Author

Christopher M. Kramer

University of Virginia Health SystemORCID 0000-0003-2057-7731Unclaimed 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 Approach:statistical model· 2 Research Focus:differential expression· 1 Assay:DNA methylation· 1 Assay:imaging· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Hugh C WatkinsiD· 2 shared Kate L. ThomsoniD· 2 shared Stefan NeubaueriD· 2 shared Adam WaringiD· 1 shared Andrew Robert HarperiD· 1 shared Anuj GoeliD· 1 shared Carolyn Yung HoiD· 1 shared Christopher GraceiD· 1 shared

Activity by Year

2020-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 35 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Hugh C WatkinsORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintJul 30, 2026

Genotype-Phenotype Correlations Identify Phenotypic Differences in Sarcomere Mutation-Positive Hypertrophic Cardiomyopathy in the NHLBI HCM Registry

Jonathan Chan, Christopher Grace, Kate L. Thomson…·Anuj Goel

The paper identifies phenotypic differences in sarcomere mutation-positive hypertrophic cardiomyopathy using CMR data from the NHLBI HCM Registry, resolving prior discrepancies through meta-analysis.

DOI 10.64898/2026.07.28.26359171

humanimaging

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GeneticsJournal of Medical GeneticsPeer-reviewedJul 30, 2020

Data-driven modelling of mutational hotspots and in-silico predictors in hypertrophic cardiomyopathy

Adam Waring, Andrew Robert Harper, Silvia Salatino…·Martin Farrall

The paper introduces methods to improve disease-gene association and variant pathogenicity interpretation by incorporating missense residue position information.

9 citations

humanDNA methylation

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