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Briefings in Bioinformatics
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December 10, 2024
BICEP: Bayesian inference for rare genomic variant causality evaluation in pedigrees
Cathal Ormond, Niamh M Ryan, Mathieu Cap, et al.
Medrxiv : the Preprint Server for Health Sciences
|
May 4, 2026
Rare protein-disrupting variants in <i>NPY5R, DLGAP1</i> and <i>MAPK8IP3</i> segregate with OCD in two multiplex pedigrees
Cathal Ormond, Mathieu Cap, Yi-Chieh Chang, et al.
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Search research articles
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Showing results (1-10 of 2) with videos related to
Sort By:
Page
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Briefings in Bioinformatics
|
December 10, 2024
BICEP: Bayesian inference for rare genomic variant causality evaluation in pedigrees
Cathal Ormond, Niamh M Ryan, Mathieu Cap, et al.
Medrxiv : the Preprint Server for Health Sciences
|
May 4, 2026
Rare protein-disrupting variants in <i>NPY5R, DLGAP1</i> and <i>MAPK8IP3</i> segregate with OCD in two multiplex pedigrees
Cathal Ormond, Mathieu Cap, Yi-Chieh Chang, et al.
Page
of 1