Donald Basel

Also affiliated with Medical College of Wisconsin, University Pathologists

Biochemistry, Genetics and Molecular BiologyMedicine

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 6 papers. Top paper: “Joint, multifaceted genomic analysis enables diagnosis of diverse, ultra-rare monogenic presentations”.

Joint, multifaceted genomic analysis enables diagnosis of diverse, ultra-rare monogenic presentations

Nature Communications(2025)10.1038/s41467-025-61712-2

N/A

0.269DataRank · unranked

5 citations

Mikhail A. Moldovan, Rebecca Reimers, Daniel Traviglia, Xinyun Li, Danielle Barnum +95 more

A deep intronic variant activates a pseudoexon in the MTM1 gene in a family with X-linked myotubular myopathy

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.05.28.122333

N/A

0DataRank · unranked

0 citations

Cori Feist, Paula Dietz, S. S. Moore, Donald Basel, Jamie Fitzgerald

Novel Genetic Diagnoses in Septo-Optic Dysplasia

Genes(2022)10.3390/genes13071165

N/A

0DataRank · unranked

18 citations

Sarah E. Seese, Mohit Maheshwari, Donald Basel, LuAnn Weik, Julie McCarrier +2 more

Variants in ZFX are associated with an X-linked neurodevelopmental disorder with recurrent facial gestalt

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.01.007

N/A

0DataRank · unranked

18 citations

Katie Hutchison, Dilan Wellalage Don, George McGillivray, Tae‐Ik Choi, Carolyn A Allan +51 more

Novel Intragenic and Genomic Variants Highlight the Phenotypic Variability in HCCS-Related Disease

Genes(2024)10.3390/genes15121636

N/A

0DataRank · unranked

2 citations

Donald Basel, Pierre Bitoun, David S. Walton, Tom Glaser, Elena V. Semina +1 more

An optimized variant prioritization process for rare disease diagnostics: recommendations for Exomiser and Genomiser

Genome Medicine(2025)10.1186/s13073-025-01546-1

N/A

0DataRank · unranked

8 citations

Shruti Marwaha, Alistair Ward, Shilpa N. Kobren, Jennefer N. Carter, Undiagnosed Diseases Network +94 more