Author

Gordon Fan-Huang

Albert Einstein College of MedicineORCID 0009-0000-4435-5602Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genomics· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Research Focus:variant calling· 2 Assay:whole-genome sequencing· 2 Research Focus:differential expression· 1 Organism:Drosophila· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Approach:statistical model· 1

Frequent Co-Authors

Alexander Y. MasloviD· 2 shared Jan VijgiD· 2 shared Moonsook LeeiD· 2 shared Shixiang SuniD· 2 shared Christina L. BoulliD· 1 shared Cristina MontagnaiD· 1 shared Elizabeth L. SchmidtiD· 1 shared Elizabeth Pan· 1 shared

Activity by Year

2024-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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2 shared papersGenomics

Alexander Y. MaslovORCID

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2 papers

Recent·Most cited

GenomicsbioRxivPreprintJul 16, 2025

Uniquely high spontaneous mutational load in blood cells of XP-C patients

Gordon Fan-Huang, Elizabeth L. Schmidt, Moonsook Lee…·Alexander Y. Maslov

The paper identifies a high spontaneous mutational load in PBMCs of XP-C patients, linked to specific mutation signatures and replication-dependent mutagenesis.

DOI 10.1101/2025.07.16.665113

humanwhole-genome sequencing

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GenomicsbioRxivPreprintAug 8, 2024

Chimera-suppressing error-corrected sequencing enables quantitative detection of rare somatic structural-variant breakpoints in human cells

Elizabeth Pan, Shixiang Sun, Johanna Heid…·Alexander Y. Maslov

This paper introduces SMM-SV-seq, a method to detect rare somatic structural-variant breakpoints in bulk DNA with high precision and recall, validated using human and Drosophila DNA mixtures and clinical treatments.

3 citations

humanDrosophila

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