Author

Natalie T Deuitch

National Institutes of HealthORCID 0000-0002-0146-1162Unclaimed ORCID profile · follow to get notified of new preprints

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

Frequent Co-Authors

Alice YoungiD· 1 shared Elizabeth T. Andrews· 1 shared Erica BrescianiiD· 1 shared Frank X. DonovaniD· 1 shared James C. MullikiniD· 1 shared Jamie Lynn Diemer· 1 shared Joie Davis· 1 shared Kai YuiD· 1 shared

Activity by Year

2023-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenomics

Alice YoungORCID

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1 paper

Recent·Most cited

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, Lea Cunningham, Joie Davis, Erica Bresciani, Jamie Lynn Diemer, Elizabeth T. Andrews, Alice Young, Frank X. Donovan, Raman B. Sood, Kathleen Craft, Shawn Chong, Settara C. Chandrasekharappa, James C. Mullikin, 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.

Blood Advances · Nov 29, 2023Peer-reviewedGenomics