Lista de obras - Sudha Iyengar - Dominio Público Uruguay

A 32 kb critical region excluding Y402H in CFH mediates risk for age-related macular degeneration

artículo científico publicado en 2011

A Genetic Contribution to Intraocular Pressure: The Beaver Dam Eye Study

artículo científico publicado en 2005

A New Method for Grading the Severity of Keratoconus

artículo científico publicado en 2006

A family-based strategy to identify genes for diabetic nephropathy.

artículo científico publicado en 2001

A genome-wide association study identifies a potential novel gene locus for keratoconus, one of the commonest causes for corneal transplantation in developed countries

artículo científico publicado en 2011

A genome-wide search for linkage of estimated glomerular filtration rate (eGFR) in the Family Investigation of Nephropathy and Diabetes (FIND).

artículo científico publicado en 2013

A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants

artículo científico publicado en 2015

A multicenter study to map genes for Fuchs endothelial corneal dystrophy: baseline characteristics and heritability

artículo científico publicado en 2012

A sarcoidosis genetic linkage consortium: the sarcoidosis genetic analysis (SAGA) study.

artículo científico publicado en 2005

A whole-genome screen of a quantitative trait of age-related maculopathy in sibships from the Beaver Dam Eye Study

artículo científico publicado en 2003

Adolescent outcomes of children with early speech sound disorders with and without language impairment

artículo científico publicado en 2015

Aldose Reductase Polymorphisms, Fasting Blood Glucose, and Age-Related Cortical Cataract

artículo científico publicado en 2018

An association between the calpastatin (CAST) gene and keratoconus

artículo científico publicado en 2013

An autosome-wide search using longitudinal data for loci linked to type 2 diabetes progression

artículo científico publicado en 2003

Analyses of cross species polymerase chain reaction products to infer the ancestral state of human polymorphisms.

artículo científico publicado en 1998

Apolipoprotein A-IV genetic polymorphism and its impact on quantitative traits in normoglycemic and non-insulin-dependent diabetic Hispanics from the San Luis Valley, Colorado

artículo científico publicado el 1 de agosto de 1992

Apolipoprotein A-IV polymorphism, and its role in determining variation in lipoprotein-lipid, glucose and insulin levels in normal and non-insulin-dependent diabetic individuals ⬇️

artículo científico publicado el 1 de noviembre de 1991

Apolipoprotein L1 gene variants associate with hypertension-attributed nephropathy and the rate of kidney function decline in African Americans

artículo científico publicado en 2013

Approaches to understanding susceptibility to nephropathy: from genetics to genomics

artículo científico publicado en 2002

Association between AVPR1A, DRD2, and ASPM and endophenotypes of communication disorders

artículo científico publicado en 2014

Association between vitamin D status and age-related macular degeneration by genetic risk

artículo científico publicado en 2015

Association of polymorphisms in the hepatocyte growth factor gene promoter with keratoconus

artículo científico publicado en 2011

Association of smoking and other risk factors with Fuchs' endothelial corneal dystrophy severity and corneal thickness

artículo científico publicado en 2013

Associations Between Methylenetetrahydrofolate Reductase Polymorphisms, Serum Homocysteine Levels, and Incident Cortical Cataract.

artículo científico publicado en 2016

CKD increases the risk of age-related macular degeneration

artículo científico publicado en 2008

Candidate gene association study for diabetic retinopathy in persons with type 2 diabetes: the Candidate gene Association Resource (CARe).

artículo científico publicado en 2011

Cigarette smoking and the natural history of age-related macular degeneration: the Beaver Dam Eye Study

artículo científico publicado en 2014

Combined effects of complement factor H genotypes, fish consumption, and inflammatory markers on long-term risk for age-related macular degeneration in a cohort

artículo científico publicado en 2008

Comparison of Sarcoidosis Phenotypes Among Affected African-American Siblings

article

Complement factor H and hemicentin-1 in age-related macular degeneration and renal phenotypes

scientific article published on 25 June 2007

Correction: A 32 kb Critical Region Excluding Y402H in CFH Mediates Risk for Age-Related Macular Degeneration

scientific article published in PLoS ONE

Detection of major genes underlying several quantitative traits associated with a common disease using different ascertainment schemes

artículo científico publicado en 1997

Diabetic nephropathy in a sibling and albuminuria predict early GFR decline: a prospective cohort study

artículo científico publicado en 2013

Differing roles for TCF4 and COL8A2 in central corneal thickness and fuchs endothelial corneal dystrophy

artículo científico publicado en 2012

Dimensions of early speech sound disorders: A factor analytic study

artículo científico

Disease severity and family history in keratoconus.

