Vance P Lemmon

17PUBLICATIONS
139CO-AUTHORS
Genetics not elsewhere classifiedCraniofacial biologyGenomicsClinical chemistry (incl. diagnostics)Gene expression (incl. microarray and other genome-wide approaches)
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Publications (17)

|Oct 23, 2026
Very Low Frequency of SCA27B Among Undiagnosed Cerebellar Ataxia Patients in Peru.

|Jan 07, 2026
Spectrum of dominant Charcot-Marie-Tooth disease due to SLC12A6 variants.

Christopher J Record, Tiffany Grider, Adriana P Rebelo

|Nov 19, 2025
Population-scale Long-read Sequencing in the All of Us Research Program.

Kiran V Garimella, Qiuhui Li, Julie Wertz

|Feb 25, 2025
The Spastic Paraplegia-Centers of Excellence Research Network (SP-CERN): Clinical Trial Readiness for Hereditary Spastic Paraplegia.

Luca Schierbaum, Vicente Quiroz, Kathryn Yang

|Feb 25, 2025
Involvement of the Superior Cerebellar Peduncles in GAA-FGF14 Ataxia.

Shihan Chen, Catherine Ashton, Rawan Sakalla

|Jan 27, 2025
Detailed tandem repeat allele profiling in 1,027 long-read genomes reveals genome-wide patterns of pathogenicity.

Matt C Danzi, Isaac R L Xu, Sarah Fazal

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Frequent Collaborators

6 joint publications

Stephan Züchner

5 joint publications

Vance P Lemmon

4 joint publications

Simone Di Giovanni

4 joint publications

John L Bixby