Author

Frank X. Donovan

National Institutes of HealthORCID 0000-0002-7712-2335Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:differential expression· 2 Organism:human· 2 Approach:statistical model· 2 Assay:whole-exome sequencing· 2 Research Focus:clustering· 1 Assay:DNA methylation· 1 Approach:experimental assay· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Settara C. ChandrasekharappaiD· 2 shared Agata SmogorzewskaiD· 1 shared Alice YoungiD· 1 shared Andrew J. DeansiD· 1 shared Arleen D. AuerbachiD· 1 shared Carlo DufouriD· 1 shared Caroline S. JiangiD· 1 shared Danielle C. Kimble· 1 shared

Activity by Year

2020-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 27 mutual co-author links

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2 shared papersGenomics

Settara C. ChandrasekharappaORCID

Mutual co-authors in cluster

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2 papers

Recent·Most cited

GenomicsBlood AdvancesPeer-reviewedNov 29, 2023

Genomic Landscape of Patients with Germline RUNX1 Variants and Familial Platelet Disorder with Myeloid Malignancies in a Natural History Study

Kai Yu, Natalie T Deuitch, Matthew Merguerian…·Paul Liu

The paper analyzes genomic data from patients with FPDMM to identify germline RUNX1 variants and somatic mutations linked to clonal hematopoiesis and myeloid malignancies.

43 citationstop 2%

humanwhole-exome sequencing

Molecular BiologyBloodPeer-reviewedFeb 27, 2020

Clinical severity in Fanconi anemia correlates with residual function of FANCB missense variants

Moonjung Jung, Ramanagouda Ramanagoudr‐Bhojappa, Sylvie van Twest…·Settara C. Chandrasekharappa

The paper correlates clinical severity in Fanconi anemia with residual function of FANCB missense variants through biochemical and cell-based assays.

37 citations

humanDNA methylation