artículo científico publicado en 2008

Dissection of genomewide-scan data in extended families reveals a major locus and oligogenic susceptibility for age-related macular degeneration

artículo científico publicado en 2003

Diversity of Ocular Surface Bacterial Microbiome Adherent to Worn Contact Lenses and Bacterial Communities Associated With Care Solution Use

scientific article published on 01 September 2019

Does losartan prevent progression of early diabetic nephropathy in American Indians with type 2 diabetes?

artículo científico publicado en 2013

EPHA2 is associated with age-related cortical cataract in mice and humans

artículo científico publicado en 2009

Early presentation of metastatic medullary carcinoma in multiple endocrine neoplasia, type IIA: Implications for therapy

scientific article published on 01 September 1996

Effect of genotyping error in model-free linkage analysis using microsatellite or single-nucleotide polymorphism marker maps

artículo científico publicado en 2005

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

artículo científico publicado en 2012

Electrocardiographic Prediction of Abnormal Genotype in Congenital Long QT Syndrome: Experience in 101 Related Family Members

article

Evidence for a major gene influence on tumor necrosis factor-alpha expression in tuberculosis: path and segregation analysis

artículo científico publicado en 2005

Examination of association with candidate genes for diabetic nephropathy in a Mexican American population

artículo científico publicado en 2010

Examining the relative influence of familial, genetic, and environmental covariate information in flexible risk models

artículo científico publicado en 2009

Exome Array Analysis of Nuclear Lens Opacity

artículo científico publicado en 2017

Exome array analysis identifies CAV1/CAV2 as a susceptibility locus for intraocular pressure

artículo científico publicado en 2014

Familial clustering of chronic kidney disease

artículo científico publicado en 2007

Family pedigrees of children with suspected childhood apraxia of speech.

artículo científico publicado en 2004

Five-year progression of unilateral age-related macular degeneration to bilateral involvement: the Three Continent AMD Consortium report.

artículo científico publicado en 2017

Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo

artículo científico publicado en 2010

Fuchs’ endothelial corneal dystrophy: fostering change in clinical care using observational data

Further evidence of pleiotropy influencing speech and language: analysis of the DYX8 region.

artículo científico publicado en 2007

Generation of Kidney Transcriptomes Using Serial Analysis of Gene Expression

article

Genetic association and gene-gene interaction analyses in African American dialysis patients with nondiabetic nephropathy

artículo científico publicado en 2011

Genetic association of COL5A1 variants in keratoconus patients suggests a complex connection between corneal thinning and keratoconus

artículo científico publicado en 2013

Genetic characterization and fine mapping of susceptibility loci for sarcoidosis in African Americans on chromosome 5.

artículo científico publicado en 2006

Genetic determinants of macular pigments in women of the Carotenoids in Age-Related Eye Disease Study

artículo científico publicado en 2013

Genetic evidence for role of carotenoids in age-related macular degeneration in the Carotenoids in Age-Related Eye Disease Study (CAREDS).

scientific article published on 29 January 2014

Genetic linkage analysis of sarcoidosis phenotypes: the sarcoidosis genetic analysis (SAGA) study

article

Genetic studies of Type 2 (non-insulin-dependent) diabetes mellitus: lack of association with seven genetic markers

artículo científico publicado en 1989

Genetic susceptibility to end-stage renal disease.

artículo científico publicado en 1999

Genetic susceptibility, dietary antioxidants, and long-term incidence of age-related macular degeneration in two populations

artículo científico publicado en 2013

Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration

artículo científico publicado en 2010

Genetics of Pigment Changes and Geographic Atrophy

article

Genetics of age-related macular degeneration (AMD).

artículo científico publicado en 2017

Genetics of age-related macular degeneration (AMD).

