Author

Joel A. Morales‐Rosado

Vanderbilt University Medical CenterORCID 0000-0002-7710-2211Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Bioinformatics· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Research Focus:drug response / drug discovery· 1 Approach:experimental assay· 1 Approach:machine learning (classical)· 1 Organism:mouse· 1 Approach:statistical model· 1

Frequent Co-Authors

Eric W. KleeiD· 2 shared Alejandro FerreriD· 1 shared Allan Micheil InnesiD· 1 shared Ana S.A. CoheniD· 1 shared Benjamin B. YaniD· 1 shared Benjamin CognéiD· 1 shared Bernt PoppiD· 1 shared Bonnie R. SullivaniD· 1 shared

Activity by Year

2024-2024 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 31 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Eric W. KleeORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintApr 24, 2024

MARK2 variants cause autism spectrum disorder via the downregulation of WNT/β-catenin signaling pathway

Maolei Gong, Jiayi Li, Yijun Liu…·Xiaoli Chen

This study identifies MARK2 variants as a cause of autism spectrum disorder by showing they disrupt the WNT/β-catenin signaling pathway and impair neural development.

DOI 10.1101/2024.04.24.24304501

humanmouse

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BioinformaticsbioRxivPreprintApr 22, 2024

Unified somatic calling and machine learning-based classification enhance the discovery of clonal hematopoiesis of indeterminate potential

Shulan Tian, Garrett Jenkinson, Alejandro Ferrer…·Eric W. Klee

UNISOM improves CHIP detection from low-coverage sequencing data by combining variant calling with machine learning classification, identifying low-VAF mutations with high sensitivity.

DOI 10.1101/2024.04.22.590586

humanwhole-genome sequencing

𝕏 PostBluesky