Author

Jiangxingzi Xu

Hospital for Sick ChildrenORCID 0009-0000-3180-3672Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Approach:experimental assay· 2 Organism:human· 2 Assay:CRISPR screen· 1 Research Focus:database / resource· 1 Research Focus:variant effect prediction· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Ana S.A. CoheniD· 1 shared Andrei Turinsky· 1 shared Angela LekiD· 1 shared Anjali JainiD· 1 shared Christine L. O’ConnoriD· 1 shared Conor KlamanniD· 1 shared Delvin So· 1 shared Emily FarrowiD· 1 shared

Activity by Year

2023-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

1 shared paperGenetic & Genomic Medicine

Ana S.A. CohenORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintSep 3, 2024

One-Sided Matching Portal (OSMP): a tool to facilitate rare disease patient matchmaking

Matthew Osmond, Emily M. Price, Orion J. Buske…·Kym M Boycott

The paper introduces OSMP, a tool for one-sided genomic matchmaking in rare disease patients, which efficiently filters variant occurrences to prioritize clinically relevant matches.

1 citation

humanwhole-genome sequencing

𝕏 PostBluesky

GeneticsbioRxivPreprintJul 12, 2023

Deep Mutational Scanning in Disease-related Genes with Saturation Mutagenesis-Reinforced Functional Assays (SMuRF)

Kaiyue Ma, Shushu Huang, Kenneth K.H. Ng…·Monkol Lek

This paper introduces SMuRF, a framework for deep mutational scanning in disease-related genes, generating functional scores for all coding variants and aiding in variant interpretation.

3 citations

humanCRISPR screen

𝕏 PostBluesky