Sudha K Iyengar

Author PubWeight™ 112.15‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 MYH9 is associated with nondiabetic end-stage renal disease in African Americans. Nat Genet 2008 9.50
2 Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration. Proc Natl Acad Sci U S A 2010 4.30
3 Seven new loci associated with age-related macular degeneration. Nat Genet 2013 3.81
4 Apolipoprotein L1 gene variants associate with hypertension-attributed nephropathy and the rate of kidney function decline in African Americans. Kidney Int 2012 3.46
5 Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia. Nat Genet 2013 2.36
6 Meta-analysis of genome scans of age-related macular degeneration. Hum Mol Genet 2005 2.34
7 Familial clustering of chronic kidney disease. Semin Dial 2007 1.95
8 The Family Investigation of Nephropathy and Diabetes (FIND): design and methods. J Diabetes Complications 2005 1.87
9 EPHA2 is associated with age-related cortical cataract in mice and humans. PLoS Genet 2009 1.82
10 Genome-wide linkage study of retinal vessel diameters in the Beaver Dam Eye Study. Hypertension 2006 1.80
11 Examining the relative influence of familial, genetic, and environmental covariate information in flexible risk models. Proc Natl Acad Sci U S A 2009 1.68
12 Genome-wide scan for estimated glomerular filtration rate in multi-ethnic diabetic populations: the Family Investigation of Nephropathy and Diabetes (FIND). Diabetes 2007 1.61
13 Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo. PLoS Genet 2010 1.57
14 A whole-genome screen of a quantitative trait of age-related maculopathy in sibships from the Beaver Dam Eye Study. Am J Hum Genet 2003 1.53
15 Mathematical assumptions versus biological reality: myths in affected sib pair linkage analysis. Am J Hum Genet 2004 1.52
16 The epidemiology of retinal reticular drusen. Am J Ophthalmol 2007 1.50
17 A new method for grading the severity of keratoconus: the Keratoconus Severity Score (KSS). Cornea 2006 1.49
18 Genome scan of M. tuberculosis infection and disease in Ugandans. PLoS One 2008 1.41
19 Pleiotropic effects of a chromosome 3 locus on speech-sound disorder and reading. Am J Hum Genet 2004 1.36
20 Association of polymorphisms in the hepatocyte growth factor gene promoter with keratoconus. Invest Ophthalmol Vis Sci 2011 1.29
21 Heritability of the severity of diabetic retinopathy: the FIND-Eye study. Invest Ophthalmol Vis Sci 2008 1.29
22 Variants in the Wilms' tumor gene are associated with focal segmental glomerulosclerosis in the African American population. Physiol Genomics 2005 1.22
23 The genetic bases of speech sound disorders: evidence from spoken and written language. J Speech Lang Hear Res 2006 1.22
24 Candidate gene association study for diabetic retinopathy in persons with type 2 diabetes: the Candidate gene Association Resource (CARe). Invest Ophthalmol Vis Sci 2011 1.22
25 Mitochondrial DNA variants of respiratory complex I that uniquely characterize haplogroup T2 are associated with increased risk of age-related macular degeneration. PLoS One 2009 1.19
26 Genetic association and gene-gene interaction analyses in African American dialysis patients with nondiabetic nephropathy. Am J Kidney Dis 2011 1.19
27 Toll-like receptor polymorphisms and age-related macular degeneration. Invest Ophthalmol Vis Sci 2008 1.18
28 A sarcoidosis genetic linkage consortium: the sarcoidosis genetic analysis (SAGA) study. Sarcoidosis Vasc Diffuse Lung Dis 2005 1.18
29 A genome-wide association study identifies a potential novel gene locus for keratoconus, one of the commonest causes for corneal transplantation in developed countries. Hum Mol Genet 2011 1.11
30 Large scale international replication and meta-analysis study confirms association of the 15q14 locus with myopia. The CREAM consortium. Hum Genet 2012 1.09