artículo científico publicado en 2017

Genome scan of M. tuberculosis infection and disease in Ugandans

artículo científico publicado en 2008

Genome-Wide Association and Trans-ethnic Meta-Analysis for Advanced Diabetic Kidney Disease: Family Investigation of Nephropathy and Diabetes (FIND)

artículo científico publicado en 2015

Genome-wide association identifies SKIV2L and MYRIP as protective factors for age-related macular degeneration ⬇️

artículo científico publicado el 23 de septiembre de 2010

Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error

artículo científico publicado en 2018

Genome-wide association study identifies three novel loci in Fuchs endothelial corneal dystrophy.

artículo científico publicado en 2017

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

artículo científico publicado en 2009

Genome-wide linkage study of retinal vessel diameters in the Beaver Dam Eye Study

artículo científico publicado en 2006

Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia

artículo científico publicado en 2013

Genome-wide scan for estimated glomerular filtration rate in multi-ethnic diabetic populations: the Family Investigation of Nephropathy and Diabetes (FIND).

artículo científico publicado en 2007

Genome-wide scans for diabetic nephropathy and albuminuria in multiethnic populations: the family investigation of nephropathy and diabetes (FIND).

artículo científico publicado en 2007

Genomewide linkage scan for diabetic renal failure and albuminuria: the FIND study

artículo científico publicado en 2011

Harmonizing the classification of age-related macular degeneration in the three-continent AMD consortium

artículo científico publicado en 2014

Heritability and longitudinal outcomes of spelling skills in individuals with histories of early speech and language disorders

Heritability estimation for speech-sound traits with developmental trajectories

artículo científico publicado en 2010

Heritability of the severity of diabetic retinopathy: the FIND-Eye study

artículo científico publicado en 2008

Homozygosity by descent for a rare mutation in the myophosphorylase gene is associated with variable phenotypes in a Druze family with McArdle disease

artículo científico publicado en 1997

Identification of a major locus for age-related cortical cataract on chromosome 6p12-q12 in the Beaver Dam Eye Study

scholarly article

Identification of nephropathy candidate genes by comparing sclerosis-prone and sclerosis-resistant mouse strain kidney transcriptomes

artículo científico publicado en 2012

Inaccuracy of clinical phenotyping parameters for hypertensive nephrosclerosis

artículo científico publicado en 2000

Inhibition of EGF signaling protects the diabetic retina from insulin-induced vascular leakage

artículo científico publicado en 2013

Joint Associations of Diet, Lifestyle, and Genes with Age-Related Macular Degeneration

artículo científico publicado en 2015

Joint Contribution of Genetic Susceptibility and Modifiable Factors to the Progression of Age-Related Macular Degeneration over 10 Years

scientific article published on 30 December 2017

Large scale international replication and meta-analysis study confirms association of the 15q14 locus with myopia. The CREAM consortium

artículo científico publicado en 2012

Linkage analysis of candidate loci for end-stage renal disease due to diabetic nephropathy

artículo científico publicado en 2003

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

artículo científico publicado en 2007

Lipids, lipid genes, and incident age-related macular degeneration: the three continent age-related macular degeneration consortium

artículo científico publicado en 2014

Literacy outcomes of children with early childhood speech sound disorders: impact of endophenotypes

artículo científico publicado en 2011

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

artículo científico publicado en 2008

Markers of inflammation, oxidative stress, and endothelial dysfunction and the 20-year cumulative incidence of early age-related macular degeneration: the Beaver Dam Eye Study

artículo científico publicado en 2014

Mathematical assumptions versus biological reality: myths in affected sib pair linkage analysis

artículo científico publicado en 2004

Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error

artículo científico publicado en 2016

Meta-analysis of genome scans of age-related macular degeneration

artículo científico publicado en 2005

Meta-analysis of genome-wide association studies in African Americans provides insights into the genetic architecture of type 2 diabetes

artículo científico publicado en 2014

Meta-analysis of genome-wide association studies in multiethnic Asians identifies two loci for age-related nuclear cataract

article

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

artículo científico publicado en 2011

Mining the genome for susceptibility to diabetic nephropathy: the role of large-scale studies and consortia

