casey S. Greene et al.   PLoS One

Runs of Homozygosity in European Populations

(2008) Ruth McQuillan et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Genome-wide association study for renal traits in the Framingham Heart and Atherosclerosis Risk in Communities Studies

(2008) Anna Kottgen et al.   BMC Medical Genetics

A comprehensive evaluation of SNP genotype imputation

(2008) Michael Nothnagel et al.   HUMAN GENETICS

Linkage analysis of glomerular filtration rate in American Indians

(2008) Amy K. Mottl et al.   KIDNEY INTERNATIONAL

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

A genome-wide search for linkage to chronic kidney disease in a community-based sample: the SAFHS

(2008) N. H. Arar et al.   NEPHROLOGY DIALYSIS TRANSPLANTATION

Estimates of Genetic and Environmental Contribution to 43 Quantitative Traits Support Sharing of a Homogeneous Environment in an Isolated Population from South Tyrol, Italy

(2007) Fabio Marroni et al.   HUMAN HEREDITY