David A. Wenger

Also affiliated with Washington University in St. Louis, Mallinckrodt (United States)

MedicineBiochemistry, Genetics and Molecular Biology

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

1in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 1 indexed paper attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

Papers

Driven by 8 papers. Top paper: “Krabbe disease: globoid cell leukodystrophy”.

Krabbe disease: globoid cell leukodystrophy

Rosenberg's Molecular and Genetic Basis of Neurological and Psychiatric Disease(2025)10.1016/b978-0-443-19041-4.00043-1

N/A

0.529DataRank · unranked

33 citations

Paola Luzi, David A. Wenger

Preclinical Four-Dimensional Functional Lung Imaging and Quantification of Regional Airflow: A New Standard in Lung Function Evaluation in Murine Models

American Journal of Respiratory Cell and Molecular Biology(2022)10.1165/rcmb.2022-0055ma

N/A

0DataRank · unranked

18 citations

Matthew Frimel, Violetta Zlojutro, Dillon Grant, Olivia Stephens, David A. Wenger +4 more

PSMC3 proteasome subunit variants are associated with neurodevelopmental delay and type I interferon production

Science Translational Medicine(2023)10.1126/scitranslmed.abo3189

N/A

0DataRank · unranked

36 citations

Sébastien Küry, Victoria Most, Cory Rosenfelt, Marie‐Pier Scott‐Boyer, Geeske M. van Woerden +69 more

Ciliopathy patient variants reveal organelle-specific functions for TUBB4B in axonemal microtubules

Science(2024)10.1126/science.adf5489

N/A

0DataRank · unranked

48 citations

Sabrina Méchaussier, Patricia L. Yeyati, Fraser McPhie, Jacob R. Anderson, Chen Jing Khoo +75 more

Metachromatic Leukodystrophy: A Case of Triplets With the Late Infantile Variant and a Systematic Review of the Literature

UNC Libraries(2021)10.17615/sf56-fx77

N/A

0DataRank · unranked

0 citations

Magdi M. Sobeih, David A. Wenger, Asif Mahmood, Maria L. Escolar, Gerald V. Raymond +2 more

Severe Neurological Presentation in Siblings With COQ5 ‐Related Primary Coenzyme Q10 Deficiency: Expanding Clinical and Molecular Spectrum

JIMD Reports(2025)10.1002/jmd2.70038

N/A

0DataRank · unranked

0 citations

Rachel M. Guerra, David A. Wenger, Samantha Toy, J Hauer, David J. Pagliarini +2 more

Phenotypic expansion of CALM1/2 -associated disorders to include neurologic phenotypes without arrhythmia

Human Molecular Genetics(2025)10.1093/hmg/ddaf195

N/A

0DataRank · unranked

0 citations

Rebecca C. Spillmann, David A. Wenger, Maria Giovanna Tedesco, Malene Brohus, Antonio Novelli +24 more

Bi-allelic LAMP3 variants in childhood interstitial lung disease: a surfactant-related disease

EBioMedicine(2025)10.1016/j.ebiom.2025.105626

N/A

0DataRank · unranked

7 citations

Tifenn Desroziers, Yohan Sorèze, M. Rodriguez, Lucie Thomas, Valérie Nau +21 more