Author

S. Vincent Rajkumar

Mayo ClinicORCID 0000-0002-5862-1833Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Organism:human· 2 Approach:statistical model· 2 Research Focus:cancer & tumor microenvironment· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Research Focus:variant calling· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Shaji Kunnathu KumariD· 2 shared Ahmet DoǧaniD· 1 shared Alexander M. LesokhiniD· 1 shared Alexandra Maria PoosiD· 1 shared Alun ThomasiD· 1 shared Anthony M. CirrincioneiD· 1 shared Bachisio ZicchedduiD· 1 shared Benjamin T. DiamondiD· 1 shared

Activity by Year

2018-2025 · peak 1/yr

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10 top collaborators · 27 mutual co-author links

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2 shared papersCancer Biology

Shaji Kunnathu KumarORCID

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2 papers

Recent·Most cited

Cancer BiologyNature GeneticsPeer-reviewedAug 20, 2025

Temporal Genomic Dynamics Shape Clinical Trajectory in Multiple Myeloma

Francesco Maura, Marcella Kaddoura, Alexandra Maria Poos…·Niels Weinhold

This study analyzes whole-genome sequencing data from multiple myeloma patients to show that the timing of genetic events, not just their presence, affects clinical outcomes.

16 citationstop 1%

humanwhole-genome sequencing

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GeneticsPLoS GeneticsPeer-reviewedFeb 1, 2018

Novel pedigree analysis implicates DNA repair and chromatin remodeling in Multiple Myeloma risk

Rosalie G. Waller, Todd M. Darlington, Xiaomu Wei…·Nicola J. Camp

This paper introduces a new pedigree analysis method to identify risk variants for complex diseases, applying it to Multiple Myeloma and finding two genes associated with DNA repair and chromatin remodeling.

42 citations

humanwhole-exome sequencing

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