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Author Details

Sudha K Iyengar
1988
196
54
PMIDPaper TitleJournal TitlePublished Year
37425708Diversity and Scale: Genetic Architecture of 2,068 Traits in the VA Million Veteran Program.medRxiv2023
36041210Reply to: Sookaromdee and Wiwanitkit.Am J Respir Crit Care Med2023
36302597Genomic Disorders in CKD across the Lifespan.J Am Soc Nephrol2023
35994124Hemizygosity can reveal variant pathogenicity on the X-chromosome.Hum Genet2023
37734154Long-Term Outcomes for Individuals With Childhood Apraxia of Speech.2023
37205546Multi-ancestry GWAS of Fuchs corneal dystrophy highlights roles of laminins, collagen, and endothelial cell regulation.Res Sq2023
36540996Diversity is key for cross-ancestry transferability of glaucoma genetic risk scores in Hispanic Veterans in the Million Veteran Program.Pac Symp Biocomput2023
37170406Association Between Fuchs Endothelial Corneal Dystrophy, Diabetes Mellitus, and Multimorbidity.Cornea2023
37043519Patterns of risk for diabetic retinopathy in the Mumbai slums: The Aditya Jyot Diabetic Retinopathy in Urban Mumbai Slums Study (AJ-DRUMSS) Report 3.2023
34822319Development and Evaluation of a Rules-based Algorithm for Primary Open-Angle Glaucoma in the VA Million Veteran Program.Ophthalmic Epidemiol2022
35771531A <i>MUC5B</i> Gene Polymorphism, rs35705950-T, Confers Protective Effects Against COVID-19 Hospitalization but Not Severe Disease or Mortality.Am J Respir Crit Care Med2022
35759254Association of Kidney Comorbidities and Acute Kidney Failure With Unfavorable Outcomes After COVID-19 in Individuals With the Sickle Cell Trait.JAMA Intern Med2022
35815717Younger Age and Albuminuria are Associated with Proliferative Diabetic Retinopathy and Diabetic Macular Edema in the South Indian GeNetics of DiAbeTic Retinopathy (SIGNATR) Study.Curr Eye Res2022
36268164Erratum: Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits-The Hispanic/Latino Anthropometry Consortium.HGG Adv2022
35482673A Phenome-Wide Association Study of genes associated with COVID-19 severity reveals shared genetics with complex diseases in the Million Veteran Program.PLoS Genet2022
36064543A translational genomics approach identifies IL10RB as the top candidate gene target for COVID-19 susceptibility.NPJ Genom Med2022
35718050Glaucoma Genetic Risk Scores in the Million Veteran Program.Ophthalmology2022
35659450Erratum to Gene Set Enrichment Analyses Identify Pathways Involved in Genetic Risk for Diabetic Retinopathy. Am J Ophthalmol 2022;233:111-123.Am J Ophthalmol2022
35399580Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits-The Hispanic/Latino Anthropometry Consortium.HGG Adv2022
34166655Gene Set Enrichment Analsyes Identify Pathways Involved in Genetic Risk for Diabetic Retinopathy.Am J Ophthalmol2022
34609155Psychosocial Comorbidities in Adolescents With Histories of Childhood Apraxia of Speech.Am J Speech Lang Pathol2021
33837377Actionable druggable genome-wide Mendelian randomization identifies repurposing opportunities for COVID-19.Nat Med2021
34100031IL10RB as a key regulator of COVID-19 host susceptibility and severity.medRxiv2021
33649486A multi-ethnic genome-wide association study implicates collagen matrix integrity and cell differentiation pathways in keratoconus.Commun Biol2021
34315907Association between genes regulating neural pathways for quantitative traits of speech and language disorders.NPJ Genom Med2021
33187500Feature-driven classification reveals potential comorbid subtypes within childhood apraxia of speech.BMC Pediatr2020
33311586Common variants in SOX-2 and congenital cataract genes contribute to age-related nuclear cataract.Commun Biol2020
30724840Diversity of Ocular Surface Bacterial Microbiome Adherent to Worn Contact Lenses and Bacterial Communities Associated With Care Solution Use.Eye and Contact Lens2019
31604025Differential Long-Term Outcomes for Individuals With Histories of Preschool Speech Sound Disorders.Am J Speech Lang Pathol2019
30487263Multiethnic Genome-Wide Association Study of Diabetic Retinopathy Using Liability Threshold Modeling of Duration of Diabetes and Glycemic Control.Diabetes2019
31419159Reading Outcomes for Individuals With Histories of Suspected Childhood Apraxia of Speech.Am J Speech Lang Pathol2019
31258967Genetically-guided algorithm development and sample size optimization for age-related macular degeneration cases and controls in electronic health records from the VA Million Veteran Program.AMIA Jt Summits Transl Sci Proc2019
31047378Joint Contribution of Genetic Susceptibility and Modifiable Factors to the Progression of Age-Related Macular Degeneration over 10 Years: The Three Continent AMD Consortium Report.Ophthalmol Retina2018
30555216Heritability and longitudinal outcomes of spelling skills in individuals with histories of early speech and language disorders.Learn Individ Differ2018
30267098Aldose Reductase Polymorphisms, Fasting Blood Glucose, and Age-Related Cortical Cataract.Invest Ophthalmol Vis Sci2018
30571798Correction: A 32 kb Critical Region Excluding Y402H in CFH Mediates Risk for Age-Related Macular Degeneration.PLoS One2018
29182452Exome Array Analysis of Nuclear Lens Opacity.Ophthalmic Epidemiol2018
29808027Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error.Nat Genet2018
28108569Five-year progression of unilateral age-related macular degeneration to bilateral involvement: the Three Continent AMD Consortium report.Br J Ophthalmol2017
28854576Genetics of age-related macular degeneration (AMD).Hum Mol Genet2017
28977452Genetics of age-related macular degeneration (AMD).Hum Mol Genet2017
28358029Genome-wide association study identifies three novel loci in Fuchs endothelial corneal dystrophy.Nat Commun2017
26691988A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants.Nat Genet2016
27440996Variation in PTCHD2, CRISP3, NAP1L4, FSCB, and AP3B2 associated with spherical equivalent.Mol Vis2016
27020472Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error.Nat Commun2016
27142425Selecting SNPs informative for African, American Indian and European Ancestry: application to the Family Investigation of Nephropathy and Diabetes (FIND).BMC Genomics2016
27032038Psychosocial co-morbidities in adolescents and adults with histories of communication disorders.J Commun Disord2016
26986182Associations Between Methylenetetrahydrofolate Reductase Polymorphisms, Serum Homocysteine Levels, and Incident Cortical Cataract.JAMA Ophthalmol2016
26305897Genome-Wide Association and Trans-ethnic Meta-Analysis for Advanced Diabetic Kidney Disease: Family Investigation of Nephropathy and Diabetes (FIND).PLoS Genet2015
25340497Severity 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.JAMA Ophthalmol2015
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