31 Variation in the lysyl oxidase (LOX) gene is associated with keratoconus in family-based and case-control studies. Invest Ophthalmol Vis Sci 2012 1.09
32 Relationship of Fuchs endothelial corneal dystrophy severity to central corneal thickness. Arch Ophthalmol 2012 1.08
33 Genomewide linkage scan for diabetic renal failure and albuminuria: the FIND study. Am J Nephrol 2011 1.07
34 The relationship of cataract and cataract extraction to age-related macular degeneration: the Beaver Dam Eye Study. Ophthalmology 2012 1.06
35 Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error. Am J Hum Genet 2013 1.06
36 A 32 kb critical region excluding Y402H in CFH mediates risk for age-related macular degeneration. PLoS One 2011 1.05
37 Evidence for a major gene influence on tumor necrosis factor-alpha expression in tuberculosis: path and segregation analysis. Hum Hered 2005 1.05
38 Linkage and association analysis of candidate genes for TB and TNFalpha cytokine expression: evidence for association with IFNGR1, IL-10, and TNF receptor 1 genes. Hum Genet 2007 1.04
39 Complement factor H and hemicentin-1 in age-related macular degeneration and renal phenotypes. Hum Mol Genet 2007 1.03
40 The distribution of long range admixture linkage disequilibrium in an African-American population. Hum Hered 2002 1.03
41 Speech sound disorder influenced by a locus in 15q14 region. Behav Genet 2006 1.02
42 Structural equation model-based genome scan for the metabolic syndrome. BMC Genet 2003 1.02
43 Prediction of age-related macular degeneration in the general population: the Three Continent AMD Consortium. Ophthalmology 2013 1.02
44 Risk alleles in CFH and ARMS2 and the long-term natural history of age-related macular degeneration: the Beaver Dam Eye Study. JAMA Ophthalmol 2013 1.01
45 Harmonizing the classification of age-related macular degeneration in the three-continent AMD consortium. Ophthalmic Epidemiol 2014 1.01
46 CKD increases the risk of age-related macular degeneration. J Am Soc Nephrol 2008 1.01
47 A multicenter study to map genes for Fuchs endothelial corneal dystrophy: baseline characteristics and heritability. Cornea 2012 1.00
48 Genetic determinants of macular pigments in women of the Carotenoids in Age-Related Eye Disease Study. Invest Ophthalmol Vis Sci 2013 0.99
49 Age-related retinal degeneration (arrd2) in a novel mouse model due to a nonsense mutation in the Mdm1 gene. Hum Mol Genet 2008 0.99
50 Dimensions of early speech sound disorders: A factor analytic study. J Commun Disord 2006 0.95
51 A genetic contribution to intraocular pressure: the beaver dam eye study. Invest Ophthalmol Vis Sci 2005 0.95
52 Genetic evidence for role of carotenoids in age-related macular degeneration in the Carotenoids in Age-Related Eye Disease Study (CAREDS). Invest Ophthalmol Vis Sci 2014 0.95
53 Differing roles for TCF4 and COL8A2 in central corneal thickness and fuchs endothelial corneal dystrophy. PLoS One 2012 0.95
54 Effect of the Y402H variant in the complement factor H gene on the incidence and progression of age-related macular degeneration: results from multistate models applied to the Beaver Dam Eye Study. Arch Ophthalmol 2012 0.93
55 Vitamin D intake and season modify the effects of the GC and CYP2R1 genes on 25-hydroxyvitamin D concentrations. J Nutr 2012 0.93
56 Examination of association with candidate genes for diabetic nephropathy in a Mexican American population. Clin J Am Soc Nephrol 2010 0.91
57 Speech and language skills of parents of children with speech sound disorders. Am J Speech Lang Pathol 2007 0.91
58 School-age follow-up of children with childhood apraxia of speech. Lang Speech Hear Serv Sch 2004 0.90
59 An association between the calpastatin (CAST) gene and keratoconus. Cornea 2013 0.89
