Author

Jazmyn L. Bess

National Institutes of HealthORCID 0009-0000-5777-9105Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:benchmarking· 1 Research Focus:differential expression· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Douglas R. StewartiD· 2 shared Jung KimiD· 2 shared Alex Pemov· 1 shared Alicia A. LivinskiiD· 1 shared Anaqa Faizer· 1 shared Gina M. NeyiD· 1 shared Lesley M. ChapmaniD· 1 shared Muzzammil AhmadzadaiD· 1 shared

Activity by Year

2024-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 30 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Douglas R. StewartORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicineGenetics in MedicinePeer-reviewedApr 6, 2025

A Literature Review and Pooled Case Analysis of Cardiofaciocutaneous Syndrome to Estimate Cancer Risk

Jazmyn L. Bess, Toniya Brown, Sonia Bhala…·Douglas R. Stewart

This paper reviews literature and analyzes case data to estimate cancer risk in Cardiofaciocutaneous Syndrome (CFC) patients, finding elevated but limited cancer risk in early childhood.

3 citations

humanstatistical model

𝕏 PostBluesky

Genetic & Genomic MedicinemedRxivPreprintNov 19, 2024

Genome-wide investigation of rare germline copy-number variants in retinoblastoma

Lesley M. Chapman, Jung Kim, Jazmyn L. Bess…·Zois Boukouvalas

The paper identifies rare germline copy-number variants associated with retinoblastoma risk outside the RB1 gene using whole-genome sequencing and statistical analysis.

DOI 10.1101/2024.11.19.24316720

humanwhole-genome sequencing

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