Author

Neil Menghani

Children's Hospital of Philadelphia

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 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Arnavaz DaneshiD· 1 shared Daniela Se Gerhard· 1 shared Douglas R. StewartiD· 1 shared Gonzalo LópeziD· 1 shared Hakon H. HakonarsoniD· 1 shared Heena DesaiiD· 1 shared Jaime M. Guidry AuviliD· 1 shared Javed Iqbal KhaniD· 1 shared

Activity by Year

2023-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Arnavaz DaneshORCID

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Author profile →

1 paper

Recent·Most cited

Germline pathogenic variants in 786 neuroblastoma patients

Jung Kim, Zalman Vaksman, Laura E. Egolf, Rebecca Kaufman, Perry Evans, Karina L. Conkrite, Arnavaz Danesh, Gonzalo López, Michael P. Randall, Maiah H. Dent, Lance M. Farra, Neil Menghani, Malwina Dymek, Heena Desai, Ryan M. Hausler, , Sharon J. Diskin

This study identifies 13.9% of neuroblastoma patients with pathogenic germline variants in cancer predisposition genes, associated with worse survival and enriched in DNA repair genes like BARD1.

medRxiv · Jan 23, 2023 · PreprintGenetic & Genomic Medicine