60 Genome-wide analyses demonstrate novel loci that predispose to drusen formation. Invest Ophthalmol Vis Sci 2005 0.88
61 Genetics of pigment changes and geographic atrophy. Invest Ophthalmol Vis Sci 2007 0.87
62 Literacy outcomes of children with early childhood speech sound disorders: impact of endophenotypes. J Speech Lang Hear Res 2011 0.87
63 An autosome-wide search using longitudinal data for loci linked to type 2 diabetes progression. BMC Genet 2003 0.87
64 Genetic association of COL5A1 variants in keratoconus patients suggests a complex connection between corneal thinning and keratoconus. Invest Ophthalmol Vis Sci 2013 0.86
65 Inhibition of EGF signaling protects the diabetic retina from insulin-induced vascular leakage. Am J Pathol 2013 0.86
66 Genome-wide linkage scans for type 2 diabetes mellitus in four ethnically diverse populations-significant evidence for linkage on chromosome 4q in African Americans: the Family Investigation of Nephropathy and Diabetes Research Group. Diabetes Metab Res Rev 2009 0.86
67 Adolescent outcomes of children with early speech sound disorders with and without language impairment. Am J Speech Lang Pathol 2015 0.85
68 Relationship Between Fuchs Endothelial Corneal Dystrophy Severity and Glaucoma and/or Ocular Hypertension. Arch Ophthalmol 2012 0.83
69 The fibromyalgia family study: a genome-wide linkage scan study. Arthritis Rheum 2013 0.83
70 Reduction of sample heterogeneity through use of population substructure: an example from a population of African American families with sarcoidosis. Am J Hum Genet 2006 0.83
71 Association of smoking and other risk factors with Fuchs' endothelial corneal dystrophy severity and corneal thickness. Invest Ophthalmol Vis Sci 2013 0.81
72 The relationship of atherosclerosis to the 10-year cumulative incidence of age-related macular degeneration: the Beaver Dam studies. Ophthalmology 2013 0.81
73 Meta-analysis of genome-wide linkage scans for renal function traits. Nephrol Dial Transplant 2011 0.81
74 Heritability estimation for speech-sound traits with developmental trajectories. Behav Genet 2010 0.79
75 Subtyping Children With Speech Sound Disorders by Endophenotypes. Top Lang Disord 2011 0.79
76 Misclassification can explain most apparent regression of age-related macular degeneration: results from multistate models with misclassification. Invest Ophthalmol Vis Sci 2014 0.79
77 Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error. Nat Commun 2016 0.78
78 Diabetic nephropathy in a sibling and albuminuria predict early GFR decline: a prospective cohort study. BMC Nephrol 2013 0.78
79 Kidney disease, genotype and the pathogenesis of vasculopathy. Curr Opin Nephrol Hypertens 2003 0.77
80 Serial analysis of gene expression. Methods Mol Med 2003 0.77
81 Generation of kidney transcriptomes using serial analysis of gene expression. Exp Nephrol 2002 0.77
82 Identification of nephropathy candidate genes by comparing sclerosis-prone and sclerosis-resistant mouse strain kidney transcriptomes. BMC Nephrol 2012 0.76
83 Association between AVPR1A, DRD2, and ASPM and endophenotypes of communication disorders. Psychiatr Genet 2014 0.76
84 Prospects of admixture linkage disequilibrium mapping in the African-American genome. Cytometry 2002 0.75
85 Optimizing the evidence for linkage by permuting marker order. BMC Genet 2005 0.75
86 Comparison of sarcoidosis phenotypes among affected African-American siblings. Chest 2006 0.75
87 Studying genetic determinants of natural variation in human gene expression using Bayesian ANOVA. BMC Proc 2007 0.75
88 Effect of genotyping error in model-free linkage analysis using microsatellite or single-nucleotide polymorphism marker maps. BMC Genet 2005 0.75
89 Does losartan prevent progression of early diabetic nephropathy in American Indians with type 2 diabetes? Diabetes 2013 0.75