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James C. Slimmer

Observed names: James C. Slimmer, Slimmer, James C.
ORCID: 0009-0003-5717-4984
Observed ORCID: 0009-0003-5717-4984
OpenAlex ID: A5102043786
Rare variation in neurological disease genes and its role in multiple sclerosis mimicry and phenotype
2025 · Nicholas B. Blackburn, Bennet J. McComish, et al. · Genome Medicine · 3
Towards standards for analysing structural variants from short-read whole genome sequencing data
2026 · James C. Slimmer, Johanna L. Jones, et al. · bioRxiv (Cold Spring Harbor Laboratory)
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Rare variation in neurological disease genes and its role in multiple sclerosis mimicry and phenotype
2025 · Blackburn, Nicholas B., McComish, Bennet J., et al. · Murdoch University Research Portal
Additional file 1 of Rare variation in neurological disease genes and its role in multiple sclerosis mimicry and phenotype
2025 · Blackburn, Nicholas B., McComish, Bennet J., et al. · Figshare
Additional file 2 of Rare variation in neurological disease genes and its role in multiple sclerosis mimicry and phenotype
2025 · Blackburn, Nicholas B., McComish, Bennet J., et al. · Murdoch University Research Portal
Investigation of Genomic Mimicry and Multimorbidity in Multiple Sclerosis Using Exome Sequencing
2024 · Nicholas B. Blackburn, Bennet J. McComish, et al. · SSRN Electronic Journal
Works count: 6
Citation count: 3
H-index: 1
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