Author

Ohad Regev

Ben-Gurion University of the NegevORCID 0000-0001-8964-5582Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Amnon HadariD· 1 shared Analya MichaelovskiiD· 1 shared Apurba ShiliD· 1 shared Dikla Zigdon· 1 shared Gal MeiriiD· 1 shared Idan MenasheiD· 1 shared Ilan DinsteiniD· 1 shared Reli Hershkovitz· 1 shared

Activity by Year

2024-2024 · peak 1/yr

Co-Author Collaboration Network

9 top collaborators · 36 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Amnon HadarORCID

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1 paper

Recent·Most cited

Genetic & Genomic MedicineJournal of Neurodevelopmental DisordersPeer-reviewedSep 30, 2024

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

Ohad Regev, Apurba Shil, Tal Bronshtein…·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.

4 citations

humanwhole-exome sequencing

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