Author

Yelena M. Kemel

Memorial Sloan Kettering Cancer CenterORCID 0000-0002-5042-5651Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Research Focus:variant effect prediction· 2 Research Focus:benchmarking· 1 Research Focus:database / resource· 1 Assay:GWAS summary statistics· 1 Approach:machine learning (classical)· 1 Research Focus:software / tool· 1 Approach:statistical model· 1

Frequent Co-Authors

Diana L. MandelkeriD· 2 shared Joseph VijaiiD· 2 shared Kenneth OffitiD· 2 shared Vignesh RavichandraniD· 2 shared Zsofia Kinga StadleriD· 2 shared Alicia J. LathamiD· 1 shared Aliya KhurramiD· 1 shared Andrew R. MardersteiniD· 1 shared

Activity by Year

2019-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Diana L. MandelkerORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintJun 22, 2026

Integrated Clinicogenomic Risk Modeling for Metachronous Second Primary Cancers

Johnathan Amsalem, Irina Ostrovnaya, Andrew R. Marderstein…·Joseph Vijai

The paper develops and validates a clinicogenomic risk model to predict second primary cancers in cancer survivors using genetic, clinical, and lifestyle factors.

DOI 10.64898/2026.06.12.26355388

humanGWAS summary statistics

𝕏 PostBluesky

GeneticsGenetics in MedicinePeer-reviewedFeb 20, 2019

Towards automation of germline variant curation in clinical cancer genetics

Vignesh Ravichandran, Zarina Shameer, Yelena M. Kemel…·Joseph Vijai

PathoMAN automates germline variant curation using ACMG guidelines, achieving high concordance with expert curation and proposing refinements for better ClinVar reporting.

48 citations

humanwhole-exome sequencing

𝕏 PostBluesky