artículo científico publicado en 2007

Misclassification can explain most apparent regression of age-related macular degeneration: results from multistate models with misclassification

artículo científico publicado en 2014

Mitochondrial DNA variants of respiratory complex I that uniquely characterize haplogroup T2 are associated with increased risk of age-related macular degeneration

artículo científico publicado en 2009

Mitochondrial polymorphism A10398G and Haplogroup I are associated with Fuchs' endothelial corneal dystrophy

artículo científico publicado en 2014

Multiethnic Genome-Wide Association Study of Diabetic Retinopathy Using Liability Threshold Modeling of Duration of Diabetes and Glycemic Control

scientific article published on 28 November 2018

Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error

artículo científico publicado en 2013

Novel characteristics of a misprocessed mutant HERG channel linked to hereditary long QT syndrome.

artículo científico publicado en 2000

Optimizing the evidence for linkage by permuting marker order

artículo científico publicado en 2005

Pleiotropic effects of a chromosome 3 locus on speech-sound disorder and reading

artículo científico publicado en 2004

Pooling data and linkage analysis in the chromosome 5q candidate region for asthma.

artículo científico publicado en 2001

Prediction of age-related macular degeneration in the general population: the Three Continent AMD Consortium

artículo científico publicado en 2013

Prospects of admixture linkage disequilibrium mapping in the African-American genome

artículo científico publicado en 2002

Psychosocial co-morbidities in adolescents and adults with histories of communication disorders

artículo científico publicado en 2016

Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degeneration

artículo científico publicado en 2014

Reduction of sample heterogeneity through use of population substructure: an example from a population of African American families with sarcoidosis

artículo científico publicado en 2006

Relationship Between Fuchs Endothelial Corneal Dystrophy Severity and Glaucoma and/or Ocular Hypertension

artículo científico publicado en 2012

Risk alleles in CFH and ARMS2 and the long-term natural history of age-related macular degeneration: the Beaver Dam Eye Study

artículo científico publicado en 2013

School-Age Follow-Up of Children With Childhood Apraxia of Speech

artículo científico publicado en 2004

Selecting SNPs informative for African, American Indian and European Ancestry: application to the Family Investigation of Nephropathy and Diabetes (FIND).

artículo científico publicado en 2016

Serial Analysis of Gene Expression

article

Seven new loci associated with age-related macular degeneration

artículo científico publicado en 2013

Severe vascular calcification and tumoral calcinosis in a family with hyperphosphatemia: a fibroblast growth factor 23 mutation identified by exome sequencing

artículo científico publicado en 2014

Severity of age-related macular degeneration in 1 eye and the incidence and progression of age-related macular degeneration in the fellow eye: the Beaver Dam Eye Study

artículo científico publicado en 2015

Small Drusen and Age-Related Macular Degeneration: The Beaver Dam Eye Study

artículo científico publicado en 2015

Speech and language skills of parents of children with speech sound disorders.

artículo científico publicado en 2007

Speech sound disorder influenced by a locus in 15q14 region

artículo científico publicado en 2006

Structural equation model-based genome scan for the metabolic syndrome

artículo científico publicado en 2003

Studying genetic determinants of natural variation in human gene expression using Bayesian ANOVA.

artículo científico publicado en 2007

Subtyping Children With Speech Sound Disorders by Endophenotypes

artículo científico publicado en 2011

Sunlight exposure, pigmentation, and incident age-related macular degeneration

artículo científico publicado en 2014

The DYX2 locus and neurochemical signaling genes contribute to speech sound disorder and related neurocognitive domains

artículo científico publicado en 2015

The Distribution of Long Range Admixture Linkage Disequilibrium in an African-American Population

artículo científico publicado en 2002

The Family Investigation of Nephropathy and Diabetes (FIND): design and methods

artículo científico publicado en 2005

The application of the HapMap to diabetic nephropathy and other causes of chronic renal failure

artículo científico publicado en 2007

The aromatase gene CYP19A1: several genetic and functional lines of evidence supporting a role in reading, speech and language

artículo científico publicado en 2012

The epidemiology of retinal reticular drusen

artículo científico publicado en 2007

The fa leptin receptor mutation and the heritability of respiratory frequency in a Brown Norway and Zucker intercross

artículo científico publicado en 2004

The fibromyalgia family study: a genome-wide linkage scan study

artículo científico publicado en 2013

The genetic bases of speech sound disorders: evidence from spoken and written language

artículo científico publicado en 2006

The genetic basis of complex traits: rare variants or "common gene, common disease"?

