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Genome Medicine
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October 22, 2025
An optimized variant prioritization process for rare disease diagnostics: recommendations for Exomiser and Genomiser
Isabelle B Cooperstein, Shruti Marwaha, Alistair Ward, et al.
Medrxiv : the Preprint Server for Health Sciences
|
February 6, 2026
Phenotype-first patient matching with SimPheny identifies diagnostic candidates beyond curated gene associations
Isabelle B Cooperstein, Alistair Ward, Shilpa N Kobren, et al.
Elife
|
April 28, 2022
Neuronal apoptosis drives remodeling states of microglia and shifts in survival pathway dependence
Sarah Rose Anderson, Jacqueline M Roberts, Nathaniel Ghena, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 3) with videos related to
Sort By:
Page
of 1
Genome Medicine
|
October 22, 2025
An optimized variant prioritization process for rare disease diagnostics: recommendations for Exomiser and Genomiser
Isabelle B Cooperstein, Shruti Marwaha, Alistair Ward, et al.
Medrxiv : the Preprint Server for Health Sciences
|
February 6, 2026
Phenotype-first patient matching with SimPheny identifies diagnostic candidates beyond curated gene associations
Isabelle B Cooperstein, Alistair Ward, Shilpa N Kobren, et al.
Elife
|
April 28, 2022
Neuronal apoptosis drives remodeling states of microglia and shifts in survival pathway dependence
Sarah Rose Anderson, Jacqueline M Roberts, Nathaniel Ghena, et al.
Page
of 1