Author

Dikla Zigdon

Ben-Gurion University of the Negev

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Assay:whole-exome sequencing· 2 Research Focus:variant calling· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Analya MichaelovskiiD· 2 shared Gal MeiriiD· 2 shared Idan MenasheiD· 2 shared Amnon HadariD· 1 shared Apurba ShiliD· 1 shared Ilan DinsteiniD· 1 shared Michal IlaniD· 1 shared Mor Dekel· 1 shared

Activity by Year

2024-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Analya MichaelovskiORCID

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2 papers

Recent·Most cited

A Novel Phenotype-based Approach for Prioritizing Candidate Genetic Variants for Autism Spectrum Disorder.

Noam Levi, Mor Dekel, Michal Ilan, Dikla Zigdon, Analya Michaelovski, Tamar Kolodny, Gal Meiri, Idan Menashe

This paper introduces a phenotype-based method to prioritize genetic variants in ASD, improving diagnostic yield and identifying novel variants in unresolved cases.

medRxiv · Jul 2, 2026 · PreprintGenetic & Genomic Medicine

Genetic Elucidation of Ultrasonography Fetal Anomalies in Children with Autism Spectrum Disorder

Ohad Regev, Apurba Shil, Tal Bronshtein, Amnon Hadar, Gal Meiri, Dikla Zigdon, Analya Michaelovski, Ilan Dinstein, Reli Hershkovitz, Idan Menashe

This study identifies genetic variants associated with fetal ultrasound anomalies in children with autism spectrum disorder using whole exome sequencing and a bioinformatics pipeline.

Journal of Neurodevelopmental Disorders · Sep 30, 2024Peer-reviewedGenetic & Genomic Medicine