Author

Martin M. Fabani

Human Longevity (United States)ORCID 0009-0001-1916-182XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genomics· 2 Cancer Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:human· 2 Approach:statistical model· 2 Research Focus:cell type annotation· 1 Research Focus:cell-cell communication· 1 Research Focus:differential expression· 1 Assay:long-read sequencing· 1 Assay:scRNA-seq· 1

Frequent Co-Authors

Eli N. Glezer· 2 shared Amalio TelentiiD· 1 shared Bharat SridhariD· 1 shared Bing ReniD· 1 shared Cameron Y. ParkiD· 1 shared Catherine J. WuiD· 1 shared Chanell MangumiD· 1 shared Christopher Wei· 1 shared

Activity by Year

2018-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 19 mutual co-author links

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2 shared papersCancer Biology

Eli N. Glezer

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3 papers

Recent·Most cited

Cancer BiologyScience ImmunologyPeer-reviewedJan 24, 2025

Coordinated Immune Cell Networks in the Bone Marrow Microenvironment Define the Graft versus Leukemia Response with Adoptive Cellular Therapy

Katie Maurer, Cameron Y. Park, Shouvik Mani…·Elham Azizi

The paper analyzes single-cell data from bone marrow samples to identify immune cell interactions that predict response to adoptive cellular therapy in myeloid leukemia.

42 citationstop 1%

humanscRNA-seq

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GenomicsbioRxivPreprintMay 10, 2022

Reconstruction of Full-length scFv Libraries with the Extended Range Targeted Sequencing Method

Christopher Wei, Sarah Criner, Bharat Sridhar…·Eli N. Glezer

The paper introduces an extended range targeted sequencing method to accurately analyze full-length scFv constructs from a commercial library.

1 citation

long-read sequencingexperimental assay

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GenomicsNature GeneticsPeer-reviewedFeb 23, 2018

The human functional genome defined by genetic diversity

Julia di Iulio, István Bartha, Emily Wong…·Amalio Telenti

The paper analyzes genetic diversity across 11,257 human genomes to identify context-dependent conserved regions and their association with disease variants.

161 citationstop 1%

humanwhole-genome sequencing

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