Author

Amnon Hadar

Soroka Medical CenterORCID 0000-0002-1576-9192Unclaimed 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

Analya MichaelovskiiD· 1 shared Apurba ShiliD· 1 shared Dikla Zigdon· 1 shared Gal MeiriiD· 1 shared Idan MenasheiD· 1 shared Ilan DinsteiniD· 1 shared Ohad RegeviD· 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

Analya MichaelovskiORCID

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1 paper

Recent·Most cited

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