Wu‐Lin Charng

Also affiliated with Washington University in St. Louis

Biochemistry, Genetics and Molecular BiologyNeuroscience

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 8 papers. Top paper: “Diverse monogenic subforms of human spermatogenic failure”.

Diverse monogenic subforms of human spermatogenic failure

Nature Communications(2022)10.1038/s41467-022-35661-z

N/A

0.655DataRank · unranked

78 citations

Alexandra M. Lopes, Wu‐Lin Charng, Brian Miller, Rytis Stakaitis, Ieva Golubickaitė +44 more

Diverse Monogenic Subforms of Human Spermatogenic Failure

medRxiv(2022)10.1101/2022.07.19.22271581

N/A

0.385DataRank · unranked

12 citations

Alexandra M. Lopes, Wu‐Lin Charng, Brian Miller, Rytis Stakaitis, Ieva Golubickaitė +44 more

Sequence variants in HECTD1 result in a variable neurodevelopmental disorder

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.01.001

N/A

0.241DataRank · unranked

4 citations

Elias Oxman, Hieu D. Hoang, Wu‐Lin Charng, Tanvitha Kotla, Weimin Yuan +49 more

Rare missense variants in FNDC1 are associated with severe adolescent idiopathic scoliosis

Journal of Medical Genetics(2025)10.1136/jmg-2024-110586

N/A

0.104DataRank · unranked

1 citations

Gabe Haller, Julia Whittle, Momchil Nikolov, Addison Avery, José A. Morcuende +12 more

Diagnostic yield of exome sequencing in congenital vertical talus

European Journal of Medical Genetics(2022)10.1016/j.ejmg.2022.104514

N/A

0DataRank · unranked

6 citations

Wu‐Lin Charng, Patricia Dickson, Matthew B. Dobbs, Christina A. Gurnett, Naeimeh Tayebi

TNPO2 variants associate with human developmental delays, neurologic deficits, and dysmorphic features and alter TNPO2 activity in Drosophila

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.06.019

N/A

0DataRank · unranked

47 citations

Heidi Cope, Zelha Nil, Thomas A. Ravenscroft, Wu‐Lin Charng, Shenzhao Lu +42 more

Whole Exome Sequencing in Individuals with Idiopathic Clubfoot Reveals a Recurrent Filamin B (FLNB) Deletion

Clinical Orthopaedics and Related Research(2021)10.1097/corr.0000000000001957

N/A

0DataRank · unranked

8 citations

Wu‐Lin Charng, Lilian Antunes, Momchil Nikolov, Xavier Bledsoe, Jacqueline T. Hecht +3 more

Mutation of CFAP57, a protein required for the asymmetric targeting of a subset of inner dynein arms in Chlamydomonas, causes primary ciliary dyskinesia

PLoS Genetics(2020)10.1371/journal.pgen.1008691

N/A

0DataRank · unranked

52 citations

Amjad Horani, Mihaela Stoyanova, Wu‐Lin Charng, Mathieu Bottier, Patrick R. Sears +9 more