Author

Vanessa Hus Bal

Rutgers, The State University of New JerseyORCID 0000-0003-0750-823XUnclaimed 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 effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Anita ThapariD· 1 shared Arthur Jeremy WillseyiD· 1 shared Belinda Lei WangiD· 1 shared Clif DuhniD· 1 shared Gary A. HeimaniD· 1 shared Hasan AlkhairoiD· 1 shared Jay A. TischfieldiD· 1 shared Jinchuan XingiD· 1 shared

Activity by Year

2022-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Anita ThaparORCID

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1 paper

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintSep 22, 2022

Rare Maternally Inherited Coding Variants on Chromosome X Carry Predominantly Male Risk in Autism, Tourette Syndrome, and Attention-deficit/Hyperactivity Disorder

Sheng Wang, Belinda Lei Wang, Vanessa Drury…·Arthur Jeremy Willsey

1 citation

humanwhole-exome sequencing

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