Author

Natalie Vena

Columbia University Irving Medical CenterORCID 0000-0003-2627-5275Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Research Focus:gene regulatory network inference· 1 Approach:statistical model· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Hila Milo RasoulyiD· 2 shared Maddalena MarasàiD· 2 shared Adele MitrottiiD· 1 shared Agnieszka SzmigielskaiD· 1 shared Aleksandra GliwińskaiD· 1 shared Ali G. GharaviiD· 1 shared Andrea Ranghino· 1 shared Andrew BeenkeniD· 1 shared

Activity by Year

2022-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 38 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Hila Milo RasoulyORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicineNature CommunicationsPeer-reviewedAug 7, 2025

Exome-wide analysis of congenital kidney anomalies reveals new genes and shared architecture with developmental disorders

Hila Milo Rasouly, Sarath Babu Krishna Murthy, Natalie Vena…·Yaşar Çalışkan

This study identifies new genes and shared genetic architecture between kidney anomalies and other developmental disorders using exome-wide analysis of clinical cohorts.

12 citationstop 2%

humanwhole-exome sequencing

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Genetic & Genomic MedicineAmerican Journal of Medical Genetics Part C Seminars in Medical GeneticsPeer-reviewedSep 1, 2022

Incorporating Genetics Services into Adult Kidney Disease Care

Kelsie Bogyo, Natalie Vena, Halie J. May…·Ali G. Gharavi

This paper describes the establishment of a Kidney Genetics Clinic to improve access to genetic services for adults with kidney disease, reporting a 42.38% yield of clinically relevant genetic findings.

21 citations

human

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