artículo científico publicado en 2007

The quest for genes causing complex traits in ocular medicine: successes, interpretations, and challenges

artículo científico publicado en 2007

The relationship of atherosclerosis to the 10-year cumulative incidence of age-related macular degeneration: the Beaver Dam studies

artículo científico publicado en 2013

The relationship of cataract and cataract extraction to age-related macular degeneration: the Beaver Dam Eye Study

artículo científico publicado en 2012

Variants in the Wilms' tumor gene are associated with focal segmental glomerulosclerosis in the African American population

artículo científico publicado en 2005

Variation in PTCHD2, CRISP3, NAP1L4, FSCB, and AP3B2 associated with spherical equivalent

artículo científico publicado en 2016

Variation in the lysyl oxidase (LOX) gene is associated with keratoconus in family-based and case-control studies

artículo científico publicado en 2012

Vitamin D intake and season modify the effects of the GC and CYP2R1 genes on 25-hydroxyvitamin D concentrations

artículo científico publicado en 2012

Lista de obras de Sudha Iyengar

A 32 kb critical region excluding Y402H in CFH mediates risk for age-related macular degeneration

A Genetic Contribution to Intraocular Pressure: The Beaver Dam Eye Study

A New Method for Grading the Severity of Keratoconus

A family-based strategy to identify genes for diabetic nephropathy.

A genome-wide association study identifies a potential novel gene locus for keratoconus, one of the commonest causes for corneal transplantation in developed countries

A genome-wide search for linkage of estimated glomerular filtration rate (eGFR) in the Family Investigation of Nephropathy and Diabetes (FIND).

A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants

A multicenter study to map genes for Fuchs endothelial corneal dystrophy: baseline characteristics and heritability

A sarcoidosis genetic linkage consortium: the sarcoidosis genetic analysis (SAGA) study.

A whole-genome screen of a quantitative trait of age-related maculopathy in sibships from the Beaver Dam Eye Study

Adolescent outcomes of children with early speech sound disorders with and without language impairment

Aldose Reductase Polymorphisms, Fasting Blood Glucose, and Age-Related Cortical Cataract

An association between the calpastatin (CAST) gene and keratoconus

An autosome-wide search using longitudinal data for loci linked to type 2 diabetes progression

Analyses of cross species polymerase chain reaction products to infer the ancestral state of human polymorphisms.

Apolipoprotein A-IV genetic polymorphism and its impact on quantitative traits in normoglycemic and non-insulin-dependent diabetic Hispanics from the San Luis Valley, Colorado

Apolipoprotein A-IV polymorphism, and its role in determining variation in lipoprotein-lipid, glucose and insulin levels in normal and non-insulin-dependent diabetic individuals ⬇️

Apolipoprotein L1 gene variants associate with hypertension-attributed nephropathy and the rate of kidney function decline in African Americans

Approaches to understanding susceptibility to nephropathy: from genetics to genomics

Association between AVPR1A, DRD2, and ASPM and endophenotypes of communication disorders

Association between vitamin D status and age-related macular degeneration by genetic risk

Association of polymorphisms in the hepatocyte growth factor gene promoter with keratoconus

Association of smoking and other risk factors with Fuchs' endothelial corneal dystrophy severity and corneal thickness

Associations Between Methylenetetrahydrofolate Reductase Polymorphisms, Serum Homocysteine Levels, and Incident Cortical Cataract.

CKD increases the risk of age-related macular degeneration

Candidate gene association study for diabetic retinopathy in persons with type 2 diabetes: the Candidate gene Association Resource (CARe).

