Author

Susan Halloran Blanton

University of MiamiORCID 0000-0002-5433-3439Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 2 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Research Focus:GWAS / association mapping· 2 Assay:GWAS summary statistics· 2 Approach:statistical model· 2 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

Adán Valladares‐SalgadoiD· 1 shared Adrienne M. StilpiD· 1 shared Ah Reum KimiD· 1 shared Aida Nourbakhsh· 1 shared Aleksandra ŽivkovićiD· 1 shared Ali G. GharaviiD· 1 shared Anders Larsson· 1 shared Andrew C. HeathiD· 1 shared

Activity by Year

2018-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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1 shared paperGenetics

Adán Valladares‐SalgadoORCID

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3 papers

Recent·Most cited

Genetic & Genomic MedicineHuman Molecular GeneticsPeer-reviewedSep 16, 2024

Identifying X-Chromosome Variants Associated with Age-Related Macular Degeneration

Michelle A. Grunin, Robert P. Igo, Yeunjoo E. Song…·Jonathan L. Haines

This study identifies X-chromosome variants associated with age-related macular degeneration using genome-wide association analysis and pathway enrichment.

2 citations

humanGWAS summary statistics

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GeneticsProceedings of the National Academy of SciencesPeer-reviewedMay 28, 2021

Mutations in TMEM43 cause autosomal dominant auditory neuropathy spectrum disorder via interaction with Connexin-mediated passive conductance channels

Minwoo Wendy Jang, Doo‐Yi Oh, Eunyoung Yi…·Byung Yoon Choi

This study identifies TMEM43 mutations as a cause of autosomal dominant auditory neuropathy spectrum disorder by showing their interaction with Connexin-mediated channels in cochlear glia-like supporting cells.

33 citations

humanexperimental assay

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GeneticsNature CommunicationsPeer-reviewedDec 28, 2018

Trans-ethnic genome-wide association study provides insight into effector genes and molecular mechanisms for kidney function and highlights a causal effect on kidney-specific disease aetiologies

Andrew P. Morris, Thu H Le, Hao Wu…·Nora Franceschini

This study identifies 93 genetic loci associated with kidney function across four ancestry groups and highlights causal effects on kidney-related diseases.

146 citations

humanGWAS summary statistics

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