Author

Danny Zeevi

Howard Hughes Medical InstituteORCID 0000-0002-6901-3737Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 2 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Assay:GWAS summary statistics· 2 Research Focus:benchmarking· 1 Research Focus:GWAS / association mapping· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Leonid KruglyakiD· 2 shared Adi Ben Yehuda· 1 shared Alex Hatzimanolis· 1 shared Dafna NathaniD· 1 shared David ZangeniD· 1 shared Dimitrios AvramopoulosiD· 1 shared Ehud KaravaniiD· 1 shared Ephrat Levy‐LahadiD· 1 shared

Activity by Year

2019-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 17 mutual co-author links

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2 shared papersGenetics

Leonid KruglyakORCID

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3 papers

Recent·Most cited

TinkerHap - A Novel Read-Based Phasing Algorithm with Integrated Multi-Method Support for Enhanced Accuracy

Uri Hartmann, Eran Shaham, Dafna Nathan, Ilana Blech, Danny Zeevi

TinkerHap improves phasing accuracy by combining read-based and external phased data, achieving high accuracy for both short and long reads.

GigaScience · Jan 1, 2025Peer-reviewedGenomics

Screening human embryos for polygenic traits has limited utility

Ehud Karavani, Or Zuk, Danny Zeevi, Nir Barzilai, Nikos C. Stefanis, Alex Hatzimanolis, Nikolaos Smyrnis, Dimitrios Avramopoulos, Leonid Kruglyak, Gil Atzmon, Max Lam, Todd Lencz, Shai Carmi

This paper evaluates the potential benefits of using polygenic scores to select embryos for traits like height and cognitive function, finding limited gains with current predictors.

Cell · Nov 1, 2019Peer-reviewedGenetics

Analysis of the genetic basis of height in large Jewish nuclear families

Danny Zeevi, Joshua S. Bloom, Meru J. Sadhu, Adi Ben Yehuda, David Zangen, Ephrat Levy‐Lahad, Leonid Kruglyak

This study identifies genetic loci contributing to height variation in a Jewish population cohort, explaining 6% of the variance through rare variants.

PLoS Genetics · Jul 8, 2019Peer-reviewedGenetics