Author

Wu‐Lin Charng

Washington University in St. LouisORCID 0000-0003-0661-4081Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 2 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Research Focus:differential expression· 2 Approach:experimental assay· 2 Research Focus:gene regulatory network inference· 2 Assay:whole-exome sequencing· 2 Research Focus:benchmarking· 1 Research Focus:cell type annotation· 1

Frequent Co-Authors

Donald F. ConradiD· 2 shared Adrian M. E. PilatziD· 1 shared Alberto BarrosiD· 1 shared Alexandra M. StendahliD· 1 shared Alexandra Manuel LopesiD· 1 shared Amjad HoraniiD· 1 shared Antoni Riera‐EscamillaiD· 1 shared Brian Miller· 1 shared

Activity by Year

2020-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 23 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Donald F. ConradORCID

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3 papers

Recent·Most cited

GeneticsbioRxivPreprintAug 2, 2025

Pathogenic DVL frameshifting variants in Robinow syndrome disrupt WNT signaling and cellular dynamics

Chaofan Zhang, Rituparna Sinha Roy, Ming Yin Lun…·Claudia M.B. Carvalho

The paper investigates how pathogenic DVL frameshifting variants in Robinow syndrome disrupt WNT signaling and cellular dynamics by altering protein structure and function.

DOI 10.1101/2025.08.02.668297

humanproteomics

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Genetic & Genomic MedicineNature CommunicationsPeer-reviewedDec 26, 2022

Diverse Monogenic Subforms of Human Spermatogenic Failure

Liina Nagirnaja, Alexandra Manuel Lopes, Wu‐Lin Charng…·Donald F. Conrad

This study identifies genetic subforms of non-obstructive azoospermia using exome sequencing and single-cell RNA sequencing, revealing molecular groups of genes involved in spermatogenesis.

89 citationstop 1%

humanwhole-exome sequencing

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GeneticsPLoS GeneticsPeer-reviewedAug 7, 2020

Mutation of CFAP57 causes primary ciliary dyskinesia by disrupting theasymmetric targeting of a subset of ciliary inner dynein arms

Ximena Minerva Bustamante-Marin, Amjad Horani, Mihaela Stoyanova…·Susan K. Dutcher

This study identifies mutations in CFAP57 as a cause of primary ciliary dyskinesia by showing they disrupt asymmetric inner dynein arm assembly in cilia.

49 citationstop 4%

humanmouse

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