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Current Cardiology Reports|June 5, 2014
Exome sequencing: new insights into lipoprotein disordersSali M K Farhan, Robert A Hegele
The Canadian Journal of Cardiology|December 4, 2012
Genetics 101 for cardiologists: rare genetic variants and monogenic cardiovascular diseaseSali M K Farhan, Robert A Hegele
Neurobiology of Aging|May 5, 2022
Lack of association of TP73 with amyotrophic lateral sclerosis in a large cohort of casesAllison A Dilliott, Guy A Rouleau, Sali M K Farhan
Human Mutation|April 14, 2025
Evaluating the Utility of REVEL and CADD for Interpreting Variants in Amyotrophic Lateral Sclerosis GenesMichael R Fiorini, Allison A Dilliott, Sali M K Farhan
Molecular Neurobiology|April 5, 2024
Transcriptomics of Human Brain Tissue in Parkinson's Disease: a Comparison of Bulk and Single-cell RNA SequencingMichael R Fiorini, Allison A Dilliott, Rhalena A Thomas, et al.
Brain : a Journal of Neurology|July 3, 2023
Characterizing proteomic and transcriptomic features of missense variants in amyotrophic lateral sclerosis genesAllison A Dilliott, Seulki Kwon, Guy A Rouleau, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 29, 2017
OPTN p.Met468Arg and ATXN2 intermediate length polyQ extension in families with C9orf72 mediated amyotrophic lateral sclerosis and frontotemporal dementiaSali M K Farhan, Tania F Gendron, Leonard Petrucelli, et al.
BMC Bioinformatics|October 1, 2024
ScRNAbox: empowering single-cell RNA sequencing on high performance computing systemsRhalena A Thomas, Michael R Fiorini, Saeid Amiri, et al.
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