Cigarette smoking and the natural history of age-related macular degeneration: the Beaver Dam Eye Study

Combined effects of complement factor H genotypes, fish consumption, and inflammatory markers on long-term risk for age-related macular degeneration in a cohort

Comparison of Sarcoidosis Phenotypes Among Affected African-American Siblings

Complement factor H and hemicentin-1 in age-related macular degeneration and renal phenotypes

Correction: A 32 kb Critical Region Excluding Y402H in CFH Mediates Risk for Age-Related Macular Degeneration

Detection of major genes underlying several quantitative traits associated with a common disease using different ascertainment schemes

Diabetic nephropathy in a sibling and albuminuria predict early GFR decline: a prospective cohort study

Differing roles for TCF4 and COL8A2 in central corneal thickness and fuchs endothelial corneal dystrophy

Dimensions of early speech sound disorders: A factor analytic study

Disease severity and family history in keratoconus.

Dissection of genomewide-scan data in extended families reveals a major locus and oligogenic susceptibility for age-related macular degeneration

Diversity of Ocular Surface Bacterial Microbiome Adherent to Worn Contact Lenses and Bacterial Communities Associated With Care Solution Use

Does losartan prevent progression of early diabetic nephropathy in American Indians with type 2 diabetes?

EPHA2 is associated with age-related cortical cataract in mice and humans

Early presentation of metastatic medullary carcinoma in multiple endocrine neoplasia, type IIA: Implications for therapy

Effect of genotyping error in model-free linkage analysis using microsatellite or single-nucleotide polymorphism marker maps

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

Electrocardiographic Prediction of Abnormal Genotype in Congenital Long QT Syndrome: Experience in 101 Related Family Members

Evidence for a major gene influence on tumor necrosis factor-alpha expression in tuberculosis: path and segregation analysis

Examination of association with candidate genes for diabetic nephropathy in a Mexican American population

Examining the relative influence of familial, genetic, and environmental covariate information in flexible risk models

Exome Array Analysis of Nuclear Lens Opacity

Exome array analysis identifies CAV1/CAV2 as a susceptibility locus for intraocular pressure

Familial clustering of chronic kidney disease

Family pedigrees of children with suspected childhood apraxia of speech.

Five-year progression of unilateral age-related macular degeneration to bilateral involvement: the Three Continent AMD Consortium report.

Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo

Fuchs’ endothelial corneal dystrophy: fostering change in clinical care using observational data

Further evidence of pleiotropy influencing speech and language: analysis of the DYX8 region.

Generation of Kidney Transcriptomes Using Serial Analysis of Gene Expression

Genetic association and gene-gene interaction analyses in African American dialysis patients with nondiabetic nephropathy

Genetic association of COL5A1 variants in keratoconus patients suggests a complex connection between corneal thinning and keratoconus

Genetic characterization and fine mapping of susceptibility loci for sarcoidosis in African Americans on chromosome 5.

Genetic determinants of macular pigments in women of the Carotenoids in Age-Related Eye Disease Study

Genetic evidence for role of carotenoids in age-related macular degeneration in the Carotenoids in Age-Related Eye Disease Study (CAREDS).

Genetic linkage analysis of sarcoidosis phenotypes: the sarcoidosis genetic analysis (SAGA) study

Genetic studies of Type 2 (non-insulin-dependent) diabetes mellitus: lack of association with seven genetic markers

Genetic susceptibility to end-stage renal disease.

Genetic susceptibility, dietary antioxidants, and long-term incidence of age-related macular degeneration in two populations

Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration

Genetics of Pigment Changes and Geographic Atrophy

Genetics of age-related macular degeneration (AMD).

Genetics of age-related macular degeneration (AMD).

Genome scan of M. tuberculosis infection and disease in Ugandans

Genome-Wide Association and Trans-ethnic Meta-Analysis for Advanced Diabetic Kidney Disease: Family Investigation of Nephropathy and Diabetes (FIND)

Genome-wide association identifies SKIV2L and MYRIP as protective factors for age-related macular degeneration ⬇️

Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error

Genome-wide association study identifies three novel loci in Fuchs endothelial corneal dystrophy.

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

Genome-wide linkage study of retinal vessel diameters in the Beaver Dam Eye Study

Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia

Genome-wide scan for estimated glomerular filtration rate in multi-ethnic diabetic populations: the Family Investigation of Nephropathy and Diabetes (FIND).

Genome-wide scans for diabetic nephropathy and albuminuria in multiethnic populations: the family investigation of nephropathy and diabetes (FIND).