Author

Rena Feinman

Hackensack University Medical CenterORCID 0000-0003-0654-7181Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genomics· 1

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:DNA methylation· 1 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

Andre Henri GoyiD· 2 shared Benjamin TyckoiD· 2 shared Catherine DoiD· 2 shared David Samuel DiCapua SiegeliD· 2 shared Emmanuel LP DumontiD· 2 shared Angela M. ChristianoiD· 1 shared Angelica M. Castano· 1 shared Ariel Alejandro AptekmanniD· 1 shared

Activity by Year

2020-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 41 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Andre Henri GoyORCID

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2 papers

Recent·Most cited

Genetic Ethnicity and Hypertension Epistatic Interaction Underlying Racial Disparities in US Multiple Myeloma Susceptibility

Emmanuel LP Dumont, Luke Han, Srisundesh Kodali, Ariel Alejandro Aptekmann, Lisa Carter‐Harris, Rena Feinman, Benjamin Tycko, David Samuel DiCapua Siegel, Andre Henri Goy, Peter D. Kaplan, Catherine Do

The paper identifies an epistatic interaction between genetic ethnicity and hypertension that explains racial disparities in multiple myeloma risk among Black and mixed-ancestry individuals.

medRxiv · Jun 1, 2024 · PreprintGenetic & Genomic Medicine

Allele-specific DNA methylation is increased in cancers and its dense mapping in normal plus neoplastic cells increases the yield of disease-associated regulatory SNPs

Catherine Do, Emmanuel LP Dumont, Martha C. Salas, Angelica M. Castano, Huthayfa Mujahed, Leonel Maldonado, Arunjot Singh, Sonia C. DaSilva‐Arnold, Govind Bhagat, Soren Lehman, Angela M. Christiano, Subha Madhavan, Péter L. Nagy, Peter H.R. Green, Rena Feinman, , Benjamin Tycko

The paper maps allele-specific DNA methylation in normal and cancer tissues, identifying disease-associated regulatory SNPs that are missed by other methods.

Genome biology · Jun 28, 2020Peer-reviewedGenomics