Author

Tal Bronshtein

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· 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 Ohad RegeviD· 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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