Author

Alba Sanchis-Juan

Broad Institute

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Genomics· 1

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

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Alexander GuseviD· 1 shared Amanda GarzaiD· 1 shared Brian D. CromptoniD· 1 shared Chris Whelan· 1 shared Eliezer M. Van AlleniD· 1 shared Emma Pierce‐Hoffman· 1 shared Harrison BrandiD· 1 shared Jaclyn LoPiccoloiD· 1 shared

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2025-2025 · peak 1/yr

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Alexander GusevORCID

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1 paper

Recent·Most cited

GenomicsSciencePeer-reviewedJan 2, 2025

Rare germline structural variants increase risk for pediatric solid tumors

Riaz Gillani, Ryan L. Collins, Jett Crowdis…·Eliezer M. Van Allen

This study identifies rare germline structural variants as risk factors for pediatric solid tumors, particularly neuroblastoma, by analyzing genome sequencing data from affected children and controls.

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humanwhole-genome sequencing